Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54331 |
| ensemblid | ENSG00000186469.9 |
| hgncid | 4404 |
| symbol | GNG2 |
| name | G protein subunit gamma 2 |
| refseq_nuc | NM_053064.5 |
| refseq_prot | NP_444292.1 |
| ensembl_nuc | ENST00000556766.6 |
| ensembl_prot | ENSP00000451231.1 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 51860612 |
| end | 51969795 |
| strand | + |
| ver | v1.2 |
| region | chr14:51860612-51969795 |
| region5000 | chr14:51855612-51974795 |
| regionname0 | GNG2_chr14_51860612_51969795 |
| regionname5000 | GNG2_chr14_51855612_51974795 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 213 | 374 | 92 | 55 | 168 | 16 | 41 | GNG2_chr14_51855612_51974795 | GNG2 | ATGGC others(208): Show |
chr14 | 51855612 | 51974795 | ||
| a0001c0002 | 0/0 | 213 | 6 | 2 | 1 | 2 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | ATGGC others(208): Show |
chr14 | 51855612 | 51974795 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3573 | 84 | 12 | 12 | 42 | 7 | 11 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3568): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0002 | 0/0 | 3572 | 57 | 12 | 8 | 35 | 0 | 2 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3567): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0003 | 0/0 | 3577 | 16 | 8 | 4 | 1 | 1 | 2 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3572): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0004 | 0/0 | 3576 | 15 | 4 | 4 | 3 | 0 | 4 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3571): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0005 | 0/0 | 3573 | 14 | 2 | 2 | 8 | 0 | 2 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3568): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0006 | 0/0 | 3574 | 12 | 0 | 3 | 4 | 0 | 5 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3569): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0007 | 1/0 | 3573 | 11 | 3 | 4 | 0 | 2 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3568): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0008 | 0/0 | 3578 | 11 | 1 | 6 | 0 | 3 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3573): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0009 | 0/0 | 3577 | 10 | 3 | 4 | 2 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3572): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0010 | 0/0 | 3577 | 9 | 0 | 0 | 9 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3572): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0011 | 0/0 | 3578 | 9 | 0 | 0 | 9 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3573): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0012 | 0/0 | 3576 | 8 | 0 | 0 | 7 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3571): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0013 | 0/0 | 3575 | 6 | 0 | 0 | 6 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3570): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0014 | 0/0 | 3576 | 6 | 4 | 0 | 0 | 1 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3571): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0015 | 0/0 | 3573 | 5 | 0 | 0 | 5 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3568): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0016 | 0/0 | 3574 | 5 | 5 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3569): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0017 | 0/0 | 3574 | 4 | 1 | 0 | 3 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3569): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0018 | 0/0 | 3575 | 4 | 4 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3570): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0019 | 0/0 | 3576 | 4 | 2 | 1 | 0 | 1 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3571): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0020 | 0/0 | 3577 | 4 | 0 | 0 | 4 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3572): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0021 | 0/0 | 3573 | 4 | 0 | 0 | 4 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3568): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0022 | 0/0 | 3571 | 3 | 0 | 0 | 3 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3566): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0023 | 0/0 | 3573 | 3 | 0 | 0 | 3 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3568): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0024 | 0/0 | 3576 | 3 | 3 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3571): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0025 | 0/0 | 3574 | 3 | 0 | 0 | 3 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3569): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0026 | 0/0 | 3576 | 3 | 0 | 0 | 1 | 0 | 2 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3571): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0027 | 0/0 | 3576 | 3 | 0 | 0 | 3 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3571): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0028 | 0/0 | 3577 | 3 | 2 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3572): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0029 | 0/0 | 3574 | 2 | 0 | 0 | 2 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3569): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0030 | 0/0 | 3573 | 2 | 0 | 2 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3568): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0031 | 0/0 | 3573 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3568): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0032 | 0/0 | 3576 | 2 | 2 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3571): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0033 | 0/0 | 3575 | 2 | 0 | 0 | 2 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3570): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0034 | 0/0 | 3576 | 2 | 2 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3571): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0035 | 0/0 | 3575 | 2 | 0 | 0 | 1 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3570): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0036 | 0/0 | 3576 | 2 | 2 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3571): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0037 | 0/0 | 3576 | 2 | 2 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3571): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0038 | 0/0 | 3578 | 2 | 2 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3573): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0039 | 0/0 | 3576 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3571): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0040 | 0/0 | 3577 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3572): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0041 | 0/0 | 3578 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3573): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0042 | 0/0 | 3572 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3567): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0043 | 0/0 | 3575 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3570): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0045 | 0/0 | 3573 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3568): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0046 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3569): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0047 | 0/0 | 3573 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3568): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0048 | 0/1 | 3574 | 1 | 0 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3569): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0049 | 0/0 | 3574 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3569): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0050 | 0/0 | 3574 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3569): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0051 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3569): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0052 | 0/0 | 3573 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3568): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0053 | 0/0 | 3573 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3568): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0054 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3569): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0055 | 0/0 | 3575 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3570): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0056 | 0/0 | 3576 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3571): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0057 | 0/0 | 3576 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3571): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0058 | 0/0 | 3576 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3571): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0059 | 0/0 | 3576 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3571): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0060 | 0/0 | 3577 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3572): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0062 | 0/0 | 3577 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3572): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0063 | 0/0 | 3577 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3572): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0064 | 0/0 | 3577 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3572): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0065 | 0/0 | 3578 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3573): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0066 | 0/0 | 3578 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3573): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0067 | 0/0 | 3577 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3572): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0068 | 0/0 | 3578 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3573): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0069 | 0/0 | 3578 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3573): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0070 | 0/0 | 3576 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3571): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0071 | 0/0 | 3578 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3573): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0075 | 0/0 | 3573 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3568): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0076 | 0/0 | 3571 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3566): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0077 | 0/0 | 3572 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3567): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0078 | 0/0 | 3573 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3568): Show |
chr14 | 51855612 | 51974795 |
| a0001c0001t0079 | 0/0 | 3573 | 1 | 0 | 0 | 0 | 1 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3568): Show |
chr14 | 51855612 | 51974795 |
| a0001c0002t0031 | 0/0 | 3573 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3568): Show |
chr14 | 51855612 | 51974795 |
| a0001c0002t0044 | 0/0 | 3572 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3567): Show |
chr14 | 51855612 | 51974795 |
| a0001c0002t0061 | 0/0 | 3576 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3571): Show |
chr14 | 51855612 | 51974795 |
| a0001c0002t0072 | 0/0 | 3573 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3568): Show |
chr14 | 51855612 | 51974795 |
| a0001c0002t0073 | 0/0 | 3572 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3567): Show |
chr14 | 51855612 | 51974795 |
| a0001c0002t0074 | 0/0 | 3572 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | AGTCC others(3567): Show |
chr14 | 51855612 | 51974795 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0002g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0003g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0003g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0003g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0003g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0004g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0004g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0004g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0005g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0005g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0005g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0005g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0005g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0006g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0006g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0006g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0006g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0006g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0006g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0006g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0006g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0006g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0006g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0006g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0007g0001 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0007g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0007g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0007g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0007g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0007g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0007g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0007g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0008g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0008g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0008g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0008g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0008g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0008g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0008g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0008g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0008g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0008g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0008g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0009g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0009g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0009g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0009g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0009g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0009g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0009g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0009g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0009g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0010g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0010g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0010g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0010g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0010g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0010g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0010g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0010g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0010g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0011g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0011g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0011g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0011g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0011g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0011g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0011g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0011g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0011g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0012g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0012g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0012g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0012g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0012g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0012g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0012g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0012g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0013g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0013g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0013g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0013g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0013g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0013g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0014g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0014g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0014g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0014g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0014g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0014g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0015g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0015g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0015g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0015g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0015g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0016g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0016g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0016g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0016g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0016g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0017g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0017g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0017g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0017g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0018g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0018g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0018g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0018g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0019g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0019g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0019g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0019g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0020g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0020g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0020g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0020g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0021g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0021g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0021g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0021g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0022g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0022g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0022g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0023g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0023g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0023g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0024g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0024g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0024g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0025g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0025g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0025g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0026g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0026g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0027g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0027g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0027g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0028g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0028g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0028g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0029g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0029g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0030g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0030g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0031g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0032g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0032g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0033g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0033g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0034g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0034g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0035g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0035g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0036g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0036g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0037g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0037g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0038g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0038g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0039g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0040g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0041g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0042g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0043g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0045g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0046g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0047g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0048g0068 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0049g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0050g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0051g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0052g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0053g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0054g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0055g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0056g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0057g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0058g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0059g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0060g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0062g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0063g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0064g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0065g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0066g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0067g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0068g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0069g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0070g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0071g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0075g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0076g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0077g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0078g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0001t0079g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0002t0031g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0002t0044g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0002t0061g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0002t0072g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0002t0073g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| a0001c0002t0074g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0183 | EUR | GBR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00280 | hp1 | a0001 | c0001 | t0007 | g0160 | EUR | FIN | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00280 | hp2 | a0001 | c0001 | t0008 | g0149 | EUR | FIN | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00323 | hp1 | a0001 | c0001 | t0079 | g0142 | EUR | FIN | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0241 | EUR | FIN | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00438 | hp1 | a0001 | c0001 | t0031 | g0112 | EAS | CHS | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | CHS | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | CHS | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | CHS | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | CHS | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | CHS | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | CHS | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00621 | hp2 | a0001 | c0001 | t0009 | g0268 | EAS | CHS | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0120 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00639 | hp2 | a0001 | c0001 | t0008 | g0195 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0177 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00735 | hp2 | a0001 | c0001 | t0007 | g0194 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00738 | hp1 | a0001 | c0001 | t0056 | g0014 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG00741 | hp2 | a0001 | c0001 | t0008 | g0170 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0308 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01074 | hp1 | a0001 | c0001 | t0019 | g0074 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01074 | hp2 | a0001 | c0001 | t0009 | g0310 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01081 | hp1 | a0001 | c0001 | t0059 | g0158 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0321 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01099 | hp1 | a0001 | c0001 | t0008 | g0141 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01099 | hp2 | a0001 | c0001 | t0009 | g0353 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01106 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01106 | hp2 | a0001 | c0001 | t0008 | g0320 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01109 | hp1 | a0001 | c0001 | t0064 | g0031 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01109 | hp2 | a0001 | c0001 | t0030 | g0130 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01175 | hp1 | a0001 | c0001 | t0008 | g0167 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01175 | hp2 | a0001 | c0001 | t0030 | g0072 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0203 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01255 | hp1 | a0001 | c0001 | t0006 | g0131 | AMR | CLM | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0017 | AMR | CLM | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01258 | hp2 | a0001 | c0001 | t0007 | g0255 | AMR | CLM | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01261 | hp1 | a0001 | c0001 | t0006 | g0343 | AMR | CLM | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0359 | AMR | CLM | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01358 | hp2 | a0001 | c0001 | t0055 | g0210 | AMR | CLM | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01361 | hp2 | a0001 | c0001 | t0007 | g0325 | AMR | CLM | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01433 | hp1 | a0001 | c0002 | t0072 | g0196 | AMR | CLM | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01433 | hp2 | a0001 | c0001 | t0008 | g0356 | AMR | CLM | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | CLM | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0197 | AMR | CLM | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01515 | hp1 | a0001 | c0001 | t0007 | g0023 | EUR | IBS | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01515 | hp2 | a0001 | c0001 | t0008 | g0016 | EUR | IBS | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0358 | EUR | IBS | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | IBS | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0015 | EUR | IBS | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | IBS | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01891 | hp1 | a0001 | c0001 | t0042 | g0282 | AFR | ACB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01891 | hp2 | a0001 | c0001 | t0009 | g0042 | AFR | ACB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0261 | AMR | PEL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0156 | AMR | PEL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0143 | AMR | PEL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01978 | hp2 | a0001 | c0001 | t0028 | g0024 | AMR | PEL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0260 | AMR | PEL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0355 | AMR | PEL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PEL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0339 | AMR | PEL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | KHV | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02027 | hp2 | a0001 | c0001 | t0011 | g0316 | EAS | KHV | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02040 | hp2 | a0001 | c0001 | t0010 | g0266 | EAS | KHV | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0375 | AFR | ACB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02056 | hp1 | a0001 | c0001 | t0035 | g0284 | EAS | KHV | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02056 | hp2 | a0001 | c0001 | t0029 | g0306 | EAS | KHV | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02074 | hp1 | a0001 | c0001 | t0020 | g0092 | EAS | KHV | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02074 | hp2 | a0001 | c0001 | t0011 | g0317 | EAS | KHV | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | KHV | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | KHV | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02132 | hp2 | a0001 | c0001 | t0010 | g0244 | EAS | KHV | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02135 | hp1 | a0001 | c0001 | t0078 | g0077 | EAS | KHV | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ACB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02155 | hp1 | a0001 | c0001 | t0006 | g0350 | EAS | CDX | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02155 | hp2 | a0001 | c0001 | t0011 | g0164 | EAS | CDX | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | CDX | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | CDX | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02257 | hp1 | a0001 | c0001 | t0028 | g0019 | AFR | ACB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0157 | AFR | ACB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02258 | hp2 | a0001 | c0001 | t0016 | g0035 | AFR | ACB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0330 | AMR | PEL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02273 | hp2 | a0001 | c0001 | t0009 | g0340 | AMR | PEL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0006 | AFR | ACB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | ACB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0331 | AMR | PEL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02293 | hp2 | a0001 | c0001 | t0005 | g0332 | AMR | PEL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02451 | hp2 | a0001 | c0001 | t0014 | g0345 | AFR | ACB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02602 | hp1 | a0001 | c0001 | t0049 | g0205 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02602 | hp2 | a0001 | c0002 | t0031 | g0030 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02615 | hp1 | a0001 | c0001 | t0037 | g0180 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0327 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0347 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02622 | hp2 | a0001 | c0001 | t0016 | g0352 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02630 | hp2 | a0001 | c0001 | t0075 | g0004 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02647 | hp1 | a0001 | c0001 | t0066 | g0032 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02683 | hp2 | a0001 | c0001 | t0008 | g0144 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0176 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0370 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0043 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02723 | hp2 | a0001 | c0001 | t0069 | g0209 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02738 | hp1 | a0001 | c0001 | t0006 | g0159 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0254 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02809 | hp1 | a0001 | c0001 | t0018 | g0323 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02809 | hp2 | a0001 | c0001 | t0028 | g0022 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02886 | hp1 | a0001 | c0001 | t0024 | g0059 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0374 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02895 | hp1 | a0001 | c0001 | t0036 | g0371 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0044 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0326 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02896 | hp2 | a0001 | c0001 | t0024 | g0063 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0046 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02897 | hp2 | a0001 | c0001 | t0024 | g0058 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | ESN | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02922 | hp2 | a0001 | c0001 | t0043 | g0336 | AFR | ESN | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02965 | hp1 | a0001 | c0001 | t0040 | g0335 | AFR | ESN | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02965 | hp2 | a0001 | c0001 | t0014 | g0344 | AFR | ESN | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02970 | hp1 | a0001 | c0001 | t0046 | g0311 | AFR | ESN | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | ESN | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02976 | hp1 | a0001 | c0001 | t0016 | g0045 | AFR | ESN | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02976 | hp2 | a0001 | c0001 | t0051 | g0342 | AFR | ESN | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03017 | hp1 | a0001 | c0001 | t0065 | g0026 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03041 | hp1 | a0001 | c0001 | t0019 | g0373 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0033 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | MSL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | ESN | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03139 | hp1 | a0001 | c0002 | t0074 | g0040 | AFR | ESN | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0041 | AFR | ESN | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0369 | AFR | ESN | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03195 | hp2 | a0001 | c0001 | t0018 | g0368 | AFR | ESN | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03209 | hp1 | a0001 | c0001 | t0054 | g0202 | AFR | MSL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0372 | AFR | MSL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03225 | hp1 | a0001 | c0001 | t0034 | g0377 | AFR | MSL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03225 | hp2 | a0001 | c0001 | t0036 | g0053 | AFR | MSL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03239 | hp1 | a0001 | c0001 | t0012 | g0337 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0173 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0055 | AFR | MSL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03453 | hp2 | a0001 | c0001 | t0018 | g0324 | AFR | MSL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0376 | AFR | MSL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03486 | hp2 | a0001 | c0001 | t0047 | g0298 | AFR | MSL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03490 | hp1 | a0001 | c0001 | t0057 | g0128 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03491 | hp1 | a0001 | c0001 | t0014 | g0020 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03491 | hp2 | a0001 | c0001 | t0026 | g0002 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03492 | hp1 | a0001 | c0001 | t0062 | g0127 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03492 | hp2 | a0001 | c0001 | t0026 | g0002 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03516 | hp2 | a0001 | c0001 | t0038 | g0297 | AFR | ESN | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03540 | hp2 | a0001 | c0001 | t0032 | g0036 | AFR | GWD | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0281 | AFR | MSL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03579 | hp2 | a0001 | c0001 | t0014 | g0018 | AFR | MSL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03654 | hp1 | a0001 | c0001 | t0006 | g0354 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0027 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03669 | hp2 | a0001 | c0001 | t0007 | g0050 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | STU | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0145 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0357 | SAS | BEB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0338 | SAS | BEB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03942 | hp2 | a0001 | c0001 | t0071 | g0118 | SAS | BEB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG04184 | hp1 | a0001 | c0001 | t0006 | g0272 | SAS | BEB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0146 | SAS | BEB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG04199 | hp1 | a0001 | c0001 | t0009 | g0070 | SAS | STU | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG04199 | hp2 | a0001 | c0001 | t0052 | g0095 | SAS | STU | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG04204 | hp1 | a0001 | c0001 | t0006 | g0122 | SAS | STU | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG04204 | hp2 | a0001 | c0001 | t0006 | g0073 | SAS | STU | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG04228 | hp1 | a0001 | c0001 | t0035 | g0378 | SAS | STU | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0117 | SAS | STU | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | YRI | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18522 | hp2 | a0001 | c0001 | t0045 | g0290 | AFR | YRI | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0307 | EAS | CHB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18747 | hp2 | a0001 | c0001 | t0021 | g0208 | EAS | CHB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18906 | hp1 | a0001 | c0001 | t0016 | g0007 | AFR | YRI | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | YRI | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18939 | hp2 | a0001 | c0001 | t0012 | g0155 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18942 | hp1 | a0001 | c0001 | t0012 | g0148 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18945 | hp1 | a0001 | c0001 | t0023 | g0108 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18946 | hp1 | a0001 | c0001 | t0015 | g0302 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18947 | hp1 | a0001 | c0001 | t0011 | g0090 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18947 | hp2 | a0001 | c0001 | t0011 | g0125 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18950 | hp2 | a0001 | c0001 | t0012 | g0163 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18951 | hp2 | a0001 | c0001 | t0005 | g0225 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18952 | hp2 | a0001 | c0001 | t0011 | g0314 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18953 | hp1 | a0001 | c0001 | t0027 | g0103 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18954 | hp1 | a0001 | c0001 | t0010 | g0100 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18954 | hp2 | a0001 | c0001 | t0017 | g0082 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18959 | hp1 | a0001 | c0001 | t0010 | g0186 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0199 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18960 | hp2 | a0001 | c0001 | t0022 | g0094 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18961 | hp2 | a0001 | c0001 | t0006 | g0226 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18962 | hp1 | a0001 | c0001 | t0039 | g0313 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18963 | hp1 | a0001 | c0001 | t0013 | g0228 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18963 | hp2 | a0001 | c0001 | t0021 | g0362 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18964 | hp1 | a0001 | c0001 | t0005 | g0080 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18964 | hp2 | a0001 | c0001 | t0070 | g0201 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18965 | hp1 | a0001 | c0001 | t0023 | g0048 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0300 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18966 | hp2 | a0001 | c0001 | t0013 | g0227 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18967 | hp2 | a0001 | c0001 | t0033 | g0363 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18968 | hp1 | a0001 | c0001 | t0010 | g0078 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18969 | hp1 | a0001 | c0001 | t0021 | g0087 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18971 | hp1 | a0001 | c0001 | t0011 | g0235 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18972 | hp1 | a0001 | c0002 | t0044 | g0133 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18975 | hp1 | a0001 | c0001 | t0029 | g0114 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0253 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18978 | hp1 | a0001 | c0001 | t0009 | g0116 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18978 | hp2 | a0001 | c0001 | t0011 | g0192 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18980 | hp2 | a0001 | c0001 | t0025 | g0213 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18981 | hp2 | a0001 | c0001 | t0077 | g0134 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18982 | hp2 | a0001 | c0001 | t0010 | g0333 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18984 | hp2 | a0001 | c0001 | t0017 | g0086 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18985 | hp1 | a0001 | c0001 | t0013 | g0230 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18985 | hp2 | a0001 | c0001 | t0005 | g0185 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18989 | hp1 | a0001 | c0001 | t0005 | g0110 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18989 | hp2 | a0001 | c0002 | t0061 | g0365 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18990 | hp1 | a0001 | c0001 | t0027 | g0104 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18991 | hp1 | a0001 | c0001 | t0020 | g0204 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18993 | hp1 | a0001 | c0001 | t0020 | g0277 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18993 | hp2 | a0001 | c0001 | t0010 | g0083 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18995 | hp1 | a0001 | c0001 | t0012 | g0246 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18995 | hp2 | a0001 | c0001 | t0013 | g0091 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18999 | hp1 | a0001 | c0001 | t0022 | g0274 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19000 | hp1 | a0001 | c0001 | t0053 | g0081 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19000 | hp2 | a0001 | c0001 | t0006 | g0166 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19001 | hp2 | a0001 | c0001 | t0013 | g0224 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19002 | hp1 | a0001 | c0001 | t0015 | g0136 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19005 | hp2 | a0001 | c0001 | t0020 | g0154 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19007 | hp1 | a0001 | c0001 | t0025 | g0273 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19007 | hp2 | a0001 | c0001 | t0010 | g0102 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19010 | hp2 | a0001 | c0001 | t0012 | g0278 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19011 | hp1 | a0001 | c0001 | t0013 | g0361 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19011 | hp2 | a0001 | c0001 | t0015 | g0132 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19030 | hp1 | a0001 | c0001 | t0067 | g0065 | AFR | LWK | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19030 | hp2 | a0001 | c0001 | t0018 | g0367 | AFR | LWK | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19043 | hp1 | a0001 | c0001 | t0032 | g0349 | AFR | LWK | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19043 | hp2 | a0001 | c0001 | t0063 | g0005 | AFR | LWK | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19054 | hp2 | a0001 | c0001 | t0017 | g0085 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19056 | hp1 | a0001 | c0001 | t0021 | g0264 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19057 | hp1 | a0001 | c0001 | t0025 | g0097 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19057 | hp2 | a0001 | c0001 | t0005 | g0129 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19058 | hp1 | a0001 | c0001 | t0006 | g0234 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19062 | hp1 | a0001 | c0001 | t0076 | g0220 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19062 | hp2 | a0001 | c0001 | t0005 | g0275 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19065 | hp1 | a0001 | c0001 | t0012 | g0229 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19066 | hp1 | a0001 | c0001 | t0011 | g0190 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19070 | hp1 | a0001 | c0001 | t0010 | g0137 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19079 | hp1 | a0001 | c0001 | t0026 | g0188 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0366 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19081 | hp2 | a0001 | c0001 | t0027 | g0179 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19082 | hp1 | a0001 | c0001 | t0012 | g0189 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19082 | hp2 | a0001 | c0001 | t0033 | g0315 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19085 | hp1 | a0001 | c0001 | t0022 | g0121 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19085 | hp2 | a0001 | c0001 | t0015 | g0138 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19086 | hp2 | a0001 | c0001 | t0023 | g0269 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19240 | hp1 | a0001 | c0001 | t0041 | g0334 | AFR | YRI | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | YRI | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA20129 | hp1 | a0001 | c0001 | t0008 | g0360 | AFR | ASW | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA20129 | hp2 | a0001 | c0001 | t0019 | g0051 | AFR | ASW | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA20752 | hp1 | a0001 | c0001 | t0019 | g0039 | EUR | TSI | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | TSI | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA20805 | hp1 | a0001 | c0001 | t0014 | g0088 | EUR | TSI | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA20805 | hp2 | a0001 | c0001 | t0008 | g0169 | EUR | TSI | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | GIH | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA20905 | hp2 | a0001 | c0001 | t0058 | g0341 | SAS | GIH | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02109 | hp1 | a0001 | c0001 | t0038 | g0346 | AFR | ACB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02109 | hp2 | a0001 | c0001 | t0060 | g0147 | AFR | ACB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02486 | hp1 | a0001 | c0002 | t0073 | g0010 | AFR | ACB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0348 | AFR | ACB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02559 | hp1 | a0001 | c0001 | t0014 | g0309 | AFR | ACB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0329 | AFR | ACB | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | MSL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG03471 | hp2 | a0001 | c0001 | t0016 | g0351 | AFR | MSL | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | USA | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| HG06807 | hp2 | a0001 | c0001 | t0068 | g0322 | AFR | USA | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18955 | hp1 | a0001 | c0001 | t0050 | g0123 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA18955 | hp2 | a0001 | c0001 | t0015 | g0139 | EAS | JPT | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | USA | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA20300 | hp2 | a0001 | c0001 | t0037 | g0028 | AFR | USA | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA21309 | hp1 | a0001 | c0001 | t0034 | g0364 | AFR | LWK | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| NA21309 | hp2 | a0001 | c0001 | t0017 | g0047 | AFR | LWK | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0048 | g0068 | REF | REF | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0001 | REF | REF | GNG2_chr14_51855612_51974795 | GNG2 | chr14 | 51855612 | 51974795 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:51860789 | A | G | 1 | a0001 | 1 | HG00323.hp1 | splice_region_variant | LOW | c.-72A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/4 | chr14 | 51860789 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:51966621 | C | T | 1 | a0001c0002 | 6 | HG01433.hp1 HG02486.hp1 HG02602.hp2 others(3): Show |
synonymous_variant | LOW | c.150C>T | p.Leu50Leu | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 399/3573 | 150/216 | 50/71 | chr14 | 51966621 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:51860713 | T | C | 1 | a0001c0001t0039 | 1 | NA18962.hp1 | 5_prime_UTR_variant | MODIFIER | c.-148T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/4 | 89966 | chr14 | 51860713 | ||||||
| chr14:51966702 | C | T | 4 | a0001c0001t0021 a0001c0001t0076 a0001c0001t0077 others(1): Show |
7 | HG02135.hp1 NA18747.hp2 NA18963.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*15C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 15 | chr14 | 51966702 | ||||||
| chr14:51966783 | G | A | 2 | a0001c0001t0040 a0001c0001t0041 |
2 | HG02965.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*96G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 96 | chr14 | 51966783 | ||||||
| chr14:51966832 | A | G | 1 | a0001c0001t0075 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*145A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 145 | chr14 | 51966832 | ||||||
| chr14:51966962 | G | GC | 13 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0017 others(10): Show |
88 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*285dupC | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 286 | INFO_REALIGN_3_PRIME | chr14 | 51966962 | |||||
| chr14:51966962 | G | GCC | 11 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0016 others(8): Show |
37 | HG01358.hp2 HG02135.hp1 HG02258.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*284_*285dupCC | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 286 | INFO_REALIGN_3_PRIME | chr14 | 51966962 | |||||
| chr14:51966962 | G | GCCC | 13 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0014 others(10): Show |
47 | HG00738.hp1 HG01074.hp1 HG01081.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*283_*285dupCCC | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 286 | INFO_REALIGN_3_PRIME | chr14 | 51966962 | |||||
| chr14:51966962 | G | GCCCC | 13 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0010 others(10): Show |
52 | HG00621.hp2 HG00639.hp1 HG01074.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*282_*285dupCCCC | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 286 | INFO_REALIGN_3_PRIME | chr14 | 51966962 | |||||
| chr14:51966962 | G | GCCCCC | 11 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0037 others(8): Show |
31 | HG00280.hp2 HG00639.hp2 HG00741.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*281_*285dupCCCCC | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 286 | INFO_REALIGN_3_PRIME | chr14 | 51966962 | |||||
| chr14:51966964 | C | T | 3 | a0001c0002t0072 a0001c0002t0073 a0001c0002t0074 |
3 | HG01433.hp1 HG02486.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*277C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 277 | chr14 | 51966964 | ||||||
| chr14:51967002 | G | A | 1 | a0001c0001t0051 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*315G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 315 | chr14 | 51967002 | ||||||
| chr14:51967337 | G | T | 31 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(28): Show |
207 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*650G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 650 | chr14 | 51967337 | ||||||
| chr14:51967646 | A | C | 2 | a0001c0001t0049 a0001c0001t0058 |
2 | HG02602.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*959A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 959 | chr14 | 51967646 | ||||||
| chr14:51967711 | A | G | 2 | a0001c0001t0024 a0001c0001t0032 |
5 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1024A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 1024 | chr14 | 51967711 | ||||||
| chr14:51967816 | AT | A | 32 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0016 others(29): Show |
114 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*1136delT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 1136 | INFO_REALIGN_3_PRIME | chr14 | 51967816 | |||||
| chr14:51967869 | G | C | 11 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0022 others(8): Show |
84 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*1182G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 1182 | chr14 | 51967869 | ||||||
| chr14:51967920 | C | T | 6 | a0001c0001t0031 a0001c0002t0031 a0001c0002t0044 others(3): Show |
6 | HG00438.hp1 HG02486.hp1 HG02602.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1233C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 1233 | chr14 | 51967920 | ||||||
| chr14:51967966 | C | T | 2 | a0001c0001t0036 a0001c0001t0067 |
3 | HG02895.hp1 HG03225.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1279C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 1279 | chr14 | 51967966 | ||||||
| chr14:51967967 | G | A | 1 | a0001c0001t0064 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1280G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 1280 | chr14 | 51967967 | ||||||
| chr14:51967984 | C | T | 1 | a0001c0002t0074 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1297C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 1297 | chr14 | 51967984 | ||||||
| chr14:51968014 | C | G | 1 | a0001c0001t0047 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1327C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 1327 | chr14 | 51968014 | ||||||
| chr14:51968053 | A | C | 1 | a0001c0001t0030 | 2 | HG01109.hp2 HG01175.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1366A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 1366 | chr14 | 51968053 | ||||||
| chr14:51968107 | C | T | 1 | a0001c0001t0016 | 5 | HG02258.hp2 HG02622.hp2 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1420C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 1420 | chr14 | 51968107 | ||||||
| chr14:51968165 | G | A | 11 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0012 others(8): Show |
44 | HG02027.hp2 HG02040.hp2 HG02074.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1478G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 1478 | chr14 | 51968165 | ||||||
| chr14:51968239 | G | T | 2 | a0001c0001t0063 a0001c0001t0069 |
2 | HG02723.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1552G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 1552 | chr14 | 51968239 | ||||||
| chr14:51968308 | A | G | 1 | a0001c0001t0016 | 5 | HG02258.hp2 HG02622.hp2 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1621A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 1621 | chr14 | 51968308 | ||||||
| chr14:51968328 | G | C | 46 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(43): Show |
158 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*1641G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 1641 | chr14 | 51968328 | ||||||
| chr14:51968341 | C | G | 11 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0022 others(8): Show |
84 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*1654C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 1654 | chr14 | 51968341 | ||||||
| chr14:51968357 | G | GT | 10 | a0001c0001t0029 a0001c0001t0034 a0001c0001t0036 others(7): Show |
13 | HG00738.hp1 HG01433.hp1 HG02056.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1680dupT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 1681 | INFO_REALIGN_3_PRIME | chr14 | 51968357 | |||||
| chr14:51968357 | G | GTTT | 3 | a0001c0001t0024 a0001c0001t0032 a0001c0001t0043 |
6 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1678_*1680dupTTT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 1681 | INFO_REALIGN_3_PRIME | chr14 | 51968357 | |||||
| chr14:51968367 | TA | T | 11 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0022 others(8): Show |
84 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*1689delA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 1689 | INFO_REALIGN_3_PRIME | chr14 | 51968367 | |||||
| chr14:51968368 | A | T | 65 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(62): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*1681A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 1681 | chr14 | 51968368 | ||||||
| chr14:51968369 | A | T | 3 | a0001c0001t0056 a0001c0001t0066 a0001c0001t0068 |
3 | HG00738.hp1 HG02647.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1682A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 1682 | chr14 | 51968369 | ||||||
| chr14:51968620 | C | T | 1 | a0001c0001t0016 | 5 | HG02258.hp2 HG02622.hp2 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1933C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 1933 | chr14 | 51968620 | ||||||
| chr14:51968730 | T | C | 1 | a0001c0001t0052 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2043T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 2043 | chr14 | 51968730 | ||||||
| chr14:51968777 | G | C | 32 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0016 others(29): Show |
114 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*2090G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 2090 | chr14 | 51968777 | ||||||
| chr14:51968851 | G | A | 1 | a0001c0001t0024 | 3 | HG02886.hp1 HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2164G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 2164 | chr14 | 51968851 | ||||||
| chr14:51968865 | C | A | 1 | a0001c0001t0053 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2178C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 2178 | chr14 | 51968865 | ||||||
| chr14:51969027 | C | A | 1 | a0001c0002t0074 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2340C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 2340 | chr14 | 51969027 | ||||||
| chr14:51969207 | C | T | 3 | a0001c0001t0014 a0001c0001t0028 a0001c0001t0060 |
10 | HG01978.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2520C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 2520 | chr14 | 51969207 | ||||||
| chr14:51969213 | A | T | 34 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0016 others(31): Show |
116 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*2526A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 2526 | chr14 | 51969213 | ||||||
| chr14:51969287 | A | C | 5 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0023 others(2): Show |
25 | HG02027.hp2 HG02040.hp2 HG02074.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2600A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 2600 | chr14 | 51969287 | ||||||
| chr14:51969336 | AT | A | 2 | a0001c0001t0036 a0001c0001t0067 |
3 | HG02895.hp1 HG03225.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2654delT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 2654 | INFO_REALIGN_3_PRIME | chr14 | 51969336 | |||||
| chr14:51969392 | C | A | 33 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0022 others(30): Show |
111 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*2705C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 2705 | chr14 | 51969392 | ||||||
| chr14:51969405 | A | G | 1 | a0001c0001t0015 | 5 | NA18946.hp1 NA18955.hp2 NA19002.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2718A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 2718 | chr14 | 51969405 | ||||||
| chr14:51969494 | C | T | 1 | a0001c0002t0072 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2807C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 2807 | chr14 | 51969494 | ||||||
| chr14:51969684 | T | C | 1 | a0001c0001t0059 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2997T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 4/4 | 2997 | chr14 | 51969684 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:51860931 | C | A | 2 | a0001c0001t0002g0003 a0001c0001t0075g0004 |
2 | HG01358.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-71+141C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51860931 | |||||||
| chr14:51860941 | A | G | 342 | a0001c0001t0001g0052 a0001c0001t0001g0057 a0001c0001t0001g0075 others(339): Show |
343 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.-71+151A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51860941 | |||||||
| chr14:51861073 | C | G | 1 | a0001c0001t0035g0378 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-71+283C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51861073 | |||||||
| chr14:51861253 | T | C | 1 | a0001c0001t0019g0039 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-71+463T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51861253 | |||||||
| chr14:51861359 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-71+569A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51861359 | |||||||
| chr14:51861401 | T | C | 7 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0007g0044 others(4): Show |
7 | HG01891.hp2 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-71+611T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51861401 | |||||||
| chr14:51861575 | G | A | 152 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0052 others(149): Show |
153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.-71+785G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51861575 | |||||||
| chr14:51861594 | T | C | 3 | a0001c0001t0009g0006 a0001c0001t0016g0007 a0001c0001t0063g0005 |
3 | HG02280.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-71+804T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51861594 | |||||||
| chr14:51861594 | T | G | 164 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0052 others(161): Show |
165 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.-71+804T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51861594 | |||||||
| chr14:51861784 | G | A | 350 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0052 others(347): Show |
351 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(348): Show |
intron_variant | MODIFIER | c.-71+994G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51861784 | |||||||
| chr14:51861808 | C | T | 123 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0098 others(120): Show |
124 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.-71+1018C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51861808 | |||||||
| chr14:51861831 | T | A | 1 | a0001c0001t0004g0197 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-71+1041T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51861831 | |||||||
| chr14:51861834 | T | A | 1 | a0001c0001t0002g0067 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-71+1044T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51861834 | |||||||
| chr14:51861931 | AAG | A | 5 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0009g0006 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-71+1145_-71+1146d others(4): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51861931 | ||||||
| chr14:51861958 | A | C | 151 | a0001c0001t0001g0052 a0001c0001t0001g0057 a0001c0001t0001g0075 others(148): Show |
152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.-71+1168A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51861958 | |||||||
| chr14:51861966 | A | T | 8 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0002g0008 others(5): Show |
8 | HG02257.hp2 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-71+1176A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51861966 | |||||||
| chr14:51861967 | A | T | 5 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0009g0006 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-71+1177A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51861967 | |||||||
| chr14:51862127 | C | T | 1 | a0001c0001t0012g0189 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-71+1337C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51862127 | |||||||
| chr14:51862344 | C | T | 2 | a0001c0001t0004g0187 a0001c0001t0026g0188 |
2 | NA18965.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-71+1554C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51862344 | |||||||
| chr14:51862383 | T | C | 350 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0052 others(347): Show |
351 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(348): Show |
intron_variant | MODIFIER | c.-71+1593T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51862383 | |||||||
| chr14:51862542 | T | C | 7 | a0001c0001t0001g0193 a0001c0001t0002g0191 a0001c0001t0007g0194 others(4): Show |
7 | HG00639.hp2 HG00735.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71+1752T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51862542 | |||||||
| chr14:51862609 | C | G | 1 | a0001c0002t0072g0196 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-71+1819C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51862609 | |||||||
| chr14:51862678 | G | A | 1 | a0001c0002t0074g0040 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-71+1888G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51862678 | |||||||
| chr14:51862829 | A | G | 6 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0009g0006 others(3): Show |
6 | HG02257.hp2 HG02280.hp1 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71+2039A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51862829 | |||||||
| chr14:51862908 | T | C | 3 | a0001c0001t0002g0200 a0001c0001t0004g0198 a0001c0001t0004g0199 |
3 | NA18944.hp1 NA18959.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-71+2118T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51862908 | |||||||
| chr14:51862984 | C | CT | 166 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0212 others(163): Show |
166 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(163): Show |
intron_variant | MODIFIER | c.-71+2209dupT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51862984 | ||||||
| chr14:51862984 | C | CTT | 161 | a0001c0001t0001g0052 a0001c0001t0001g0057 a0001c0001t0001g0075 others(158): Show |
162 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.-71+2208_-71+2209d others(4): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51862984 | ||||||
| chr14:51862984 | C | CTTT | 13 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0182 others(10): Show |
13 | HG00140.hp1 HG01358.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-71+2207_-71+2209d others(5): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51862984 | ||||||
| chr14:51863147 | A | G | 1 | a0001c0001t0027g0179 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-71+2357A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51863147 | |||||||
| chr14:51863490 | C | T | 3 | a0001c0001t0001g0178 a0001c0001t0003g0176 a0001c0001t0006g0177 |
3 | HG00642.hp1 HG01243.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-71+2700C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51863490 | |||||||
| chr14:51863588 | C | T | 2 | a0001c0001t0013g0361 a0001c0001t0021g0362 |
2 | NA18963.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-71+2798C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51863588 | |||||||
| chr14:51864115 | A | C | 248 | a0001c0001t0001g0052 a0001c0001t0001g0057 a0001c0001t0001g0075 others(245): Show |
249 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.-71+3325A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51864115 | |||||||
| chr14:51864198 | A | G | 8 | a0001c0001t0001g0355 a0001c0001t0001g0357 a0001c0001t0001g0358 others(5): Show |
8 | HG01261.hp2 HG01433.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.-71+3408A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51864198 | |||||||
| chr14:51864225 | T | C | 7 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0007g0044 others(4): Show |
7 | HG01891.hp2 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-71+3435T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51864225 | |||||||
| chr14:51864262 | C | T | 103 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0038 others(100): Show |
103 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.-71+3472C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51864262 | |||||||
| chr14:51864300 | A | G | 2 | a0001c0001t0002g0003 a0001c0001t0075g0004 |
2 | HG01358.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-71+3510A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51864300 | |||||||
| chr14:51864380 | T | C | 2 | a0001c0001t0017g0047 a0001c0002t0073g0010 |
2 | HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-71+3590T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51864380 | |||||||
| chr14:51864469 | C | T | 5 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0009g0006 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-71+3679C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51864469 | |||||||
| chr14:51864506 | C | T | 149 | a0001c0001t0001g0052 a0001c0001t0001g0057 a0001c0001t0001g0075 others(146): Show |
150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-71+3716C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51864506 | |||||||
| chr14:51864673 | G | A | 1 | a0001c0001t0033g0363 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-71+3883G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51864673 | |||||||
| chr14:51864678 | C | T | 1 | a0001c0001t0033g0363 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-71+3888C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51864678 | |||||||
| chr14:51864680 | C | G | 1 | a0001c0001t0033g0363 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-71+3890C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51864680 | |||||||
| chr14:51864681 | T | A | 1 | a0001c0001t0033g0363 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-71+3891T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51864681 | |||||||
| chr14:51864682 | A | T | 1 | a0001c0001t0033g0363 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-71+3892A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51864682 | |||||||
| chr14:51864685 | G | C | 1 | a0001c0001t0033g0363 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-71+3895G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51864685 | |||||||
| chr14:51864686 | A | G | 1 | a0001c0001t0033g0363 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-71+3896A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51864686 | |||||||
| chr14:51864687 | G | T | 1 | a0001c0001t0033g0363 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-71+3897G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51864687 | |||||||
| chr14:51864689 | C | T | 1 | a0001c0001t0033g0363 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-71+3899C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51864689 | |||||||
| chr14:51864690 | A | T | 1 | a0001c0001t0033g0363 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-71+3900A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51864690 | |||||||
| chr14:51864816 | G | A | 86 | a0001c0001t0001g0037 a0001c0001t0001g0206 a0001c0001t0001g0207 others(83): Show |
86 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.-71+4026G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51864816 | |||||||
| chr14:51865274 | T | A | 2 | a0001c0001t0002g0280 a0001c0001t0002g0366 |
2 | NA19074.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-71+4484T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51865274 | |||||||
| chr14:51865307 | C | T | 356 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0037 others(353): Show |
357 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.-71+4517C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51865307 | |||||||
| chr14:51865406 | A | C | 87 | a0001c0001t0001g0283 a0001c0001t0001g0289 a0001c0001t0001g0291 others(84): Show |
87 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-71+4616A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51865406 | |||||||
| chr14:51865684 | ATTGT | A | 7 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0007g0044 others(4): Show |
7 | HG01891.hp2 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-71+4899_-71+4902d others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51865684 | ||||||
| chr14:51865697 | C | G | 6 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0007g0044 others(3): Show |
6 | HG01891.hp2 HG02717.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-71+4907C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51865697 | |||||||
| chr14:51865790 | G | A | 352 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0038 others(349): Show |
353 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.-71+5000G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51865790 | |||||||
| chr14:51865906 | G | A | 1 | a0001c0001t0005g0013 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-71+5116G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51865906 | |||||||
| chr14:51865949 | GA | G | 15 | a0001c0001t0001g0369 a0001c0001t0002g0008 a0001c0001t0002g0009 others(12): Show |
15 | HG02055.hp1 HG02257.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-71+5171delA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51865949 | ||||||
| chr14:51865949 | GAA | G | 333 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0038 others(330): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.-71+5170_-71+5171d others(4): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51865949 | ||||||
| chr14:51865967 | C | T | 139 | a0001c0001t0001g0052 a0001c0001t0001g0057 a0001c0001t0001g0075 others(136): Show |
140 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-71+5177C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51865967 | |||||||
| chr14:51866171 | G | A | 7 | a0001c0001t0001g0193 a0001c0001t0002g0191 a0001c0001t0007g0194 others(4): Show |
7 | HG00639.hp2 HG00735.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71+5381G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51866171 | |||||||
| chr14:51866192 | C | A | 1 | a0001c0001t0002g0003 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-71+5402C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51866192 | |||||||
| chr14:51866274 | C | G | 94 | a0001c0001t0001g0193 a0001c0001t0001g0206 a0001c0001t0001g0207 others(91): Show |
94 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.-71+5484C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51866274 | |||||||
| chr14:51866400 | G | A | 349 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0038 others(346): Show |
350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.-71+5610G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51866400 | |||||||
| chr14:51866403 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-71+5613C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51866403 | |||||||
| chr14:51866426 | G | A | 7 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0007g0044 others(4): Show |
7 | HG01891.hp2 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-71+5636G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51866426 | |||||||
| chr14:51866493 | C | T | 333 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0038 others(330): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.-71+5703C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51866493 | |||||||
| chr14:51866732 | A | G | 2 | a0001c0001t0016g0035 a0001c0001t0032g0036 |
2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-71+5942A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51866732 | |||||||
| chr14:51866844 | G | C | 344 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0038 others(341): Show |
345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.-71+6054G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51866844 | |||||||
| chr14:51866851 | G | A | 343 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0038 others(340): Show |
344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.-71+6061G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51866851 | |||||||
| chr14:51866890 | A | T | 8 | a0001c0001t0001g0369 a0001c0001t0002g0376 a0001c0001t0003g0372 others(5): Show |
8 | HG02055.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-71+6100A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51866890 | |||||||
| chr14:51867007 | T | C | 7 | a0001c0001t0001g0369 a0001c0001t0004g0041 a0001c0001t0004g0043 others(4): Show |
7 | HG01891.hp2 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-71+6217T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51867007 | |||||||
| chr14:51867027 | G | C | 1 | a0001c0001t0020g0204 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-71+6237G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51867027 | |||||||
| chr14:51867095 | A | T | 1 | a0001c0001t0001g0369 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-71+6305A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51867095 | |||||||
| chr14:51867107 | T | C | 2 | a0001c0001t0002g0003 a0001c0001t0018g0368 |
2 | HG01358.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-71+6317T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51867107 | |||||||
| chr14:51867257 | G | T | 1 | a0001c0001t0016g0352 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-71+6467G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51867257 | |||||||
| chr14:51867357 | A | T | 1 | a0001c0001t0002g0003 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-71+6567A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51867357 | |||||||
| chr14:51867371 | A | G | 224 | a0001c0001t0001g0012 a0001c0001t0001g0052 a0001c0001t0001g0057 others(221): Show |
225 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.-71+6581A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51867371 | |||||||
| chr14:51867446 | T | C | 68 | a0001c0001t0001g0052 a0001c0001t0001g0098 a0001c0001t0001g0099 others(65): Show |
69 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.-71+6656T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51867446 | |||||||
| chr14:51867485 | A | G | 224 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0052 others(221): Show |
225 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.-71+6695A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51867485 | |||||||
| chr14:51867507 | G | A | 11 | a0001c0001t0003g0054 a0001c0001t0003g0372 a0001c0001t0003g0374 others(8): Show |
11 | HG01891.hp2 HG02717.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.-71+6717G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51867507 | |||||||
| chr14:51867524 | A | C | 146 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0052 others(143): Show |
146 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.-71+6734A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51867524 | |||||||
| chr14:51867536 | T | C | 1 | a0001c0001t0001g0369 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-71+6746T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51867536 | |||||||
| chr14:51867598 | G | A | 6 | a0001c0001t0001g0289 a0001c0001t0002g0285 a0001c0001t0002g0286 others(3): Show |
6 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71+6808G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51867598 | |||||||
| chr14:51867620 | C | T | 1 | a0001c0002t0074g0040 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-71+6830C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51867620 | |||||||
| chr14:51867639 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-71+6849G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51867639 | |||||||
| chr14:51867696 | C | T | 260 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0037 others(257): Show |
261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.-71+6906C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51867696 | |||||||
| chr14:51867834 | T | A | 33 | a0001c0001t0001g0037 a0001c0001t0001g0052 a0001c0001t0001g0328 others(30): Show |
33 | HG00140.hp2 HG00735.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-71+7044T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51867834 | |||||||
| chr14:51867871 | T | C | 131 | a0001c0001t0001g0034 a0001c0001t0001g0057 a0001c0001t0001g0098 others(128): Show |
132 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-71+7081T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51867871 | |||||||
| chr14:51867900 | A | AT | 8 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0293 others(5): Show |
8 | HG00544.hp2 HG02027.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.-71+7121dupT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51867900 | ||||||
| chr14:51867913 | A | G | 1 | a0001c0001t0011g0316 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-71+7123A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51867913 | |||||||
| chr14:51868069 | C | G | 2 | a0001c0001t0002g0232 a0001c0001t0002g0293 |
2 | HG00544.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.-71+7279C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51868069 | |||||||
| chr14:51868213 | C | T | 71 | a0001c0001t0001g0075 a0001c0001t0001g0098 a0001c0001t0001g0099 others(68): Show |
72 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.-71+7423C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51868213 | |||||||
| chr14:51868219 | G | A | 1 | a0001c0001t0002g0191 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-71+7429G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51868219 | |||||||
| chr14:51868261 | C | CA | 4 | a0001c0001t0016g0007 a0001c0001t0016g0352 a0001c0001t0040g0335 others(1): Show |
4 | HG02622.hp2 HG02965.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-71+7472dupA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51868261 | ||||||
| chr14:51868263 | G | A | 119 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0038 others(116): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.-71+7473G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51868263 | |||||||
| chr14:51868488 | C | T | 1 | a0001c0001t0009g0070 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-71+7698C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51868488 | |||||||
| chr14:51868615 | G | A | 1 | a0001c0001t0002g0049 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-71+7825G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51868615 | |||||||
| chr14:51868622 | G | C | 1 | a0001c0001t0017g0047 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-71+7832G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51868622 | |||||||
| chr14:51868694 | A | T | 1 | a0001c0001t0016g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-71+7904A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51868694 | |||||||
| chr14:51868951 | T | A | 1 | a0001c0001t0004g0198 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-71+8161T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51868951 | |||||||
| chr14:51869114 | T | C | 3 | a0001c0001t0003g0176 a0001c0001t0006g0131 a0001c0001t0008g0195 |
3 | HG00639.hp2 HG01255.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-71+8324T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51869114 | |||||||
| chr14:51869158 | G | C | 1 | a0001c0001t0056g0014 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-71+8368G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51869158 | |||||||
| chr14:51869483 | G | C | 2 | a0001c0001t0002g0008 a0001c0001t0002g0009 |
2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-70-8134G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51869483 | |||||||
| chr14:51869499 | C | A | 1 | a0001c0001t0002g0231 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-70-8118C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51869499 | |||||||
| chr14:51869703 | G | C | 2 | a0001c0001t0037g0180 a0001c0001t0051g0342 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-70-7914G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51869703 | |||||||
| chr14:51869714 | T | C | 1 | a0001c0001t0016g0352 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-70-7903T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51869714 | |||||||
| chr14:51869813 | G | A | 35 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(32): Show |
35 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.-70-7804G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51869813 | |||||||
| chr14:51869870 | C | T | 70 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0135 others(67): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-70-7747C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51869870 | |||||||
| chr14:51869964 | G | T | 177 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0038 others(174): Show |
178 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.-70-7653G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51869964 | |||||||
| chr14:51870003 | G | C | 6 | a0001c0001t0003g0372 a0001c0001t0003g0374 a0001c0001t0003g0375 others(3): Show |
6 | HG02055.hp1 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-70-7614G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51870003 | |||||||
| chr14:51870178 | C | T | 4 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0034g0377 others(1): Show |
4 | HG01433.hp1 HG03225.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70-7439C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51870178 | |||||||
| chr14:51870227 | C | G | 1 | a0001c0001t0023g0269 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-70-7390C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51870227 | |||||||
| chr14:51870241 | A | G | 1 | a0001c0001t0006g0159 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-70-7376A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51870241 | |||||||
| chr14:51870250 | G | GA | 62 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0106 others(59): Show |
63 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.-70-7357dupA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51870250 | ||||||
| chr14:51870320 | AAC | A | 7 | a0001c0001t0001g0075 a0001c0001t0016g0007 a0001c0001t0016g0035 others(4): Show |
7 | HG02258.hp2 HG02622.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-70-7293_-70-7292d others(4): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51870320 | ||||||
| chr14:51870366 | A | T | 1 | a0001c0001t0009g0070 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-70-7251A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51870366 | |||||||
| chr14:51870749 | G | A | 1 | a0001c0001t0046g0311 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-70-6868G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51870749 | |||||||
| chr14:51870824 | A | G | 7 | a0001c0001t0001g0075 a0001c0001t0016g0007 a0001c0001t0016g0352 others(4): Show |
7 | HG02622.hp2 HG02965.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.-70-6793A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51870824 | |||||||
| chr14:51871057 | A | G | 12 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0007g0044 others(9): Show |
12 | HG01243.hp1 HG01433.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-70-6560A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51871057 | |||||||
| chr14:51871084 | G | GA | 59 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0106 others(56): Show |
60 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.-70-6527dupA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51871084 | ||||||
| chr14:51871180 | C | T | 2 | a0001c0001t0002g0232 a0001c0001t0002g0293 |
2 | HG00544.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.-70-6437C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51871180 | |||||||
| chr14:51871240 | T | C | 1 | a0001c0001t0003g0054 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-70-6377T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51871240 | |||||||
| chr14:51871331 | C | CA | 188 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0038 others(185): Show |
189 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.-70-6275dupA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51871331 | ||||||
| chr14:51871331 | C | CAA | 81 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0075 others(78): Show |
81 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.-70-6276_-70-6275d others(4): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51871331 | ||||||
| chr14:51871332 | A | C | 2 | a0001c0001t0002g0109 a0001c0001t0005g0110 |
2 | NA18989.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-70-6285A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51871332 | |||||||
| chr14:51871423 | T | C | 1 | a0001c0001t0009g0353 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-70-6194T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51871423 | |||||||
| chr14:51871499 | C | T | 7 | a0001c0001t0005g0225 a0001c0001t0006g0226 a0001c0001t0012g0229 others(4): Show |
7 | NA18951.hp2 NA18961.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.-70-6118C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51871499 | |||||||
| chr14:51871500 | C | T | 10 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0007g0044 others(7): Show |
10 | HG01433.hp1 HG01891.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-70-6117C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51871500 | |||||||
| chr14:51871526 | A | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0369 a0001c0001t0002g0281 others(3): Show |
6 | HG01891.hp1 HG03195.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-70-6091A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51871526 | |||||||
| chr14:51871675 | G | A | 15 | a0001c0001t0001g0012 a0001c0001t0001g0075 a0001c0001t0001g0369 others(12): Show |
15 | HG01891.hp1 HG02258.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.-70-5942G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51871675 | |||||||
| chr14:51871676 | A | C | 1 | a0001c0001t0023g0108 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-70-5941A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51871676 | |||||||
| chr14:51871696 | A | C | 10 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0007g0044 others(7): Show |
10 | HG01433.hp1 HG01891.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-70-5921A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51871696 | |||||||
| chr14:51871739 | A | G | 36 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(33): Show |
36 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.-70-5878A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51871739 | |||||||
| chr14:51871877 | A | G | 1 | a0001c0001t0002g0003 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-70-5740A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51871877 | |||||||
| chr14:51871956 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-70-5661G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51871956 | |||||||
| chr14:51872010 | A | T | 1 | a0001c0001t0002g0327 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-70-5607A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51872010 | |||||||
| chr14:51872019 | G | A | 72 | a0001c0001t0001g0034 a0001c0001t0001g0111 a0001c0001t0001g0126 others(69): Show |
72 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.-70-5598G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51872019 | |||||||
| chr14:51872118 | C | T | 10 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0007g0044 others(7): Show |
10 | HG01433.hp1 HG01891.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-70-5499C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51872118 | |||||||
| chr14:51872124 | A | G | 1 | a0001c0001t0001g0270 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-70-5493A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51872124 | |||||||
| chr14:51872310 | T | TTG | 6 | a0001c0001t0001g0258 a0001c0001t0002g0107 a0001c0001t0003g0027 others(3): Show |
6 | HG03225.hp2 HG03654.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.-70-5283_-70-5282d others(4): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51872310 | ||||||
| chr14:51872310 | T | TTGTGTGT others(3): Show |
1 | a0001c0002t0072g0196 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-70-5291_-70-5282d others(12): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51872310 | ||||||
| chr14:51872310 | T | TTGTGTGT others(5): Show |
6 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0007g0044 others(3): Show |
6 | HG01891.hp2 HG02717.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-70-5293_-70-5282d others(14): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51872310 | ||||||
| chr14:51872310 | T | TTGTGTGT others(7): Show |
1 | a0001c0001t0034g0377 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-70-5295_-70-5282d others(16): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51872310 | ||||||
| chr14:51872310 | T | TTGTGTGT others(9): Show |
1 | a0001c0001t0034g0364 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-70-5297_-70-5282d others(18): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51872310 | ||||||
| chr14:51872310 | T | TTGTGTGT others(17): Show |
1 | a0001c0001t0032g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-70-5305_-70-5282d others(26): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51872310 | ||||||
| chr14:51872310 | TTG | T | 78 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0075 others(75): Show |
78 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.-70-5283_-70-5282d others(4): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51872310 | ||||||
| chr14:51872448 | T | C | 1 | a0001c0001t0032g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-70-5169T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51872448 | |||||||
| chr14:51872472 | G | A | 2 | a0001c0001t0004g0017 a0001c0001t0055g0210 |
2 | HG01255.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.-70-5145G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51872472 | |||||||
| chr14:51872488 | T | G | 148 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0075 others(145): Show |
149 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.-70-5129T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51872488 | |||||||
| chr14:51872535 | C | T | 1 | a0001c0001t0011g0314 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-70-5082C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51872535 | |||||||
| chr14:51872582 | T | C | 12 | a0001c0001t0002g0049 a0001c0001t0004g0041 a0001c0001t0004g0043 others(9): Show |
12 | HG01433.hp1 HG01891.hp2 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.-70-5035T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51872582 | |||||||
| chr14:51872633 | G | A | 72 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0135 others(69): Show |
72 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.-70-4984G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51872633 | |||||||
| chr14:51872743 | AATG | A | 3 | a0001c0001t0002g0281 a0001c0001t0002g0376 a0001c0001t0042g0282 |
3 | HG01891.hp1 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-70-4871_-70-4869d others(5): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51872743 | ||||||
| chr14:51872746 | G | A | 7 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0007g0044 others(4): Show |
7 | HG01891.hp2 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-70-4871G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51872746 | |||||||
| chr14:51873435 | T | C | 5 | a0001c0001t0009g0203 a0001c0001t0034g0364 a0001c0001t0034g0377 others(2): Show |
5 | HG01243.hp1 HG01433.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-70-4182T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51873435 | |||||||
| chr14:51873459 | A | G | 1 | a0001c0001t0071g0118 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-70-4158A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51873459 | |||||||
| chr14:51873638 | C | T | 6 | a0001c0001t0003g0372 a0001c0001t0003g0374 a0001c0001t0003g0375 others(3): Show |
6 | HG02055.hp1 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-70-3979C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51873638 | |||||||
| chr14:51873885 | C | T | 30 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0291 others(27): Show |
30 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.-70-3732C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51873885 | |||||||
| chr14:51873956 | G | A | 35 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(32): Show |
35 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.-70-3661G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51873956 | |||||||
| chr14:51873959 | A | G | 46 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0106 others(43): Show |
47 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.-70-3658A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51873959 | |||||||
| chr14:51873961 | C | T | 6 | a0001c0001t0003g0372 a0001c0001t0003g0374 a0001c0001t0003g0375 others(3): Show |
6 | HG02055.hp1 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-70-3656C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51873961 | |||||||
| chr14:51874023 | A | G | 1 | a0001c0001t0034g0364 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-70-3594A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51874023 | |||||||
| chr14:51874039 | AGTATGAT others(5): Show |
A | 2 | a0001c0001t0002g0109 a0001c0001t0005g0110 |
2 | NA18989.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-70-3575_-70-3564d others(14): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51874039 | ||||||
| chr14:51874126 | T | C | 2 | a0001c0001t0003g0321 a0001c0001t0008g0320 |
2 | HG01081.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.-70-3491T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51874126 | |||||||
| chr14:51874140 | C | T | 180 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0038 others(177): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.-70-3477C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51874140 | |||||||
| chr14:51874153 | A | G | 3 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 |
3 | HG00609.hp2 NA18941.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.-70-3464A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51874153 | |||||||
| chr14:51874164 | C | T | 2 | a0001c0001t0003g0054 a0001c0002t0074g0040 |
2 | HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-70-3453C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51874164 | |||||||
| chr14:51874297 | C | T | 2 | a0001c0001t0013g0361 a0001c0001t0021g0362 |
2 | NA18963.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-70-3320C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51874297 | |||||||
| chr14:51874318 | G | A | 1 | a0001c0001t0043g0336 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-70-3299G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51874318 | |||||||
| chr14:51874341 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-70-3276C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51874341 | |||||||
| chr14:51874424 | C | CA | 86 | a0001c0001t0001g0111 a0001c0001t0001g0135 a0001c0001t0001g0140 others(83): Show |
86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.-70-3175dupA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51874424 | ||||||
| chr14:51874424 | C | CAA | 10 | a0001c0001t0001g0057 a0001c0001t0001g0242 a0001c0001t0003g0372 others(7): Show |
10 | HG01243.hp1 HG02622.hp1 HG03209.hp1 others(7): Show |
intron_variant | MODIFIER | c.-70-3176_-70-3175d others(4): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51874424 | ||||||
| chr14:51874424 | CA | C | 49 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0106 others(46): Show |
50 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.-70-3175delA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51874424 | ||||||
| chr14:51874424 | CAA | C | 34 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(31): Show |
34 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.-70-3176_-70-3175d others(4): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51874424 | ||||||
| chr14:51874592 | C | T | 2 | a0001c0001t0009g0203 a0001c0001t0054g0202 |
2 | HG01243.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-70-3025C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51874592 | |||||||
| chr14:51874722 | A | C | 3 | a0001c0001t0002g0089 a0001c0001t0009g0268 a0001c0001t0021g0208 |
3 | HG00621.hp2 HG02165.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.-70-2895A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51874722 | |||||||
| chr14:51874844 | C | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0355 a0001c0002t0031g0030 |
3 | HG01981.hp2 HG02602.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-70-2773C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51874844 | |||||||
| chr14:51874869 | A | G | 39 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(36): Show |
39 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.-70-2748A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51874869 | |||||||
| chr14:51875101 | A | C | 1 | a0001c0001t0002g0232 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-70-2516A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51875101 | |||||||
| chr14:51875138 | G | A | 39 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(36): Show |
39 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.-70-2479G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51875138 | |||||||
| chr14:51875142 | G | A | 1 | a0001c0001t0002g0049 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-70-2475G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51875142 | |||||||
| chr14:51875298 | T | C | 2 | a0001c0001t0003g0054 a0001c0002t0074g0040 |
2 | HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-70-2319T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51875298 | |||||||
| chr14:51875464 | T | C | 63 | a0001c0001t0001g0034 a0001c0001t0001g0111 a0001c0001t0001g0126 others(60): Show |
63 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-70-2153T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51875464 | |||||||
| chr14:51875539 | A | G | 1 | a0001c0001t0014g0345 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-70-2078A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51875539 | |||||||
| chr14:51875850 | A | C | 13 | a0001c0001t0003g0372 a0001c0001t0003g0374 a0001c0001t0003g0375 others(10): Show |
13 | HG01891.hp2 HG02055.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-70-1767A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51875850 | |||||||
| chr14:51875947 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0030g0130 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-70-1664_-70-1663i others(12): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51875947 | ||||||
| chr14:51875947 | C | CTTTTTTT others(4): Show |
36 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0291 others(33): Show |
36 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.-70-1664_-70-1663i others(13): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51875947 | ||||||
| chr14:51875947 | C | CTTTTTTT others(5): Show |
65 | a0001c0001t0001g0052 a0001c0001t0001g0140 a0001c0001t0001g0150 others(62): Show |
65 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.-70-1664_-70-1663i others(14): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51875947 | ||||||
| chr14:51875947 | C | CTTTTTTT others(6): Show |
68 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0075 others(65): Show |
69 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.-70-1664_-70-1663i others(15): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51875947 | ||||||
| chr14:51875947 | C | CTTTTTTT others(7): Show |
6 | a0001c0001t0002g0376 a0001c0001t0009g0203 a0001c0001t0011g0316 others(3): Show |
6 | HG01243.hp1 HG02027.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-70-1664_-70-1663i others(16): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51875947 | ||||||
| chr14:51876023 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-70-1594A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51876023 | |||||||
| chr14:51876072 | G | A | 1 | a0001c0001t0070g0201 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-70-1545G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51876072 | |||||||
| chr14:51876243 | T | TAAATTTC others(332): Show |
1 | a0001c0001t0054g0202 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-70-1359_-70-1358i others(341): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51876243 | ||||||
| chr14:51876243 | T | TAAATTTC others(333): Show |
1 | a0001c0001t0009g0203 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-70-1359_-70-1358i others(342): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 51876243 | ||||||
| chr14:51876260 | T | C | 1 | a0001c0001t0002g0003 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-70-1357T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51876260 | |||||||
| chr14:51876295 | T | C | 4 | a0001c0001t0001g0369 a0001c0001t0002g0281 a0001c0001t0002g0376 others(1): Show |
4 | HG01891.hp1 HG03195.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-70-1322T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51876295 | |||||||
| chr14:51876360 | C | T | 3 | a0001c0001t0001g0207 a0001c0001t0001g0233 a0001c0001t0006g0234 |
3 | NA18951.hp1 NA19009.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.-70-1257C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51876360 | |||||||
| chr14:51876438 | G | A | 1 | a0001c0001t0007g0011 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-70-1179G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51876438 | |||||||
| chr14:51876509 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0035g0378 |
2 | HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-70-1108C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51876509 | |||||||
| chr14:51876543 | C | T | 32 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0291 others(29): Show |
32 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.-70-1074C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51876543 | |||||||
| chr14:51876620 | T | C | 1 | a0001c0001t0019g0373 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-70-997T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51876620 | |||||||
| chr14:51876640 | A | T | 15 | a0001c0001t0001g0279 a0001c0001t0002g0200 a0001c0001t0004g0187 others(12): Show |
15 | HG00438.hp1 HG02109.hp1 HG02273.hp2 others(12): Show |
intron_variant | MODIFIER | c.-70-977A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51876640 | |||||||
| chr14:51876680 | A | G | 2 | a0001c0001t0009g0203 a0001c0001t0054g0202 |
2 | HG01243.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-70-937A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51876680 | |||||||
| chr14:51876693 | A | G | 2 | a0001c0001t0009g0203 a0001c0001t0054g0202 |
2 | HG01243.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-70-924A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51876693 | |||||||
| chr14:51876694 | T | C | 4 | a0001c0001t0002g0200 a0001c0001t0004g0187 a0001c0001t0004g0198 others(1): Show |
4 | NA18944.hp1 NA18959.hp2 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70-923T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51876694 | |||||||
| chr14:51876757 | G | A | 4 | a0001c0001t0001g0369 a0001c0001t0002g0281 a0001c0001t0002g0376 others(1): Show |
4 | HG01891.hp1 HG03195.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-70-860G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51876757 | |||||||
| chr14:51876799 | C | G | 1 | a0001c0001t0004g0156 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-70-818C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51876799 | |||||||
| chr14:51876939 | T | A | 2 | a0001c0001t0034g0377 a0001c0002t0072g0196 |
2 | HG01433.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-70-678T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51876939 | |||||||
| chr14:51876972 | A | G | 1 | a0001c0001t0014g0088 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-70-645A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51876972 | |||||||
| chr14:51877032 | C | G | 2 | a0001c0001t0004g0326 a0001c0001t0068g0322 |
2 | HG02896.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-70-585C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51877032 | |||||||
| chr14:51877065 | G | A | 1 | a0001c0001t0016g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-70-552G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51877065 | |||||||
| chr14:51877087 | A | G | 1 | a0001c0001t0013g0224 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-70-530A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51877087 | |||||||
| chr14:51877118 | T | G | 32 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0291 others(29): Show |
32 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.-70-499T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51877118 | |||||||
| chr14:51877235 | T | C | 2 | a0001c0001t0001g0029 a0001c0002t0031g0030 |
2 | HG02602.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-70-382T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51877235 | |||||||
| chr14:51877283 | A | T | 1 | a0001c0001t0068g0322 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-70-334A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 1/3 | chr14 | 51877283 | |||||||
| chr14:51877720 | A | G | 5 | a0001c0001t0003g0372 a0001c0001t0003g0374 a0001c0001t0003g0375 others(2): Show |
5 | HG02055.hp1 HG02886.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+63A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51877720 | |||||||
| chr14:51877795 | T | C | 2 | a0001c0001t0046g0311 a0001c0001t0065g0026 |
2 | HG02970.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-30+138T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51877795 | |||||||
| chr14:51877825 | T | C | 53 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(50): Show |
53 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.-30+168T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51877825 | |||||||
| chr14:51877889 | C | T | 40 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(37): Show |
40 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.-30+232C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51877889 | |||||||
| chr14:51877961 | T | C | 1 | a0001c0001t0016g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-30+304T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51877961 | |||||||
| chr14:51878050 | T | C | 73 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0135 others(70): Show |
73 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.-30+393T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51878050 | |||||||
| chr14:51878138 | T | C | 5 | a0001c0001t0001g0299 a0001c0001t0016g0007 a0001c0001t0016g0352 others(2): Show |
5 | HG00438.hp2 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+481T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51878138 | |||||||
| chr14:51878377 | A | G | 93 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0075 others(90): Show |
93 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.-30+720A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51878377 | |||||||
| chr14:51878493 | A | G | 70 | a0001c0001t0001g0034 a0001c0001t0001g0111 a0001c0001t0001g0126 others(67): Show |
70 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.-30+836A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51878493 | |||||||
| chr14:51878599 | C | T | 66 | a0001c0001t0001g0034 a0001c0001t0001g0111 a0001c0001t0001g0126 others(63): Show |
66 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.-30+942C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51878599 | |||||||
| chr14:51878836 | C | T | 9 | a0001c0001t0001g0162 a0001c0001t0001g0174 a0001c0001t0001g0299 others(6): Show |
9 | HG00438.hp2 HG00609.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.-30+1179C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51878836 | |||||||
| chr14:51878909 | G | A | 1 | a0001c0001t0019g0051 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-30+1252G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51878909 | |||||||
| chr14:51878946 | G | A | 1 | a0001c0001t0004g0197 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-30+1289G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51878946 | |||||||
| chr14:51879083 | C | T | 2 | a0001c0001t0005g0254 a0001c0001t0007g0255 |
2 | HG01258.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-30+1426C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51879083 | |||||||
| chr14:51879154 | T | C | 102 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(99): Show |
103 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.-30+1497T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51879154 | |||||||
| chr14:51879443 | G | A | 5 | a0001c0001t0001g0135 a0001c0001t0010g0137 a0001c0001t0015g0132 others(2): Show |
5 | HG02132.hp1 NA19002.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30+1786G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51879443 | |||||||
| chr14:51879585 | T | G | 3 | a0001c0001t0001g0075 a0001c0001t0012g0337 a0001c0001t0035g0378 |
3 | HG03239.hp1 HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-30+1928T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51879585 | |||||||
| chr14:51879586 | G | A | 1 | a0001c0001t0004g0197 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-30+1929G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51879586 | |||||||
| chr14:51879926 | A | G | 7 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0007g0044 others(4): Show |
7 | HG01891.hp2 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30+2269A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51879926 | |||||||
| chr14:51879953 | A | C | 4 | a0001c0001t0016g0007 a0001c0001t0016g0352 a0001c0001t0040g0335 others(1): Show |
4 | HG02622.hp2 HG02965.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+2296A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51879953 | |||||||
| chr14:51879977 | A | G | 66 | a0001c0001t0001g0057 a0001c0001t0001g0135 a0001c0001t0001g0140 others(63): Show |
66 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.-30+2320A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51879977 | |||||||
| chr14:51880044 | C | G | 72 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0135 others(69): Show |
72 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.-30+2387C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51880044 | |||||||
| chr14:51880244 | A | G | 86 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(83): Show |
87 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.-30+2587A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51880244 | |||||||
| chr14:51880299 | A | G | 1 | a0001c0001t0002g0049 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-30+2642A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51880299 | |||||||
| chr14:51880478 | C | G | 1 | a0001c0001t0034g0364 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-30+2821C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51880478 | |||||||
| chr14:51880513 | A | T | 2 | a0001c0001t0009g0203 a0001c0001t0054g0202 |
2 | HG01243.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-30+2856A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51880513 | |||||||
| chr14:51880753 | A | G | 1 | a0001c0001t0006g0166 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-30+3096A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51880753 | |||||||
| chr14:51880769 | C | T | 4 | a0001c0001t0016g0007 a0001c0001t0016g0352 a0001c0001t0040g0335 others(1): Show |
4 | HG02622.hp2 HG02965.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+3112C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51880769 | |||||||
| chr14:51880848 | C | T | 1 | a0001c0001t0026g0188 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-30+3191C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51880848 | |||||||
| chr14:51880867 | C | A | 1 | a0001c0001t0021g0264 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-30+3210C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51880867 | |||||||
| chr14:51880932 | G | A | 1 | a0001c0001t0002g0049 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-30+3275G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51880932 | |||||||
| chr14:51880967 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-30+3310G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51880967 | |||||||
| chr14:51880967 | G | GA | 123 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0037 others(120): Show |
123 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.-30+3331dupA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51880967 | ||||||
| chr14:51880967 | G | GAA | 106 | a0001c0001t0001g0057 a0001c0001t0001g0098 a0001c0001t0001g0099 others(103): Show |
107 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.-30+3330_-30+3331d others(4): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51880967 | ||||||
| chr14:51880967 | G | GAAA | 19 | a0001c0001t0001g0106 a0001c0001t0001g0135 a0001c0001t0001g0140 others(16): Show |
19 | HG00621.hp2 HG02074.hp1 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.-30+3329_-30+3331d others(5): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51880967 | ||||||
| chr14:51880967 | GA | G | 9 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0002g0124 others(6): Show |
9 | HG01109.hp2 NA18747.hp1 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.-30+3331delA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51880967 | ||||||
| chr14:51880977 | A | AC | 6 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0007g0044 others(3): Show |
6 | HG01891.hp2 HG02717.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+3320_-30+3321i others(3): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51880977 | |||||||
| chr14:51881005 | T | C | 4 | a0001c0001t0001g0052 a0001c0001t0019g0051 a0001c0001t0036g0053 others(1): Show |
4 | HG03098.hp1 HG03225.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+3348T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51881005 | |||||||
| chr14:51881062 | G | T | 3 | a0001c0001t0001g0075 a0001c0001t0012g0337 a0001c0001t0035g0378 |
3 | HG03239.hp1 HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-30+3405G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51881062 | |||||||
| chr14:51881316 | T | C | 3 | a0001c0001t0001g0075 a0001c0001t0012g0337 a0001c0001t0035g0378 |
3 | HG03239.hp1 HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-30+3659T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51881316 | |||||||
| chr14:51881386 | G | A | 2 | a0001c0001t0009g0203 a0001c0001t0054g0202 |
2 | HG01243.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-30+3729G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51881386 | |||||||
| chr14:51881424 | C | G | 7 | a0001c0001t0002g0084 a0001c0001t0010g0083 a0001c0001t0017g0082 others(4): Show |
7 | NA18954.hp2 NA18969.hp1 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30+3767C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51881424 | |||||||
| chr14:51881482 | T | G | 1 | a0001c0001t0006g0131 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-30+3825T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51881482 | |||||||
| chr14:51881508 | G | A | 182 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0038 others(179): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.-30+3851G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51881508 | |||||||
| chr14:51881517 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-30+3860C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51881517 | |||||||
| chr14:51881701 | C | CT | 35 | a0001c0001t0001g0038 a0001c0001t0001g0135 a0001c0001t0001g0182 others(32): Show |
35 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.-30+4067dupT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51881701 | ||||||
| chr14:51881701 | C | CTT | 55 | a0001c0001t0001g0012 a0001c0001t0001g0140 a0001c0001t0001g0150 others(52): Show |
55 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.-30+4066_-30+4067d others(4): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51881701 | ||||||
| chr14:51881701 | C | CTTT | 8 | a0001c0001t0001g0057 a0001c0001t0001g0168 a0001c0001t0002g0066 others(5): Show |
8 | HG01891.hp1 HG02135.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30+4065_-30+4067d others(5): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51881701 | ||||||
| chr14:51881701 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0016g0007 a0001c0001t0040g0335 a0001c0001t0041g0334 |
3 | HG02965.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-30+4056_-30+4067d others(14): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51881701 | ||||||
| chr14:51881701 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0016g0352 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-30+4055_-30+4067d others(15): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51881701 | ||||||
| chr14:51881701 | CT | C | 27 | a0001c0001t0001g0052 a0001c0001t0001g0075 a0001c0001t0001g0126 others(24): Show |
27 | HG00280.hp1 HG01433.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.-30+4067delT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51881701 | ||||||
| chr14:51881724 | T | A | 3 | a0001c0001t0002g0093 a0001c0001t0027g0179 a0001c0001t0033g0363 |
3 | NA18967.hp2 NA19072.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-30+4067T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51881724 | |||||||
| chr14:51881724 | T | TA | 43 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0106 others(40): Show |
44 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.-30+4069dupA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51881724 | ||||||
| chr14:51881881 | A | C | 1 | a0001c0001t0005g0013 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-30+4224A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51881881 | |||||||
| chr14:51881944 | A | G | 1 | a0001c0001t0016g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-30+4287A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51881944 | |||||||
| chr14:51881967 | C | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0369 a0001c0001t0002g0281 others(2): Show |
5 | HG01891.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+4310C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51881967 | |||||||
| chr14:51882100 | A | G | 1 | a0001c0001t0075g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-30+4443A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51882100 | |||||||
| chr14:51882261 | A | G | 2 | a0001c0001t0009g0203 a0001c0001t0054g0202 |
2 | HG01243.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-30+4604A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51882261 | |||||||
| chr14:51882374 | C | T | 4 | a0001c0001t0017g0082 a0001c0001t0017g0085 a0001c0001t0017g0086 others(1): Show |
4 | NA18954.hp2 NA18969.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+4717C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51882374 | |||||||
| chr14:51882555 | T | C | 1 | a0001c0001t0034g0364 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-30+4898T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51882555 | |||||||
| chr14:51882692 | C | T | 6 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0007g0044 others(3): Show |
6 | HG01891.hp2 HG02717.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+5035C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51882692 | |||||||
| chr14:51882766 | T | C | 46 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0106 others(43): Show |
47 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.-30+5109T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51882766 | |||||||
| chr14:51882792 | G | T | 8 | a0001c0001t0001g0052 a0001c0001t0016g0007 a0001c0001t0016g0352 others(5): Show |
8 | HG02622.hp2 HG02965.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30+5135G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51882792 | |||||||
| chr14:51882881 | A | G | 1 | a0001c0001t0016g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-30+5224A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51882881 | |||||||
| chr14:51882887 | G | T | 1 | a0001c0001t0018g0367 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-30+5230G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51882887 | |||||||
| chr14:51882952 | G | T | 2 | a0001c0001t0034g0377 a0001c0002t0072g0196 |
2 | HG01433.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-30+5295G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51882952 | |||||||
| chr14:51883009 | C | CA | 8 | a0001c0001t0001g0076 a0001c0001t0002g0064 a0001c0001t0002g0260 others(5): Show |
8 | HG01070.hp2 HG01928.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30+5365dupA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51883009 | ||||||
| chr14:51883056 | A | T | 177 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0038 others(174): Show |
178 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.-30+5399A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51883056 | |||||||
| chr14:51883158 | C | T | 1 | a0001c0001t0023g0108 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-30+5501C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51883158 | |||||||
| chr14:51883441 | G | A | 46 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0106 others(43): Show |
47 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.-30+5784G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51883441 | |||||||
| chr14:51883577 | AG | A | 54 | a0001c0001t0001g0052 a0001c0001t0001g0098 a0001c0001t0001g0099 others(51): Show |
55 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.-30+5922delG | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51883577 | ||||||
| chr14:51883679 | G | A | 46 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0106 others(43): Show |
47 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.-30+6022G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51883679 | |||||||
| chr14:51883688 | A | G | 1 | a0001c0001t0009g0070 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-30+6031A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51883688 | |||||||
| chr14:51883768 | T | C | 1 | a0001c0001t0018g0367 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-30+6111T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51883768 | |||||||
| chr14:51883910 | T | A | 1 | a0001c0001t0001g0212 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-30+6253T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51883910 | |||||||
| chr14:51883930 | G | A | 1 | a0001c0001t0010g0137 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-30+6273G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51883930 | |||||||
| chr14:51883984 | C | T | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | NA18971.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.-30+6327C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51883984 | |||||||
| chr14:51884003 | C | T | 46 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0106 others(43): Show |
47 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.-30+6346C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51884003 | |||||||
| chr14:51884220 | A | G | 54 | a0001c0001t0001g0052 a0001c0001t0001g0098 a0001c0001t0001g0099 others(51): Show |
55 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.-30+6563A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51884220 | |||||||
| chr14:51884221 | C | T | 1 | a0001c0001t0006g0073 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-30+6564C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51884221 | |||||||
| chr14:51884254 | G | A | 1 | a0001c0001t0016g0352 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-30+6597G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51884254 | |||||||
| chr14:51884361 | T | A | 1 | a0001c0001t0034g0364 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-30+6704T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51884361 | |||||||
| chr14:51884461 | G | A | 1 | a0001c0001t0016g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-30+6804G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51884461 | |||||||
| chr14:51884550 | C | A | 2 | a0001c0001t0003g0055 a0001c0001t0003g0056 |
2 | HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-30+6893C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51884550 | |||||||
| chr14:51884573 | G | A | 8 | a0001c0001t0001g0052 a0001c0001t0016g0007 a0001c0001t0016g0352 others(5): Show |
8 | HG02622.hp2 HG02965.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30+6916G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51884573 | |||||||
| chr14:51884635 | C | T | 1 | a0001c0001t0002g0049 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-30+6978C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51884635 | |||||||
| chr14:51884651 | A | G | 1 | a0001c0001t0002g0049 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-30+6994A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51884651 | |||||||
| chr14:51884736 | A | T | 1 | a0001c0001t0030g0130 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-30+7079A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51884736 | |||||||
| chr14:51884761 | C | T | 1 | a0001c0001t0003g0307 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-30+7104C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51884761 | |||||||
| chr14:51884890 | G | A | 2 | a0001c0001t0034g0377 a0001c0002t0072g0196 |
2 | HG01433.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-30+7233G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51884890 | |||||||
| chr14:51884973 | C | A | 46 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0106 others(43): Show |
47 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.-30+7316C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51884973 | |||||||
| chr14:51885188 | T | C | 1 | a0001c0001t0027g0179 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-30+7531T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51885188 | |||||||
| chr14:51885309 | G | A | 54 | a0001c0001t0001g0052 a0001c0001t0001g0098 a0001c0001t0001g0099 others(51): Show |
55 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.-30+7652G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51885309 | |||||||
| chr14:51885314 | G | GTAT | 54 | a0001c0001t0001g0052 a0001c0001t0001g0098 a0001c0001t0001g0099 others(51): Show |
55 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.-30+7659_-30+7661d others(5): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51885314 | ||||||
| chr14:51885387 | G | A | 3 | a0001c0001t0007g0044 a0001c0001t0007g0046 a0001c0001t0016g0045 |
3 | HG02895.hp2 HG02897.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-30+7730G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51885387 | |||||||
| chr14:51885589 | T | A | 2 | a0001c0001t0009g0203 a0001c0001t0054g0202 |
2 | HG01243.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-30+7932T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51885589 | |||||||
| chr14:51885590 | A | AAC | 103 | a0001c0001t0001g0034 a0001c0001t0001g0111 a0001c0001t0001g0113 others(100): Show |
104 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.-30+7952_-30+7953d others(4): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51885590 | ||||||
| chr14:51885611 | C | A | 1 | a0001c0001t0011g0090 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-30+7954C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51885611 | |||||||
| chr14:51885738 | A | G | 36 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0291 others(33): Show |
36 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.-30+8081A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51885738 | |||||||
| chr14:51885820 | AG | A | 46 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0106 others(43): Show |
47 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.-30+8164delG | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51885820 | |||||||
| chr14:51885966 | T | G | 1 | a0001c0001t0076g0220 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-30+8309T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51885966 | |||||||
| chr14:51886060 | C | G | 1 | a0001c0001t0058g0341 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-30+8403C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51886060 | |||||||
| chr14:51886119 | C | T | 1 | a0001c0001t0011g0190 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-30+8462C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51886119 | |||||||
| chr14:51886194 | A | G | 103 | a0001c0001t0001g0034 a0001c0001t0001g0111 a0001c0001t0001g0113 others(100): Show |
103 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.-30+8537A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51886194 | |||||||
| chr14:51886232 | A | T | 100 | a0001c0001t0001g0034 a0001c0001t0001g0111 a0001c0001t0001g0113 others(97): Show |
100 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.-30+8575A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51886232 | |||||||
| chr14:51886242 | A | G | 4 | a0001c0001t0016g0007 a0001c0001t0016g0352 a0001c0001t0040g0335 others(1): Show |
4 | HG02622.hp2 HG02965.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+8585A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51886242 | |||||||
| chr14:51886300 | C | T | 1 | a0001c0001t0016g0351 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-30+8643C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51886300 | |||||||
| chr14:51886489 | G | C | 2 | a0001c0001t0025g0213 a0001c0001t0025g0273 |
2 | NA18980.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-30+8832G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51886489 | |||||||
| chr14:51886674 | G | C | 2 | a0001c0001t0009g0203 a0001c0001t0054g0202 |
2 | HG01243.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-30+9017G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51886674 | |||||||
| chr14:51886747 | C | A | 1 | a0001c0001t0001g0126 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-30+9090C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51886747 | |||||||
| chr14:51886930 | C | T | 2 | a0001c0001t0020g0154 a0001c0002t0044g0133 |
2 | NA18972.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-30+9273C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51886930 | |||||||
| chr14:51886946 | C | T | 1 | a0001c0001t0002g0330 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-30+9289C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51886946 | |||||||
| chr14:51886947 | G | A | 31 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0291 others(28): Show |
31 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.-30+9290G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51886947 | |||||||
| chr14:51887240 | C | A | 31 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0291 others(28): Show |
31 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.-30+9583C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51887240 | |||||||
| chr14:51887259 | T | A | 1 | a0001c0001t0066g0032 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-30+9602T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51887259 | |||||||
| chr14:51887281 | G | A | 4 | a0001c0001t0001g0052 a0001c0001t0019g0051 a0001c0001t0036g0053 others(1): Show |
4 | HG03098.hp1 HG03225.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+9624G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51887281 | |||||||
| chr14:51887510 | T | G | 106 | a0001c0001t0001g0034 a0001c0001t0001g0111 a0001c0001t0001g0113 others(103): Show |
106 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.-30+9853T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51887510 | |||||||
| chr14:51887540 | A | G | 1 | a0001c0001t0071g0118 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-30+9883A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51887540 | |||||||
| chr14:51887601 | G | C | 1 | a0001c0001t0016g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-30+9944G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51887601 | |||||||
| chr14:51887613 | C | T | 11 | a0001c0001t0001g0357 a0001c0001t0001g0358 a0001c0001t0003g0015 others(8): Show |
11 | HG00280.hp1 HG00741.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.-30+9956C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51887613 | |||||||
| chr14:51887633 | A | T | 1 | a0001c0001t0001g0291 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-30+9976A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51887633 | |||||||
| chr14:51887674 | T | A | 1 | a0001c0001t0055g0210 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-30+10017T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51887674 | |||||||
| chr14:51887674 | T | C | 1 | a0001c0001t0034g0364 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-30+10017T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51887674 | |||||||
| chr14:51887686 | A | G | 142 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0038 others(139): Show |
142 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.-30+10029A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51887686 | |||||||
| chr14:51887762 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-30+10105G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51887762 | |||||||
| chr14:51887989 | G | A | 368 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0034 others(365): Show |
369 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.-30+10332G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51887989 | |||||||
| chr14:51888068 | A | C | 4 | a0001c0001t0014g0018 a0001c0001t0014g0344 a0001c0001t0014g0345 others(1): Show |
4 | HG02257.hp1 HG02451.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+10411A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51888068 | |||||||
| chr14:51888077 | A | G | 1 | a0001c0001t0002g0064 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-30+10420A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51888077 | |||||||
| chr14:51888138 | A | T | 1 | a0001c0001t0002g0064 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-30+10481A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51888138 | |||||||
| chr14:51888261 | T | C | 4 | a0001c0001t0001g0115 a0001c0001t0001g0279 a0001c0001t0009g0116 others(1): Show |
4 | NA18942.hp2 NA18975.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+10604T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51888261 | |||||||
| chr14:51888302 | TTTTG | T | 24 | a0001c0001t0001g0259 a0001c0001t0001g0265 a0001c0001t0001g0267 others(21): Show |
24 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.-30+10657_-30+1066 others(8): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51888302 | ||||||
| chr14:51888378 | A | G | 73 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0135 others(70): Show |
73 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.-30+10721A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51888378 | |||||||
| chr14:51888475 | C | T | 1 | a0001c0001t0051g0342 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-30+10818C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51888475 | |||||||
| chr14:51888523 | T | C | 5 | a0001c0001t0003g0372 a0001c0001t0003g0374 a0001c0001t0003g0375 others(2): Show |
5 | HG02055.hp1 HG02886.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+10866T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51888523 | |||||||
| chr14:51888669 | A | G | 73 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0135 others(70): Show |
73 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.-30+11012A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51888669 | |||||||
| chr14:51888681 | C | T | 39 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0106 others(36): Show |
40 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.-30+11024C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51888681 | |||||||
| chr14:51888718 | C | T | 1 | a0001c0001t0034g0364 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-30+11061C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51888718 | |||||||
| chr14:51888872 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-30+11215A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51888872 | |||||||
| chr14:51889015 | A | G | 87 | a0001c0001t0001g0034 a0001c0001t0001g0111 a0001c0001t0001g0126 others(84): Show |
87 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.-30+11358A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51889015 | |||||||
| chr14:51889020 | C | G | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-30+11363C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51889020 | |||||||
| chr14:51889108 | G | GC | 3 | a0001c0001t0004g0338 a0001c0001t0006g0272 a0001c0001t0029g0306 |
3 | HG02056.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-30+11452dupC | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51889108 | ||||||
| chr14:51889109 | C | CT | 11 | a0001c0001t0001g0140 a0001c0001t0001g0152 a0001c0001t0001g0184 others(8): Show |
11 | HG01891.hp2 HG01928.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-30+11473dupT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51889109 | ||||||
| chr14:51889109 | CT | C | 47 | a0001c0001t0001g0038 a0001c0001t0001g0098 a0001c0001t0001g0106 others(44): Show |
48 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.-30+11473delT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51889109 | ||||||
| chr14:51889110 | T | C | 79 | a0001c0001t0001g0034 a0001c0001t0001g0111 a0001c0001t0001g0126 others(76): Show |
79 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-30+11453T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51889110 | |||||||
| chr14:51889111 | T | C | 2 | a0001c0001t0001g0303 a0001c0001t0003g0015 |
2 | HG01517.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.-30+11454T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51889111 | |||||||
| chr14:51889166 | A | C | 2 | a0001c0001t0025g0213 a0001c0001t0025g0273 |
2 | NA18980.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-30+11509A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51889166 | |||||||
| chr14:51889198 | C | T | 87 | a0001c0001t0001g0034 a0001c0001t0001g0111 a0001c0001t0001g0126 others(84): Show |
87 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.-30+11541C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51889198 | |||||||
| chr14:51889269 | C | T | 78 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(75): Show |
79 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.-30+11612C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51889269 | |||||||
| chr14:51889297 | G | A | 3 | a0001c0001t0001g0152 a0001c0001t0001g0182 a0001c0001t0001g0183 |
3 | HG00140.hp1 HG02735.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-30+11640G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51889297 | |||||||
| chr14:51889324 | G | T | 8 | a0001c0001t0001g0221 a0001c0001t0002g0124 a0001c0001t0003g0307 others(5): Show |
8 | NA18747.hp1 NA18947.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30+11667G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51889324 | |||||||
| chr14:51889449 | A | G | 2 | a0001c0001t0009g0203 a0001c0001t0054g0202 |
2 | HG01243.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-30+11792A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51889449 | |||||||
| chr14:51889482 | A | C | 5 | a0001c0001t0001g0135 a0001c0001t0010g0137 a0001c0001t0015g0132 others(2): Show |
5 | HG02132.hp1 NA19002.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30+11825A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51889482 | |||||||
| chr14:51889745 | C | T | 1 | a0001c0001t0010g0244 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-30+12088C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51889745 | |||||||
| chr14:51889767 | G | A | 1 | a0001c0001t0004g0156 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-30+12110G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51889767 | |||||||
| chr14:51889892 | A | G | 1 | a0001c0001t0042g0282 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-30+12235A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51889892 | |||||||
| chr14:51889945 | A | G | 91 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(88): Show |
92 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.-30+12288A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51889945 | |||||||
| chr14:51890030 | T | A | 2 | a0001c0001t0040g0335 a0001c0001t0041g0334 |
2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-30+12373T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51890030 | |||||||
| chr14:51890118 | G | C | 1 | a0001c0001t0016g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-30+12461G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51890118 | |||||||
| chr14:51890150 | T | A | 10 | a0001c0001t0001g0037 a0001c0001t0003g0055 a0001c0001t0003g0056 others(7): Show |
10 | HG00140.hp2 HG00735.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.-30+12493T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51890150 | |||||||
| chr14:51890314 | T | C | 12 | a0001c0001t0003g0372 a0001c0001t0003g0374 a0001c0001t0003g0375 others(9): Show |
12 | HG01891.hp2 HG02055.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.-30+12657T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51890314 | |||||||
| chr14:51890758 | G | A | 12 | a0001c0001t0003g0372 a0001c0001t0003g0374 a0001c0001t0003g0375 others(9): Show |
12 | HG01891.hp2 HG02055.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.-30+13101G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51890758 | |||||||
| chr14:51890782 | A | G | 30 | a0001c0001t0001g0057 a0001c0001t0001g0135 a0001c0001t0001g0168 others(27): Show |
30 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.-30+13125A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51890782 | |||||||
| chr14:51890900 | T | TAC | 179 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0038 others(176): Show |
180 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.-30+13244_-30+1324 others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51890900 | ||||||
| chr14:51890902 | T | C | 179 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0038 others(176): Show |
180 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.-30+13245T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51890902 | |||||||
| chr14:51890905 | G | GGGAGACA others(3): Show |
179 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0038 others(176): Show |
180 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.-30+13248_-30+1324 others(14): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51890905 | |||||||
| chr14:51890907 | A | AGG | 179 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0038 others(176): Show |
180 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.-30+13250_-30+1325 others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51890907 | |||||||
| chr14:51890960 | C | T | 1 | a0001c0001t0002g0049 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-30+13303C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51890960 | |||||||
| chr14:51890979 | C | A | 1 | a0001c0001t0003g0120 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-30+13322C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51890979 | |||||||
| chr14:51891086 | C | T | 1 | a0001c0001t0016g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-30+13429C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51891086 | |||||||
| chr14:51891094 | T | C | 4 | a0001c0001t0002g0064 a0001c0001t0002g0348 a0001c0001t0005g0347 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+13437T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51891094 | |||||||
| chr14:51891288 | T | A | 2 | a0001c0001t0001g0328 a0001c0001t0002g0329 |
2 | HG02559.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-30+13631T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51891288 | |||||||
| chr14:51891537 | C | G | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-30+13880C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51891537 | |||||||
| chr14:51891727 | G | T | 39 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0106 others(36): Show |
40 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.-30+14070G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51891727 | |||||||
| chr14:51891785 | A | G | 1 | a0001c0001t0011g0316 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-30+14128A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51891785 | |||||||
| chr14:51892050 | T | G | 89 | a0001c0001t0001g0034 a0001c0001t0001g0111 a0001c0001t0001g0113 others(86): Show |
89 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.-30+14393T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51892050 | |||||||
| chr14:51892095 | G | A | 1 | a0001c0001t0079g0142 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-30+14438G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51892095 | |||||||
| chr14:51892104 | AT | A | 37 | a0001c0001t0001g0140 a0001c0001t0001g0150 a0001c0001t0001g0151 others(34): Show |
37 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.-30+14451delT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51892104 | ||||||
| chr14:51892106 | T | C | 37 | a0001c0001t0001g0140 a0001c0001t0001g0150 a0001c0001t0001g0151 others(34): Show |
37 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.-30+14449T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51892106 | |||||||
| chr14:51892145 | G | T | 165 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0038 others(162): Show |
166 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.-30+14488G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51892145 | |||||||
| chr14:51892149 | A | G | 1 | a0001c0001t0002g0064 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-30+14492A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51892149 | |||||||
| chr14:51892176 | A | G | 182 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0038 others(179): Show |
183 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.-30+14519A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51892176 | |||||||
| chr14:51892199 | G | A | 196 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0038 others(193): Show |
197 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.-30+14542G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51892199 | |||||||
| chr14:51892241 | G | A | 80 | a0001c0001t0001g0034 a0001c0001t0001g0111 a0001c0001t0001g0113 others(77): Show |
80 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.-30+14584G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51892241 | |||||||
| chr14:51892304 | T | A | 1 | a0001c0001t0051g0342 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-30+14647T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51892304 | |||||||
| chr14:51892314 | A | T | 1 | a0001c0001t0012g0189 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-30+14657A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51892314 | |||||||
| chr14:51892319 | A | T | 61 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0057 others(58): Show |
61 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.-30+14662A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51892319 | |||||||
| chr14:51892372 | C | T | 36 | a0001c0001t0001g0057 a0001c0001t0001g0075 a0001c0001t0001g0135 others(33): Show |
36 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-30+14715C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51892372 | |||||||
| chr14:51892423 | T | C | 1 | a0001c0001t0023g0108 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-30+14766T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51892423 | |||||||
| chr14:51892436 | A | G | 40 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(37): Show |
40 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.-30+14779A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51892436 | |||||||
| chr14:51892445 | A | G | 1 | a0001c0001t0034g0364 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-30+14788A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51892445 | |||||||
| chr14:51892536 | T | C | 88 | a0001c0001t0001g0034 a0001c0001t0001g0111 a0001c0001t0001g0113 others(85): Show |
88 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.-30+14879T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51892536 | |||||||
| chr14:51892582 | A | G | 128 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0038 others(125): Show |
128 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.-30+14925A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51892582 | |||||||
| chr14:51892716 | C | T | 1 | a0001c0001t0047g0298 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-30+15059C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51892716 | |||||||
| chr14:51892739 | T | C | 2 | a0001c0001t0034g0377 a0001c0002t0072g0196 |
2 | HG01433.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-30+15082T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51892739 | |||||||
| chr14:51892748 | G | C | 3 | a0001c0001t0003g0143 a0001c0001t0008g0141 a0001c0001t0008g0144 |
3 | HG01099.hp1 HG01943.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.-30+15091G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51892748 | |||||||
| chr14:51892762 | G | A | 79 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(76): Show |
80 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.-30+15105G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51892762 | |||||||
| chr14:51892922 | A | T | 40 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(37): Show |
40 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.-30+15265A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51892922 | |||||||
| chr14:51893043 | T | C | 10 | a0001c0001t0003g0054 a0001c0001t0004g0041 a0001c0001t0004g0043 others(7): Show |
10 | HG01433.hp1 HG01891.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-30+15386T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51893043 | |||||||
| chr14:51893091 | A | T | 1 | a0001c0002t0074g0040 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-30+15434A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51893091 | |||||||
| chr14:51893352 | A | G | 1 | a0001c0001t0059g0158 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-30+15695A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51893352 | |||||||
| chr14:51893378 | T | G | 8 | a0001c0001t0002g0079 a0001c0001t0002g0084 a0001c0001t0005g0080 others(5): Show |
8 | NA18954.hp2 NA18964.hp1 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30+15721T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51893378 | |||||||
| chr14:51893386 | C | T | 1 | a0001c0001t0002g0049 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-30+15729C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51893386 | |||||||
| chr14:51893498 | C | T | 10 | a0001c0001t0003g0054 a0001c0001t0004g0041 a0001c0001t0004g0043 others(7): Show |
10 | HG01433.hp1 HG01891.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-30+15841C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51893498 | |||||||
| chr14:51893852 | T | G | 2 | a0001c0001t0009g0203 a0001c0001t0054g0202 |
2 | HG01243.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-30+16195T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51893852 | |||||||
| chr14:51893861 | A | G | 1 | a0001c0001t0019g0039 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-30+16204A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51893861 | |||||||
| chr14:51893907 | T | C | 105 | a0001c0001t0001g0034 a0001c0001t0001g0111 a0001c0001t0001g0113 others(102): Show |
105 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.-30+16250T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51893907 | |||||||
| chr14:51893971 | G | A | 196 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0038 others(193): Show |
197 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.-30+16314G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51893971 | |||||||
| chr14:51894073 | A | AT | 50 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(47): Show |
50 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.-30+16422dupT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51894073 | ||||||
| chr14:51894095 | A | C | 28 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(25): Show |
28 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.-30+16438A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51894095 | |||||||
| chr14:51894266 | G | C | 1 | a0001c0001t0034g0377 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-30+16609G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51894266 | |||||||
| chr14:51894389 | A | ACT | 105 | a0001c0001t0001g0034 a0001c0001t0001g0111 a0001c0001t0001g0113 others(102): Show |
105 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.-30+16733_-30+1673 others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51894389 | ||||||
| chr14:51894647 | GT | G | 40 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0106 others(37): Show |
41 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.-30+16999delT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51894647 | ||||||
| chr14:51894715 | G | A | 105 | a0001c0001t0001g0034 a0001c0001t0001g0111 a0001c0001t0001g0113 others(102): Show |
105 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.-30+17058G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51894715 | |||||||
| chr14:51894749 | C | T | 2 | a0001c0001t0009g0203 a0001c0001t0054g0202 |
2 | HG01243.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-30+17092C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51894749 | |||||||
| chr14:51894774 | AGT | A | 8 | a0001c0001t0001g0075 a0001c0001t0001g0207 a0001c0001t0001g0233 others(5): Show |
8 | HG03688.hp2 HG04228.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.-30+17118_-30+1711 others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51894774 | |||||||
| chr14:51894797 | T | G | 74 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0135 others(71): Show |
74 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.-30+17140T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51894797 | |||||||
| chr14:51894838 | C | T | 4 | a0001c0001t0001g0052 a0001c0001t0019g0051 a0001c0001t0036g0053 others(1): Show |
4 | HG03098.hp1 HG03225.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+17181C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51894838 | |||||||
| chr14:51894840 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-30+17183G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51894840 | |||||||
| chr14:51894883 | C | G | 1 | a0001c0001t0043g0336 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-30+17226C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51894883 | |||||||
| chr14:51895042 | A | AG | 18 | a0001c0001t0002g0200 a0001c0001t0004g0187 a0001c0001t0004g0198 others(15): Show |
18 | HG00438.hp1 HG01993.hp2 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.-30+17387dupG | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51895042 | ||||||
| chr14:51895044 | G | GA | 171 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0057 others(168): Show |
171 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.-30+17397dupA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51895044 | ||||||
| chr14:51895150 | A | G | 1 | a0001c0001t0007g0255 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-30+17493A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51895150 | |||||||
| chr14:51895409 | T | G | 2 | a0001c0001t0009g0203 a0001c0001t0054g0202 |
2 | HG01243.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-30+17752T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51895409 | |||||||
| chr14:51895806 | G | T | 1 | a0001c0001t0023g0269 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-30+18149G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51895806 | |||||||
| chr14:51895828 | C | T | 166 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0038 others(163): Show |
167 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.-30+18171C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51895828 | |||||||
| chr14:51895848 | A | C | 39 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0106 others(36): Show |
40 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.-30+18191A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51895848 | |||||||
| chr14:51895913 | G | A | 1 | a0001c0001t0075g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-30+18256G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51895913 | |||||||
| chr14:51895926 | T | TA | 17 | a0001c0001t0002g0200 a0001c0001t0004g0187 a0001c0001t0004g0198 others(14): Show |
17 | HG00438.hp1 HG01993.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.-30+18270dupA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51895926 | ||||||
| chr14:51895970 | A | G | 1 | a0001c0001t0030g0072 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-30+18313A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51895970 | |||||||
| chr14:51896024 | G | A | 1 | a0001c0001t0009g0340 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-30+18367G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51896024 | |||||||
| chr14:51896078 | A | C | 6 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0007g0044 others(3): Show |
6 | HG01891.hp2 HG02717.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+18421A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51896078 | |||||||
| chr14:51896209 | C | T | 38 | a0001c0001t0001g0140 a0001c0001t0001g0150 a0001c0001t0001g0151 others(35): Show |
38 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.-30+18552C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51896209 | |||||||
| chr14:51896256 | G | C | 2 | a0001c0001t0034g0377 a0001c0002t0072g0196 |
2 | HG01433.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-30+18599G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51896256 | |||||||
| chr14:51896265 | T | C | 1 | a0001c0001t0014g0088 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-30+18608T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51896265 | |||||||
| chr14:51896281 | A | C | 1 | a0001c0001t0003g0054 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-30+18624A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51896281 | |||||||
| chr14:51896340 | T | A | 1 | a0001c0001t0002g0191 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-30+18683T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51896340 | |||||||
| chr14:51896425 | G | T | 111 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0038 others(108): Show |
111 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.-30+18768G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51896425 | |||||||
| chr14:51896579 | G | A | 1 | a0001c0001t0001g0355 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-30+18922G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51896579 | |||||||
| chr14:51896631 | G | C | 183 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0057 others(180): Show |
184 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.-30+18974G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51896631 | |||||||
| chr14:51896745 | C | A | 1 | a0001c0001t0023g0108 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-30+19088C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51896745 | |||||||
| chr14:51897037 | A | T | 2 | a0001c0001t0003g0054 a0001c0002t0074g0040 |
2 | HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-30+19380A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51897037 | |||||||
| chr14:51897118 | G | A | 1 | a0001c0001t0016g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-30+19461G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51897118 | |||||||
| chr14:51897175 | T | C | 1 | a0001c0001t0016g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-30+19518T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51897175 | |||||||
| chr14:51897219 | A | G | 3 | a0001c0001t0001g0034 a0001c0001t0001g0161 a0001c0001t0006g0354 |
3 | HG00735.hp1 HG01258.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-30+19562A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51897219 | |||||||
| chr14:51897237 | G | A | 1 | a0001c0001t0034g0364 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-30+19580G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51897237 | |||||||
| chr14:51897251 | A | G | 7 | a0001c0001t0005g0225 a0001c0001t0006g0226 a0001c0001t0012g0229 others(4): Show |
7 | NA18951.hp2 NA18961.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30+19594A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51897251 | |||||||
| chr14:51897446 | C | T | 1 | a0001c0001t0016g0007 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-30+19789C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51897446 | |||||||
| chr14:51897536 | TA | T | 3 | a0001c0001t0003g0143 a0001c0001t0008g0141 a0001c0001t0008g0144 |
3 | HG01099.hp1 HG01943.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.-30+19881delA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51897536 | ||||||
| chr14:51897538 | A | T | 3 | a0001c0001t0003g0143 a0001c0001t0008g0141 a0001c0001t0008g0144 |
3 | HG01099.hp1 HG01943.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.-30+19881A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51897538 | |||||||
| chr14:51897612 | G | T | 1 | a0001c0001t0002g0329 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-30+19955G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51897612 | |||||||
| chr14:51897709 | A | G | 5 | a0001c0001t0001g0135 a0001c0001t0010g0137 a0001c0001t0015g0132 others(2): Show |
5 | HG02132.hp1 NA19002.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30+20052A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51897709 | |||||||
| chr14:51897735 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-30+20078G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51897735 | |||||||
| chr14:51897751 | G | T | 1 | a0001c0001t0034g0364 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-30+20094G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51897751 | |||||||
| chr14:51897977 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-30+20320A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51897977 | |||||||
| chr14:51897990 | C | T | 169 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0038 others(166): Show |
170 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.-30+20333C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51897990 | |||||||
| chr14:51898036 | C | T | 35 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0291 others(32): Show |
35 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.-30+20379C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51898036 | |||||||
| chr14:51898115 | C | T | 4 | a0001c0001t0001g0052 a0001c0001t0019g0051 a0001c0001t0036g0053 others(1): Show |
4 | HG03098.hp1 HG03225.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+20458C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51898115 | |||||||
| chr14:51898378 | G | A | 4 | a0001c0001t0001g0052 a0001c0001t0019g0051 a0001c0001t0036g0053 others(1): Show |
4 | HG03098.hp1 HG03225.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+20721G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51898378 | |||||||
| chr14:51898384 | T | C | 1 | a0001c0001t0049g0205 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-30+20727T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51898384 | |||||||
| chr14:51898429 | G | C | 4 | a0001c0001t0001g0052 a0001c0001t0019g0051 a0001c0001t0036g0053 others(1): Show |
4 | HG03098.hp1 HG03225.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+20772G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51898429 | |||||||
| chr14:51898518 | A | G | 1 | a0001c0001t0003g0157 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-30+20861A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51898518 | |||||||
| chr14:51898766 | G | C | 1 | a0001c0001t0038g0346 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-30+21109G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51898766 | |||||||
| chr14:51899021 | G | T | 10 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0296 others(7): Show |
10 | HG00738.hp1 HG01261.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-30+21364G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51899021 | |||||||
| chr14:51899056 | A | G | 110 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0057 others(107): Show |
110 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.-30+21399A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51899056 | |||||||
| chr14:51899103 | C | A | 1 | a0001c0001t0002g0079 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-30+21446C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51899103 | |||||||
| chr14:51899263 | C | T | 1 | a0001c0001t0034g0377 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-30+21606C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51899263 | |||||||
| chr14:51899294 | C | T | 1 | a0001c0001t0059g0158 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-30+21637C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51899294 | |||||||
| chr14:51899389 | T | G | 2 | a0001c0001t0001g0369 a0001c0001t0016g0035 |
2 | HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-30+21732T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51899389 | |||||||
| chr14:51899458 | T | C | 1 | a0001c0001t0018g0368 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-30+21801T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51899458 | |||||||
| chr14:51899612 | C | A | 90 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(87): Show |
91 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.-30+21955C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51899612 | |||||||
| chr14:51899636 | C | A | 9 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0062 others(6): Show |
9 | HG02280.hp2 HG02615.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-30+21979C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51899636 | |||||||
| chr14:51899643 | C | T | 1 | a0001c0001t0046g0311 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-30+21986C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51899643 | |||||||
| chr14:51899748 | G | A | 1 | a0001c0001t0002g0049 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-30+22091G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51899748 | |||||||
| chr14:51899780 | G | C | 1 | a0001c0001t0001g0271 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-30+22123G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51899780 | |||||||
| chr14:51899822 | G | A | 1 | a0001c0001t0047g0298 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-30+22165G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51899822 | |||||||
| chr14:51899859 | C | G | 244 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0037 others(241): Show |
245 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.-30+22202C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51899859 | |||||||
| chr14:51899902 | A | T | 1 | a0001c0001t0016g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-30+22245A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51899902 | |||||||
| chr14:51899987 | T | C | 3 | a0001c0001t0002g0281 a0001c0001t0002g0376 a0001c0001t0042g0282 |
3 | HG01891.hp1 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-30+22330T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51899987 | |||||||
| chr14:51900016 | T | C | 1 | a0001c0001t0043g0336 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-30+22359T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51900016 | |||||||
| chr14:51900058 | G | C | 191 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0037 others(188): Show |
191 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.-30+22401G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51900058 | |||||||
| chr14:51900357 | C | T | 189 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0038 others(186): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.-30+22700C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51900357 | |||||||
| chr14:51900385 | G | T | 1 | a0001c0001t0043g0336 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-30+22728G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51900385 | |||||||
| chr14:51900452 | C | A | 1 | a0001c0001t0068g0322 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-30+22795C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51900452 | |||||||
| chr14:51900587 | A | G | 1 | a0001c0001t0006g0272 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-30+22930A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51900587 | |||||||
| chr14:51900623 | C | G | 1 | a0001c0001t0012g0337 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-30+22966C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51900623 | |||||||
| chr14:51900637 | G | C | 45 | a0001c0001t0001g0098 a0001c0001t0001g0106 a0001c0001t0001g0165 others(42): Show |
46 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.-30+22980G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51900637 | |||||||
| chr14:51900736 | T | G | 16 | a0001c0001t0001g0219 a0001c0001t0001g0270 a0001c0001t0004g0187 others(13): Show |
16 | HG01099.hp2 HG01175.hp2 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.-30+23079T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51900736 | |||||||
| chr14:51900745 | A | C | 2 | a0001c0001t0003g0054 a0001c0002t0074g0040 |
2 | HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-30+23088A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51900745 | |||||||
| chr14:51900779 | G | T | 1 | a0001c0001t0001g0369 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-30+23122G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51900779 | |||||||
| chr14:51901038 | T | A | 2 | a0001c0001t0003g0055 a0001c0001t0003g0056 |
2 | HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-30+23381T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51901038 | |||||||
| chr14:51901114 | G | A | 1 | a0001c0001t0002g0049 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-30+23457G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51901114 | |||||||
| chr14:51901129 | T | C | 8 | a0001c0001t0001g0099 a0001c0001t0005g0225 a0001c0001t0006g0226 others(5): Show |
8 | NA18951.hp2 NA18961.hp2 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30+23472T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51901129 | |||||||
| chr14:51901186 | CT | C | 38 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(35): Show |
38 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.-30+23540delT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51901186 | ||||||
| chr14:51901225 | G | T | 15 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0007g0044 others(12): Show |
15 | HG01891.hp2 HG02717.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.-30+23568G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51901225 | |||||||
| chr14:51901335 | C | A | 1 | a0001c0001t0001g0113 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-30+23678C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51901335 | |||||||
| chr14:51901354 | T | A | 88 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0075 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.-30+23697T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51901354 | |||||||
| chr14:51901356 | T | C | 1 | a0001c0001t0002g0049 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-30+23699T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51901356 | |||||||
| chr14:51901469 | C | T | 79 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0075 others(76): Show |
79 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.-30+23812C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51901469 | |||||||
| chr14:51901484 | A | G | 2 | a0001c0001t0009g0203 a0001c0001t0054g0202 |
2 | HG01243.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-30+23827A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51901484 | |||||||
| chr14:51901486 | G | A | 3 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0002t0073g0010 |
3 | HG02257.hp2 HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-30+23829G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51901486 | |||||||
| chr14:51901722 | T | G | 79 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0075 others(76): Show |
79 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.-30+24065T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51901722 | |||||||
| chr14:51901734 | G | A | 6 | a0001c0001t0012g0163 a0001c0001t0012g0189 a0001c0001t0012g0246 others(3): Show |
6 | HG03239.hp1 HG04228.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+24077G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51901734 | |||||||
| chr14:51901752 | G | A | 37 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(34): Show |
37 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.-30+24095G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51901752 | |||||||
| chr14:51901752 | G | C | 1 | a0001c0001t0068g0322 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-30+24095G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51901752 | |||||||
| chr14:51901811 | A | G | 2 | a0001c0001t0001g0168 a0001c0001t0001g0263 |
2 | HG02135.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-30+24154A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51901811 | |||||||
| chr14:51901841 | A | G | 350 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0034 others(347): Show |
351 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.-30+24184A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51901841 | |||||||
| chr14:51901870 | G | A | 68 | a0001c0001t0001g0098 a0001c0001t0001g0106 a0001c0001t0001g0165 others(65): Show |
69 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.-30+24213G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51901870 | |||||||
| chr14:51901895 | A | G | 6 | a0001c0001t0012g0163 a0001c0001t0012g0189 a0001c0001t0012g0246 others(3): Show |
6 | HG03239.hp1 HG04228.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+24238A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51901895 | |||||||
| chr14:51901949 | A | G | 14 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0009g0042 others(11): Show |
14 | HG01891.hp2 HG02717.hp2 HG02976.hp1 others(11): Show |
intron_variant | MODIFIER | c.-30+24292A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51901949 | |||||||
| chr14:51901963 | TA | T | 10 | a0001c0001t0001g0219 a0001c0001t0002g0281 a0001c0001t0002g0376 others(7): Show |
10 | HG01515.hp1 HG01978.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.-30+24335delA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51901963 | ||||||
| chr14:51901963 | TAA | T | 53 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0052 others(50): Show |
53 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.-30+24334_-30+2433 others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51901963 | ||||||
| chr14:51901963 | TAAA | T | 246 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0034 others(243): Show |
246 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.-30+24333_-30+2433 others(7): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51901963 | ||||||
| chr14:51901963 | TAAAA | T | 48 | a0001c0001t0001g0098 a0001c0001t0001g0106 a0001c0001t0001g0165 others(45): Show |
49 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.-30+24332_-30+2433 others(8): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51901963 | ||||||
| chr14:51901963 | TAAAAAAA others(5): Show |
T | 2 | a0001c0001t0003g0054 a0001c0002t0074g0040 |
2 | HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-30+24324_-30+2433 others(16): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51901963 | ||||||
| chr14:51902295 | A | G | 1 | a0001c0001t0009g0268 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-30+24638A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51902295 | |||||||
| chr14:51902360 | A | G | 1 | a0001c0001t0005g0185 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-30+24703A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51902360 | |||||||
| chr14:51902520 | C | T | 3 | a0001c0001t0002g0281 a0001c0001t0002g0376 a0001c0001t0042g0282 |
3 | HG01891.hp1 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-30+24863C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51902520 | |||||||
| chr14:51902555 | C | T | 2 | a0001c0001t0016g0007 a0001c0001t0016g0352 |
2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-30+24898C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51902555 | |||||||
| chr14:51902692 | G | C | 4 | a0001c0001t0003g0054 a0001c0001t0009g0203 a0001c0001t0054g0202 others(1): Show |
4 | HG01243.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+25035G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51902692 | |||||||
| chr14:51902807 | G | A | 6 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0221 others(3): Show |
6 | HG02080.hp1 NA18946.hp2 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+25150G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51902807 | |||||||
| chr14:51902820 | C | G | 1 | a0001c0001t0016g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-30+25163C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51902820 | |||||||
| chr14:51902923 | GAGAA | G | 64 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(61): Show |
65 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(62): Show |
intron_variant | MODIFIER | c.-30+25272_-30+2527 others(8): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51902923 | ||||||
| chr14:51902945 | G | T | 4 | a0001c0001t0007g0050 a0001c0001t0016g0035 a0001c0001t0026g0002 others(1): Show |
5 | HG02258.hp2 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30+25288G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51902945 | |||||||
| chr14:51903029 | C | T | 1 | a0001c0001t0005g0013 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-30+25372C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51903029 | |||||||
| chr14:51903038 | A | G | 1 | a0001c0001t0002g0049 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-30+25381A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51903038 | |||||||
| chr14:51903108 | A | T | 32 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(29): Show |
32 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.-30+25451A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51903108 | |||||||
| chr14:51903233 | C | A | 1 | a0001c0001t0003g0027 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-30+25576C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51903233 | |||||||
| chr14:51903359 | C | G | 1 | a0001c0001t0012g0337 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-30+25702C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51903359 | |||||||
| chr14:51903471 | C | T | 1 | a0001c0001t0010g0137 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-30+25814C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51903471 | |||||||
| chr14:51903650 | A | G | 1 | a0001c0001t0004g0197 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-30+25993A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51903650 | |||||||
| chr14:51903817 | G | A | 1 | a0001c0001t0019g0074 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-30+26160G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51903817 | |||||||
| chr14:51903906 | G | T | 3 | a0001c0001t0002g0281 a0001c0001t0002g0376 a0001c0001t0042g0282 |
3 | HG01891.hp1 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-30+26249G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51903906 | |||||||
| chr14:51904145 | C | G | 1 | a0001c0001t0016g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-30+26488C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51904145 | |||||||
| chr14:51904161 | C | T | 54 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(51): Show |
55 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.-30+26504C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51904161 | |||||||
| chr14:51904260 | C | T | 3 | a0001c0001t0007g0050 a0001c0001t0026g0002 a0001c0001t0052g0095 |
4 | HG03491.hp2 HG03492.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+26603C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51904260 | |||||||
| chr14:51904294 | G | C | 51 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(48): Show |
51 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.-30+26637G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51904294 | |||||||
| chr14:51904387 | G | C | 1 | a0001c0001t0001g0369 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-30+26730G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51904387 | |||||||
| chr14:51904553 | CATGATCT others(7): Show |
C | 3 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0002t0073g0010 |
3 | HG02257.hp2 HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-30+26897_-30+2691 others(18): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51904553 | |||||||
| chr14:51904568 | G | T | 3 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0002t0073g0010 |
3 | HG02257.hp2 HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-30+26911G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51904568 | |||||||
| chr14:51904595 | T | C | 334 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0034 others(331): Show |
335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.-30+26938T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51904595 | |||||||
| chr14:51904716 | C | T | 50 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(47): Show |
51 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.-30+27059C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51904716 | |||||||
| chr14:51904816 | T | C | 1 | a0001c0001t0023g0048 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-30+27159T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51904816 | |||||||
| chr14:51904888 | G | A | 4 | a0001c0001t0002g0281 a0001c0001t0002g0376 a0001c0001t0016g0035 others(1): Show |
4 | HG01891.hp1 HG02258.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+27231G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51904888 | |||||||
| chr14:51904993 | T | C | 73 | a0001c0001t0001g0029 a0001c0001t0001g0076 a0001c0001t0001g0099 others(70): Show |
73 | HG00544.hp2 HG00597.hp1 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.-30+27336T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51904993 | |||||||
| chr14:51905222 | A | G | 11 | a0001c0001t0001g0140 a0001c0001t0001g0171 a0001c0001t0001g0172 others(8): Show |
11 | HG01081.hp1 HG02083.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-30+27565A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51905222 | |||||||
| chr14:51905236 | T | A | 2 | a0001c0001t0009g0203 a0001c0001t0054g0202 |
2 | HG01243.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-30+27579T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51905236 | |||||||
| chr14:51905351 | T | C | 81 | a0001c0001t0001g0057 a0001c0001t0001g0075 a0001c0001t0001g0113 others(78): Show |
81 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.-30+27694T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51905351 | |||||||
| chr14:51905373 | C | T | 1 | a0001c0001t0005g0300 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-30+27716C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51905373 | |||||||
| chr14:51905424 | A | C | 34 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(31): Show |
34 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.-30+27767A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51905424 | |||||||
| chr14:51905533 | C | A | 61 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(58): Show |
61 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.-30+27876C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51905533 | |||||||
| chr14:51905721 | G | A | 1 | a0001c0001t0035g0378 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-30+28064G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51905721 | |||||||
| chr14:51905800 | G | A | 4 | a0001c0001t0012g0163 a0001c0001t0012g0189 a0001c0001t0012g0246 others(1): Show |
4 | HG04228.hp1 NA18950.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+28143G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51905800 | |||||||
| chr14:51905829 | G | C | 7 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0009g0042 others(4): Show |
7 | HG01891.hp2 HG02717.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30+28172G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51905829 | |||||||
| chr14:51905832 | C | T | 1 | a0001c0001t0002g0218 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-30+28175C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51905832 | |||||||
| chr14:51905902 | A | G | 26 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0281 others(23): Show |
26 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.-30+28245A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51905902 | |||||||
| chr14:51905915 | A | T | 4 | a0001c0001t0002g0281 a0001c0001t0002g0376 a0001c0001t0016g0035 others(1): Show |
4 | HG01891.hp1 HG02258.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+28258A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51905915 | |||||||
| chr14:51906127 | A | C | 2 | a0001c0001t0004g0041 a0001c0001t0004g0043 |
2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-30+28470A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51906127 | |||||||
| chr14:51906494 | T | TA | 4 | a0001c0001t0001g0052 a0001c0001t0045g0290 a0001c0001t0063g0005 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+28839dupA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51906494 | ||||||
| chr14:51906635 | T | G | 299 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0037 others(296): Show |
300 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.-30+28978T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51906635 | |||||||
| chr14:51906709 | A | G | 2 | a0001c0001t0002g0348 a0001c0001t0005g0347 |
2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-30+29052A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51906709 | |||||||
| chr14:51906735 | C | T | 9 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0003g0372 others(6): Show |
9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-30+29078C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51906735 | |||||||
| chr14:51906757 | C | CT | 8 | a0001c0001t0001g0012 a0001c0001t0002g0286 a0001c0001t0004g0199 others(5): Show |
8 | HG01099.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-30+29116dupT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51906757 | ||||||
| chr14:51906757 | C | CTT | 79 | a0001c0001t0001g0057 a0001c0001t0001g0075 a0001c0001t0001g0113 others(76): Show |
79 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.-30+29115_-30+2911 others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51906757 | ||||||
| chr14:51906757 | C | CTTTTTTT others(4): Show |
39 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0099 others(36): Show |
40 | HG00140.hp2 HG00735.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.-30+29106_-30+2911 others(15): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51906757 | ||||||
| chr14:51906757 | C | CTTTTTTT others(5): Show |
151 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0052 others(148): Show |
151 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-30+29105_-30+2911 others(16): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51906757 | ||||||
| chr14:51906757 | C | CTTTTTTT others(6): Show |
41 | a0001c0001t0001g0076 a0001c0001t0001g0115 a0001c0001t0001g0119 others(38): Show |
41 | HG01074.hp2 HG01496.hp1 HG01978.hp1 others(38): Show |
intron_variant | MODIFIER | c.-30+29104_-30+2911 others(17): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51906757 | ||||||
| chr14:51906757 | C | CTTTTTTT others(7): Show |
3 | a0001c0001t0002g0181 a0001c0001t0002g0239 a0001c0001t0023g0269 |
3 | HG01993.hp1 NA18967.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-30+29103_-30+2911 others(18): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51906757 | ||||||
| chr14:51906757 | C | CTTTTTTT others(9): Show |
2 | a0001c0001t0003g0054 a0001c0002t0074g0040 |
2 | HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-30+29101_-30+2911 others(20): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51906757 | ||||||
| chr14:51906757 | C | CTTTTTTT others(18): Show |
1 | a0001c0001t0016g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-30+29116_-30+2911 others(29): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51906757 | ||||||
| chr14:51906971 | G | T | 2 | a0001c0001t0001g0249 a0001c0001t0019g0074 |
2 | HG01074.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-30+29314G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51906971 | |||||||
| chr14:51907172 | C | T | 1 | a0001c0002t0072g0196 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-30+29515C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51907172 | |||||||
| chr14:51907198 | A | G | 10 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0003g0372 others(7): Show |
10 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-30+29541A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51907198 | |||||||
| chr14:51907325 | A | G | 1 | a0001c0001t0002g0049 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-30+29668A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51907325 | |||||||
| chr14:51907417 | C | T | 3 | a0001c0001t0004g0326 a0001c0001t0009g0033 a0001c0001t0068g0322 |
3 | HG02896.hp1 HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-30+29760C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51907417 | |||||||
| chr14:51907620 | C | A | 1 | a0001c0001t0003g0176 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-30+29963C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51907620 | |||||||
| chr14:51907739 | A | G | 5 | a0001c0001t0003g0372 a0001c0001t0003g0374 a0001c0001t0003g0375 others(2): Show |
5 | HG02055.hp1 HG02886.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+30082A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51907739 | |||||||
| chr14:51907746 | C | T | 1 | a0001c0001t0002g0181 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-30+30089C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51907746 | |||||||
| chr14:51907765 | C | T | 4 | a0001c0001t0001g0098 a0001c0001t0001g0106 a0001c0001t0002g0109 others(1): Show |
4 | NA18989.hp1 NA19065.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+30108C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51907765 | |||||||
| chr14:51907773 | C | T | 3 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0002t0073g0010 |
3 | HG02257.hp2 HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-30+30116C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51907773 | |||||||
| chr14:51907837 | G | A | 1 | a0001c0001t0032g0349 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-30+30180G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51907837 | |||||||
| chr14:51907982 | T | G | 1 | a0001c0001t0010g0244 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-30+30325T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51907982 | |||||||
| chr14:51908140 | C | T | 217 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0037 others(214): Show |
218 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.-30+30483C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51908140 | |||||||
| chr14:51908153 | G | A | 1 | a0001c0001t0014g0088 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-30+30496G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51908153 | |||||||
| chr14:51908164 | A | T | 1 | a0001c0001t0034g0364 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-30+30507A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51908164 | |||||||
| chr14:51908206 | G | A | 1 | a0001c0001t0075g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-30+30549G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51908206 | |||||||
| chr14:51908407 | A | C | 3 | a0001c0001t0002g0281 a0001c0001t0002g0376 a0001c0001t0042g0282 |
3 | HG01891.hp1 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-30+30750A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51908407 | |||||||
| chr14:51908527 | G | GATCT | 56 | a0001c0001t0001g0113 a0001c0001t0001g0135 a0001c0001t0001g0140 others(53): Show |
56 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.-30+30902_-30+3090 others(8): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51908527 | ||||||
| chr14:51908527 | G | GATCTATC others(1): Show |
41 | a0001c0001t0001g0012 a0001c0001t0001g0168 a0001c0001t0001g0171 others(38): Show |
41 | HG00323.hp2 HG00597.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.-30+30898_-30+3090 others(12): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51908527 | ||||||
| chr14:51908527 | G | GATCTATC others(5): Show |
10 | a0001c0001t0001g0184 a0001c0001t0001g0247 a0001c0001t0001g0357 others(7): Show |
10 | HG00280.hp2 HG00642.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.-30+30894_-30+3090 others(16): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51908527 | ||||||
| chr14:51908527 | GATCT | G | 7 | a0001c0001t0002g0064 a0001c0001t0002g0348 a0001c0001t0009g0203 others(4): Show |
7 | HG01243.hp1 HG02132.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30+30902_-30+3090 others(8): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51908527 | ||||||
| chr14:51908527 | GATCTATC others(1): Show |
G | 185 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0076 others(182): Show |
186 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.-30+30898_-30+3090 others(12): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51908527 | ||||||
| chr14:51908527 | GATCTATC others(5): Show |
G | 31 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(28): Show |
31 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.-30+30894_-30+3090 others(16): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51908527 | ||||||
| chr14:51908531 | T | G | 3 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0002t0073g0010 |
3 | HG02257.hp2 HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-30+30874T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51908531 | |||||||
| chr14:51908551 | TATCTATC others(5): Show |
T | 1 | a0001c0001t0037g0180 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-30+30897_-30+3090 others(16): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51908551 | ||||||
| chr14:51908559 | T | C | 1 | a0001c0001t0005g0347 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-30+30902T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51908559 | |||||||
| chr14:51908571 | T | G | 90 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0075 others(87): Show |
90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.-30+30914T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51908571 | |||||||
| chr14:51908573 | G | T | 85 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0034 others(82): Show |
86 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.-30+30916G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51908573 | |||||||
| chr14:51908575 | G | T | 7 | a0001c0001t0001g0207 a0001c0001t0002g0003 a0001c0001t0002g0049 others(4): Show |
7 | HG00738.hp1 HG01358.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30+30918G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51908575 | |||||||
| chr14:51908577 | G | T | 1 | a0001c0001t0007g0050 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-30+30920G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51908577 | |||||||
| chr14:51908594 | G | A | 215 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0037 others(212): Show |
216 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.-30+30937G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51908594 | |||||||
| chr14:51908594 | G | C | 3 | a0001c0001t0001g0106 a0001c0001t0002g0109 a0001c0001t0005g0110 |
3 | NA18989.hp1 NA19065.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-30+30937G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51908594 | |||||||
| chr14:51908667 | TC | T | 174 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0076 others(171): Show |
174 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.-30+31011delC | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51908667 | |||||||
| chr14:51908736 | A | ATTT | 6 | a0001c0001t0004g0197 a0001c0001t0009g0310 a0001c0001t0018g0323 others(3): Show |
6 | HG01074.hp2 HG01496.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+31100_-30+3110 others(7): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51908736 | ||||||
| chr14:51908736 | A | ATTTT | 27 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(24): Show |
28 | HG00140.hp2 HG00735.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.-30+31099_-30+3110 others(8): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51908736 | ||||||
| chr14:51908736 | A | ATTTTTTT others(1): Show |
68 | a0001c0001t0001g0029 a0001c0001t0001g0119 a0001c0001t0001g0175 others(65): Show |
68 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.-30+31095_-30+3110 others(12): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51908736 | ||||||
| chr14:51908736 | A | ATTTTTTT others(2): Show |
103 | a0001c0001t0001g0057 a0001c0001t0001g0075 a0001c0001t0001g0076 others(100): Show |
103 | HG00280.hp1 HG00558.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.-30+31094_-30+3110 others(13): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51908736 | ||||||
| chr14:51908736 | A | ATTTTTTT others(3): Show |
46 | a0001c0001t0001g0098 a0001c0001t0001g0106 a0001c0001t0001g0113 others(43): Show |
46 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.-30+31093_-30+3110 others(14): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51908736 | ||||||
| chr14:51908736 | A | ATTTTTTT others(4): Show |
19 | a0001c0001t0001g0034 a0001c0001t0001g0279 a0001c0001t0001g0319 others(16): Show |
19 | HG00438.hp1 HG00735.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.-30+31092_-30+3110 others(15): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51908736 | ||||||
| chr14:51908736 | A | ATTTTTTT others(5): Show |
3 | a0001c0001t0003g0372 a0001c0001t0005g0253 a0001c0001t0054g0202 |
3 | HG03209.hp1 HG03209.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.-30+31091_-30+3110 others(16): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51908736 | ||||||
| chr14:51908736 | A | ATTTTTTT others(6): Show |
2 | a0001c0001t0009g0203 a0001c0001t0016g0351 |
2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-30+31090_-30+3110 others(17): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51908736 | ||||||
| chr14:51908736 | A | ATTTTTTT others(7): Show |
1 | a0001c0001t0026g0188 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-30+31089_-30+3110 others(18): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51908736 | ||||||
| chr14:51908736 | A | ATTTTTTT others(11): Show |
1 | a0001c0001t0075g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-30+31085_-30+3110 others(22): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51908736 | ||||||
| chr14:51908736 | ATTTT | A | 7 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0009g0042 others(4): Show |
7 | HG01891.hp2 HG02717.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30+31099_-30+3110 others(8): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51908736 | ||||||
| chr14:51908889 | T | G | 3 | a0001c0001t0009g0203 a0001c0001t0043g0336 a0001c0001t0054g0202 |
3 | HG01243.hp1 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-30+31232T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51908889 | |||||||
| chr14:51909283 | CT | C | 3 | a0001c0001t0009g0310 a0001c0001t0018g0323 a0001c0001t0018g0324 |
3 | HG01074.hp2 HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-30+31631delT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51909283 | ||||||
| chr14:51909337 | T | C | 1 | a0001c0001t0010g0266 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-30+31680T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51909337 | |||||||
| chr14:51909534 | G | A | 2 | a0001c0001t0040g0335 a0001c0001t0041g0334 |
2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-30+31877G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51909534 | |||||||
| chr14:51909596 | G | C | 218 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0037 others(215): Show |
219 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.-30+31939G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51909596 | |||||||
| chr14:51909629 | G | A | 31 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(28): Show |
31 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.-30+31972G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51909629 | |||||||
| chr14:51910030 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-30+32373C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51910030 | |||||||
| chr14:51910089 | C | G | 1 | a0001c0001t0001g0369 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-30+32432C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51910089 | |||||||
| chr14:51910109 | T | A | 39 | a0001c0001t0001g0140 a0001c0001t0001g0152 a0001c0001t0001g0171 others(36): Show |
39 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.-30+32452T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51910109 | |||||||
| chr14:51910140 | A | C | 180 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0076 others(177): Show |
180 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.-30+32483A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51910140 | |||||||
| chr14:51910142 | A | G | 180 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0076 others(177): Show |
180 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.-30+32485A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51910142 | |||||||
| chr14:51910228 | G | C | 1 | a0001c0001t0052g0095 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-30+32571G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51910228 | |||||||
| chr14:51910230 | T | C | 41 | a0001c0001t0001g0012 a0001c0001t0001g0140 a0001c0001t0001g0152 others(38): Show |
41 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.-30+32573T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51910230 | |||||||
| chr14:51910331 | G | A | 1 | a0001c0001t0043g0336 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-30+32674G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51910331 | |||||||
| chr14:51910417 | C | T | 9 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0003g0372 others(6): Show |
9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-30+32760C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51910417 | |||||||
| chr14:51910524 | C | T | 1 | a0001c0001t0003g0176 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-30+32867C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51910524 | |||||||
| chr14:51910961 | G | A | 35 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(32): Show |
36 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.-30+33304G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51910961 | |||||||
| chr14:51911021 | C | T | 118 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0038 others(115): Show |
119 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-30+33364C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51911021 | |||||||
| chr14:51911093 | C | G | 52 | a0001c0001t0001g0012 a0001c0001t0001g0140 a0001c0001t0001g0152 others(49): Show |
52 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.-30+33436C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51911093 | |||||||
| chr14:51911174 | A | G | 7 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0009g0042 others(4): Show |
7 | HG01891.hp2 HG02717.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30+33517A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51911174 | |||||||
| chr14:51911196 | A | T | 151 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0038 others(148): Show |
152 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.-30+33539A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51911196 | |||||||
| chr14:51911302 | G | A | 37 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(34): Show |
38 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.-30+33645G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51911302 | |||||||
| chr14:51911356 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0032g0036 |
2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-30+33699C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51911356 | |||||||
| chr14:51911405 | T | G | 3 | a0001c0001t0002g0124 a0001c0001t0011g0125 a0001c0001t0050g0123 |
3 | NA18947.hp2 NA18955.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.-30+33748T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51911405 | |||||||
| chr14:51911413 | G | C | 1 | a0001c0001t0002g0049 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-30+33756G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51911413 | |||||||
| chr14:51911450 | G | A | 1 | a0001c0001t0016g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-30+33793G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51911450 | |||||||
| chr14:51911473 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0032g0036 |
2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-30+33816G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51911473 | |||||||
| chr14:51911545 | C | CT | 20 | a0001c0001t0001g0219 a0001c0001t0001g0270 a0001c0001t0001g0276 others(17): Show |
20 | HG01099.hp2 HG01175.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.-30+33902dupT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51911545 | ||||||
| chr14:51911545 | CT | C | 19 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0003g0372 others(16): Show |
20 | HG01433.hp1 HG02055.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.-30+33902delT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51911545 | ||||||
| chr14:51911545 | CTT | C | 46 | a0001c0001t0001g0057 a0001c0001t0001g0075 a0001c0001t0001g0113 others(43): Show |
46 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.-30+33901_-30+3390 others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51911545 | ||||||
| chr14:51911625 | CCTCTAAC others(552): Show |
C | 60 | a0001c0001t0001g0057 a0001c0001t0001g0075 a0001c0001t0001g0113 others(57): Show |
60 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.-30+33970_-30+3452 others(4): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51911625 | ||||||
| chr14:51911627 | T | C | 1 | a0001c0001t0006g0272 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-30+33970T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51911627 | |||||||
| chr14:51911746 | C | T | 3 | a0001c0001t0002g0281 a0001c0001t0002g0376 a0001c0001t0042g0282 |
3 | HG01891.hp1 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-30+34089C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51911746 | |||||||
| chr14:51911761 | C | T | 10 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0003g0372 others(7): Show |
10 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-30+34104C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51911761 | |||||||
| chr14:51911855 | C | A | 25 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0002g0003 others(22): Show |
25 | HG00738.hp1 HG01358.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.-30+34198C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51911855 | |||||||
| chr14:51911866 | G | GT | 17 | a0001c0001t0001g0038 a0001c0001t0001g0126 a0001c0001t0001g0291 others(14): Show |
17 | HG01261.hp1 HG01891.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-30+34221dupT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51911866 | ||||||
| chr14:51911866 | GT | G | 35 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0002g0003 others(32): Show |
35 | HG00738.hp1 HG01358.hp1 HG01361.hp1 others(32): Show |
intron_variant | MODIFIER | c.-30+34221delT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51911866 | ||||||
| chr14:51911874 | T | G | 25 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0002g0003 others(22): Show |
25 | HG00738.hp1 HG01358.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.-30+34217T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51911874 | |||||||
| chr14:51911876 | T | G | 1 | a0001c0001t0035g0284 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-30+34219T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51911876 | |||||||
| chr14:51911876 | T | TG | 24 | a0001c0001t0001g0037 a0001c0001t0001g0052 a0001c0001t0002g0049 others(21): Show |
25 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.-30+34219_-30+3422 others(5): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51911876 | |||||||
| chr14:51911950 | A | G | 21 | a0001c0001t0001g0025 a0001c0001t0002g0003 a0001c0001t0002g0064 others(18): Show |
21 | HG00738.hp1 HG01358.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.-30+34293A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51911950 | |||||||
| chr14:51911954 | A | T | 5 | a0001c0001t0003g0372 a0001c0001t0003g0374 a0001c0001t0003g0375 others(2): Show |
5 | HG02055.hp1 HG02886.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+34297A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51911954 | |||||||
| chr14:51912016 | A | G | 35 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(32): Show |
36 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.-30+34359A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51912016 | |||||||
| chr14:51912082 | A | G | 54 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(51): Show |
55 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.-30+34425A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51912082 | |||||||
| chr14:51912229 | G | A | 1 | a0001c0001t0004g0197 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-30+34572G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51912229 | |||||||
| chr14:51912340 | T | C | 51 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(48): Show |
52 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.-30+34683T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51912340 | |||||||
| chr14:51912563 | C | T | 32 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(29): Show |
32 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.-30+34906C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51912563 | |||||||
| chr14:51912735 | G | A | 104 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(101): Show |
104 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-30+35078G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51912735 | |||||||
| chr14:51912854 | G | T | 1 | a0001c0001t0023g0269 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-30+35197G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51912854 | |||||||
| chr14:51912856 | G | T | 1 | a0001c0001t0023g0269 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-30+35199G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51912856 | |||||||
| chr14:51912861 | G | C | 59 | a0001c0001t0001g0057 a0001c0001t0001g0075 a0001c0001t0001g0113 others(56): Show |
59 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.-30+35204G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51912861 | |||||||
| chr14:51912957 | C | T | 1 | a0001c0001t0008g0360 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-30+35300C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51912957 | |||||||
| chr14:51913297 | C | T | 104 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(101): Show |
104 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-30+35640C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51913297 | |||||||
| chr14:51913306 | T | G | 104 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(101): Show |
104 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-30+35649T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51913306 | |||||||
| chr14:51913438 | C | T | 3 | a0001c0001t0004g0339 a0001c0001t0009g0340 a0001c0001t0009g0353 |
3 | HG01099.hp2 HG01993.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.-30+35781C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51913438 | |||||||
| chr14:51913469 | G | A | 105 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(102): Show |
105 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.-30+35812G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51913469 | |||||||
| chr14:51913615 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-30+35958T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51913615 | |||||||
| chr14:51913779 | A | T | 108 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(105): Show |
108 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.-30+36122A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51913779 | |||||||
| chr14:51913817 | T | G | 7 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0009g0042 others(4): Show |
7 | HG01891.hp2 HG02717.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30+36160T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51913817 | |||||||
| chr14:51914116 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-30+36459T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51914116 | |||||||
| chr14:51914295 | C | A | 1 | a0001c0001t0006g0122 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-29-36355C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51914295 | |||||||
| chr14:51914310 | C | T | 1 | a0001c0001t0007g0325 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-29-36340C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51914310 | |||||||
| chr14:51914396 | T | C | 18 | a0001c0001t0001g0037 a0001c0001t0003g0055 a0001c0001t0003g0056 others(15): Show |
18 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.-29-36254T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51914396 | |||||||
| chr14:51914414 | A | C | 7 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0009g0042 others(4): Show |
7 | HG01891.hp2 HG02258.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-36236A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51914414 | |||||||
| chr14:51914433 | G | A | 1 | a0001c0001t0010g0333 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-29-36217G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51914433 | |||||||
| chr14:51914447 | T | C | 1 | a0001c0001t0007g0255 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-29-36203T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51914447 | |||||||
| chr14:51914460 | C | A | 196 | a0001c0001t0001g0057 a0001c0001t0001g0098 a0001c0001t0001g0099 others(193): Show |
196 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.-29-36190C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51914460 | |||||||
| chr14:51914473 | A | T | 1 | a0001c0001t0004g0197 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-29-36177A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51914473 | |||||||
| chr14:51914506 | C | T | 278 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0034 others(275): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.-29-36144C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51914506 | |||||||
| chr14:51914526 | G | A | 128 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0038 others(125): Show |
128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.-29-36124G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51914526 | |||||||
| chr14:51914589 | A | T | 1 | a0001c0001t0009g0070 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-29-36061A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51914589 | |||||||
| chr14:51914677 | G | A | 71 | a0001c0001t0001g0025 a0001c0001t0001g0126 a0001c0001t0001g0140 others(68): Show |
71 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.-29-35973G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51914677 | |||||||
| chr14:51914887 | T | C | 1 | a0001c0001t0037g0180 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-29-35763T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51914887 | |||||||
| chr14:51915191 | T | C | 1 | a0001c0001t0022g0274 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-29-35459T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51915191 | |||||||
| chr14:51915212 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-29-35438C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51915212 | |||||||
| chr14:51915515 | T | G | 2 | a0001c0001t0002g0216 a0001c0001t0005g0275 |
2 | NA18968.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-29-35135T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51915515 | |||||||
| chr14:51915560 | A | C | 1 | a0001c0001t0012g0278 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-29-35090A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51915560 | |||||||
| chr14:51915576 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0017g0047 |
2 | HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-29-35074G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51915576 | |||||||
| chr14:51915677 | G | A | 374 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(371): Show |
375 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(372): Show |
intron_variant | MODIFIER | c.-29-34973G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51915677 | |||||||
| chr14:51915714 | G | T | 2 | a0001c0001t0018g0323 a0001c0001t0018g0324 |
2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-29-34936G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51915714 | |||||||
| chr14:51915771 | T | C | 1 | a0001c0001t0030g0130 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-29-34879T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51915771 | |||||||
| chr14:51915789 | A | C | 1 | a0001c0001t0001g0369 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-29-34861A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51915789 | |||||||
| chr14:51915797 | A | T | 1 | a0001c0001t0001g0369 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-29-34853A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51915797 | |||||||
| chr14:51915876 | T | A | 1 | a0001c0001t0001g0037 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-29-34774T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51915876 | |||||||
| chr14:51915959 | C | T | 1 | a0001c0002t0044g0133 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-29-34691C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51915959 | |||||||
| chr14:51916097 | T | C | 102 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0140 others(99): Show |
102 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.-29-34553T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51916097 | |||||||
| chr14:51916119 | A | C | 3 | a0001c0001t0019g0051 a0001c0001t0032g0036 a0001c0001t0067g0065 |
3 | HG03540.hp2 NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-29-34531A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51916119 | |||||||
| chr14:51916411 | G | A | 1 | a0001c0001t0006g0073 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-29-34239G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51916411 | |||||||
| chr14:51916420 | T | C | 3 | a0001c0001t0001g0357 a0001c0001t0002g0222 a0001c0002t0044g0133 |
3 | HG03834.hp2 NA18950.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.-29-34230T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51916420 | |||||||
| chr14:51916510 | GA | G | 208 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(205): Show |
208 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(205): Show |
intron_variant | MODIFIER | c.-29-34129delA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51916510 | ||||||
| chr14:51916517 | A | G | 1 | a0001c0001t0070g0201 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-29-34133A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51916517 | |||||||
| chr14:51916563 | C | T | 4 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0009g0042 others(1): Show |
4 | HG01891.hp2 HG02717.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-34087C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51916563 | |||||||
| chr14:51916579 | G | A | 19 | a0001c0001t0002g0281 a0001c0001t0002g0376 a0001c0001t0003g0054 others(16): Show |
19 | HG00735.hp2 HG01074.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-29-34071G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51916579 | |||||||
| chr14:51916739 | G | T | 3 | a0001c0001t0001g0369 a0001c0001t0018g0367 a0001c0001t0037g0180 |
3 | HG02615.hp1 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-29-33911G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51916739 | |||||||
| chr14:51916963 | A | G | 3 | a0001c0001t0003g0015 a0001c0001t0008g0016 a0001c0001t0008g0170 |
3 | HG00741.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-29-33687A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51916963 | |||||||
| chr14:51917207 | T | C | 1 | a0001c0002t0073g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-29-33443T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51917207 | |||||||
| chr14:51917296 | G | A | 76 | a0001c0001t0001g0057 a0001c0001t0001g0075 a0001c0001t0001g0113 others(73): Show |
76 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.-29-33354G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51917296 | |||||||
| chr14:51917300 | A | C | 3 | a0001c0001t0014g0020 a0001c0001t0028g0024 a0001c0001t0060g0147 |
3 | HG01978.hp2 HG02109.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.-29-33350A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51917300 | |||||||
| chr14:51917360 | A | AATCG | 9 | a0001c0001t0002g0064 a0001c0001t0002g0348 a0001c0001t0005g0347 others(6): Show |
9 | HG02486.hp2 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29-33289_-29-3328 others(8): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51917360 | ||||||
| chr14:51917375 | G | C | 76 | a0001c0001t0001g0057 a0001c0001t0001g0075 a0001c0001t0001g0113 others(73): Show |
76 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.-29-33275G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51917375 | |||||||
| chr14:51917441 | C | T | 9 | a0001c0001t0002g0064 a0001c0001t0002g0348 a0001c0001t0005g0347 others(6): Show |
9 | HG02486.hp2 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29-33209C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51917441 | |||||||
| chr14:51917443 | T | C | 1 | a0001c0001t0005g0275 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-29-33207T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51917443 | |||||||
| chr14:51917740 | C | T | 1 | a0001c0001t0002g0049 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-29-32910C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51917740 | |||||||
| chr14:51917806 | G | A | 1 | a0001c0001t0043g0336 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-29-32844G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51917806 | |||||||
| chr14:51917961 | GGTTGCAC others(12): Show |
G | 1 | a0001c0001t0009g0268 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-29-32686_-29-3266 others(23): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51917961 | ||||||
| chr14:51917971 | C | T | 1 | a0001c0001t0051g0342 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-29-32679C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51917971 | |||||||
| chr14:51918037 | CA | C | 53 | a0001c0001t0001g0012 a0001c0001t0001g0111 a0001c0001t0001g0162 others(50): Show |
53 | HG01099.hp2 HG01243.hp1 HG01496.hp2 others(50): Show |
intron_variant | MODIFIER | c.-29-32596delA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51918037 | ||||||
| chr14:51918037 | CAA | C | 91 | a0001c0001t0001g0057 a0001c0001t0001g0075 a0001c0001t0001g0113 others(88): Show |
91 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.-29-32597_-29-3259 others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51918037 | ||||||
| chr14:51918307 | G | C | 2 | a0001c0001t0018g0323 a0001c0001t0018g0324 |
2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-29-32343G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51918307 | |||||||
| chr14:51918314 | G | C | 1 | a0001c0001t0008g0167 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-29-32336G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51918314 | |||||||
| chr14:51918432 | A | G | 2 | a0001c0001t0018g0323 a0001c0001t0018g0324 |
2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-29-32218A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51918432 | |||||||
| chr14:51918435 | C | T | 1 | a0001c0001t0027g0103 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-29-32215C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51918435 | |||||||
| chr14:51918506 | C | T | 1 | a0001c0001t0075g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-29-32144C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51918506 | |||||||
| chr14:51918613 | CTT | C | 18 | a0001c0001t0002g0281 a0001c0001t0002g0376 a0001c0001t0003g0054 others(15): Show |
18 | HG00735.hp2 HG01074.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.-29-32036_-29-3203 others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51918613 | |||||||
| chr14:51918617 | T | C | 1 | a0001c0001t0075g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-29-32033T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51918617 | |||||||
| chr14:51919112 | A | C | 1 | a0001c0001t0001g0252 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-29-31538A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51919112 | |||||||
| chr14:51919114 | C | T | 1 | a0001c0001t0004g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-29-31536C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51919114 | |||||||
| chr14:51919140 | GATTTTAC others(13): Show |
G | 113 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0075 others(110): Show |
113 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.-29-31488_-29-3146 others(24): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51919140 | ||||||
| chr14:51919145 | T | C | 19 | a0001c0001t0002g0281 a0001c0001t0002g0376 a0001c0001t0003g0054 others(16): Show |
19 | HG00735.hp2 HG01074.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-29-31505T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51919145 | |||||||
| chr14:51919209 | C | T | 2 | a0001c0001t0018g0367 a0001c0001t0037g0180 |
2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-29-31441C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51919209 | |||||||
| chr14:51919244 | A | G | 200 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(197): Show |
200 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.-29-31406A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51919244 | |||||||
| chr14:51919340 | T | C | 18 | a0001c0001t0002g0281 a0001c0001t0002g0376 a0001c0001t0003g0054 others(15): Show |
18 | HG00735.hp2 HG01074.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.-29-31310T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51919340 | |||||||
| chr14:51919385 | A | G | 1 | a0001c0001t0034g0377 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-29-31265A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51919385 | |||||||
| chr14:51919394 | A | C | 1 | a0001c0001t0001g0171 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-29-31256A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51919394 | |||||||
| chr14:51919485 | T | C | 2 | a0001c0001t0002g0348 a0001c0001t0005g0347 |
2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-29-31165T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51919485 | |||||||
| chr14:51919493 | C | T | 1 | a0001c0001t0018g0368 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-29-31157C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51919493 | |||||||
| chr14:51919521 | G | T | 1 | a0001c0002t0074g0040 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-29-31129G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51919521 | |||||||
| chr14:51919549 | A | C | 9 | a0001c0001t0003g0372 a0001c0001t0003g0374 a0001c0001t0003g0375 others(6): Show |
9 | HG02055.hp1 HG02109.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29-31101A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51919549 | |||||||
| chr14:51919670 | C | A | 2 | a0001c0001t0018g0323 a0001c0001t0018g0324 |
2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-29-30980C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51919670 | |||||||
| chr14:51919676 | C | A | 2 | a0001c0001t0018g0323 a0001c0001t0018g0324 |
2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-29-30974C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51919676 | |||||||
| chr14:51919708 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-29-30942G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51919708 | |||||||
| chr14:51919897 | A | T | 2 | a0001c0001t0018g0367 a0001c0001t0037g0180 |
2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-29-30753A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51919897 | |||||||
| chr14:51919945 | A | C | 1 | a0001c0001t0018g0368 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-29-30705A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51919945 | |||||||
| chr14:51919975 | G | A | 2 | a0001c0001t0003g0055 a0001c0001t0003g0056 |
2 | HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-29-30675G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51919975 | |||||||
| chr14:51919975 | G | T | 1 | a0001c0001t0002g0239 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-29-30675G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51919975 | |||||||
| chr14:51920169 | G | A | 1 | a0001c0001t0016g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-29-30481G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51920169 | |||||||
| chr14:51920174 | A | G | 1 | a0001c0001t0043g0336 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-29-30476A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51920174 | |||||||
| chr14:51920232 | C | T | 3 | a0001c0001t0003g0143 a0001c0001t0008g0141 a0001c0001t0008g0144 |
3 | HG01099.hp1 HG01943.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.-29-30418C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51920232 | |||||||
| chr14:51920347 | T | C | 2 | a0001c0001t0018g0367 a0001c0001t0037g0180 |
2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-29-30303T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51920347 | |||||||
| chr14:51920395 | GTAAA | G | 3 | a0001c0001t0001g0369 a0001c0001t0018g0367 a0001c0001t0037g0180 |
3 | HG02615.hp1 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-29-30252_-29-3024 others(8): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51920395 | ||||||
| chr14:51920465 | C | T | 12 | a0001c0001t0001g0025 a0001c0001t0003g0021 a0001c0001t0014g0018 others(9): Show |
12 | HG00738.hp1 HG01361.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.-29-30185C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51920465 | |||||||
| chr14:51920517 | C | T | 1 | a0001c0001t0051g0342 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-29-30133C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51920517 | |||||||
| chr14:51920642 | G | A | 3 | a0001c0001t0003g0143 a0001c0001t0008g0141 a0001c0001t0008g0144 |
3 | HG01099.hp1 HG01943.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.-29-30008G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51920642 | |||||||
| chr14:51920732 | A | G | 3 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0006g0177 |
3 | HG00642.hp1 HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-29-29918A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51920732 | |||||||
| chr14:51921208 | T | C | 1 | a0001c0001t0067g0065 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-29-29442T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51921208 | |||||||
| chr14:51921209 | C | G | 1 | a0001c0001t0067g0065 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-29-29441C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51921209 | |||||||
| chr14:51921220 | G | A | 1 | a0001c0001t0056g0014 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-29-29430G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51921220 | |||||||
| chr14:51921472 | T | C | 4 | a0001c0001t0018g0323 a0001c0001t0018g0324 a0001c0001t0075g0004 others(1): Show |
4 | HG02630.hp2 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-29178T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51921472 | |||||||
| chr14:51921482 | A | G | 1 | a0001c0001t0032g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-29-29168A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51921482 | |||||||
| chr14:51921589 | G | T | 1 | a0001c0001t0018g0368 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-29-29061G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51921589 | |||||||
| chr14:51921596 | A | C | 1 | a0001c0001t0046g0311 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-29-29054A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51921596 | |||||||
| chr14:51921609 | A | G | 1 | a0001c0001t0007g0255 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-29-29041A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51921609 | |||||||
| chr14:51921623 | G | C | 1 | a0001c0001t0016g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-29-29027G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51921623 | |||||||
| chr14:51921921 | C | A | 19 | a0001c0001t0002g0281 a0001c0001t0002g0376 a0001c0001t0003g0054 others(16): Show |
19 | HG00735.hp2 HG01074.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-29-28729C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51921921 | |||||||
| chr14:51921946 | C | A | 1 | a0001c0001t0018g0368 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-29-28704C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51921946 | |||||||
| chr14:51922069 | A | C | 1 | a0001c0001t0018g0368 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-29-28581A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51922069 | |||||||
| chr14:51922073 | A | C | 1 | a0001c0001t0018g0368 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-29-28577A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51922073 | |||||||
| chr14:51922113 | C | T | 16 | a0001c0001t0001g0172 a0001c0001t0001g0219 a0001c0001t0001g0270 others(13): Show |
16 | HG01099.hp2 HG01993.hp2 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.-29-28537C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51922113 | |||||||
| chr14:51922163 | G | A | 2 | a0001c0001t0051g0342 a0001c0002t0072g0196 |
2 | HG01433.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-29-28487G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51922163 | |||||||
| chr14:51922209 | AAG | A | 7 | a0001c0001t0003g0321 a0001c0001t0007g0194 a0001c0001t0007g0325 others(4): Show |
7 | HG00735.hp2 HG01074.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-28433_-29-2843 others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51922209 | ||||||
| chr14:51922225 | T | G | 1 | a0001c0001t0034g0377 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-29-28425T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51922225 | |||||||
| chr14:51922328 | A | G | 1 | a0001c0001t0018g0368 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-29-28322A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51922328 | |||||||
| chr14:51922482 | A | C | 1 | a0001c0001t0001g0248 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-29-28168A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51922482 | |||||||
| chr14:51922539 | A | C | 202 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(199): Show |
202 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(199): Show |
intron_variant | MODIFIER | c.-29-28111A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51922539 | |||||||
| chr14:51922585 | C | G | 3 | a0001c0001t0003g0321 a0001c0001t0008g0320 a0001c0001t0030g0130 |
3 | HG01081.hp2 HG01106.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.-29-28065C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51922585 | |||||||
| chr14:51922624 | C | T | 1 | a0001c0001t0002g0293 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-29-28026C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51922624 | |||||||
| chr14:51922658 | C | T | 2 | a0001c0001t0025g0097 a0001c0001t0033g0363 |
2 | NA18967.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-29-27992C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51922658 | |||||||
| chr14:51922670 | T | C | 35 | a0001c0001t0001g0012 a0001c0001t0001g0172 a0001c0001t0001g0219 others(32): Show |
35 | HG01074.hp2 HG01099.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.-29-27980T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51922670 | |||||||
| chr14:51922751 | A | T | 1 | a0001c0001t0018g0368 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-29-27899A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51922751 | |||||||
| chr14:51922781 | C | T | 2 | a0001c0001t0019g0051 a0001c0001t0036g0053 |
2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-29-27869C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51922781 | |||||||
| chr14:51922891 | G | A | 19 | a0001c0001t0001g0075 a0001c0001t0002g0281 a0001c0001t0002g0376 others(16): Show |
19 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.-29-27759G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51922891 | |||||||
| chr14:51922987 | C | G | 2 | a0001c0001t0018g0323 a0001c0001t0018g0324 |
2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-29-27663C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51922987 | |||||||
| chr14:51923091 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0009g0116 |
2 | NA18942.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.-29-27559A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51923091 | |||||||
| chr14:51923123 | A | T | 1 | a0001c0001t0002g0153 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-29-27527A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51923123 | |||||||
| chr14:51923337 | T | A | 3 | a0001c0001t0025g0213 a0001c0001t0025g0273 a0001c0001t0033g0315 |
3 | NA18980.hp2 NA19007.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-29-27313T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51923337 | |||||||
| chr14:51923341 | A | T | 16 | a0001c0001t0001g0172 a0001c0001t0001g0219 a0001c0001t0001g0270 others(13): Show |
16 | HG01099.hp2 HG01993.hp2 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.-29-27309A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51923341 | |||||||
| chr14:51923355 | G | T | 1 | a0001c0001t0003g0054 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-29-27295G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51923355 | |||||||
| chr14:51923438 | C | T | 35 | a0001c0001t0001g0012 a0001c0001t0001g0172 a0001c0001t0001g0219 others(32): Show |
35 | HG01074.hp2 HG01099.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.-29-27212C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51923438 | |||||||
| chr14:51923442 | A | AAT | 3 | a0001c0001t0001g0369 a0001c0001t0043g0336 a0001c0001t0051g0342 |
3 | HG02922.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-29-27194_-29-2719 others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51923442 | ||||||
| chr14:51923452 | T | A | 1 | a0001c0001t0018g0368 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-29-27198T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51923452 | |||||||
| chr14:51923513 | GTA | G | 81 | a0001c0001t0001g0057 a0001c0001t0001g0075 a0001c0001t0001g0113 others(78): Show |
81 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.-29-27129_-29-2712 others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51923513 | ||||||
| chr14:51923525 | G | A | 3 | a0001c0001t0024g0058 a0001c0001t0024g0059 a0001c0001t0024g0063 |
3 | HG02886.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-29-27125G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51923525 | |||||||
| chr14:51923537 | A | G | 16 | a0001c0001t0002g0281 a0001c0001t0002g0376 a0001c0001t0003g0321 others(13): Show |
16 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.-29-27113A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51923537 | |||||||
| chr14:51923567 | T | TAC | 194 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0038 others(191): Show |
194 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.-29-27065_-29-2706 others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51923567 | ||||||
| chr14:51923567 | T | TACACACA others(3): Show |
1 | a0001c0001t0001g0369 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-29-27073_-29-2706 others(14): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51923567 | ||||||
| chr14:51923567 | TAC | T | 58 | a0001c0001t0001g0025 a0001c0001t0001g0168 a0001c0001t0001g0171 others(55): Show |
58 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-29-27065_-29-2706 others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51923567 | ||||||
| chr14:51923772 | T | C | 81 | a0001c0001t0001g0057 a0001c0001t0001g0075 a0001c0001t0001g0113 others(78): Show |
81 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.-29-26878T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51923772 | |||||||
| chr14:51923906 | C | T | 1 | a0001c0001t0035g0378 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-29-26744C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51923906 | |||||||
| chr14:51924159 | C | G | 16 | a0001c0001t0002g0281 a0001c0001t0002g0376 a0001c0001t0003g0321 others(13): Show |
16 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.-29-26491C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51924159 | |||||||
| chr14:51924315 | G | T | 2 | a0001c0001t0002g0348 a0001c0001t0005g0347 |
2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-29-26335G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51924315 | |||||||
| chr14:51924473 | T | C | 60 | a0001c0001t0001g0025 a0001c0001t0001g0152 a0001c0001t0001g0168 others(57): Show |
60 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.-29-26177T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51924473 | |||||||
| chr14:51924533 | G | A | 1 | a0001c0001t0018g0368 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-29-26117G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51924533 | |||||||
| chr14:51924534 | A | G | 1 | a0001c0001t0018g0368 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-29-26116A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51924534 | |||||||
| chr14:51924609 | A | G | 1 | a0001c0001t0067g0065 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-29-26041A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51924609 | |||||||
| chr14:51924803 | A | G | 3 | a0001c0001t0001g0057 a0001c0001t0003g0054 a0001c0001t0017g0047 |
3 | HG03516.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-29-25847A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51924803 | |||||||
| chr14:51924901 | G | A | 2 | a0001c0001t0018g0367 a0001c0001t0037g0180 |
2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-29-25749G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51924901 | |||||||
| chr14:51924919 | T | C | 1 | a0001c0001t0034g0377 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-29-25731T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51924919 | |||||||
| chr14:51925114 | A | T | 1 | a0001c0001t0043g0336 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-29-25536A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51925114 | |||||||
| chr14:51925205 | A | G | 3 | a0001c0001t0003g0143 a0001c0001t0008g0141 a0001c0001t0008g0144 |
3 | HG01099.hp1 HG01943.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.-29-25445A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51925205 | |||||||
| chr14:51925251 | C | A | 17 | a0001c0001t0002g0281 a0001c0001t0002g0376 a0001c0001t0003g0321 others(14): Show |
17 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.-29-25399C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51925251 | |||||||
| chr14:51925410 | A | T | 1 | a0001c0001t0001g0212 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-29-25240A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51925410 | |||||||
| chr14:51925547 | G | A | 1 | a0001c0001t0030g0072 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-29-25103G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51925547 | |||||||
| chr14:51925611 | T | C | 2 | a0001c0001t0018g0367 a0001c0001t0037g0180 |
2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-29-25039T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51925611 | |||||||
| chr14:51925745 | G | A | 79 | a0001c0001t0001g0057 a0001c0001t0001g0075 a0001c0001t0001g0113 others(76): Show |
79 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.-29-24905G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51925745 | |||||||
| chr14:51925787 | AT | A | 191 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(188): Show |
191 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(188): Show |
intron_variant | MODIFIER | c.-29-24849delT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51925787 | ||||||
| chr14:51925935 | A | G | 1 | a0001c0001t0006g0073 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-29-24715A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51925935 | |||||||
| chr14:51926240 | A | G | 4 | a0001c0001t0003g0372 a0001c0001t0003g0374 a0001c0001t0003g0375 others(1): Show |
4 | HG02055.hp1 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-24410A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51926240 | |||||||
| chr14:51926509 | C | A | 1 | a0001c0001t0008g0149 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-29-24141C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51926509 | |||||||
| chr14:51926582 | G | A | 1 | a0001c0001t0071g0118 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-29-24068G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51926582 | |||||||
| chr14:51926646 | C | T | 1 | a0001c0001t0014g0088 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-29-24004C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51926646 | |||||||
| chr14:51926647 | G | A | 1 | a0001c0001t0006g0073 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-29-24003G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51926647 | |||||||
| chr14:51926661 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-29-23989G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51926661 | |||||||
| chr14:51926679 | T | C | 79 | a0001c0001t0001g0057 a0001c0001t0001g0075 a0001c0001t0001g0113 others(76): Show |
79 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.-29-23971T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51926679 | |||||||
| chr14:51926694 | G | T | 115 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0075 others(112): Show |
115 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.-29-23956G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51926694 | |||||||
| chr14:51926695 | A | C | 115 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0075 others(112): Show |
115 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.-29-23955A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51926695 | |||||||
| chr14:51926751 | A | G | 1 | a0001c0001t0001g0369 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-29-23899A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51926751 | |||||||
| chr14:51926754 | G | A | 1 | a0001c0001t0001g0369 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-29-23896G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51926754 | |||||||
| chr14:51926787 | A | G | 20 | a0001c0001t0002g0281 a0001c0001t0002g0376 a0001c0001t0003g0321 others(17): Show |
20 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-29-23863A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51926787 | |||||||
| chr14:51926797 | T | G | 11 | a0001c0001t0002g0003 a0001c0001t0002g0064 a0001c0001t0002g0348 others(8): Show |
11 | HG01358.hp1 HG02486.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-29-23853T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51926797 | |||||||
| chr14:51926854 | A | AC | 4 | a0001c0001t0005g0347 a0001c0001t0042g0282 a0001c0001t0060g0147 others(1): Show |
4 | HG01891.hp1 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-23792dupC | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51926854 | ||||||
| chr14:51927018 | G | A | 1 | a0001c0001t0001g0369 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-29-23632G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51927018 | |||||||
| chr14:51927311 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-29-23339C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51927311 | |||||||
| chr14:51927448 | A | G | 1 | a0001c0001t0031g0112 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-29-23202A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51927448 | |||||||
| chr14:51927546 | A | G | 1 | a0001c0001t0016g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-29-23104A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51927546 | |||||||
| chr14:51927696 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-29-22954G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51927696 | |||||||
| chr14:51927738 | G | T | 1 | a0001c0001t0001g0294 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-29-22912G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51927738 | |||||||
| chr14:51927858 | T | TTTG | 3 | a0001c0001t0001g0012 a0001c0001t0016g0351 a0001c0002t0073g0010 |
3 | HG02486.hp1 HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-29-22768_-29-2276 others(7): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51927858 | ||||||
| chr14:51927858 | TTTG | T | 17 | a0001c0001t0002g0281 a0001c0001t0002g0376 a0001c0001t0003g0321 others(14): Show |
17 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.-29-22768_-29-2276 others(7): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51927858 | ||||||
| chr14:51928026 | C | CT | 8 | a0001c0001t0001g0052 a0001c0001t0001g0178 a0001c0001t0002g0069 others(5): Show |
8 | HG01175.hp2 HG01243.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29-22603dupT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51928026 | ||||||
| chr14:51928026 | CT | C | 76 | a0001c0001t0001g0075 a0001c0001t0001g0135 a0001c0001t0001g0221 others(73): Show |
76 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.-29-22603delT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51928026 | ||||||
| chr14:51928026 | CTT | C | 108 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0152 others(105): Show |
108 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.-29-22604_-29-2260 others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51928026 | ||||||
| chr14:51928026 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0193 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-29-22613_-29-2260 others(15): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51928026 | ||||||
| chr14:51928027 | T | TC | 5 | a0001c0001t0001g0113 a0001c0001t0001g0240 a0001c0001t0001g0271 others(2): Show |
5 | HG00621.hp1 HG02056.hp2 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29-22623_-29-2262 others(5): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928027 | |||||||
| chr14:51928028 | T | C | 2 | a0001c0001t0009g0268 a0001c0001t0018g0368 |
2 | HG00621.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-29-22622T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928028 | |||||||
| chr14:51928313 | G | C | 9 | a0001c0001t0003g0372 a0001c0001t0003g0374 a0001c0001t0003g0375 others(6): Show |
9 | HG01074.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29-22337G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928313 | |||||||
| chr14:51928348 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-29-22302G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928348 | |||||||
| chr14:51928366 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0011g0192 |
2 | NA18941.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.-29-22284G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928366 | |||||||
| chr14:51928399 | T | A | 1 | a0001c0001t0034g0377 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-29-22251T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928399 | |||||||
| chr14:51928514 | A | G | 1 | a0001c0001t0004g0197 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-29-22136A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928514 | |||||||
| chr14:51928517 | A | G | 1 | a0001c0001t0004g0197 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-29-22133A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928517 | |||||||
| chr14:51928521 | A | G | 1 | a0001c0001t0004g0197 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-29-22129A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928521 | |||||||
| chr14:51928530 | C | T | 1 | a0001c0001t0004g0197 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-29-22120C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928530 | |||||||
| chr14:51928558 | A | G | 1 | a0001c0001t0004g0197 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-29-22092A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928558 | |||||||
| chr14:51928572 | G | A | 1 | a0001c0001t0004g0197 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-29-22078G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928572 | |||||||
| chr14:51928604 | C | T | 1 | a0001c0001t0004g0197 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-29-22046C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928604 | |||||||
| chr14:51928619 | C | T | 20 | a0001c0001t0001g0369 a0001c0001t0002g0281 a0001c0001t0002g0376 others(17): Show |
20 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-29-22031C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928619 | |||||||
| chr14:51928631 | A | T | 1 | a0001c0001t0004g0197 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-29-22019A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928631 | |||||||
| chr14:51928673 | G | A | 1 | a0001c0001t0032g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-29-21977G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928673 | |||||||
| chr14:51928683 | G | T | 2 | a0001c0001t0016g0351 a0001c0002t0073g0010 |
2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-29-21967G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928683 | |||||||
| chr14:51928702 | C | T | 1 | a0001c0001t0003g0307 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-29-21948C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928702 | |||||||
| chr14:51928762 | A | G | 1 | a0001c0001t0067g0065 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-29-21888A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928762 | |||||||
| chr14:51928806 | G | A | 1 | a0001c0001t0007g0325 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-29-21844G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928806 | |||||||
| chr14:51928853 | G | A | 6 | a0001c0001t0001g0207 a0001c0001t0002g0084 a0001c0001t0002g0181 others(3): Show |
6 | NA18951.hp2 NA18967.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29-21797G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928853 | |||||||
| chr14:51928863 | G | A | 1 | a0001c0001t0018g0324 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-29-21787G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928863 | |||||||
| chr14:51928873 | G | A | 1 | a0001c0001t0065g0026 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-29-21777G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928873 | |||||||
| chr14:51928901 | C | A | 2 | a0001c0001t0018g0367 a0001c0001t0037g0180 |
2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-29-21749C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928901 | |||||||
| chr14:51928927 | G | A | 1 | a0001c0001t0003g0054 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-29-21723G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928927 | |||||||
| chr14:51928929 | C | A | 1 | a0001c0001t0067g0065 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-29-21721C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928929 | |||||||
| chr14:51928963 | C | T | 2 | a0001c0001t0018g0367 a0001c0001t0037g0180 |
2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-29-21687C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51928963 | |||||||
| chr14:51929150 | C | A | 1 | a0001c0001t0067g0065 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-29-21500C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51929150 | |||||||
| chr14:51929264 | A | G | 1 | a0001c0001t0001g0369 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-29-21386A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51929264 | |||||||
| chr14:51929292 | C | T | 6 | a0001c0001t0001g0215 a0001c0001t0002g0079 a0001c0001t0005g0080 others(3): Show |
6 | NA18964.hp1 NA18969.hp1 NA19056.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29-21358C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51929292 | |||||||
| chr14:51929329 | G | A | 197 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(194): Show |
197 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(194): Show |
intron_variant | MODIFIER | c.-29-21321G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51929329 | |||||||
| chr14:51929394 | G | A | 1 | a0001c0001t0008g0149 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-29-21256G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51929394 | |||||||
| chr14:51929411 | A | G | 1 | a0001c0001t0018g0368 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-29-21239A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51929411 | |||||||
| chr14:51929412 | G | A | 1 | a0001c0001t0018g0368 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-29-21238G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51929412 | |||||||
| chr14:51929413 | A | T | 1 | a0001c0001t0005g0129 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-29-21237A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51929413 | |||||||
| chr14:51929486 | G | A | 36 | a0001c0001t0001g0012 a0001c0001t0001g0172 a0001c0001t0001g0219 others(33): Show |
36 | HG01074.hp2 HG01099.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.-29-21164G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51929486 | |||||||
| chr14:51929496 | G | T | 1 | a0001c0001t0001g0369 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-29-21154G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51929496 | |||||||
| chr14:51929515 | G | A | 79 | a0001c0001t0001g0057 a0001c0001t0001g0075 a0001c0001t0001g0113 others(76): Show |
79 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.-29-21135G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51929515 | |||||||
| chr14:51929559 | A | G | 1 | a0001c0001t0011g0316 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-29-21091A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51929559 | |||||||
| chr14:51929563 | G | A | 3 | a0001c0001t0004g0339 a0001c0001t0009g0340 a0001c0001t0009g0353 |
3 | HG01099.hp2 HG01993.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.-29-21087G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51929563 | |||||||
| chr14:51929679 | T | A | 36 | a0001c0001t0001g0012 a0001c0001t0001g0172 a0001c0001t0001g0219 others(33): Show |
36 | HG01074.hp2 HG01099.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.-29-20971T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51929679 | |||||||
| chr14:51929779 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-29-20871A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51929779 | |||||||
| chr14:51929826 | G | A | 140 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0001c0001t0001g0075 others(137): Show |
140 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.-29-20824G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51929826 | |||||||
| chr14:51929939 | A | C | 2 | a0001c0001t0018g0367 a0001c0001t0037g0180 |
2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-29-20711A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51929939 | |||||||
| chr14:51929968 | G | A | 2 | a0001c0001t0001g0369 a0001c0001t0004g0197 |
2 | HG01496.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-29-20682G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51929968 | |||||||
| chr14:51929984 | A | G | 4 | a0001c0001t0015g0132 a0001c0001t0015g0136 a0001c0001t0015g0138 others(1): Show |
4 | NA18946.hp1 NA19002.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-20666A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51929984 | |||||||
| chr14:51930009 | T | C | 1 | a0001c0001t0021g0208 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-29-20641T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51930009 | |||||||
| chr14:51930183 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-29-20467G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51930183 | |||||||
| chr14:51930414 | G | A | 17 | a0001c0001t0002g0281 a0001c0001t0002g0376 a0001c0001t0003g0321 others(14): Show |
17 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.-29-20236G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51930414 | |||||||
| chr14:51930605 | G | A | 1 | a0001c0001t0004g0117 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-29-20045G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51930605 | |||||||
| chr14:51930697 | A | G | 1 | a0001c0001t0001g0369 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-29-19953A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51930697 | |||||||
| chr14:51930778 | C | T | 79 | a0001c0001t0001g0057 a0001c0001t0001g0075 a0001c0001t0001g0113 others(76): Show |
79 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.-29-19872C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51930778 | |||||||
| chr14:51930821 | G | A | 1 | a0001c0001t0001g0369 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-29-19829G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51930821 | |||||||
| chr14:51930843 | A | G | 1 | a0001c0001t0025g0097 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-29-19807A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51930843 | |||||||
| chr14:51930937 | G | A | 2 | a0001c0001t0018g0367 a0001c0001t0037g0180 |
2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-29-19713G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51930937 | |||||||
| chr14:51930946 | A | G | 58 | a0001c0001t0001g0025 a0001c0001t0001g0152 a0001c0001t0001g0168 others(55): Show |
58 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.-29-19704A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51930946 | |||||||
| chr14:51931008 | A | T | 2 | a0001c0001t0016g0351 a0001c0002t0073g0010 |
2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-29-19642A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51931008 | |||||||
| chr14:51931065 | T | C | 1 | a0001c0001t0047g0298 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-29-19585T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51931065 | |||||||
| chr14:51931073 | G | C | 1 | a0001c0001t0034g0364 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-29-19577G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51931073 | |||||||
| chr14:51931114 | G | A | 64 | a0001c0001t0001g0025 a0001c0001t0001g0152 a0001c0001t0001g0168 others(61): Show |
64 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.-29-19536G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51931114 | |||||||
| chr14:51931192 | G | C | 1 | a0001c0001t0034g0377 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-29-19458G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51931192 | |||||||
| chr14:51931285 | C | G | 1 | a0001c0001t0001g0233 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-29-19365C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51931285 | |||||||
| chr14:51931286 | T | C | 63 | a0001c0001t0001g0025 a0001c0001t0001g0152 a0001c0001t0001g0168 others(60): Show |
63 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.-29-19364T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51931286 | |||||||
| chr14:51931287 | G | C | 64 | a0001c0001t0001g0025 a0001c0001t0001g0152 a0001c0001t0001g0168 others(61): Show |
64 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.-29-19363G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51931287 | |||||||
| chr14:51931412 | G | A | 1 | a0001c0001t0067g0065 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-29-19238G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51931412 | |||||||
| chr14:51931514 | A | G | 1 | a0001c0001t0001g0369 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-29-19136A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51931514 | |||||||
| chr14:51931556 | T | G | 200 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(197): Show |
200 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.-29-19094T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51931556 | |||||||
| chr14:51931613 | G | A | 2 | a0001c0001t0001g0249 a0001c0001t0019g0074 |
2 | HG01074.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-29-19037G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51931613 | |||||||
| chr14:51931737 | G | C | 201 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(198): Show |
201 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.-29-18913G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51931737 | |||||||
| chr14:51931973 | G | A | 2 | a0001c0001t0019g0051 a0001c0001t0036g0053 |
2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-29-18677G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51931973 | |||||||
| chr14:51931974 | C | T | 198 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(195): Show |
198 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.-29-18676C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51931974 | |||||||
| chr14:51931985 | G | A | 1 | a0001c0001t0002g0060 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-29-18665G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51931985 | |||||||
| chr14:51931986 | C | G | 198 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(195): Show |
198 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.-29-18664C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51931986 | |||||||
| chr14:51932074 | G | A | 1 | a0001c0001t0075g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-29-18576G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51932074 | |||||||
| chr14:51932074 | G | C | 1 | a0001c0001t0012g0189 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-29-18576G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51932074 | |||||||
| chr14:51932150 | G | A | 1 | a0001c0001t0001g0369 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-29-18500G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51932150 | |||||||
| chr14:51932246 | C | CA | 23 | a0001c0001t0001g0052 a0001c0001t0001g0140 a0001c0001t0001g0150 others(20): Show |
23 | HG00323.hp1 HG00544.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.-29-18378dupA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51932246 | ||||||
| chr14:51932246 | CAAAA | C | 11 | a0001c0001t0002g0003 a0001c0001t0002g0064 a0001c0001t0002g0348 others(8): Show |
11 | HG01358.hp1 HG02486.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-29-18381_-29-1837 others(8): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51932246 | ||||||
| chr14:51932246 | CAAAAAA | C | 17 | a0001c0001t0002g0281 a0001c0001t0002g0376 a0001c0001t0003g0321 others(14): Show |
17 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.-29-18383_-29-1837 others(10): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51932246 | ||||||
| chr14:51932269 | A | G | 17 | a0001c0001t0002g0281 a0001c0001t0002g0376 a0001c0001t0003g0321 others(14): Show |
17 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.-29-18381A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51932269 | |||||||
| chr14:51932271 | A | AAAAAAG | 31 | a0001c0001t0001g0171 a0001c0001t0001g0212 a0001c0001t0001g0263 others(28): Show |
31 | HG00621.hp2 HG00741.hp2 HG02027.hp2 others(28): Show |
intron_variant | MODIFIER | c.-29-18378_-29-1837 others(10): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51932271 | ||||||
| chr14:51932271 | A | AAAAAG | 96 | a0001c0001t0001g0025 a0001c0001t0001g0075 a0001c0001t0001g0113 others(93): Show |
96 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.-29-18378_-29-1837 others(9): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51932271 | ||||||
| chr14:51932271 | A | AAAAG | 17 | a0001c0001t0001g0057 a0001c0001t0001g0357 a0001c0001t0002g0222 others(14): Show |
17 | HG01243.hp1 HG01891.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.-29-18378_-29-1837 others(8): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51932271 | ||||||
| chr14:51932271 | A | AAAG | 19 | a0001c0001t0001g0012 a0001c0001t0001g0172 a0001c0001t0001g0219 others(16): Show |
19 | HG01099.hp2 HG01993.hp2 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.-29-18378_-29-1837 others(7): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51932271 | ||||||
| chr14:51932271 | A | AAG | 13 | a0001c0001t0001g0369 a0001c0001t0003g0372 a0001c0001t0003g0374 others(10): Show |
13 | HG01074.hp2 HG01496.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-29-18377_-29-1837 others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51932271 | ||||||
| chr14:51932271 | A | G | 19 | a0001c0001t0002g0281 a0001c0001t0002g0376 a0001c0001t0003g0321 others(16): Show |
19 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.-29-18379A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51932271 | |||||||
| chr14:51932284 | A | G | 198 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(195): Show |
198 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.-29-18366A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51932284 | |||||||
| chr14:51932515 | C | T | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-29-18135C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51932515 | |||||||
| chr14:51932528 | G | A | 5 | a0001c0001t0002g0281 a0001c0001t0002g0376 a0001c0001t0007g0044 others(2): Show |
5 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29-18122G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51932528 | |||||||
| chr14:51932555 | T | A | 1 | a0001c0001t0012g0337 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-29-18095T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51932555 | |||||||
| chr14:51932613 | G | C | 2 | a0001c0001t0002g0329 a0001c0001t0005g0013 |
2 | HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-29-18037G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51932613 | |||||||
| chr14:51932639 | A | T | 2 | a0001c0001t0004g0145 a0001c0001t0004g0146 |
2 | HG03704.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-29-18011A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51932639 | |||||||
| chr14:51932662 | A | G | 132 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0075 others(129): Show |
132 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.-29-17988A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51932662 | |||||||
| chr14:51932683 | C | T | 1 | a0001c0001t0027g0104 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-29-17967C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51932683 | |||||||
| chr14:51932721 | C | A | 5 | a0001c0001t0007g0194 a0001c0001t0007g0325 a0001c0001t0030g0130 others(2): Show |
5 | HG00735.hp2 HG01109.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29-17929C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51932721 | |||||||
| chr14:51932775 | A | G | 57 | a0001c0001t0001g0025 a0001c0001t0001g0152 a0001c0001t0001g0168 others(54): Show |
57 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.-29-17875A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51932775 | |||||||
| chr14:51933066 | G | T | 1 | a0001c0001t0001g0057 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-29-17584G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51933066 | |||||||
| chr14:51933075 | C | T | 81 | a0001c0001t0001g0057 a0001c0001t0001g0075 a0001c0001t0001g0113 others(78): Show |
81 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.-29-17575C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51933075 | |||||||
| chr14:51933241 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-29-17409G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51933241 | |||||||
| chr14:51933318 | A | G | 80 | a0001c0001t0001g0057 a0001c0001t0001g0075 a0001c0001t0001g0113 others(77): Show |
80 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.-29-17332A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51933318 | |||||||
| chr14:51933336 | C | T | 124 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0075 others(121): Show |
124 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.-29-17314C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51933336 | |||||||
| chr14:51933514 | T | A | 1 | a0001c0001t0018g0367 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-29-17136T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51933514 | |||||||
| chr14:51933621 | G | C | 49 | a0001c0001t0001g0012 a0001c0001t0001g0172 a0001c0001t0002g0003 others(46): Show |
49 | HG01074.hp2 HG01099.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-29-17029G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51933621 | |||||||
| chr14:51933659 | G | A | 193 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(190): Show |
193 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(190): Show |
intron_variant | MODIFIER | c.-29-16991G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51933659 | |||||||
| chr14:51933679 | G | T | 4 | a0001c0001t0012g0163 a0001c0001t0012g0189 a0001c0001t0012g0246 others(1): Show |
4 | NA18950.hp2 NA18995.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-16971G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51933679 | |||||||
| chr14:51933775 | G | C | 1 | a0001c0001t0002g0153 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-29-16875G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51933775 | |||||||
| chr14:51934350 | A | G | 337 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0034 others(334): Show |
338 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.-29-16300A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51934350 | |||||||
| chr14:51934477 | A | G | 1 | a0001c0001t0001g0283 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-29-16173A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51934477 | |||||||
| chr14:51934479 | C | T | 1 | a0001c0001t0003g0120 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-29-16171C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51934479 | |||||||
| chr14:51934494 | G | T | 29 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(26): Show |
29 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.-29-16156G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51934494 | |||||||
| chr14:51934860 | C | T | 1 | a0001c0001t0009g0116 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-29-15790C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51934860 | |||||||
| chr14:51935021 | C | CT | 68 | a0001c0001t0001g0052 a0001c0001t0001g0140 a0001c0001t0001g0206 others(65): Show |
68 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.-29-15626dupT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51935021 | ||||||
| chr14:51935021 | C | CTT | 17 | a0001c0001t0002g0009 a0001c0001t0002g0071 a0001c0001t0002g0089 others(14): Show |
17 | HG00597.hp1 HG01070.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.-29-15627_-29-1562 others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51935021 | ||||||
| chr14:51935021 | C | CTTT | 3 | a0001c0001t0002g0366 a0001c0001t0005g0253 a0001c0001t0033g0363 |
3 | NA18967.hp2 NA18975.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-29-15628_-29-1562 others(7): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51935021 | ||||||
| chr14:51935023 | TTC | T | 32 | a0001c0001t0001g0175 a0001c0001t0001g0289 a0001c0001t0002g0061 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-29-15625_-29-1562 others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51935023 | ||||||
| chr14:51935024 | TC | T | 110 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0001c0001t0001g0152 others(107): Show |
110 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.-29-15625delC | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51935024 | |||||||
| chr14:51935025 | C | T | 216 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0034 others(213): Show |
216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.-29-15625C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51935025 | |||||||
| chr14:51935027 | T | C | 1 | a0001c0001t0051g0342 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-29-15623T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51935027 | |||||||
| chr14:51935041 | T | G | 6 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0009g0042 others(3): Show |
6 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-15609T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51935041 | |||||||
| chr14:51935056 | G | C | 1 | a0001c0001t0046g0311 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-29-15594G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51935056 | |||||||
| chr14:51935073 | G | A | 31 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(28): Show |
31 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.-29-15577G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51935073 | |||||||
| chr14:51935073 | G | T | 1 | a0001c0001t0042g0282 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-29-15577G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51935073 | |||||||
| chr14:51935085 | C | T | 92 | a0001c0001t0001g0025 a0001c0001t0001g0152 a0001c0001t0001g0168 others(89): Show |
92 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.-29-15565C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51935085 | |||||||
| chr14:51935103 | T | C | 1 | a0001c0001t0002g0214 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-29-15547T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51935103 | |||||||
| chr14:51935129 | G | A | 31 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(28): Show |
31 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.-29-15521G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51935129 | |||||||
| chr14:51935231 | TAGTC | T | 8 | a0001c0001t0001g0057 a0001c0001t0003g0054 a0001c0001t0004g0326 others(5): Show |
8 | HG01074.hp2 HG02258.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29-15416_-29-1541 others(8): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51935231 | ||||||
| chr14:51935239 | A | T | 70 | a0001c0001t0001g0206 a0001c0001t0001g0215 a0001c0001t0001g0270 others(67): Show |
70 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.-29-15411A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51935239 | |||||||
| chr14:51935241 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-29-15409A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51935241 | |||||||
| chr14:51935260 | C | T | 1 | a0001c0001t0002g0293 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-29-15390C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51935260 | |||||||
| chr14:51935316 | C | T | 85 | a0001c0001t0001g0025 a0001c0001t0001g0168 a0001c0001t0001g0175 others(82): Show |
85 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.-29-15334C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51935316 | |||||||
| chr14:51935325 | C | A | 30 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(27): Show |
30 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.-29-15325C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51935325 | |||||||
| chr14:51935728 | GT | G | 31 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(28): Show |
31 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.-29-14920delT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51935728 | ||||||
| chr14:51935759 | G | A | 6 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0009g0042 others(3): Show |
6 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-14891G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51935759 | |||||||
| chr14:51935766 | G | A | 7 | a0001c0001t0003g0021 a0001c0001t0014g0018 a0001c0001t0014g0309 others(4): Show |
7 | HG02257.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-14884G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51935766 | |||||||
| chr14:51935773 | T | C | 6 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0009g0042 others(3): Show |
6 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-14877T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51935773 | |||||||
| chr14:51935855 | G | A | 15 | a0001c0001t0001g0057 a0001c0001t0003g0054 a0001c0001t0004g0041 others(12): Show |
15 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.-29-14795G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51935855 | |||||||
| chr14:51935857 | G | T | 31 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(28): Show |
31 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.-29-14793G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51935857 | |||||||
| chr14:51935924 | A | T | 31 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(28): Show |
31 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.-29-14726A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51935924 | |||||||
| chr14:51935991 | A | G | 1 | a0001c0001t0066g0032 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-29-14659A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51935991 | |||||||
| chr14:51936064 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-29-14586A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51936064 | |||||||
| chr14:51936169 | G | C | 1 | a0001c0001t0035g0378 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-29-14481G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51936169 | |||||||
| chr14:51936409 | G | T | 5 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0009g0042 others(2): Show |
5 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29-14241G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51936409 | |||||||
| chr14:51936427 | TAAATAGC others(6): Show |
T | 1 | a0001c0001t0075g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-29-14211_-29-1419 others(17): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51936427 | ||||||
| chr14:51936446 | G | A | 1 | a0001c0001t0019g0051 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-29-14204G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51936446 | |||||||
| chr14:51936515 | C | CT | 171 | a0001c0001t0001g0025 a0001c0001t0001g0168 a0001c0001t0001g0175 others(168): Show |
171 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.-29-14120dupT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51936515 | ||||||
| chr14:51936515 | C | CTT | 8 | a0001c0001t0001g0057 a0001c0001t0003g0054 a0001c0001t0004g0326 others(5): Show |
8 | HG01074.hp2 HG02258.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29-14121_-29-1412 others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51936515 | ||||||
| chr14:51936515 | CT | C | 33 | a0001c0001t0001g0289 a0001c0001t0001g0304 a0001c0001t0002g0061 others(30): Show |
33 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.-29-14120delT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51936515 | ||||||
| chr14:51936540 | A | AT | 80 | a0001c0001t0001g0206 a0001c0001t0001g0215 a0001c0001t0001g0270 others(77): Show |
80 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.-29-14098dupT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51936540 | ||||||
| chr14:51936540 | AT | A | 31 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(28): Show |
31 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.-29-14098delT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51936540 | ||||||
| chr14:51936603 | C | G | 8 | a0001c0001t0001g0057 a0001c0001t0003g0054 a0001c0001t0004g0326 others(5): Show |
8 | HG01074.hp2 HG02258.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29-14047C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51936603 | |||||||
| chr14:51936604 | G | A | 124 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0037 others(121): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.-29-14046G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51936604 | |||||||
| chr14:51936626 | T | C | 1 | a0001c0001t0008g0141 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-29-14024T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51936626 | |||||||
| chr14:51936708 | G | A | 84 | a0001c0001t0001g0025 a0001c0001t0001g0168 a0001c0001t0001g0175 others(81): Show |
84 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.-29-13942G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51936708 | |||||||
| chr14:51936791 | T | C | 33 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(30): Show |
33 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.-29-13859T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51936791 | |||||||
| chr14:51936838 | T | C | 33 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(30): Show |
33 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.-29-13812T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51936838 | |||||||
| chr14:51936902 | G | T | 1 | a0001c0001t0005g0300 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-29-13748G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51936902 | |||||||
| chr14:51936966 | C | T | 33 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(30): Show |
33 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.-29-13684C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51936966 | |||||||
| chr14:51937033 | T | C | 70 | a0001c0001t0001g0206 a0001c0001t0001g0215 a0001c0001t0001g0270 others(67): Show |
70 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.-29-13617T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51937033 | |||||||
| chr14:51937063 | C | A | 1 | a0001c0001t0001g0029 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-29-13587C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51937063 | |||||||
| chr14:51937108 | C | A | 68 | a0001c0001t0001g0206 a0001c0001t0001g0270 a0001c0001t0001g0299 others(65): Show |
68 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.-29-13542C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51937108 | |||||||
| chr14:51937215 | G | A | 1 | a0001c0001t0027g0179 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-29-13435G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51937215 | |||||||
| chr14:51937255 | A | C | 104 | a0001c0001t0001g0206 a0001c0001t0001g0215 a0001c0001t0001g0270 others(101): Show |
104 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.-29-13395A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51937255 | |||||||
| chr14:51937258 | A | C | 14 | a0001c0001t0001g0057 a0001c0001t0003g0054 a0001c0001t0004g0041 others(11): Show |
14 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-29-13392A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51937258 | |||||||
| chr14:51937298 | A | T | 1 | a0001c0001t0001g0168 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-29-13352A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51937298 | |||||||
| chr14:51937336 | A | G | 118 | a0001c0001t0001g0057 a0001c0001t0001g0206 a0001c0001t0001g0215 others(115): Show |
118 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.-29-13314A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51937336 | |||||||
| chr14:51937339 | G | A | 1 | a0001c0001t0046g0311 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-29-13311G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51937339 | |||||||
| chr14:51937375 | A | T | 33 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(30): Show |
33 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.-29-13275A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51937375 | |||||||
| chr14:51937413 | T | C | 85 | a0001c0001t0001g0057 a0001c0001t0001g0206 a0001c0001t0001g0215 others(82): Show |
85 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.-29-13237T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51937413 | |||||||
| chr14:51937422 | G | A | 6 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0009g0042 others(3): Show |
6 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-13228G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51937422 | |||||||
| chr14:51937429 | T | C | 60 | a0001c0001t0001g0206 a0001c0001t0001g0215 a0001c0001t0001g0270 others(57): Show |
60 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.-29-13221T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51937429 | |||||||
| chr14:51937578 | G | A | 1 | a0001c0001t0078g0077 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-29-13072G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51937578 | |||||||
| chr14:51937614 | AAATACAT others(118): Show |
A | 116 | a0001c0001t0001g0057 a0001c0001t0001g0206 a0001c0001t0001g0215 others(113): Show |
116 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.-29-13022_-29-1289 others(4): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51937614 | ||||||
| chr14:51937623 | A | AT | 47 | a0001c0001t0001g0358 a0001c0001t0002g0008 a0001c0001t0002g0009 others(44): Show |
47 | HG00621.hp2 HG00741.hp2 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.-29-13012dupT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51937623 | ||||||
| chr14:51937623 | A | ATT | 22 | a0001c0001t0001g0212 a0001c0001t0002g0348 a0001c0001t0003g0021 others(19): Show |
22 | HG00639.hp2 HG00738.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.-29-13013_-29-1301 others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51937623 | ||||||
| chr14:51937623 | A | ATTT | 54 | a0001c0001t0001g0025 a0001c0001t0001g0168 a0001c0001t0001g0175 others(51): Show |
54 | HG00323.hp2 HG00642.hp2 HG01255.hp1 others(51): Show |
intron_variant | MODIFIER | c.-29-13014_-29-1301 others(7): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51937623 | ||||||
| chr14:51937623 | AT | A | 112 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0034 others(109): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.-29-13012delT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51937623 | ||||||
| chr14:51937623 | ATT | A | 18 | a0001c0001t0001g0075 a0001c0001t0001g0140 a0001c0001t0001g0150 others(15): Show |
18 | HG00323.hp1 HG00609.hp2 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.-29-13013_-29-1301 others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51937623 | ||||||
| chr14:51937848 | T | C | 4 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0009g0042 others(1): Show |
4 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-12802T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51937848 | |||||||
| chr14:51937866 | C | T | 1 | a0001c0001t0075g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-29-12784C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51937866 | |||||||
| chr14:51937932 | T | G | 69 | a0001c0001t0001g0206 a0001c0001t0001g0215 a0001c0001t0001g0270 others(66): Show |
69 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.-29-12718T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51937932 | |||||||
| chr14:51937973 | C | T | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-29-12677C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51937973 | |||||||
| chr14:51937988 | A | G | 15 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0003g0055 others(12): Show |
15 | HG01496.hp2 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-29-12662A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51937988 | |||||||
| chr14:51938005 | G | A | 78 | a0001c0001t0001g0057 a0001c0001t0001g0206 a0001c0001t0001g0215 others(75): Show |
78 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-29-12645G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51938005 | |||||||
| chr14:51938023 | G | A | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-29-12627G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51938023 | |||||||
| chr14:51938161 | C | G | 110 | a0001c0001t0001g0057 a0001c0001t0001g0206 a0001c0001t0001g0215 others(107): Show |
110 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.-29-12489C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51938161 | |||||||
| chr14:51938194 | C | T | 223 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0001c0001t0001g0168 others(220): Show |
223 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.-29-12456C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51938194 | |||||||
| chr14:51938200 | C | A | 1 | a0001c0001t0006g0073 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-29-12450C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51938200 | |||||||
| chr14:51938238 | T | C | 3 | a0001c0001t0018g0323 a0001c0001t0018g0324 a0001c0001t0047g0298 |
3 | HG02809.hp1 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-29-12412T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51938238 | |||||||
| chr14:51938294 | C | A | 70 | a0001c0001t0001g0206 a0001c0001t0001g0215 a0001c0001t0001g0270 others(67): Show |
70 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.-29-12356C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51938294 | |||||||
| chr14:51938375 | G | A | 1 | a0001c0001t0016g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-29-12275G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51938375 | |||||||
| chr14:51938505 | T | G | 102 | a0001c0001t0001g0206 a0001c0001t0001g0215 a0001c0001t0001g0270 others(99): Show |
102 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.-29-12145T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51938505 | |||||||
| chr14:51938544 | G | T | 109 | a0001c0001t0001g0057 a0001c0001t0001g0206 a0001c0001t0001g0215 others(106): Show |
109 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.-29-12106G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51938544 | |||||||
| chr14:51938560 | T | G | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-29-12090T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51938560 | |||||||
| chr14:51938570 | C | T | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-29-12080C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51938570 | |||||||
| chr14:51938781 | T | G | 2 | a0001c0001t0043g0336 a0001c0001t0051g0342 |
2 | HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-29-11869T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51938781 | |||||||
| chr14:51938871 | G | C | 2 | a0001c0001t0012g0148 a0001c0001t0012g0155 |
2 | NA18939.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.-29-11779G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51938871 | |||||||
| chr14:51938914 | G | A | 7 | a0001c0001t0001g0057 a0001c0001t0004g0326 a0001c0001t0009g0033 others(4): Show |
7 | HG01074.hp2 HG02258.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-11736G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51938914 | |||||||
| chr14:51938939 | A | G | 1 | a0001c0001t0005g0254 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-29-11711A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51938939 | |||||||
| chr14:51938979 | T | G | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-29-11671T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51938979 | |||||||
| chr14:51939156 | C | T | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-29-11494C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51939156 | |||||||
| chr14:51939267 | T | G | 3 | a0001c0001t0045g0290 a0001c0001t0063g0005 a0001c0001t0069g0209 |
3 | HG02723.hp2 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-29-11383T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51939267 | |||||||
| chr14:51939271 | A | G | 83 | a0001c0001t0001g0057 a0001c0001t0001g0206 a0001c0001t0001g0215 others(80): Show |
83 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.-29-11379A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51939271 | |||||||
| chr14:51939290 | C | G | 1 | a0001c0001t0038g0346 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-29-11360C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51939290 | |||||||
| chr14:51939319 | A | T | 1 | a0001c0001t0063g0005 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-29-11331A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51939319 | |||||||
| chr14:51939415 | T | C | 34 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(31): Show |
34 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.-29-11235T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51939415 | |||||||
| chr14:51939518 | C | T | 83 | a0001c0001t0001g0057 a0001c0001t0001g0206 a0001c0001t0001g0215 others(80): Show |
83 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.-29-11132C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51939518 | |||||||
| chr14:51939771 | T | TG | 84 | a0001c0001t0001g0057 a0001c0001t0001g0206 a0001c0001t0001g0215 others(81): Show |
84 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.-29-10878dupG | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51939771 | ||||||
| chr14:51939800 | G | A | 4 | a0001c0001t0018g0323 a0001c0001t0018g0324 a0001c0001t0047g0298 others(1): Show |
4 | HG02647.hp1 HG02809.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-10850G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51939800 | |||||||
| chr14:51939886 | G | A | 1 | a0001c0001t0075g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-29-10764G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51939886 | |||||||
| chr14:51940082 | T | C | 3 | a0001c0001t0001g0140 a0001c0001t0001g0276 a0001c0001t0006g0159 |
3 | HG02738.hp1 HG03688.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-29-10568T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51940082 | |||||||
| chr14:51940130 | G | T | 20 | a0001c0001t0001g0057 a0001c0001t0004g0041 a0001c0001t0004g0043 others(17): Show |
20 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-29-10520G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51940130 | |||||||
| chr14:51940146 | T | C | 352 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(349): Show |
353 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.-29-10504T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51940146 | |||||||
| chr14:51940213 | CTGTTT | C | 15 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0003g0055 others(12): Show |
15 | HG01496.hp2 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-29-10422_-29-1041 others(9): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51940213 | ||||||
| chr14:51940230 | G | T | 34 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(31): Show |
34 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.-29-10420G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51940230 | |||||||
| chr14:51940260 | C | T | 1 | a0001c0001t0002g0064 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-29-10390C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51940260 | |||||||
| chr14:51940261 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0023g0108 |
2 | NA18945.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.-29-10389G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51940261 | |||||||
| chr14:51940279 | C | T | 84 | a0001c0001t0001g0057 a0001c0001t0001g0206 a0001c0001t0001g0215 others(81): Show |
84 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.-29-10371C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51940279 | |||||||
| chr14:51940378 | G | A | 2 | a0001c0001t0036g0053 a0001c0001t0067g0065 |
2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-29-10272G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51940378 | |||||||
| chr14:51940381 | G | C | 1 | a0001c0001t0075g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-29-10269G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51940381 | |||||||
| chr14:51940423 | T | C | 87 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(84): Show |
87 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.-29-10227T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51940423 | |||||||
| chr14:51940592 | G | A | 14 | a0001c0001t0001g0057 a0001c0001t0004g0326 a0001c0001t0009g0033 others(11): Show |
14 | HG01074.hp2 HG02258.hp2 HG02886.hp1 others(11): Show |
intron_variant | MODIFIER | c.-29-10058G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51940592 | |||||||
| chr14:51940604 | C | T | 1 | a0001c0001t0066g0032 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-29-10046C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51940604 | |||||||
| chr14:51940622 | A | G | 121 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0037 others(118): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-29-10028A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51940622 | |||||||
| chr14:51940653 | T | C | 1 | a0001c0001t0030g0072 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-29-9997T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51940653 | |||||||
| chr14:51940722 | C | A | 19 | a0001c0001t0001g0057 a0001c0001t0004g0041 a0001c0001t0004g0043 others(16): Show |
19 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-29-9928C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51940722 | |||||||
| chr14:51941015 | A | G | 11 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0003g0055 others(8): Show |
11 | HG01496.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-29-9635A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51941015 | |||||||
| chr14:51941076 | G | C | 1 | a0001c0001t0005g0300 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-29-9574G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51941076 | |||||||
| chr14:51941178 | C | A | 1 | a0001c0001t0022g0094 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-29-9472C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51941178 | |||||||
| chr14:51941461 | C | G | 1 | a0001c0001t0005g0300 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-29-9189C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51941461 | |||||||
| chr14:51941548 | C | G | 91 | a0001c0001t0001g0057 a0001c0001t0001g0206 a0001c0001t0001g0215 others(88): Show |
91 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.-29-9102C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51941548 | |||||||
| chr14:51941662 | A | G | 83 | a0001c0001t0001g0057 a0001c0001t0001g0206 a0001c0001t0001g0215 others(80): Show |
83 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.-29-8988A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51941662 | |||||||
| chr14:51941756 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-29-8894G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51941756 | |||||||
| chr14:51941784 | TCTC | T | 5 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0009g0042 others(2): Show |
5 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29-8862_-29-8860d others(5): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51941784 | ||||||
| chr14:51942000 | C | T | 9 | a0001c0001t0003g0015 a0001c0001t0003g0176 a0001c0001t0003g0359 others(6): Show |
9 | HG00639.hp2 HG00741.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29-8650C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51942000 | |||||||
| chr14:51942099 | C | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0263 |
2 | HG00642.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-29-8551C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51942099 | |||||||
| chr14:51942113 | G | C | 221 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(218): Show |
221 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(218): Show |
intron_variant | MODIFIER | c.-29-8537G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51942113 | |||||||
| chr14:51942145 | T | C | 1 | a0001c0001t0002g0101 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-29-8505T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51942145 | |||||||
| chr14:51942191 | A | T | 7 | a0001c0001t0001g0057 a0001c0001t0004g0326 a0001c0001t0009g0033 others(4): Show |
7 | HG01074.hp2 HG02258.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-8459A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51942191 | |||||||
| chr14:51942269 | G | A | 221 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(218): Show |
221 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(218): Show |
intron_variant | MODIFIER | c.-29-8381G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51942269 | |||||||
| chr14:51942297 | T | A | 85 | a0001c0001t0001g0057 a0001c0001t0001g0206 a0001c0001t0001g0215 others(82): Show |
85 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.-29-8353T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51942297 | |||||||
| chr14:51942414 | T | C | 1 | a0001c0001t0066g0032 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-29-8236T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51942414 | |||||||
| chr14:51942480 | G | A | 1 | a0001c0001t0075g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-29-8170G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51942480 | |||||||
| chr14:51942571 | C | CTCTTTCT others(5): Show |
18 | a0001c0001t0002g0049 a0001c0001t0002g0109 a0001c0001t0004g0017 others(15): Show |
18 | HG00621.hp2 HG01099.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.-29-8069_-29-8058d others(14): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942571 | ||||||
| chr14:51942571 | C | CTCTTTCT others(41): Show |
1 | a0001c0001t0001g0295 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-29-8064_-29-8063i others(50): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942571 | ||||||
| chr14:51942571 | C | CTCTTTCT others(45): Show |
3 | a0001c0001t0001g0174 a0001c0001t0001g0221 a0001c0001t0003g0307 |
3 | NA18747.hp1 NA18945.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-29-8064_-29-8063i others(54): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942571 | ||||||
| chr14:51942571 | C | CTCTTTCT others(49): Show |
3 | a0001c0001t0001g0162 a0001c0001t0001g0219 a0001c0001t0001g0248 |
3 | NA18961.hp1 NA18972.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-29-8064_-29-8063i others(58): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942571 | ||||||
| chr14:51942571 | C | CTCTTTCT others(53): Show |
4 | a0001c0001t0001g0165 a0001c0001t0001g0223 a0001c0001t0001g0242 others(1): Show |
4 | NA18969.hp2 NA18980.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-8064_-29-8063i others(62): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942571 | ||||||
| chr14:51942571 | C | CTCTTTCT others(57): Show |
1 | a0001c0001t0023g0108 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-29-8064_-29-8063i others(66): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942571 | ||||||
| chr14:51942571 | C | CTCTTTCT others(13): Show |
1 | a0001c0001t0039g0313 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-29-8077_-29-8058d others(22): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942571 | ||||||
| chr14:51942571 | C | CTCTTTCT others(41): Show |
1 | a0001c0001t0001g0037 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-29-8058_-29-8057i others(50): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942571 | ||||||
| chr14:51942571 | C | CTCTTTCT others(21): Show |
1 | a0001c0001t0009g0006 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-29-8058_-29-8057i others(30): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942571 | ||||||
| chr14:51942571 | C | CTCTTTCT others(25): Show |
3 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0015g0139 |
3 | HG00609.hp2 NA18941.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(34): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942571 | ||||||
| chr14:51942571 | C | CTCTTTCT others(29): Show |
4 | a0001c0001t0001g0250 a0001c0001t0001g0279 a0001c0001t0001g0319 others(1): Show |
4 | HG01070.hp1 HG01943.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(38): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942571 | ||||||
| chr14:51942571 | C | CTCTTTCT others(33): Show |
8 | a0001c0001t0001g0038 a0001c0001t0001g0259 a0001c0001t0001g0265 others(5): Show |
8 | HG00738.hp2 HG00741.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(42): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942571 | ||||||
| chr14:51942571 | C | CTCTTTCT others(37): Show |
19 | a0001c0001t0001g0135 a0001c0001t0001g0161 a0001c0001t0001g0171 others(16): Show |
19 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(46): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942571 | ||||||
| chr14:51942571 | C | CTCTTTCT others(41): Show |
7 | a0001c0001t0001g0034 a0001c0001t0001g0152 a0001c0001t0001g0292 others(4): Show |
8 | HG00735.hp1 HG02922.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(50): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942571 | ||||||
| chr14:51942571 | C | CTCTTTCT others(45): Show |
9 | a0001c0001t0001g0076 a0001c0001t0001g0151 a0001c0001t0001g0183 others(6): Show |
9 | HG00140.hp1 HG00621.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(54): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942571 | ||||||
| chr14:51942571 | C | CTCTTTCT others(49): Show |
4 | a0001c0001t0001g0113 a0001c0001t0002g0124 a0001c0001t0042g0282 others(1): Show |
4 | HG00323.hp1 HG01891.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(58): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942571 | ||||||
| chr14:51942571 | C | CTCTTTCT others(53): Show |
4 | a0001c0001t0001g0184 a0001c0001t0001g0291 a0001c0001t0006g0122 others(1): Show |
4 | HG02145.hp1 HG02145.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(62): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942571 | ||||||
| chr14:51942571 | C | CTCTTTCT others(27): Show |
1 | a0001c0002t0074g0040 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-29-8062_-29-8061i others(36): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942571 | ||||||
| chr14:51942571 | C | CTTTTTCT others(9): Show |
1 | a0001c0001t0003g0143 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-29-8078_-29-8077i others(18): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942571 | ||||||
| chr14:51942571 | C | CTTTTTCT others(17): Show |
4 | a0001c0001t0002g0329 a0001c0001t0002g0330 a0001c0001t0005g0331 others(1): Show |
4 | HG02056.hp1 HG02273.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-8078_-29-8077i others(26): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942571 | ||||||
| chr14:51942571 | C | CTTTTTCT others(21): Show |
23 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(20): Show |
23 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.-29-8078_-29-8077i others(30): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942571 | ||||||
| chr14:51942571 | C | CTTTTTCT others(25): Show |
1 | a0001c0001t0020g0277 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-29-8078_-29-8077i others(34): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942571 | ||||||
| chr14:51942571 | C | CTTTTTCT others(29): Show |
2 | a0001c0001t0005g0129 a0001c0001t0013g0361 |
2 | NA19011.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-29-8078_-29-8077i others(38): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942571 | ||||||
| chr14:51942573 | C | CTTTCTTT others(19): Show |
1 | a0001c0001t0043g0336 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-29-8058_-29-8057i others(28): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942573 | ||||||
| chr14:51942573 | C | T | 188 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(185): Show |
188 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(185): Show |
intron_variant | MODIFIER | c.-29-8077C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51942573 | |||||||
| chr14:51942585 | C | CTTTCTTT others(35): Show |
1 | a0001c0001t0001g0249 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-29-8058_-29-8057i others(44): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942585 | ||||||
| chr14:51942587 | T | G | 7 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0119 others(4): Show |
7 | HG02080.hp1 NA18944.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-8063T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51942587 | |||||||
| chr14:51942589 | C | CTTTCTCT others(81): Show |
1 | a0001c0001t0016g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-29-8058_-29-8057i others(90): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | CTTTCTCT others(69): Show |
1 | a0001c0001t0018g0367 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-29-8058_-29-8057i others(78): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | CTTTCTCT others(57): Show |
1 | a0001c0001t0001g0057 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-29-8058_-29-8057i others(66): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | CTTTCTCT others(49): Show |
3 | a0001c0001t0004g0326 a0001c0001t0009g0033 a0001c0001t0068g0322 |
3 | HG02896.hp1 HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(58): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | CTTTCTTT others(6): Show |
2 | a0001c0001t0001g0012 a0001c0001t0010g0137 |
2 | HG06807.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(15): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | CTTTCTTT others(73): Show |
1 | a0001c0001t0009g0310 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-29-8058_-29-8057i others(82): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | CTTTCTTT others(10): Show |
55 | a0001c0001t0001g0025 a0001c0001t0001g0168 a0001c0001t0001g0212 others(52): Show |
55 | HG00323.hp2 HG00642.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(19): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | CTTTCTTT others(11): Show |
3 | a0001c0001t0008g0195 a0001c0001t0018g0324 a0001c0001t0021g0362 |
3 | HG00639.hp2 HG03453.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(20): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | CTTTCTTT others(14): Show |
25 | a0001c0001t0001g0175 a0001c0001t0002g0093 a0001c0001t0003g0054 others(22): Show |
25 | HG00738.hp1 HG02027.hp2 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(23): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | CTTTCTTT others(15): Show |
1 | a0001c0001t0010g0083 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-29-8058_-29-8057i others(24): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | CTTTCTTT others(18): Show |
2 | a0001c0001t0011g0090 a0001c0001t0011g0125 |
2 | NA18947.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(27): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | CTTTCTTT others(22): Show |
2 | a0001c0001t0005g0300 a0001c0002t0061g0365 |
2 | NA18966.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(31): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | CTTTCTTT others(26): Show |
2 | a0001c0001t0001g0303 a0001c0001t0001g0328 |
2 | HG02630.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(35): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | CTTTCTTT others(30): Show |
1 | a0001c0001t0067g0065 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-29-8058_-29-8057i others(39): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | CTTTCTTT others(34): Show |
1 | a0001c0001t0001g0296 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-29-8058_-29-8057i others(43): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | CTTTCTTT others(38): Show |
7 | a0001c0001t0001g0140 a0001c0001t0001g0257 a0001c0001t0003g0027 others(4): Show |
7 | HG01081.hp2 HG01175.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(47): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | CTTTCTTT others(42): Show |
5 | a0001c0001t0001g0106 a0001c0001t0001g0301 a0001c0001t0008g0356 others(2): Show |
5 | HG01433.hp2 HG02080.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(51): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | CTTTCTTT others(46): Show |
1 | a0001c0001t0037g0180 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-29-8058_-29-8057i others(55): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | CTTTCTTT others(50): Show |
1 | a0001c0001t0001g0115 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-29-8058_-29-8057i others(59): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | CTTTCTTT others(54): Show |
1 | a0001c0001t0001g0029 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-29-8058_-29-8057i others(63): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | CTTTCTTT others(27): Show |
2 | a0001c0001t0002g0008 a0001c0001t0002g0009 |
2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(36): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | CTTTCTTT others(23): Show |
7 | a0001c0001t0003g0055 a0001c0001t0004g0197 a0001c0001t0017g0047 others(4): Show |
7 | HG01496.hp2 HG02965.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(32): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | CTTTCTTT others(24): Show |
1 | a0001c0001t0003g0056 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-29-8058_-29-8057i others(33): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | CTTTCTTT others(25): Show |
1 | a0001c0001t0038g0346 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-29-8058_-29-8057i others(34): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | CTTTTT | 74 | a0001c0001t0001g0206 a0001c0001t0001g0215 a0001c0001t0001g0270 others(71): Show |
74 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.-29-8048_-29-8044d others(7): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | CTTTTTT | 8 | a0001c0001t0002g0084 a0001c0001t0006g0226 a0001c0001t0013g0224 others(5): Show |
8 | NA18961.hp2 NA18963.hp1 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.-29-8049_-29-8044d others(8): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942589 | ||||||
| chr14:51942589 | C | T | 1 | a0001c0001t0024g0058 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-29-8061C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51942589 | |||||||
| chr14:51942590 | T | TTTCTTTC others(4): Show |
1 | a0001c0001t0004g0198 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-29-8058_-29-8057i others(13): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942590 | ||||||
| chr14:51942590 | T | TTTCTTTC others(8): Show |
1 | a0001c0001t0046g0311 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-29-8058_-29-8057i others(17): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942590 | ||||||
| chr14:51942590 | T | TTTCTTTC others(36): Show |
2 | a0001c0001t0015g0132 a0001c0001t0038g0297 |
2 | HG03516.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(45): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942590 | ||||||
| chr14:51942590 | T | TTTCTTTC others(40): Show |
4 | a0001c0001t0001g0207 a0001c0001t0001g0240 a0001c0001t0006g0159 others(1): Show |
4 | HG01433.hp1 HG02738.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(49): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942590 | ||||||
| chr14:51942590 | T | TTTCTTTC others(44): Show |
4 | a0001c0001t0001g0052 a0001c0001t0002g0060 a0001c0001t0015g0302 others(1): Show |
4 | HG01109.hp1 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(53): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942590 | ||||||
| chr14:51942590 | T | TTTCTTTC others(48): Show |
1 | a0001c0001t0001g0276 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-29-8058_-29-8057i others(57): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942590 | ||||||
| chr14:51942590 | T | TTTCTTTC others(52): Show |
1 | a0001c0001t0001g0126 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-29-8058_-29-8057i others(61): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942590 | ||||||
| chr14:51942590 | T | TTTCTTTC others(56): Show |
1 | a0001c0001t0001g0251 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-29-8058_-29-8057i others(65): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942590 | ||||||
| chr14:51942591 | T | TTCTTTCT others(35): Show |
3 | a0001c0001t0001g0075 a0001c0001t0001g0355 a0001c0001t0031g0112 |
3 | HG00438.hp1 HG01981.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(44): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942591 | ||||||
| chr14:51942591 | T | TTCTTTCT others(39): Show |
4 | a0001c0001t0001g0233 a0001c0001t0016g0352 a0001c0001t0022g0094 others(1): Show |
4 | HG02486.hp1 HG02622.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(48): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942591 | ||||||
| chr14:51942591 | T | TTCTTTCT others(47): Show |
4 | a0001c0001t0001g0099 a0001c0001t0001g0150 a0001c0001t0006g0177 others(1): Show |
4 | HG00642.hp1 HG01517.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(56): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942591 | ||||||
| chr14:51942591 | T | TTCTTTCT others(51): Show |
2 | a0001c0001t0001g0256 a0001c0001t0006g0166 |
2 | NA18944.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(60): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51942591 | ||||||
| chr14:51942592 | T | TCTTTCTT others(10): Show |
1 | a0001c0001t0035g0378 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-29-8058_-29-8057i others(19): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51942592 | |||||||
| chr14:51942592 | T | TCTTTCTT others(34): Show |
1 | a0001c0001t0006g0073 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-29-8058_-29-8057i others(43): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51942592 | |||||||
| chr14:51942592 | T | TCTTTCTT others(38): Show |
1 | a0001c0001t0001g0243 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-29-8058_-29-8057i others(47): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51942592 | |||||||
| chr14:51942592 | T | TCTTTCTT others(42): Show |
2 | a0001c0001t0001g0193 a0001c0001t0001g0357 |
2 | HG03834.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(51): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51942592 | |||||||
| chr14:51942592 | T | TCTTTCTT others(46): Show |
3 | a0001c0001t0001g0098 a0001c0001t0001g0111 a0001c0001t0001g0178 |
3 | HG01243.hp2 NA18946.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-29-8058_-29-8057i others(55): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51942592 | |||||||
| chr14:51942592 | T | TCTTTCTT others(50): Show |
1 | a0001c0001t0001g0119 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-29-8058_-29-8057i others(59): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51942592 | |||||||
| chr14:51942594 | T | C | 1 | a0001c0001t0038g0297 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-29-8056T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51942594 | |||||||
| chr14:51942607 | A | T | 7 | a0001c0001t0001g0057 a0001c0001t0004g0326 a0001c0001t0009g0033 others(4): Show |
7 | HG01074.hp2 HG02258.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-8043A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51942607 | |||||||
| chr14:51942652 | G | A | 2 | a0001c0001t0066g0032 a0001c0001t0075g0004 |
2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-29-7998G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51942652 | |||||||
| chr14:51942720 | G | A | 3 | a0001c0001t0001g0243 a0001c0001t0001g0249 a0001c0001t0064g0031 |
3 | HG01109.hp1 HG02055.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-29-7930G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51942720 | |||||||
| chr14:51942786 | G | A | 2 | a0001c0001t0036g0371 a0001c0001t0037g0028 |
2 | HG02895.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-29-7864G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51942786 | |||||||
| chr14:51943028 | C | T | 6 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0009g0042 others(3): Show |
6 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-7622C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51943028 | |||||||
| chr14:51943059 | T | A | 1 | a0001c0001t0004g0197 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-29-7591T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51943059 | |||||||
| chr14:51943098 | G | C | 87 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(84): Show |
87 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.-29-7552G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51943098 | |||||||
| chr14:51943100 | G | T | 1 | a0001c0001t0046g0311 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-29-7550G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51943100 | |||||||
| chr14:51943113 | A | G | 7 | a0001c0001t0001g0057 a0001c0001t0004g0326 a0001c0001t0009g0033 others(4): Show |
7 | HG01074.hp2 HG02258.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-7537A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51943113 | |||||||
| chr14:51943202 | G | T | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-29-7448G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51943202 | |||||||
| chr14:51943248 | G | A | 1 | a0001c0001t0008g0169 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-29-7402G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51943248 | |||||||
| chr14:51943255 | G | T | 7 | a0001c0001t0001g0057 a0001c0001t0004g0326 a0001c0001t0009g0033 others(4): Show |
7 | HG01074.hp2 HG02258.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-7395G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51943255 | |||||||
| chr14:51943283 | T | C | 7 | a0001c0001t0001g0057 a0001c0001t0004g0326 a0001c0001t0009g0033 others(4): Show |
7 | HG01074.hp2 HG02258.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-7367T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51943283 | |||||||
| chr14:51943427 | A | G | 2 | a0001c0001t0066g0032 a0001c0001t0075g0004 |
2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-29-7223A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51943427 | |||||||
| chr14:51943526 | T | C | 7 | a0001c0001t0001g0057 a0001c0001t0004g0326 a0001c0001t0009g0033 others(4): Show |
7 | HG01074.hp2 HG02258.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-7124T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51943526 | |||||||
| chr14:51943727 | G | A | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-29-6923G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51943727 | |||||||
| chr14:51943727 | G | C | 1 | a0001c0001t0075g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-29-6923G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51943727 | |||||||
| chr14:51943804 | AT | A | 86 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(83): Show |
86 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.-29-6845delT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51943804 | |||||||
| chr14:51943845 | G | C | 226 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(223): Show |
226 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(223): Show |
intron_variant | MODIFIER | c.-29-6805G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51943845 | |||||||
| chr14:51944019 | A | G | 1 | a0001c0001t0022g0274 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-29-6631A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51944019 | |||||||
| chr14:51944211 | C | CA | 78 | a0001c0001t0001g0057 a0001c0001t0001g0206 a0001c0001t0001g0215 others(75): Show |
78 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-29-6429dupA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51944211 | ||||||
| chr14:51944225 | A | G | 127 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(124): Show |
127 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.-29-6425A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51944225 | |||||||
| chr14:51944243 | A | G | 120 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(117): Show |
120 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.-29-6407A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51944243 | |||||||
| chr14:51944291 | T | A | 1 | a0001c0001t0075g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-29-6359T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51944291 | |||||||
| chr14:51944350 | G | A | 128 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(125): Show |
128 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-29-6300G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51944350 | |||||||
| chr14:51944624 | C | T | 1 | a0001c0001t0001g0294 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-29-6026C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51944624 | |||||||
| chr14:51944835 | G | A | 214 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(211): Show |
214 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(211): Show |
intron_variant | MODIFIER | c.-29-5815G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51944835 | |||||||
| chr14:51945133 | C | CAAA | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-29-5511_-29-5509d others(5): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51945133 | ||||||
| chr14:51945133 | C | CAAAAA | 83 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(80): Show |
83 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.-29-5513_-29-5509d others(7): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51945133 | ||||||
| chr14:51945232 | T | G | 2 | a0001c0001t0002g0008 a0001c0001t0002g0009 |
2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-29-5418T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51945232 | |||||||
| chr14:51945278 | A | T | 2 | a0001c0001t0002g0008 a0001c0001t0002g0009 |
2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-29-5372A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51945278 | |||||||
| chr14:51945408 | T | C | 2 | a0001c0001t0001g0178 a0001c0001t0006g0177 |
2 | HG00642.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.-29-5242T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51945408 | |||||||
| chr14:51945518 | CA | C | 121 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(118): Show |
121 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.-29-5131delA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51945518 | |||||||
| chr14:51945624 | A | C | 2 | a0001c0001t0002g0008 a0001c0001t0002g0009 |
2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-29-5026A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51945624 | |||||||
| chr14:51945642 | A | G | 2 | a0001c0002t0044g0133 a0001c0002t0061g0365 |
2 | NA18972.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.-29-5008A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51945642 | |||||||
| chr14:51945780 | G | A | 128 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(125): Show |
128 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-29-4870G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51945780 | |||||||
| chr14:51945784 | GTGTA | G | 3 | a0001c0001t0018g0323 a0001c0001t0018g0324 a0001c0001t0047g0298 |
3 | HG02809.hp1 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-29-4862_-29-4859d others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51945784 | ||||||
| chr14:51945788 | A | ATG | 90 | a0001c0001t0001g0206 a0001c0001t0001g0215 a0001c0001t0001g0270 others(87): Show |
90 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.-29-4847_-29-4846d others(4): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51945788 | ||||||
| chr14:51945788 | ATG | A | 128 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(125): Show |
128 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-29-4847_-29-4846d others(4): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51945788 | ||||||
| chr14:51945841 | C | CTCTT | 128 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(125): Show |
128 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-29-4808_-29-4805d others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51945841 | ||||||
| chr14:51945898 | G | GTTGT | 42 | a0001c0001t0001g0057 a0001c0001t0001g0289 a0001c0001t0002g0061 others(39): Show |
42 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.-29-4733_-29-4730d others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51945898 | ||||||
| chr14:51945898 | G | GTTGTTTG others(1): Show |
85 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(82): Show |
85 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.-29-4737_-29-4730d others(10): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51945898 | ||||||
| chr14:51945898 | G | GTTGTTTG others(5): Show |
1 | a0001c0001t0021g0362 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-29-4741_-29-4730d others(14): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51945898 | ||||||
| chr14:51946078 | G | A | 1 | a0001c0001t0066g0032 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-29-4572G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51946078 | |||||||
| chr14:51946114 | A | G | 7 | a0001c0001t0024g0058 a0001c0001t0024g0059 a0001c0001t0024g0063 others(4): Show |
7 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-4536A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51946114 | |||||||
| chr14:51946233 | T | C | 7 | a0001c0001t0001g0057 a0001c0001t0004g0326 a0001c0001t0009g0033 others(4): Show |
7 | HG01074.hp2 HG02258.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-4417T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51946233 | |||||||
| chr14:51946277 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-29-4373C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51946277 | |||||||
| chr14:51946321 | A | G | 88 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(85): Show |
88 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.-29-4329A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51946321 | |||||||
| chr14:51946433 | C | G | 70 | a0001c0001t0001g0206 a0001c0001t0001g0215 a0001c0001t0001g0270 others(67): Show |
70 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.-29-4217C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51946433 | |||||||
| chr14:51946642 | A | G | 1 | a0001c0001t0054g0202 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-29-4008A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51946642 | |||||||
| chr14:51946688 | C | T | 2 | a0001c0001t0036g0053 a0001c0001t0067g0065 |
2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-29-3962C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51946688 | |||||||
| chr14:51946727 | C | T | 6 | a0001c0001t0024g0058 a0001c0001t0024g0059 a0001c0001t0024g0063 others(3): Show |
6 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-3923C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51946727 | |||||||
| chr14:51946803 | C | T | 1 | a0001c0001t0017g0047 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-29-3847C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51946803 | |||||||
| chr14:51946855 | T | C | 210 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(207): Show |
210 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(207): Show |
intron_variant | MODIFIER | c.-29-3795T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51946855 | |||||||
| chr14:51946857 | C | G | 1 | a0001c0001t0009g0310 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-29-3793C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51946857 | |||||||
| chr14:51946945 | G | A | 5 | a0001c0001t0025g0097 a0001c0001t0025g0213 a0001c0001t0025g0273 others(2): Show |
5 | NA18967.hp2 NA18980.hp2 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29-3705G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51946945 | |||||||
| chr14:51946951 | A | G | 89 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(86): Show |
89 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.-29-3699A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51946951 | |||||||
| chr14:51947043 | G | A | 2 | a0001c0001t0049g0205 a0001c0001t0058g0341 |
2 | HG02602.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-29-3607G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51947043 | |||||||
| chr14:51947061 | G | T | 6 | a0001c0001t0001g0135 a0001c0001t0015g0132 a0001c0001t0015g0136 others(3): Show |
6 | HG02132.hp1 NA18946.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-3589G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51947061 | |||||||
| chr14:51947250 | A | G | 1 | a0001c0001t0037g0180 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-29-3400A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51947250 | |||||||
| chr14:51947350 | C | T | 89 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(86): Show |
89 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.-29-3300C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51947350 | |||||||
| chr14:51947351 | C | G | 121 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(118): Show |
121 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.-29-3299C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51947351 | |||||||
| chr14:51947369 | C | T | 6 | a0001c0001t0024g0058 a0001c0001t0024g0059 a0001c0001t0024g0063 others(3): Show |
6 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-3281C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51947369 | |||||||
| chr14:51947395 | A | C | 1 | a0001c0001t0075g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-29-3255A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51947395 | |||||||
| chr14:51947531 | C | T | 352 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(349): Show |
353 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.-29-3119C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51947531 | |||||||
| chr14:51947690 | C | T | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-29-2960C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51947690 | |||||||
| chr14:51947710 | T | A | 121 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(118): Show |
121 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.-29-2940T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51947710 | |||||||
| chr14:51947746 | G | A | 1 | a0001c0001t0034g0377 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-29-2904G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51947746 | |||||||
| chr14:51947784 | G | T | 1 | a0001c0001t0002g0109 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-29-2866G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51947784 | |||||||
| chr14:51947805 | C | T | 1 | a0001c0001t0066g0032 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-29-2845C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51947805 | |||||||
| chr14:51947830 | A | T | 121 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(118): Show |
121 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.-29-2820A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51947830 | |||||||
| chr14:51947937 | G | C | 1 | a0001c0001t0075g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-29-2713G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51947937 | |||||||
| chr14:51948010 | T | C | 1 | a0001c0001t0002g0329 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-29-2640T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51948010 | |||||||
| chr14:51948037 | G | T | 141 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(138): Show |
141 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.-29-2613G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51948037 | |||||||
| chr14:51948137 | C | T | 2 | a0001c0001t0023g0269 a0001c0001t0050g0123 |
2 | NA18955.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-29-2513C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51948137 | |||||||
| chr14:51948263 | C | T | 6 | a0001c0001t0024g0058 a0001c0001t0024g0059 a0001c0001t0024g0063 others(3): Show |
6 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-2387C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51948263 | |||||||
| chr14:51948336 | C | T | 1 | a0001c0001t0002g0222 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-29-2314C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51948336 | |||||||
| chr14:51948405 | C | T | 68 | a0001c0001t0001g0206 a0001c0001t0001g0215 a0001c0001t0001g0270 others(65): Show |
68 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.-29-2245C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51948405 | |||||||
| chr14:51948427 | C | A | 2 | a0001c0001t0010g0083 a0001c0001t0012g0189 |
2 | NA18993.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-29-2223C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51948427 | |||||||
| chr14:51948427 | C | G | 119 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(116): Show |
119 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.-29-2223C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51948427 | |||||||
| chr14:51948428 | A | T | 121 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(118): Show |
121 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.-29-2222A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51948428 | |||||||
| chr14:51948579 | T | C | 7 | a0001c0001t0001g0057 a0001c0001t0004g0326 a0001c0001t0009g0033 others(4): Show |
7 | HG01074.hp2 HG02258.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-2071T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51948579 | |||||||
| chr14:51948848 | G | A | 1 | a0001c0001t0075g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-29-1802G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51948848 | |||||||
| chr14:51948948 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-29-1702C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51948948 | |||||||
| chr14:51949039 | T | C | 70 | a0001c0001t0001g0206 a0001c0001t0001g0215 a0001c0001t0001g0270 others(67): Show |
70 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.-29-1611T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51949039 | |||||||
| chr14:51949077 | C | T | 5 | a0001c0001t0034g0377 a0001c0001t0036g0053 a0001c0001t0043g0336 others(2): Show |
5 | HG02922.hp2 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29-1573C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51949077 | |||||||
| chr14:51949078 | G | A | 121 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(118): Show |
121 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.-29-1572G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51949078 | |||||||
| chr14:51949116 | G | A | 121 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(118): Show |
121 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.-29-1534G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51949116 | |||||||
| chr14:51949120 | C | CA | 9 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0009g0042 others(6): Show |
9 | HG01243.hp1 HG01891.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29-1514dupA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51949120 | ||||||
| chr14:51949120 | CA | C | 19 | a0001c0001t0001g0215 a0001c0001t0002g0008 a0001c0001t0002g0009 others(16): Show |
19 | HG01496.hp2 HG02109.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-29-1514delA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 51949120 | ||||||
| chr14:51949166 | G | C | 121 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(118): Show |
121 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.-29-1484G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51949166 | |||||||
| chr14:51949239 | G | A | 3 | a0001c0001t0003g0176 a0001c0001t0003g0359 a0001c0001t0008g0195 |
3 | HG00639.hp2 HG01261.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-29-1411G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51949239 | |||||||
| chr14:51949297 | A | AGAACTTG others(6): Show |
32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-29-1353_-29-1352i others(15): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51949297 | |||||||
| chr14:51949299 | A | G | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-29-1351A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51949299 | |||||||
| chr14:51949311 | C | G | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-29-1339C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51949311 | |||||||
| chr14:51949619 | C | G | 89 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(86): Show |
89 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.-29-1031C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51949619 | |||||||
| chr14:51949694 | G | A | 151 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(148): Show |
151 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.-29-956G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51949694 | |||||||
| chr14:51949773 | G | A | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-29-877G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51949773 | |||||||
| chr14:51949806 | T | C | 39 | a0001c0001t0001g0057 a0001c0001t0001g0289 a0001c0001t0002g0061 others(36): Show |
39 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.-29-844T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51949806 | |||||||
| chr14:51949826 | A | G | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-29-824A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51949826 | |||||||
| chr14:51949843 | G | A | 1 | a0001c0002t0074g0040 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-29-807G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51949843 | |||||||
| chr14:51949875 | G | T | 1 | a0001c0001t0004g0041 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-29-775G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51949875 | |||||||
| chr14:51949892 | T | C | 128 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(125): Show |
128 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-29-758T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51949892 | |||||||
| chr14:51949911 | G | A | 11 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0003g0055 others(8): Show |
11 | HG01496.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-29-739G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51949911 | |||||||
| chr14:51949930 | G | A | 1 | a0001c0001t0022g0274 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-29-720G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51949930 | |||||||
| chr14:51949989 | C | T | 1 | a0001c0001t0066g0032 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-29-661C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51949989 | |||||||
| chr14:51950018 | A | G | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-29-632A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51950018 | |||||||
| chr14:51950049 | A | G | 4 | a0001c0001t0015g0132 a0001c0001t0015g0136 a0001c0001t0015g0138 others(1): Show |
4 | NA18946.hp1 NA19002.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-601A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51950049 | |||||||
| chr14:51950382 | C | A | 19 | a0001c0001t0001g0057 a0001c0001t0004g0041 a0001c0001t0004g0043 others(16): Show |
19 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-29-268C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51950382 | |||||||
| chr14:51950401 | T | C | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-29-249T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51950401 | |||||||
| chr14:51950570 | A | T | 2 | a0001c0001t0002g0330 a0001c0001t0005g0331 |
2 | HG02273.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-29-80A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51950570 | |||||||
| chr14:51950627 | C | G | 38 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(35): Show |
38 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.-29-23C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 2/3 | chr14 | 51950627 | |||||||
| chr14:51950938 | G | A | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.87+173G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51950938 | |||||||
| chr14:51950971 | C | A | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.87+206C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51950971 | |||||||
| chr14:51950986 | C | CA | 7 | a0001c0001t0005g0254 a0001c0001t0006g0159 a0001c0001t0006g0226 others(4): Show |
7 | HG02738.hp1 HG02738.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.87+231dupA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51950986 | ||||||
| chr14:51950988 | A | C | 1 | a0001c0001t0002g0214 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.87+223A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51950988 | |||||||
| chr14:51950989 | A | C | 121 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(118): Show |
121 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.87+224A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51950989 | |||||||
| chr14:51951061 | C | T | 1 | a0001c0001t0020g0204 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.87+296C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51951061 | |||||||
| chr14:51951062 | A | G | 121 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(118): Show |
121 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.87+297A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51951062 | |||||||
| chr14:51951152 | C | T | 11 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0003g0055 others(8): Show |
11 | HG01496.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.87+387C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51951152 | |||||||
| chr14:51951153 | G | A | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.87+388G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51951153 | |||||||
| chr14:51951189 | G | A | 12 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0003g0055 others(9): Show |
12 | HG01496.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.87+424G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51951189 | |||||||
| chr14:51951202 | T | G | 39 | a0001c0001t0001g0057 a0001c0001t0001g0289 a0001c0001t0002g0061 others(36): Show |
39 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.87+437T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51951202 | |||||||
| chr14:51951369 | C | A | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.87+604C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51951369 | |||||||
| chr14:51951464 | G | A | 11 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0003g0055 others(8): Show |
11 | HG01496.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.87+699G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51951464 | |||||||
| chr14:51951468 | T | C | 7 | a0001c0001t0001g0057 a0001c0001t0004g0326 a0001c0001t0009g0033 others(4): Show |
7 | HG01074.hp2 HG02258.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.87+703T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51951468 | |||||||
| chr14:51951476 | T | A | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.87+711T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51951476 | |||||||
| chr14:51951698 | G | C | 6 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0009g0042 others(3): Show |
6 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+933G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51951698 | |||||||
| chr14:51951742 | A | G | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | NA18971.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.87+977A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51951742 | |||||||
| chr14:51951753 | G | T | 7 | a0001c0001t0001g0057 a0001c0001t0004g0326 a0001c0001t0009g0033 others(4): Show |
7 | HG01074.hp2 HG02258.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.87+988G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51951753 | |||||||
| chr14:51951869 | T | C | 38 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(35): Show |
38 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.87+1104T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51951869 | |||||||
| chr14:51951899 | C | T | 38 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(35): Show |
38 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.87+1134C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51951899 | |||||||
| chr14:51951918 | G | T | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.87+1153G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51951918 | |||||||
| chr14:51951935 | G | A | 12 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0003g0055 others(9): Show |
12 | HG01496.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.87+1170G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51951935 | |||||||
| chr14:51951937 | G | A | 89 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(86): Show |
89 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.87+1172G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51951937 | |||||||
| chr14:51952041 | T | A | 6 | a0001c0001t0024g0058 a0001c0001t0024g0059 a0001c0001t0024g0063 others(3): Show |
6 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+1276T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51952041 | |||||||
| chr14:51952061 | A | G | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.87+1296A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51952061 | |||||||
| chr14:51952092 | T | C | 70 | a0001c0001t0001g0206 a0001c0001t0001g0215 a0001c0001t0001g0270 others(67): Show |
70 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.87+1327T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51952092 | |||||||
| chr14:51952097 | T | A | 5 | a0001c0001t0025g0097 a0001c0001t0025g0213 a0001c0001t0025g0273 others(2): Show |
5 | NA18967.hp2 NA18980.hp2 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.87+1332T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51952097 | |||||||
| chr14:51952127 | C | T | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.87+1362C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51952127 | |||||||
| chr14:51952341 | C | T | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.87+1576C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51952341 | |||||||
| chr14:51952415 | A | T | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.87+1650A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51952415 | |||||||
| chr14:51952443 | A | G | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.87+1678A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51952443 | |||||||
| chr14:51952481 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.87+1716G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51952481 | |||||||
| chr14:51952566 | C | T | 88 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(85): Show |
88 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.87+1801C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51952566 | |||||||
| chr14:51952579 | C | T | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.87+1814C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51952579 | |||||||
| chr14:51952625 | C | T | 9 | a0001c0001t0003g0015 a0001c0001t0003g0176 a0001c0001t0003g0359 others(6): Show |
9 | HG00639.hp2 HG00741.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.87+1860C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51952625 | |||||||
| chr14:51952652 | A | G | 39 | a0001c0001t0001g0057 a0001c0001t0001g0289 a0001c0001t0002g0061 others(36): Show |
39 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.87+1887A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51952652 | |||||||
| chr14:51952799 | T | C | 236 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0037 others(233): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.87+2034T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51952799 | |||||||
| chr14:51952934 | C | T | 1 | a0001c0001t0035g0284 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.87+2169C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51952934 | |||||||
| chr14:51952949 | C | A | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.87+2184C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51952949 | |||||||
| chr14:51953013 | T | C | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.87+2248T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51953013 | |||||||
| chr14:51953019 | A | C | 32 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(29): Show |
32 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.87+2254A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51953019 | |||||||
| chr14:51953189 | T | A | 1 | a0001c0001t0030g0072 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.87+2424T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51953189 | |||||||
| chr14:51953344 | C | G | 1 | a0001c0001t0004g0197 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.87+2579C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51953344 | |||||||
| chr14:51953388 | C | T | 51 | a0001c0001t0001g0289 a0001c0001t0002g0008 a0001c0001t0002g0009 others(48): Show |
51 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.87+2623C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51953388 | |||||||
| chr14:51953398 | A | G | 160 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0037 others(157): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.87+2633A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51953398 | |||||||
| chr14:51953403 | C | T | 39 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(36): Show |
39 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.87+2638C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51953403 | |||||||
| chr14:51953424 | G | T | 3 | a0001c0002t0072g0196 a0001c0002t0073g0010 a0001c0002t0074g0040 |
3 | HG01433.hp1 HG02486.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.87+2659G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51953424 | |||||||
| chr14:51953426 | G | C | 39 | a0001c0001t0001g0289 a0001c0001t0002g0061 a0001c0001t0002g0062 others(36): Show |
39 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.87+2661G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51953426 | |||||||
| chr14:51953730 | G | A | 3 | a0001c0001t0018g0323 a0001c0001t0018g0324 a0001c0001t0047g0298 |
3 | HG02809.hp1 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.87+2965G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51953730 | |||||||
| chr14:51954191 | G | C | 89 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(86): Show |
89 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.87+3426G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51954191 | |||||||
| chr14:51954313 | T | C | 100 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0057 others(97): Show |
100 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(97): Show |
intron_variant | MODIFIER | c.87+3548T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51954313 | |||||||
| chr14:51954559 | G | T | 355 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(352): Show |
355 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.87+3794G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51954559 | |||||||
| chr14:51954604 | T | G | 92 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0168 others(89): Show |
92 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.87+3839T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51954604 | |||||||
| chr14:51954668 | C | T | 4 | a0001c0001t0034g0377 a0001c0001t0036g0053 a0001c0001t0043g0336 others(1): Show |
4 | HG02922.hp2 HG03225.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.87+3903C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51954668 | |||||||
| chr14:51954678 | G | A | 1 | a0001c0001t0002g0329 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.87+3913G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51954678 | |||||||
| chr14:51954781 | A | G | 1 | a0001c0002t0073g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.87+4016A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51954781 | |||||||
| chr14:51954877 | T | C | 241 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(238): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.87+4112T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51954877 | |||||||
| chr14:51954952 | A | G | 1 | a0001c0001t0034g0364 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.87+4187A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51954952 | |||||||
| chr14:51955168 | A | T | 90 | a0001c0001t0001g0025 a0001c0001t0001g0168 a0001c0001t0001g0212 others(87): Show |
90 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(87): Show |
intron_variant | MODIFIER | c.87+4403A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51955168 | |||||||
| chr14:51955175 | T | TCTCATTT others(3): Show |
94 | a0001c0001t0001g0175 a0001c0001t0001g0206 a0001c0001t0001g0215 others(91): Show |
94 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.87+4412_87+4421dup others(10): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51955175 | ||||||
| chr14:51955322 | A | G | 2 | a0001c0001t0003g0157 a0001c0001t0019g0039 |
2 | HG02258.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.87+4557A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51955322 | |||||||
| chr14:51955435 | A | C | 156 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0034 others(153): Show |
156 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.87+4670A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51955435 | |||||||
| chr14:51955475 | A | G | 1 | a0001c0001t0075g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.87+4710A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51955475 | |||||||
| chr14:51955512 | G | A | 7 | a0001c0001t0004g0326 a0001c0001t0009g0006 a0001c0001t0009g0033 others(4): Show |
7 | HG01074.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.87+4747G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51955512 | |||||||
| chr14:51955861 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.87+5096T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51955861 | |||||||
| chr14:51955975 | G | A | 1 | a0001c0001t0004g0338 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.87+5210G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51955975 | |||||||
| chr14:51956003 | A | G | 1 | a0001c0001t0071g0118 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.87+5238A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51956003 | |||||||
| chr14:51956063 | C | A | 1 | a0001c0001t0005g0129 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.87+5298C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51956063 | |||||||
| chr14:51956076 | G | A | 7 | a0001c0001t0024g0058 a0001c0001t0024g0059 a0001c0001t0024g0063 others(4): Show |
7 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.87+5311G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51956076 | |||||||
| chr14:51956389 | T | C | 129 | a0001c0001t0001g0025 a0001c0001t0001g0168 a0001c0001t0001g0212 others(126): Show |
129 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(126): Show |
intron_variant | MODIFIER | c.87+5624T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51956389 | |||||||
| chr14:51956406 | T | A | 109 | a0001c0001t0001g0025 a0001c0001t0001g0168 a0001c0001t0001g0212 others(106): Show |
109 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(106): Show |
intron_variant | MODIFIER | c.87+5641T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51956406 | |||||||
| chr14:51956424 | G | A | 1 | a0001c0001t0075g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.87+5659G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51956424 | |||||||
| chr14:51956426 | A | G | 109 | a0001c0001t0001g0025 a0001c0001t0001g0168 a0001c0001t0001g0212 others(106): Show |
109 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(106): Show |
intron_variant | MODIFIER | c.87+5661A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51956426 | |||||||
| chr14:51956468 | G | T | 92 | a0001c0001t0001g0175 a0001c0001t0001g0206 a0001c0001t0001g0215 others(89): Show |
92 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.87+5703G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51956468 | |||||||
| chr14:51956565 | T | G | 5 | a0001c0001t0001g0168 a0001c0001t0001g0241 a0001c0001t0001g0247 others(2): Show |
5 | HG00323.hp2 HG00642.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.87+5800T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51956565 | |||||||
| chr14:51956715 | C | T | 1 | a0001c0001t0051g0342 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.87+5950C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51956715 | |||||||
| chr14:51956730 | G | A | 94 | a0001c0001t0001g0175 a0001c0001t0001g0206 a0001c0001t0001g0215 others(91): Show |
94 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.87+5965G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51956730 | |||||||
| chr14:51956892 | C | A | 6 | a0001c0001t0016g0007 a0001c0001t0016g0351 a0001c0001t0016g0352 others(3): Show |
6 | HG02622.hp2 HG02723.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+6127C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51956892 | |||||||
| chr14:51957011 | A | G | 347 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(344): Show |
348 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.87+6246A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51957011 | |||||||
| chr14:51957055 | G | A | 38 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0003g0055 others(35): Show |
38 | HG01243.hp1 HG01496.hp2 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.87+6290G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51957055 | |||||||
| chr14:51957067 | T | A | 109 | a0001c0001t0001g0025 a0001c0001t0001g0168 a0001c0001t0001g0212 others(106): Show |
109 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(106): Show |
intron_variant | MODIFIER | c.87+6302T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51957067 | |||||||
| chr14:51957156 | G | GATCC | 109 | a0001c0001t0001g0025 a0001c0001t0001g0168 a0001c0001t0001g0212 others(106): Show |
109 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(106): Show |
intron_variant | MODIFIER | c.87+6392_87+6395dup others(4): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51957156 | ||||||
| chr14:51957567 | G | A | 98 | a0001c0001t0001g0025 a0001c0001t0001g0168 a0001c0001t0001g0212 others(95): Show |
98 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.87+6802G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51957567 | |||||||
| chr14:51957603 | T | C | 3 | a0001c0002t0031g0030 a0001c0002t0044g0133 a0001c0002t0061g0365 |
3 | HG02602.hp2 NA18972.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.87+6838T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51957603 | |||||||
| chr14:51957611 | T | C | 3 | a0001c0001t0001g0119 a0001c0001t0001g0242 a0001c0001t0001g0251 |
3 | NA18969.hp2 NA18981.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.87+6846T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51957611 | |||||||
| chr14:51957624 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.87+6859G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51957624 | |||||||
| chr14:51957775 | C | T | 94 | a0001c0001t0001g0025 a0001c0001t0001g0168 a0001c0001t0001g0212 others(91): Show |
94 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.87+7010C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51957775 | |||||||
| chr14:51957776 | G | A | 19 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0003g0055 others(16): Show |
19 | HG01496.hp2 HG02109.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.87+7011G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51957776 | |||||||
| chr14:51958251 | C | T | 94 | a0001c0001t0001g0175 a0001c0001t0001g0206 a0001c0001t0001g0215 others(91): Show |
94 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.87+7486C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51958251 | |||||||
| chr14:51958280 | A | G | 2 | a0001c0001t0003g0027 a0001c0001t0064g0031 |
2 | HG01109.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.87+7515A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51958280 | |||||||
| chr14:51958366 | GC | G | 107 | a0001c0001t0001g0025 a0001c0001t0001g0168 a0001c0001t0001g0212 others(104): Show |
107 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.87+7607delC | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51958366 | ||||||
| chr14:51958412 | C | A | 1 | a0001c0002t0072g0196 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.87+7647C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51958412 | |||||||
| chr14:51958415 | T | A | 1 | a0001c0001t0029g0306 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.87+7650T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51958415 | |||||||
| chr14:51958426 | C | T | 1 | a0001c0001t0054g0202 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.87+7661C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51958426 | |||||||
| chr14:51958437 | G | A | 3 | a0001c0001t0004g0145 a0001c0001t0004g0146 a0001c0001t0054g0202 |
3 | HG03209.hp1 HG03704.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.87+7672G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51958437 | |||||||
| chr14:51958439 | T | TC | 103 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0034 others(100): Show |
103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.87+7684dupC | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51958439 | ||||||
| chr14:51958439 | T | TCC | 16 | a0001c0001t0001g0075 a0001c0001t0001g0240 a0001c0001t0001g0243 others(13): Show |
16 | HG00597.hp2 HG01070.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.87+7683_87+7684dup others(2): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51958439 | ||||||
| chr14:51958439 | TC | T | 116 | a0001c0001t0001g0025 a0001c0001t0001g0168 a0001c0001t0001g0212 others(113): Show |
116 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(113): Show |
intron_variant | MODIFIER | c.87+7684delC | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51958439 | ||||||
| chr14:51958562 | G | A | 1 | a0001c0001t0032g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.87+7797G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51958562 | |||||||
| chr14:51958602 | C | A | 6 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0009g0042 others(3): Show |
6 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+7837C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51958602 | |||||||
| chr14:51958706 | T | C | 106 | a0001c0001t0001g0025 a0001c0001t0001g0168 a0001c0001t0001g0212 others(103): Show |
106 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.88-7853T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51958706 | |||||||
| chr14:51958724 | C | T | 119 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0034 others(116): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.88-7835C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51958724 | |||||||
| chr14:51958727 | C | T | 1 | a0001c0001t0054g0202 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.88-7832C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51958727 | |||||||
| chr14:51958788 | A | G | 107 | a0001c0001t0001g0025 a0001c0001t0001g0168 a0001c0001t0001g0212 others(104): Show |
107 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.88-7771A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51958788 | |||||||
| chr14:51958874 | T | G | 1 | a0001c0001t0005g0013 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.88-7685T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51958874 | |||||||
| chr14:51958921 | T | G | 19 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0003g0055 others(16): Show |
19 | HG01496.hp2 HG02109.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.88-7638T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51958921 | |||||||
| chr14:51958952 | C | T | 1 | a0001c0001t0025g0213 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.88-7607C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51958952 | |||||||
| chr14:51959014 | T | C | 19 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0003g0055 others(16): Show |
19 | HG01496.hp2 HG02109.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.88-7545T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51959014 | |||||||
| chr14:51959105 | T | C | 1 | a0001c0001t0001g0263 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.88-7454T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51959105 | |||||||
| chr14:51959115 | C | A | 94 | a0001c0001t0001g0175 a0001c0001t0001g0206 a0001c0001t0001g0215 others(91): Show |
94 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.88-7444C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51959115 | |||||||
| chr14:51959159 | C | T | 5 | a0001c0001t0001g0126 a0001c0001t0001g0140 a0001c0001t0001g0276 others(2): Show |
5 | HG02738.hp1 HG03017.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.88-7400C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51959159 | |||||||
| chr14:51959192 | C | T | 3 | a0001c0001t0018g0323 a0001c0001t0018g0324 a0001c0001t0047g0298 |
3 | HG02809.hp1 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.88-7367C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51959192 | |||||||
| chr14:51959249 | C | T | 1 | a0001c0001t0007g0255 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.88-7310C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51959249 | |||||||
| chr14:51959498 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.88-7061C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51959498 | |||||||
| chr14:51959524 | G | T | 2 | a0001c0001t0040g0335 a0001c0001t0041g0334 |
2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.88-7035G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51959524 | |||||||
| chr14:51959643 | A | G | 130 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0034 others(127): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.88-6916A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51959643 | |||||||
| chr14:51959671 | TG | T | 130 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0034 others(127): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.88-6887delG | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51959671 | |||||||
| chr14:51959682 | G | C | 3 | a0001c0001t0018g0323 a0001c0001t0018g0324 a0001c0001t0047g0298 |
3 | HG02809.hp1 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.88-6877G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51959682 | |||||||
| chr14:51959732 | A | AGATT | 129 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0034 others(126): Show |
129 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.88-6826_88-6823dup others(4): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51959732 | ||||||
| chr14:51959734 | A | ATTGC | 103 | a0001c0001t0001g0025 a0001c0001t0001g0075 a0001c0001t0001g0168 others(100): Show |
103 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.88-6823_88-6822ins others(4): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51959734 | ||||||
| chr14:51959735 | T | TTGA | 19 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0003g0055 others(16): Show |
19 | HG01496.hp2 HG02109.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.88-6823_88-6822ins others(3): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51959735 | ||||||
| chr14:51959962 | G | A | 1 | a0001c0001t0029g0306 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.88-6597G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51959962 | |||||||
| chr14:51960064 | A | T | 213 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0034 others(210): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.88-6495A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51960064 | |||||||
| chr14:51960070 | T | C | 213 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0034 others(210): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.88-6489T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51960070 | |||||||
| chr14:51960174 | A | AT | 111 | a0001c0001t0001g0025 a0001c0001t0001g0168 a0001c0001t0001g0212 others(108): Show |
111 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(108): Show |
intron_variant | MODIFIER | c.88-6375dupT | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51960174 | ||||||
| chr14:51960223 | C | A | 5 | a0001c0001t0034g0377 a0001c0001t0036g0053 a0001c0001t0043g0336 others(2): Show |
5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.88-6336C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51960223 | |||||||
| chr14:51960247 | ATCTT | A | 9 | a0001c0001t0018g0323 a0001c0001t0018g0324 a0001c0001t0034g0377 others(6): Show |
9 | HG02809.hp1 HG02922.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.88-6307_88-6304del others(4): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51960247 | ||||||
| chr14:51960436 | G | A | 126 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0034 others(123): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.88-6123G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51960436 | |||||||
| chr14:51960459 | A | G | 84 | a0001c0001t0001g0025 a0001c0001t0001g0168 a0001c0001t0001g0212 others(81): Show |
84 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.88-6100A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51960459 | |||||||
| chr14:51960473 | T | C | 1 | a0001c0001t0002g0280 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.88-6086T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51960473 | |||||||
| chr14:51960479 | C | G | 3 | a0001c0001t0018g0323 a0001c0001t0018g0324 a0001c0001t0047g0298 |
3 | HG02809.hp1 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.88-6080C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51960479 | |||||||
| chr14:51960566 | T | G | 1 | a0001c0001t0001g0135 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.88-5993T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51960566 | |||||||
| chr14:51960582 | C | T | 4 | a0001c0001t0015g0132 a0001c0001t0015g0136 a0001c0001t0015g0138 others(1): Show |
4 | NA18946.hp1 NA19002.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.88-5977C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51960582 | |||||||
| chr14:51960587 | T | TTAACAAT others(25): Show |
100 | a0001c0001t0001g0175 a0001c0001t0001g0206 a0001c0001t0001g0215 others(97): Show |
100 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.88-5959_88-5928dup others(32): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51960587 | ||||||
| chr14:51960587 | T | TTAACAAT others(57): Show |
6 | a0001c0001t0004g0041 a0001c0001t0004g0043 a0001c0001t0009g0042 others(3): Show |
6 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-5928_88-5927ins others(64): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51960587 | ||||||
| chr14:51960657 | T | TTAAAA | 337 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(334): Show |
337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.88-5899_88-5898ins others(5): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51960657 | ||||||
| chr14:51960804 | G | A | 2 | a0001c0001t0007g0044 a0001c0001t0007g0046 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.88-5755G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51960804 | |||||||
| chr14:51960854 | A | G | 106 | a0001c0001t0001g0175 a0001c0001t0001g0206 a0001c0001t0001g0215 others(103): Show |
106 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.88-5705A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51960854 | |||||||
| chr14:51960907 | T | C | 337 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(334): Show |
337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.88-5652T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51960907 | |||||||
| chr14:51960913 | G | A | 6 | a0001c0002t0031g0030 a0001c0002t0044g0133 a0001c0002t0061g0365 others(3): Show |
6 | HG01433.hp1 HG02486.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-5646G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51960913 | |||||||
| chr14:51960936 | C | T | 337 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(334): Show |
337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.88-5623C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51960936 | |||||||
| chr14:51960941 | G | A | 337 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(334): Show |
337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.88-5618G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51960941 | |||||||
| chr14:51960949 | T | C | 337 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(334): Show |
337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.88-5610T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51960949 | |||||||
| chr14:51961068 | G | C | 100 | a0001c0001t0001g0175 a0001c0001t0001g0206 a0001c0001t0001g0215 others(97): Show |
100 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.88-5491G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51961068 | |||||||
| chr14:51961113 | C | T | 337 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(334): Show |
337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.88-5446C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51961113 | |||||||
| chr14:51961234 | A | G | 106 | a0001c0001t0001g0175 a0001c0001t0001g0206 a0001c0001t0001g0215 others(103): Show |
106 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.88-5325A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51961234 | |||||||
| chr14:51961384 | G | A | 144 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0034 others(141): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.88-5175G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51961384 | |||||||
| chr14:51961394 | A | G | 334 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(331): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.88-5165A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51961394 | |||||||
| chr14:51961413 | G | T | 334 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(331): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.88-5146G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51961413 | |||||||
| chr14:51961456 | C | A | 106 | a0001c0001t0001g0175 a0001c0001t0001g0206 a0001c0001t0001g0215 others(103): Show |
106 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.88-5103C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51961456 | |||||||
| chr14:51961456 | C | T | 7 | a0001c0001t0004g0326 a0001c0001t0009g0006 a0001c0001t0009g0033 others(4): Show |
7 | HG01074.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.88-5103C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51961456 | |||||||
| chr14:51961490 | C | G | 3 | a0001c0002t0031g0030 a0001c0002t0044g0133 a0001c0002t0061g0365 |
3 | HG02602.hp2 NA18972.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.88-5069C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51961490 | |||||||
| chr14:51961490 | C | T | 334 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(331): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.88-5069C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51961490 | |||||||
| chr14:51961569 | A | C | 334 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(331): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.88-4990A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51961569 | |||||||
| chr14:51961587 | G | A | 1 | a0001c0002t0074g0040 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.88-4972G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51961587 | |||||||
| chr14:51961625 | A | G | 3 | a0001c0001t0003g0055 a0001c0001t0003g0056 a0001c0001t0019g0051 |
3 | HG03453.hp1 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.88-4934A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51961625 | |||||||
| chr14:51961627 | A | T | 11 | a0001c0001t0003g0055 a0001c0001t0003g0056 a0001c0001t0004g0197 others(8): Show |
11 | HG01496.hp2 HG02109.hp1 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.88-4932A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51961627 | |||||||
| chr14:51961699 | G | A | 1 | a0001c0001t0002g0330 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.88-4860G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51961699 | |||||||
| chr14:51961708 | T | C | 337 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(334): Show |
337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.88-4851T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51961708 | |||||||
| chr14:51961776 | G | A | 3 | a0001c0002t0031g0030 a0001c0002t0044g0133 a0001c0002t0061g0365 |
3 | HG02602.hp2 NA18972.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.88-4783G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51961776 | |||||||
| chr14:51961848 | T | G | 41 | a0001c0001t0002g0049 a0001c0001t0002g0109 a0001c0001t0003g0307 others(38): Show |
42 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.88-4711T>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51961848 | |||||||
| chr14:51961915 | A | T | 334 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(331): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.88-4644A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51961915 | |||||||
| chr14:51962023 | T | A | 1 | a0001c0001t0004g0197 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.88-4536T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51962023 | |||||||
| chr14:51962041 | A | G | 353 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(350): Show |
353 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.88-4518A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51962041 | |||||||
| chr14:51962105 | C | G | 1 | a0001c0001t0054g0202 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.88-4454C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51962105 | |||||||
| chr14:51962118 | T | A | 334 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(331): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.88-4441T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51962118 | |||||||
| chr14:51962157 | A | T | 1 | a0001c0001t0022g0094 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.88-4402A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51962157 | |||||||
| chr14:51962171 | G | T | 7 | a0001c0001t0024g0058 a0001c0001t0024g0059 a0001c0001t0024g0063 others(4): Show |
7 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.88-4388G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51962171 | |||||||
| chr14:51962208 | T | TTCTTTAA others(2): Show |
334 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(331): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.88-4350_88-4349ins others(9): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51962208 | ||||||
| chr14:51962235 | A | G | 1 | a0001c0001t0034g0364 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.88-4324A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51962235 | |||||||
| chr14:51962241 | G | A | 4 | a0001c0001t0034g0377 a0001c0001t0036g0053 a0001c0001t0043g0336 others(1): Show |
4 | HG02922.hp2 HG03225.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.88-4318G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51962241 | |||||||
| chr14:51962297 | C | G | 11 | a0001c0001t0024g0058 a0001c0001t0024g0059 a0001c0001t0024g0063 others(8): Show |
11 | HG01433.hp1 HG02486.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.88-4262C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51962297 | |||||||
| chr14:51962329 | G | A | 334 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(331): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.88-4230G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51962329 | |||||||
| chr14:51962401 | A | G | 106 | a0001c0001t0001g0175 a0001c0001t0001g0206 a0001c0001t0001g0215 others(103): Show |
106 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.88-4158A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51962401 | |||||||
| chr14:51962469 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.88-4090G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51962469 | |||||||
| chr14:51962484 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.88-4075A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51962484 | |||||||
| chr14:51962524 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.88-4035C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51962524 | |||||||
| chr14:51962534 | C | T | 334 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(331): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.88-4025C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51962534 | |||||||
| chr14:51962758 | C | G | 334 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(331): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.88-3801C>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51962758 | |||||||
| chr14:51962830 | G | A | 1 | a0001c0001t0054g0202 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.88-3729G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51962830 | |||||||
| chr14:51962855 | C | A | 334 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(331): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.88-3704C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51962855 | |||||||
| chr14:51962879 | T | C | 1 | a0001c0001t0004g0017 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.88-3680T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51962879 | |||||||
| chr14:51962901 | A | G | 334 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(331): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.88-3658A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51962901 | |||||||
| chr14:51962939 | G | T | 3 | a0001c0002t0031g0030 a0001c0002t0044g0133 a0001c0002t0061g0365 |
3 | HG02602.hp2 NA18972.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.88-3620G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51962939 | |||||||
| chr14:51963175 | G | A | 334 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(331): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.88-3384G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963175 | |||||||
| chr14:51963331 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.88-3228C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963331 | |||||||
| chr14:51963359 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.88-3200C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963359 | |||||||
| chr14:51963360 | G | A | 2 | a0001c0001t0002g0109 a0001c0001t0005g0110 |
2 | NA18989.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.88-3199G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963360 | |||||||
| chr14:51963387 | C | T | 334 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(331): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.88-3172C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963387 | |||||||
| chr14:51963494 | T | C | 334 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(331): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.88-3065T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963494 | |||||||
| chr14:51963692 | C | T | 1 | a0001c0001t0043g0336 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.88-2867C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963692 | |||||||
| chr14:51963769 | T | A | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2790T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963769 | |||||||
| chr14:51963772 | C | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2787C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963772 | |||||||
| chr14:51963773 | A | G | 18 | a0001c0001t0003g0055 a0001c0001t0003g0056 a0001c0001t0004g0197 others(15): Show |
18 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.88-2786A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963773 | |||||||
| chr14:51963775 | C | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2784C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963775 | |||||||
| chr14:51963777 | A | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2782A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963777 | |||||||
| chr14:51963781 | A | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2778A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963781 | |||||||
| chr14:51963782 | A | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2777A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963782 | |||||||
| chr14:51963784 | G | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2775G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963784 | |||||||
| chr14:51963786 | G | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2773G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963786 | |||||||
| chr14:51963787 | G | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2772G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963787 | |||||||
| chr14:51963797 | C | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2762C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963797 | |||||||
| chr14:51963801 | C | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2758C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963801 | |||||||
| chr14:51963802 | C | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2757C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963802 | |||||||
| chr14:51963803 | T | A | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2756T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963803 | |||||||
| chr14:51963804 | C | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2755C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963804 | |||||||
| chr14:51963806 | G | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2753G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963806 | |||||||
| chr14:51963807 | G | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2752G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963807 | |||||||
| chr14:51963811 | A | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2748A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963811 | |||||||
| chr14:51963812 | C | A | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2747C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963812 | |||||||
| chr14:51963814 | G | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2745G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963814 | |||||||
| chr14:51963816 | G | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2743G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963816 | |||||||
| chr14:51963817 | A | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2742A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963817 | |||||||
| chr14:51963819 | G | A | 1 | a0001c0001t0003g0021 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.88-2740G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963819 | |||||||
| chr14:51963819 | G | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2740G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963819 | |||||||
| chr14:51963822 | C | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2737C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963822 | |||||||
| chr14:51963824 | A | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2735A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963824 | |||||||
| chr14:51963825 | A | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2734A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963825 | |||||||
| chr14:51963826 | A | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2733A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963826 | |||||||
| chr14:51963828 | A | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2731A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963828 | |||||||
| chr14:51963829 | G | A | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2730G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963829 | |||||||
| chr14:51963830 | G | A | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2729G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963830 | |||||||
| chr14:51963831 | A | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2728A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963831 | |||||||
| chr14:51963832 | A | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2727A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963832 | |||||||
| chr14:51963836 | T | A | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2723T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963836 | |||||||
| chr14:51963837 | A | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2722A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963837 | |||||||
| chr14:51963839 | C | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2720C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963839 | |||||||
| chr14:51963841 | C | A | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2718C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963841 | |||||||
| chr14:51963842 | A | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2717A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963842 | |||||||
| chr14:51963845 | G | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2714G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963845 | |||||||
| chr14:51963846 | TCTGGAAC others(3): Show |
T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2712_88-2703del others(10): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963846 | |||||||
| chr14:51963858 | T | C | 333 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(330): Show |
333 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.88-2701T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963858 | |||||||
| chr14:51963859 | A | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2700A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963859 | |||||||
| chr14:51963860 | A | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2699A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963860 | |||||||
| chr14:51963861 | G | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2698G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963861 | |||||||
| chr14:51963862 | G | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2697G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963862 | |||||||
| chr14:51963865 | A | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2694A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963865 | |||||||
| chr14:51963867 | A | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2692A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963867 | |||||||
| chr14:51963870 | A | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2689A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963870 | |||||||
| chr14:51963871 | A | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2688A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963871 | |||||||
| chr14:51963872 | A | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2687A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963872 | |||||||
| chr14:51963873 | A | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2686A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963873 | |||||||
| chr14:51963881 | T | A | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2678T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963881 | |||||||
| chr14:51963882 | G | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2677G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963882 | |||||||
| chr14:51963885 | A | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2674A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963885 | |||||||
| chr14:51963886 | G | A | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2673G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963886 | |||||||
| chr14:51963889 | C | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2670C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963889 | |||||||
| chr14:51963891 | G | A | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2668G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963891 | |||||||
| chr14:51963894 | A | T | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2665A>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963894 | |||||||
| chr14:51963896 | G | A | 1 | a0001c0001t0021g0087 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.88-2663G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963896 | |||||||
| chr14:51963993 | G | A | 334 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(331): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.88-2566G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51963993 | |||||||
| chr14:51964088 | T | A | 334 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(331): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.88-2471T>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51964088 | |||||||
| chr14:51964118 | C | T | 1 | a0001c0001t0029g0114 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.88-2441C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51964118 | |||||||
| chr14:51964151 | T | C | 334 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(331): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.88-2408T>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51964151 | |||||||
| chr14:51964223 | A | G | 3 | a0001c0001t0018g0323 a0001c0001t0018g0324 a0001c0001t0047g0298 |
3 | HG02809.hp1 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.88-2336A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51964223 | |||||||
| chr14:51964421 | G | A | 107 | a0001c0001t0001g0175 a0001c0001t0001g0206 a0001c0001t0001g0215 others(104): Show |
107 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.88-2138G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51964421 | |||||||
| chr14:51964650 | G | A | 3 | a0001c0002t0072g0196 a0001c0002t0073g0010 a0001c0002t0074g0040 |
3 | HG01433.hp1 HG02486.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.88-1909G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51964650 | |||||||
| chr14:51964770 | G | A | 1 | a0001c0001t0075g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.88-1789G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51964770 | |||||||
| chr14:51964837 | C | A | 328 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(325): Show |
328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.88-1722C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51964837 | |||||||
| chr14:51965303 | G | A | 2 | a0001c0001t0004g0145 a0001c0001t0054g0202 |
2 | HG03209.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.88-1256G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51965303 | |||||||
| chr14:51965307 | G | A | 1 | a0001c0001t0036g0053 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.88-1252G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51965307 | |||||||
| chr14:51965432 | G | A | 5 | a0001c0001t0034g0377 a0001c0001t0036g0053 a0001c0001t0043g0336 others(2): Show |
5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.88-1127G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51965432 | |||||||
| chr14:51965456 | C | T | 96 | a0001c0001t0001g0175 a0001c0001t0001g0206 a0001c0001t0001g0215 others(93): Show |
96 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.88-1103C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51965456 | |||||||
| chr14:51965576 | C | T | 15 | a0001c0001t0002g0089 a0001c0001t0002g0218 a0001c0001t0002g0260 others(12): Show |
15 | HG00597.hp1 HG01070.hp2 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.88-983C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51965576 | |||||||
| chr14:51965579 | C | A | 1 | a0001c0001t0002g0153 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.88-980C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51965579 | |||||||
| chr14:51965605 | C | A | 103 | a0001c0001t0001g0175 a0001c0001t0001g0206 a0001c0001t0001g0215 others(100): Show |
103 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.88-954C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51965605 | |||||||
| chr14:51965702 | C | A | 334 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(331): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.88-857C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51965702 | |||||||
| chr14:51965930 | C | T | 1 | a0001c0001t0066g0032 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.88-629C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51965930 | |||||||
| chr14:51965968 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.88-591G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51965968 | |||||||
| chr14:51965985 | G | C | 7 | a0001c0001t0024g0058 a0001c0001t0024g0059 a0001c0001t0024g0063 others(4): Show |
7 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.88-574G>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51965985 | |||||||
| chr14:51966030 | G | A | 7 | a0001c0001t0024g0058 a0001c0001t0024g0059 a0001c0001t0024g0063 others(4): Show |
7 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.88-529G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51966030 | |||||||
| chr14:51966044 | A | G | 7 | a0001c0001t0004g0326 a0001c0001t0009g0006 a0001c0001t0009g0033 others(4): Show |
7 | HG01074.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.88-515A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51966044 | |||||||
| chr14:51966084 | C | T | 1 | a0001c0002t0074g0040 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.88-475C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51966084 | |||||||
| chr14:51966132 | C | T | 1 | a0001c0002t0074g0040 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.88-427C>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51966132 | |||||||
| chr14:51966156 | G | A | 1 | a0001c0001t0051g0342 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.88-403G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51966156 | |||||||
| chr14:51966209 | C | CA | 60 | a0001c0001t0001g0206 a0001c0001t0001g0289 a0001c0001t0001g0299 others(57): Show |
60 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.88-322dupA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51966209 | ||||||
| chr14:51966209 | C | CAA | 17 | a0001c0001t0009g0042 a0001c0001t0009g0203 a0001c0001t0009g0310 others(14): Show |
17 | HG01074.hp2 HG01099.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.88-323_88-322dupAA | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51966209 | ||||||
| chr14:51966209 | C | CAAA | 19 | a0001c0001t0003g0056 a0001c0001t0004g0197 a0001c0001t0004g0326 others(16): Show |
19 | HG01496.hp2 HG02622.hp2 HG02647.hp1 others(16): Show |
intron_variant | MODIFIER | c.88-324_88-322dupAA others(1): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51966209 | ||||||
| chr14:51966209 | C | CAAAA | 34 | a0001c0001t0001g0025 a0001c0001t0001g0212 a0001c0001t0001g0247 others(31): Show |
34 | HG00642.hp2 HG01361.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.88-325_88-322dupAA others(2): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51966209 | ||||||
| chr14:51966209 | C | CAAAAA | 39 | a0001c0001t0001g0168 a0001c0001t0001g0241 a0001c0001t0003g0054 others(36): Show |
39 | HG00323.hp2 HG00639.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.88-326_88-322dupAA others(3): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51966209 | ||||||
| chr14:51966209 | C | CAAAAAA | 10 | a0001c0001t0003g0143 a0001c0001t0003g0176 a0001c0001t0003g0372 others(7): Show |
10 | HG00741.hp2 HG01515.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.88-327_88-322dupAA others(4): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51966209 | ||||||
| chr14:51966209 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0011g0090 a0001c0001t0011g0125 |
2 | NA18947.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.88-332_88-322delAA others(9): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51966209 | ||||||
| chr14:51966218 | A | AAAAAAAG | 9 | a0001c0001t0001g0029 a0001c0001t0001g0075 a0001c0001t0001g0126 others(6): Show |
9 | HG02698.hp2 HG02738.hp1 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.88-335_88-334insGA others(5): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51966218 | ||||||
| chr14:51966227 | A | AAAAAAAA others(4): Show |
1 | a0001c0002t0072g0196 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.88-328_88-318dupAA others(9): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51966227 | ||||||
| chr14:51966227 | A | AAAAAAAA others(3): Show |
1 | a0001c0002t0073g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.88-323_88-322insCA others(8): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51966227 | ||||||
| chr14:51966227 | A | C | 1 | a0001c0002t0074g0040 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.88-332A>C | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51966227 | |||||||
| chr14:51966231 | A | AAAAAAAA others(1): Show |
21 | a0001c0001t0001g0052 a0001c0001t0001g0113 a0001c0001t0001g0184 others(18): Show |
21 | HG00597.hp2 HG00738.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.88-322_88-321insAG others(6): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51966231 | ||||||
| chr14:51966231 | A | AAAAAAAG | 74 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0038 others(71): Show |
74 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.88-322_88-321insGA others(5): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51966231 | ||||||
| chr14:51966231 | A | AAAAAAG | 8 | a0001c0001t0001g0037 a0001c0001t0001g0151 a0001c0001t0007g0011 others(5): Show |
8 | HG00140.hp2 HG00735.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.88-323_88-322insGA others(4): Show |
GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 51966231 | ||||||
| chr14:51966231 | A | G | 15 | a0001c0001t0001g0029 a0001c0001t0001g0075 a0001c0001t0001g0126 others(12): Show |
15 | HG00140.hp1 HG00639.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.88-328A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51966231 | |||||||
| chr14:51966247 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.88-312G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51966247 | |||||||
| chr14:51966252 | A | G | 18 | a0001c0001t0004g0326 a0001c0001t0009g0006 a0001c0001t0009g0033 others(15): Show |
18 | HG01074.hp2 HG02258.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.88-307A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51966252 | |||||||
| chr14:51966265 | G | T | 1 | a0001c0001t0037g0180 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.88-294G>T | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51966265 | |||||||
| chr14:51966353 | C | A | 1 | a0001c0001t0001g0294 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.88-206C>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51966353 | |||||||
| chr14:51966385 | A | G | 245 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(242): Show |
245 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.88-174A>G | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51966385 | |||||||
| chr14:51966397 | G | A | 245 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0029 others(242): Show |
245 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.88-162G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51966397 | |||||||
| chr14:51966461 | G | A | 108 | a0001c0001t0001g0175 a0001c0001t0001g0206 a0001c0001t0001g0215 others(105): Show |
108 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.88-98G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51966461 | |||||||
| chr14:51966517 | G | A | 13 | a0001c0001t0003g0055 a0001c0001t0003g0056 a0001c0001t0004g0197 others(10): Show |
13 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.88-42G>A | GNG2 | ENSG00000186469.9 | transcript | ENST00000556766.6 | protein_coding | 3/3 | chr14 | 51966517 |