Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2743 |
| ensemblid | ENSG00000109738.11 |
| hgncid | 4329 |
| symbol | GLRB |
| name | glycine receptor beta |
| refseq_nuc | NM_000824.5 |
| refseq_prot | NP_000815.1 |
| ensembl_nuc | ENST00000264428.9 |
| ensembl_prot | ENSP00000264428.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 157076150 |
| end | 157172090 |
| strand | + |
| ver | v1.2 |
| region | chr4:157076150-157172090 |
| region5000 | chr4:157071150-157177090 |
| regionname0 | GLRB_chr4_157076150_157172090 |
| regionname5000 | GLRB_chr4_157071150_157177090 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 497 | 302 | 90 | 46 | 135 | 4 | 25 | 103 | GLRB_chr4_157071150_157177090 | GLRB | MKFLL others(492): Show |
chr4 | 157071150 | 157177090 |
| a0002 | 0/0 | 497 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GLRB_chr4_157071150_157177090 | GLRB | MKFLL others(492): Show |
chr4 | 157071150 | 157177090 |
| a0003 | 0/0 | 497 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GLRB_chr4_157071150_157177090 | GLRB | MKFLL others(492): Show |
chr4 | 157071150 | 157177090 |
| a0004 | 0/0 | 497 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GLRB_chr4_157071150_157177090 | GLRB | MKFLL others(492): Show |
chr4 | 157071150 | 157177090 |
| a0005 | 0/0 | 497 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | MKFLL others(492): Show |
chr4 | 157071150 | 157177090 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1491 | 279 | 76 | 46 | 130 | 3 | 23 | GLRB_chr4_157071150_157177090 | GLRB | ATGAA others(1486): Show |
chr4 | 157071150 | 157177090 | ||
| a0001c0002 | 0/0 | 1491 | 14 | 7 | 0 | 4 | 1 | 2 | GLRB_chr4_157071150_157177090 | GLRB | ATGAA others(1486): Show |
chr4 | 157071150 | 157177090 | ||
| a0001c0003 | 1/0 | 1491 | 7 | 6 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | ATGAA others(1486): Show |
chr4 | 157071150 | 157177090 | ||
| a0001c0007 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | ATGAA others(1486): Show |
chr4 | 157071150 | 157177090 | ||
| a0001c0008 | 0/0 | 1491 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | ATGAA others(1486): Show |
chr4 | 157071150 | 157177090 | ||
| a0002c0005 | 0/0 | 1491 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | ATGAA others(1486): Show |
chr4 | 157071150 | 157177090 | ||
| a0003c0009 | 0/0 | 1491 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | ATGAA others(1486): Show |
chr4 | 157071150 | 157177090 | ||
| a0004c0004 | 0/0 | 1491 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | ATGAA others(1486): Show |
chr4 | 157071150 | 157177090 | ||
| a0005c0006 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | ATGAA others(1486): Show |
chr4 | 157071150 | 157177090 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3033 | 92 | 9 | 21 | 48 | 2 | 11 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0001t0002 | 0/0 | 3033 | 63 | 8 | 7 | 39 | 1 | 8 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0001t0003 | 0/0 | 3033 | 45 | 29 | 10 | 3 | 0 | 3 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0001t0004 | 0/0 | 3033 | 24 | 0 | 0 | 24 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0001t0005 | 0/0 | 3033 | 15 | 7 | 0 | 7 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0001t0006 | 0/0 | 3033 | 7 | 6 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0001t0007 | 0/0 | 3033 | 7 | 5 | 2 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0001t0009 | 0/0 | 3033 | 4 | 0 | 0 | 4 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0001t0010 | 0/0 | 3033 | 3 | 3 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0001t0011 | 0/0 | 3033 | 3 | 0 | 0 | 3 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0001t0012 | 0/0 | 3033 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0001t0013 | 0/0 | 3033 | 3 | 3 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0001t0014 | 0/0 | 3033 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0001t0015 | 0/0 | 3033 | 2 | 0 | 2 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0001t0016 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0001t0017 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0001t0018 | 0/0 | 3033 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0001t0019 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0001t0020 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0001t0021 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0001t0022 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0001t0023 | 0/0 | 3033 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0001t0025 | 0/0 | 3033 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0002t0006 | 0/0 | 3033 | 6 | 0 | 0 | 4 | 0 | 2 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0002t0008 | 0/0 | 3033 | 6 | 6 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0002t0012 | 0/0 | 3033 | 2 | 1 | 0 | 0 | 1 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0003t0001 | 1/0 | 3033 | 6 | 5 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0003t0014 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0007t0002 | 0/0 | 3033 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0001c0008t0024 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0002c0005t0006 | 0/0 | 3033 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0003c0009t0009 | 0/0 | 3033 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0004c0004t0002 | 0/0 | 3033 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| a0005c0006t0002 | 0/0 | 3033 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | AGGCG others(3028): Show |
chr4 | 157071150 | 157177090 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0004g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0005g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0005g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0005g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0006g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0006g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0006g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0007g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0007g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0007g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0007g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0007g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0007g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0009g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0009g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0009g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0009g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0010g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0010g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0010g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0011g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0011g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0011g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0012g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0013g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0013g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0013g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0014g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0015g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0015g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0016g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0017g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0018g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0019g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0020g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0021g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0022g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0023g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0001t0025g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0002t0006g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0002t0006g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0002t0006g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0002t0006g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0002t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0002t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0002t0008g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0002t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0002t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0002t0008g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0002t0008g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0002t0008g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0002t0012g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0002t0012g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0003t0001g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0003t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0003t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0003t0014g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0007t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0001c0008t0024g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0002c0005t0006g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0003c0009t0009g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0004c0004t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| a0005c0006t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0193 | EUR | FIN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | FIN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0280 | EAS | CHS | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | CHS | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | CHS | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG00544 | hp2 | a0001 | c0002 | t0006 | g0188 | EAS | CHS | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | CHS | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0047 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG00639 | hp2 | a0001 | c0001 | t0012 | g0091 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01081 | hp2 | a0001 | c0001 | t0006 | g0159 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01192 | hp1 | a0001 | c0001 | t0007 | g0219 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01255 | hp1 | a0001 | c0001 | t0014 | g0253 | AMR | CLM | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | CLM | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01496 | hp2 | a0001 | c0001 | t0025 | g0120 | AMR | CLM | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01515 | hp1 | a0001 | c0002 | t0012 | g0107 | EUR | IBS | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | IBS | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01952 | hp2 | a0001 | c0001 | t0015 | g0186 | AMR | PEL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0288 | AMR | PEL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | PEL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01981 | hp1 | a0001 | c0001 | t0007 | g0192 | AMR | PEL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | PEL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0289 | AMR | PEL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02015 | hp1 | a0001 | c0002 | t0006 | g0179 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0287 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0269 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02080 | hp2 | a0001 | c0002 | t0006 | g0180 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CDX | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0150 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02258 | hp2 | a0001 | c0008 | t0024 | g0286 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02280 | hp1 | a0001 | c0002 | t0008 | g0163 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02293 | hp2 | a0001 | c0001 | t0015 | g0239 | AMR | PEL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0115 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0161 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0249 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02647 | hp1 | a0001 | c0001 | t0010 | g0257 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02683 | hp1 | a0002 | c0005 | t0006 | g0204 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02698 | hp1 | a0001 | c0001 | t0005 | g0167 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0238 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0182 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02735 | hp1 | a0001 | c0002 | t0006 | g0176 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02809 | hp2 | a0001 | c0001 | t0016 | g0175 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0218 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02895 | hp1 | a0001 | c0001 | t0019 | g0240 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0260 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0072 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0057 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0086 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0259 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0160 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0172 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0261 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0155 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0202 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0254 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0242 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03139 | hp1 | a0001 | c0002 | t0008 | g0162 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0250 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03195 | hp1 | a0001 | c0002 | t0008 | g0025 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03195 | hp2 | a0001 | c0001 | t0021 | g0252 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0026 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03225 | hp1 | a0001 | c0002 | t0008 | g0156 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0251 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0229 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0170 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03486 | hp1 | a0001 | c0001 | t0010 | g0255 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03486 | hp2 | a0001 | c0001 | t0022 | g0142 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03492 | hp2 | a0003 | c0009 | t0009 | g0106 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0217 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03540 | hp2 | a0001 | c0001 | t0013 | g0019 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03579 | hp1 | a0001 | c0002 | t0012 | g0153 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | STU | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | STU | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0033 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03927 | hp1 | a0004 | c0004 | t0002 | g0244 | SAS | BEB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0029 | SAS | STU | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG04115 | hp2 | a0001 | c0002 | t0006 | g0177 | SAS | STU | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | STU | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0070 | SAS | STU | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18522 | hp1 | a0001 | c0003 | t0014 | g0258 | AFR | YRI | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | YRI | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0283 | EAS | CHB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18906 | hp1 | a0001 | c0001 | t0013 | g0037 | AFR | YRI | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0079 | AFR | YRI | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18939 | hp2 | a0001 | c0001 | t0011 | g0264 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0285 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18952 | hp1 | a0001 | c0007 | t0002 | g0185 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18957 | hp2 | a0001 | c0001 | t0011 | g0278 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18965 | hp2 | a0001 | c0001 | t0005 | g0214 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0268 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18971 | hp1 | a0001 | c0001 | t0011 | g0265 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18974 | hp2 | a0001 | c0001 | t0005 | g0248 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18975 | hp1 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18977 | hp1 | a0001 | c0001 | t0005 | g0209 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0213 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0275 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18985 | hp2 | a0001 | c0001 | t0009 | g0074 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0277 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0281 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18998 | hp2 | a0001 | c0001 | t0023 | g0272 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0279 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0282 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19030 | hp1 | a0001 | c0002 | t0008 | g0015 | AFR | LWK | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0215 | AFR | LWK | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | LWK | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19056 | hp1 | a0001 | c0001 | t0009 | g0075 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0284 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19070 | hp1 | a0001 | c0001 | t0018 | g0234 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19074 | hp1 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19081 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19081 | hp2 | a0001 | c0001 | t0009 | g0093 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19082 | hp1 | a0001 | c0002 | t0006 | g0178 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19084 | hp1 | a0001 | c0001 | t0005 | g0212 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19084 | hp2 | a0001 | c0001 | t0009 | g0076 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19085 | hp2 | a0005 | c0006 | t0002 | g0199 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19091 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0067 | AFR | YRI | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0181 | AFR | YRI | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0158 | AFR | ASW | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA20129 | hp2 | a0001 | c0001 | t0010 | g0256 | AFR | ASW | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | GIH | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0194 | SAS | GIH | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02109 | hp1 | a0001 | c0001 | t0020 | g0174 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02109 | hp2 | a0001 | c0001 | t0017 | g0021 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0157 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0173 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0168 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG03471 | hp2 | a0001 | c0002 | t0008 | g0024 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | USA | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| HG06807 | hp2 | a0001 | c0001 | t0013 | g0018 | AFR | USA | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0136 | AFR | LWK | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | LWK | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0058 | REF | REF | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0066 | REF | REF | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:157136671 | G | A | 1 | a0004 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.500G>A | p.Arg167His | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 5/10 | 677/3033 | 500/1494 | 167/497 | chr4 | 157136671 | |||
| chr4:157136883 | A | G | 1 | a0003 | 1 | HG03492.hp2 | missense_variant | MODERATE | c.607A>G | p.Ser203Gly | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/10 | 784/3033 | 607/1494 | 203/497 | chr4 | 157136883 | |||
| chr4:157138811 | G | A | 1 | a0002 | 1 | HG02683.hp1 | missense_variant&splice_region_variant | MODERATE | c.613G>A | p.Gly205Ser | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/10 | 790/3033 | 613/1494 | 205/497 | chr4 | 157138811 | |||
| chr4:157170619 | C | G | 1 | a0005 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.1385C>G | p.Ala462Gly | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 1562/3033 | 1385/1494 | 462/497 | chr4 | 157170619 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:157143820 | C | T | 1 | a0001c0008 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.765C>T | p.Cys255Cys | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/10 | 942/3033 | 765/1494 | 255/497 | chr4 | 157143820 | |||
| chr4:157143886 | T | C | 8 | a0001c0001 a0001c0002 a0001c0007 others(5): Show |
298 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(295): Show |
synonymous_variant | LOW | c.831T>C | p.Thr277Thr | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/10 | 1008/3033 | 831/1494 | 277/497 | chr4 | 157143886 | |||
| chr4:157152761 | T | C | 1 | a0001c0002 | 14 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(11): Show |
synonymous_variant | LOW | c.948T>C | p.Leu316Leu | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/10 | 1125/3033 | 948/1494 | 316/497 | chr4 | 157152761 | |||
| chr4:157152857 | A | G | 1 | a0001c0007 | 1 | NA18952.hp1 | synonymous_variant | LOW | c.1044A>G | p.Ala348Ala | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/10 | 1221/3033 | 1044/1494 | 348/497 | chr4 | 157152857 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:157076225 | T | C | 26 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(23): Show |
196 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(193): Show |
5_prime_UTR_variant | MODIFIER | c.-102T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/10 | 1800 | chr4 | 157076225 | ||||||
| chr4:157076258 | C | T | 4 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0023 others(1): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-69C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/10 | 1767 | chr4 | 157076258 | ||||||
| chr4:157076270 | C | T | 1 | a0001c0008t0024 | 1 | HG02258.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-57C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/10 | chr4 | 157076270 | |||||||
| chr4:157077999 | G | T | 1 | a0001c0001t0015 | 2 | HG01952.hp2 HG02293.hp2 |
5_prime_UTR_variant | MODIFIER | c.-26G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/10 | 26 | chr4 | 157077999 | ||||||
| chr4:157078009 | A | T | 5 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0021 others(2): Show |
7 | HG01255.hp1 HG02647.hp1 HG03195.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-16A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/10 | 16 | chr4 | 157078009 | ||||||
| chr4:157170761 | C | T | 1 | a0001c0001t0020 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*33C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 33 | chr4 | 157170761 | ||||||
| chr4:157170851 | T | C | 1 | a0001c0008t0024 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*123T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 123 | chr4 | 157170851 | ||||||
| chr4:157170888 | G | A | 5 | a0001c0001t0006 a0001c0001t0012 a0001c0002t0006 others(2): Show |
17 | HG00544.hp2 HG00639.hp2 HG01081.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*160G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 160 | chr4 | 157170888 | ||||||
| chr4:157170979 | A | G | 1 | a0001c0001t0025 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*251A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 251 | chr4 | 157170979 | ||||||
| chr4:157171233 | T | A | 4 | a0001c0001t0010 a0001c0001t0016 a0001c0001t0017 others(1): Show |
6 | HG02109.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*505T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 505 | chr4 | 157171233 | ||||||
| chr4:157171270 | T | A | 26 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(23): Show |
188 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*542T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 542 | chr4 | 157171270 | ||||||
| chr4:157171303 | T | C | 1 | a0001c0001t0007 | 7 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*575T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 575 | chr4 | 157171303 | ||||||
| chr4:157171310 | G | A | 1 | a0001c0001t0018 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*582G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 582 | chr4 | 157171310 | ||||||
| chr4:157171581 | T | C | 6 | a0001c0001t0006 a0001c0001t0012 a0001c0002t0006 others(3): Show |
23 | HG00544.hp2 HG00639.hp2 HG01081.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*853T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 853 | chr4 | 157171581 | ||||||
| chr4:157171631 | T | C | 2 | a0001c0001t0010 a0001c0001t0016 |
4 | HG02647.hp1 HG02809.hp2 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*903T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 903 | chr4 | 157171631 | ||||||
| chr4:157171635 | T | A | 1 | a0001c0008t0024 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*907T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 907 | chr4 | 157171635 | ||||||
| chr4:157171691 | T | C | 1 | a0001c0001t0019 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*963T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 963 | chr4 | 157171691 | ||||||
| chr4:157171768 | A | G | 6 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0013 others(3): Show |
58 | HG00639.hp1 HG00733.hp1 HG00738.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1040A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 1040 | chr4 | 157171768 | ||||||
| chr4:157171909 | C | T | 6 | a0001c0001t0006 a0001c0001t0012 a0001c0002t0006 others(3): Show |
23 | HG00544.hp2 HG00639.hp2 HG01081.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1181C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 1181 | chr4 | 157171909 | ||||||
| chr4:157172073 | A | G | 1 | a0001c0001t0011 | 3 | NA18939.hp2 NA18957.hp2 NA18971.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1345A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 1345 | chr4 | 157172073 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:157076333 | G | T | 2 | a0001c0001t0003g0288 a0001c0001t0003g0289 |
2 | HG01975.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.-30+36G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076333 | |||||||
| chr4:157076334 | C | T | 1 | a0001c0001t0003g0287 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-30+37C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076334 | |||||||
| chr4:157076346 | G | T | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-30+49G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076346 | |||||||
| chr4:157076392 | G | A | 1 | a0001c0002t0008g0015 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-30+95G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076392 | |||||||
| chr4:157076408 | G | T | 3 | a0001c0001t0006g0259 a0001c0001t0006g0260 a0001c0001t0006g0261 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-30+111G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076408 | |||||||
| chr4:157076437 | C | A | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-30+140C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076437 | |||||||
| chr4:157076438 | C | G | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-30+141C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076438 | |||||||
| chr4:157076458 | TGCGCGGG others(6): Show |
T | 7 | a0001c0001t0003g0254 a0001c0001t0010g0255 a0001c0001t0010g0256 others(4): Show |
7 | HG01255.hp1 HG02647.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30+169_-30+181del others(13): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 157076458 | ||||||
| chr4:157076542 | A | G | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-30+245A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076542 | |||||||
| chr4:157076568 | A | G | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-30+271A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076568 | |||||||
| chr4:157076641 | C | G | 4 | a0001c0001t0010g0255 a0001c0001t0010g0256 a0001c0001t0010g0257 others(1): Show |
4 | HG02647.hp1 HG03486.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+344C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076641 | |||||||
| chr4:157076677 | G | T | 95 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(92): Show |
103 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.-30+380G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076677 | |||||||
| chr4:157076728 | C | G | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-30+431C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076728 | |||||||
| chr4:157076745 | A | C | 13 | a0001c0001t0003g0157 a0001c0001t0003g0160 a0001c0001t0006g0155 others(10): Show |
13 | HG01081.hp2 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-30+448A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076745 | |||||||
| chr4:157076757 | T | TG | 27 | a0001c0001t0001g0154 a0001c0001t0004g0001 a0001c0001t0004g0262 others(24): Show |
30 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(27): Show |
intron_variant | MODIFIER | c.-30+460_-30+461ins others(1): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076757 | |||||||
| chr4:157076827 | T | C | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-30+530T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076827 | |||||||
| chr4:157076972 | T | G | 1 | a0001c0001t0001g0016 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-30+675T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076972 | |||||||
| chr4:157076972 | T | TG | 61 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0080 others(58): Show |
64 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.-30+689dupG | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 157076972 | ||||||
| chr4:157076972 | T | TGG | 68 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0104 others(65): Show |
74 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.-30+688_-30+689dup others(2): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 157076972 | ||||||
| chr4:157076972 | T | TGGG | 23 | a0001c0001t0001g0008 a0001c0001t0001g0143 a0001c0001t0001g0144 others(20): Show |
25 | HG00738.hp2 HG01109.hp1 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.-30+687_-30+689dup others(3): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 157076972 | ||||||
| chr4:157076972 | TG | T | 33 | a0001c0001t0001g0035 a0001c0001t0001g0044 a0001c0001t0002g0183 others(30): Show |
35 | HG00738.hp1 HG01168.hp2 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.-30+689delG | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 157076972 | ||||||
| chr4:157076972 | TGG | T | 50 | a0001c0001t0001g0017 a0001c0001t0003g0003 a0001c0001t0003g0020 others(47): Show |
54 | HG00408.hp1 HG00558.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.-30+688_-30+689del others(2): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 157076972 | ||||||
| chr4:157076980 | G | A | 14 | a0001c0001t0001g0017 a0001c0001t0003g0157 a0001c0001t0003g0160 others(11): Show |
14 | HG01081.hp2 HG02280.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-30+683G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076980 | |||||||
| chr4:157076980 | G | GC | 4 | a0001c0001t0002g0164 a0001c0001t0002g0165 a0001c0001t0002g0166 others(1): Show |
4 | HG01069.hp1 HG01993.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+683_-30+684ins others(1): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076980 | |||||||
| chr4:157076980 | G | T | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-30+683G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076980 | |||||||
| chr4:157076985 | G | A | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-30+688G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076985 | |||||||
| chr4:157076986 | G | A | 44 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(41): Show |
47 | HG00408.hp1 HG00558.hp1 HG02015.hp1 others(44): Show |
intron_variant | MODIFIER | c.-30+689G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076986 | |||||||
| chr4:157076987 | A | G | 1 | a0001c0001t0002g0220 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-30+690A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076987 | |||||||
| chr4:157077050 | G | A | 2 | a0001c0001t0004g0262 a0001c0001t0004g0263 |
2 | NA18995.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-30+753G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157077050 | |||||||
| chr4:157077067 | G | T | 2 | a0001c0002t0008g0015 a0001c0002t0008g0163 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-30+770G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157077067 | |||||||
| chr4:157077114 | G | C | 25 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(22): Show |
28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.-30+817G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157077114 | |||||||
| chr4:157077123 | G | A | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-30+826G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157077123 | |||||||
| chr4:157077248 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-29-748C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157077248 | |||||||
| chr4:157077278 | G | T | 1 | a0001c0001t0001g0044 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-29-718G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157077278 | |||||||
| chr4:157077369 | G | T | 8 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(5): Show |
8 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-29-627G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157077369 | |||||||
| chr4:157077644 | T | C | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-29-352T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157077644 | |||||||
| chr4:157077795 | C | A | 1 | a0001c0001t0006g0155 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-29-201C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157077795 | |||||||
| chr4:157077938 | A | G | 8 | a0001c0001t0005g0251 a0001c0001t0007g0192 a0001c0001t0007g0217 others(5): Show |
8 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-29-58A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157077938 | |||||||
| chr4:157078150 | T | A | 25 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(22): Show |
28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
splice_region_variant&intron_variant | LOW | c.122+4T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157078150 | |||||||
| chr4:157078230 | A | G | 6 | a0001c0001t0002g0183 a0001c0001t0002g0189 a0001c0001t0002g0190 others(3): Show |
6 | HG01123.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+84A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157078230 | |||||||
| chr4:157078296 | G | A | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+150G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157078296 | |||||||
| chr4:157078302 | G | A | 3 | a0001c0001t0003g0045 a0001c0002t0008g0024 a0001c0002t0008g0025 |
3 | HG02559.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.122+156G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157078302 | |||||||
| chr4:157078376 | T | C | 92 | a0001c0001t0001g0104 a0001c0001t0002g0002 a0001c0001t0002g0009 others(89): Show |
99 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.122+230T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157078376 | |||||||
| chr4:157078395 | CTG | C | 18 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(15): Show |
21 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.122+251_122+252del others(2): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157078395 | ||||||
| chr4:157078504 | G | GT | 10 | a0001c0001t0002g0211 a0001c0001t0005g0168 a0001c0001t0005g0181 others(7): Show |
10 | HG00544.hp2 HG01192.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.122+367dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157078504 | ||||||
| chr4:157078513 | T | A | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+367T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157078513 | |||||||
| chr4:157078522 | C | A | 1 | a0001c0001t0001g0104 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.122+376C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157078522 | |||||||
| chr4:157078610 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.122+464A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157078610 | |||||||
| chr4:157078703 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.122+557G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157078703 | |||||||
| chr4:157078865 | CG | C | 8 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(5): Show |
8 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.122+722delG | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157078865 | ||||||
| chr4:157079020 | C | T | 1 | a0001c0001t0003g0036 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.122+874C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157079020 | |||||||
| chr4:157079056 | G | T | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+910G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157079056 | |||||||
| chr4:157079060 | C | T | 1 | a0001c0002t0012g0153 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.122+914C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157079060 | |||||||
| chr4:157079591 | A | G | 2 | a0001c0001t0005g0168 a0001c0001t0005g0181 |
2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.122+1445A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157079591 | |||||||
| chr4:157079896 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.122+1750C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157079896 | |||||||
| chr4:157079927 | G | C | 7 | a0001c0002t0006g0176 a0001c0002t0006g0177 a0001c0002t0006g0178 others(4): Show |
7 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+1781G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157079927 | |||||||
| chr4:157079935 | G | C | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+1789G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157079935 | |||||||
| chr4:157079985 | C | A | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+1839C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157079985 | |||||||
| chr4:157080326 | A | G | 25 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(22): Show |
28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.122+2180A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157080326 | |||||||
| chr4:157080485 | T | C | 1 | a0001c0002t0008g0015 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.122+2339T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157080485 | |||||||
| chr4:157080554 | A | C | 111 | a0001c0001t0001g0104 a0001c0001t0002g0002 a0001c0001t0002g0009 others(108): Show |
121 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.122+2408A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157080554 | |||||||
| chr4:157080703 | A | G | 3 | a0001c0002t0006g0178 a0001c0002t0006g0179 a0001c0002t0006g0180 |
3 | HG02015.hp1 HG02080.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.122+2557A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157080703 | |||||||
| chr4:157080714 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.122+2568C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157080714 | |||||||
| chr4:157080733 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.122+2587A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157080733 | |||||||
| chr4:157080758 | A | G | 1 | a0001c0001t0007g0219 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.122+2612A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157080758 | |||||||
| chr4:157080768 | C | A | 4 | a0001c0001t0003g0027 a0001c0001t0003g0072 a0001c0001t0003g0073 others(1): Show |
4 | HG02145.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+2622C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157080768 | |||||||
| chr4:157081040 | G | C | 80 | a0001c0001t0001g0104 a0001c0001t0002g0002 a0001c0001t0002g0009 others(77): Show |
87 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.122+2894G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157081040 | |||||||
| chr4:157081050 | T | C | 1 | a0001c0001t0002g0221 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.122+2904T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157081050 | |||||||
| chr4:157081059 | T | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0108 |
2 | HG00733.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.122+2913T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157081059 | |||||||
| chr4:157081193 | G | A | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+3047G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157081193 | |||||||
| chr4:157081218 | T | A | 12 | a0001c0001t0003g0020 a0001c0001t0003g0028 a0001c0001t0003g0029 others(9): Show |
12 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.122+3072T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157081218 | |||||||
| chr4:157081417 | G | A | 6 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(3): Show |
6 | HG02486.hp2 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+3271G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157081417 | |||||||
| chr4:157081659 | G | A | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+3513G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157081659 | |||||||
| chr4:157081744 | C | T | 127 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(124): Show |
137 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.122+3598C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157081744 | |||||||
| chr4:157081755 | A | C | 1 | a0001c0001t0001g0151 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.122+3609A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157081755 | |||||||
| chr4:157081925 | A | G | 1 | a0001c0001t0005g0167 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.122+3779A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157081925 | |||||||
| chr4:157081949 | C | G | 1 | a0001c0001t0002g0183 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.122+3803C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157081949 | |||||||
| chr4:157081973 | G | A | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+3827G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157081973 | |||||||
| chr4:157082008 | T | A | 5 | a0001c0001t0010g0255 a0001c0001t0010g0256 a0001c0001t0010g0257 others(2): Show |
5 | HG02647.hp1 HG03195.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+3862T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082008 | |||||||
| chr4:157082042 | A | G | 1 | a0001c0001t0002g0241 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.122+3896A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082042 | |||||||
| chr4:157082074 | A | G | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+3928A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082074 | |||||||
| chr4:157082133 | G | A | 286 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(283): Show |
303 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.122+3987G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082133 | |||||||
| chr4:157082139 | A | G | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+3993A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082139 | |||||||
| chr4:157082213 | A | G | 80 | a0001c0001t0001g0104 a0001c0001t0002g0002 a0001c0001t0002g0009 others(77): Show |
87 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.122+4067A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082213 | |||||||
| chr4:157082309 | A | G | 4 | a0001c0001t0003g0027 a0001c0001t0003g0072 a0001c0001t0003g0073 others(1): Show |
4 | HG02145.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+4163A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082309 | |||||||
| chr4:157082312 | G | T | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+4166G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082312 | |||||||
| chr4:157082323 | A | G | 1 | a0001c0001t0002g0210 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.122+4177A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082323 | |||||||
| chr4:157082364 | C | A | 10 | a0001c0001t0003g0045 a0001c0001t0003g0048 a0001c0001t0003g0254 others(7): Show |
10 | HG01255.hp1 HG02559.hp2 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.122+4218C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082364 | |||||||
| chr4:157082441 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.122+4295A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082441 | |||||||
| chr4:157082456 | T | G | 1 | a0001c0001t0003g0046 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.122+4310T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082456 | |||||||
| chr4:157082628 | A | C | 1 | a0001c0001t0001g0102 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.122+4482A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082628 | |||||||
| chr4:157082639 | T | C | 128 | a0001c0001t0001g0104 a0001c0001t0002g0002 a0001c0001t0002g0009 others(125): Show |
138 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.122+4493T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082639 | |||||||
| chr4:157082671 | G | A | 1 | a0001c0001t0003g0287 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122+4525G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082671 | |||||||
| chr4:157082685 | A | G | 36 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(33): Show |
39 | HG00733.hp1 HG00738.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.122+4539A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082685 | |||||||
| chr4:157082964 | T | A | 6 | a0001c0001t0001g0044 a0001c0001t0001g0078 a0001c0001t0001g0080 others(3): Show |
6 | HG00733.hp2 HG01123.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+4818T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082964 | |||||||
| chr4:157082964 | T | TTA | 23 | a0001c0001t0001g0016 a0001c0001t0001g0099 a0001c0001t0001g0100 others(20): Show |
23 | HG00544.hp1 HG01255.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.122+4843_122+4844d others(4): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | ||||||
| chr4:157082964 | T | TTATA | 11 | a0001c0001t0003g0045 a0001c0001t0003g0157 a0001c0001t0003g0160 others(8): Show |
11 | HG01081.hp2 HG02486.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.122+4841_122+4844d others(6): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | ||||||
| chr4:157082964 | T | TTATATA | 13 | a0001c0001t0001g0064 a0001c0001t0004g0001 a0001c0001t0004g0266 others(10): Show |
16 | HG00558.hp1 HG00597.hp1 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.122+4839_122+4844d others(8): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | ||||||
| chr4:157082964 | T | TTATATAT others(1): Show |
6 | a0001c0001t0004g0271 a0001c0001t0004g0273 a0001c0001t0004g0274 others(3): Show |
6 | HG02080.hp2 NA18965.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+4837_122+4844d others(10): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | ||||||
| chr4:157082964 | T | TTATATAT others(3): Show |
7 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0276 others(4): Show |
7 | HG00408.hp1 NA18957.hp2 NA18989.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+4835_122+4844d others(12): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | ||||||
| chr4:157082964 | T | TTATATAT others(5): Show |
4 | a0001c0001t0004g0281 a0001c0001t0004g0282 a0001c0002t0008g0024 others(1): Show |
4 | HG03195.hp1 HG03471.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+4833_122+4844d others(14): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | ||||||
| chr4:157082964 | T | TTATATAT others(7): Show |
3 | a0001c0001t0004g0283 a0001c0001t0004g0284 a0001c0001t0016g0175 |
3 | HG02809.hp2 NA18612.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.122+4831_122+4844d others(16): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | ||||||
| chr4:157082964 | T | TTATATAT others(9): Show |
1 | a0001c0001t0003g0287 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122+4829_122+4844d others(18): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | ||||||
| chr4:157082964 | T | TTATATAT others(11): Show |
1 | a0001c0001t0004g0285 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.122+4827_122+4844d others(20): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | ||||||
| chr4:157082964 | T | TTTTA | 2 | a0001c0001t0001g0007 a0001c0001t0005g0170 |
3 | HG01255.hp2 HG01981.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.122+4819_122+4820i others(6): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | ||||||
| chr4:157082964 | T | TTTTATA | 6 | a0001c0001t0003g0171 a0001c0001t0005g0168 a0001c0001t0005g0181 others(3): Show |
6 | HG00544.hp2 HG01515.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+4819_122+4820i others(8): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | ||||||
| chr4:157082964 | T | TTTTATAT others(1): Show |
3 | a0001c0001t0003g0172 a0001c0001t0003g0173 a0001c0001t0003g0182 |
3 | HG02486.hp2 HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.122+4819_122+4820i others(10): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | ||||||
| chr4:157082964 | TTA | T | 97 | a0001c0001t0001g0049 a0001c0001t0001g0071 a0001c0001t0001g0081 others(94): Show |
104 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.122+4843_122+4844d others(4): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | ||||||
| chr4:157082966 | A | T | 16 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(13): Show |
18 | HG01256.hp2 HG01258.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.122+4820A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082966 | |||||||
| chr4:157083000 | T | A | 81 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(78): Show |
88 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.122+4854T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083000 | |||||||
| chr4:157083042 | C | T | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+4896C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083042 | |||||||
| chr4:157083113 | G | T | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+4967G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083113 | |||||||
| chr4:157083114 | C | T | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+4968C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083114 | |||||||
| chr4:157083225 | CAT | C | 9 | a0001c0001t0003g0005 a0001c0001t0003g0041 a0001c0001t0003g0042 others(6): Show |
10 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.122+5082_122+5083d others(4): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157083225 | ||||||
| chr4:157083403 | T | TG | 127 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(124): Show |
137 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.122+5257_122+5258i others(3): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083403 | |||||||
| chr4:157083404 | T | A | 127 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(124): Show |
137 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.122+5258T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083404 | |||||||
| chr4:157083525 | A | T | 4 | a0001c0001t0004g0279 a0001c0001t0004g0280 a0001c0001t0004g0281 others(1): Show |
4 | HG00408.hp1 NA18994.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+5379A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083525 | |||||||
| chr4:157083532 | C | T | 18 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(15): Show |
21 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.122+5386C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083532 | |||||||
| chr4:157083533 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.122+5387G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083533 | |||||||
| chr4:157083553 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.122+5407T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083553 | |||||||
| chr4:157083556 | T | C | 85 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(82): Show |
92 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.122+5410T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083556 | |||||||
| chr4:157083607 | G | A | 185 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(182): Show |
198 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.122+5461G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083607 | |||||||
| chr4:157083786 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.122+5640A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083786 | |||||||
| chr4:157083834 | C | T | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+5688C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083834 | |||||||
| chr4:157083901 | C | T | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+5755C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083901 | |||||||
| chr4:157084032 | A | G | 2 | a0001c0001t0002g0208 a0001c0001t0019g0240 |
2 | HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.122+5886A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157084032 | |||||||
| chr4:157084061 | A | G | 25 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(22): Show |
28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.122+5915A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157084061 | |||||||
| chr4:157084146 | T | G | 1 | a0001c0001t0002g0193 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.122+6000T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157084146 | |||||||
| chr4:157084251 | A | G | 81 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(78): Show |
88 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.122+6105A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157084251 | |||||||
| chr4:157084306 | C | T | 1 | a0001c0001t0003g0040 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.122+6160C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157084306 | |||||||
| chr4:157084488 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0098 |
2 | HG00741.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.122+6342C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157084488 | |||||||
| chr4:157084516 | A | C | 4 | a0001c0001t0003g0027 a0001c0001t0003g0072 a0001c0001t0003g0073 others(1): Show |
4 | HG02145.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+6370A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157084516 | |||||||
| chr4:157084525 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.122+6379A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157084525 | |||||||
| chr4:157084688 | A | G | 18 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(15): Show |
21 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.122+6542A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157084688 | |||||||
| chr4:157084724 | G | A | 79 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(76): Show |
86 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.122+6578G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157084724 | |||||||
| chr4:157084761 | C | T | 9 | a0001c0001t0005g0168 a0001c0001t0005g0181 a0001c0002t0006g0176 others(6): Show |
9 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+6615C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157084761 | |||||||
| chr4:157084810 | G | A | 8 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(5): Show |
8 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.122+6664G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157084810 | |||||||
| chr4:157085130 | A | G | 1 | a0001c0002t0006g0177 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.122+6984A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157085130 | |||||||
| chr4:157085175 | C | G | 2 | a0001c0001t0003g0034 a0001c0001t0003g0036 |
2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.122+7029C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157085175 | |||||||
| chr4:157085182 | A | G | 12 | a0001c0001t0003g0020 a0001c0001t0003g0028 a0001c0001t0003g0029 others(9): Show |
12 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.122+7036A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157085182 | |||||||
| chr4:157085229 | G | T | 1 | a0001c0001t0003g0005 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.122+7083G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157085229 | |||||||
| chr4:157085320 | C | T | 9 | a0001c0001t0005g0168 a0001c0001t0005g0181 a0001c0002t0006g0176 others(6): Show |
9 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+7174C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157085320 | |||||||
| chr4:157085374 | G | C | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+7228G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157085374 | |||||||
| chr4:157085411 | T | C | 1 | a0001c0001t0003g0287 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122+7265T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157085411 | |||||||
| chr4:157085495 | G | T | 1 | a0001c0001t0002g0009 | 2 | HG00558.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.122+7349G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157085495 | |||||||
| chr4:157085680 | G | A | 8 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(5): Show |
8 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.122+7534G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157085680 | |||||||
| chr4:157085944 | T | C | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+7798T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157085944 | |||||||
| chr4:157086085 | T | G | 127 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(124): Show |
137 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.122+7939T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086085 | |||||||
| chr4:157086101 | G | A | 83 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(80): Show |
90 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.122+7955G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086101 | |||||||
| chr4:157086110 | G | A | 1 | a0001c0001t0004g0283 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.122+7964G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086110 | |||||||
| chr4:157086161 | G | A | 80 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(77): Show |
87 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.122+8015G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086161 | |||||||
| chr4:157086164 | G | T | 12 | a0001c0001t0003g0020 a0001c0001t0003g0028 a0001c0001t0003g0029 others(9): Show |
12 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.122+8018G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086164 | |||||||
| chr4:157086200 | C | T | 2 | a0001c0001t0007g0192 a0001c0001t0007g0219 |
2 | HG01192.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.122+8054C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086200 | |||||||
| chr4:157086350 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.122+8204G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086350 | |||||||
| chr4:157086366 | A | T | 6 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0270 others(3): Show |
6 | NA18612.hp2 NA18951.hp2 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+8220A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086366 | |||||||
| chr4:157086433 | T | C | 14 | a0001c0001t0001g0035 a0001c0001t0001g0050 a0001c0001t0001g0051 others(11): Show |
14 | HG01952.hp1 HG02135.hp1 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.122+8287T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086433 | |||||||
| chr4:157086528 | C | T | 4 | a0001c0001t0003g0027 a0001c0001t0003g0072 a0001c0001t0003g0073 others(1): Show |
4 | HG02145.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+8382C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086528 | |||||||
| chr4:157086529 | G | A | 8 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(5): Show |
8 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.122+8383G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086529 | |||||||
| chr4:157086620 | A | T | 1 | a0001c0001t0003g0033 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.122+8474A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086620 | |||||||
| chr4:157086661 | C | T | 9 | a0001c0001t0005g0168 a0001c0001t0005g0181 a0001c0002t0006g0176 others(6): Show |
9 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+8515C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086661 | |||||||
| chr4:157086730 | G | C | 2 | a0001c0001t0003g0048 a0001c0001t0005g0079 |
2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.122+8584G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086730 | |||||||
| chr4:157086797 | C | T | 5 | a0001c0001t0003g0169 a0001c0001t0003g0172 a0001c0001t0003g0173 others(2): Show |
5 | HG02486.hp2 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.122+8651C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086797 | |||||||
| chr4:157087143 | G | T | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+8997G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157087143 | |||||||
| chr4:157087198 | G | T | 32 | a0001c0001t0002g0002 a0001c0001t0002g0164 a0001c0001t0002g0165 others(29): Show |
34 | HG00408.hp2 HG00438.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.122+9052G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157087198 | |||||||
| chr4:157087255 | G | A | 79 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(76): Show |
86 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.122+9109G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157087255 | |||||||
| chr4:157087323 | T | C | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+9177T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157087323 | |||||||
| chr4:157087417 | T | A | 1 | a0001c0001t0001g0135 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.122+9271T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157087417 | |||||||
| chr4:157087580 | C | T | 1 | a0001c0001t0005g0251 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.122+9434C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157087580 | |||||||
| chr4:157087632 | C | G | 25 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(22): Show |
28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.122+9486C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157087632 | |||||||
| chr4:157087673 | G | GGTA | 9 | a0001c0001t0005g0168 a0001c0001t0005g0181 a0001c0002t0006g0176 others(6): Show |
9 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+9528_122+9530d others(5): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157087673 | ||||||
| chr4:157087744 | C | G | 9 | a0001c0001t0003g0005 a0001c0001t0003g0041 a0001c0001t0003g0042 others(6): Show |
10 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.122+9598C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157087744 | |||||||
| chr4:157087773 | T | C | 2 | a0001c0001t0010g0257 a0001c0003t0014g0258 |
2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.122+9627T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157087773 | |||||||
| chr4:157087787 | C | CT | 78 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(75): Show |
85 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.122+9651dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157087787 | ||||||
| chr4:157087852 | G | A | 12 | a0001c0001t0003g0020 a0001c0001t0003g0028 a0001c0001t0003g0029 others(9): Show |
12 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.122+9706G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157087852 | |||||||
| chr4:157087859 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.122+9713A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157087859 | |||||||
| chr4:157087959 | T | C | 1 | a0001c0001t0005g0167 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.122+9813T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157087959 | |||||||
| chr4:157088043 | T | C | 2 | a0001c0001t0002g0202 a0001c0001t0002g0229 |
2 | HG03017.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.122+9897T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088043 | |||||||
| chr4:157088126 | A | C | 2 | a0001c0001t0015g0186 a0001c0001t0015g0239 |
2 | HG01952.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.122+9980A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088126 | |||||||
| chr4:157088217 | G | A | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+10071G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088217 | |||||||
| chr4:157088281 | TG | T | 18 | a0001c0001t0003g0157 a0001c0001t0003g0160 a0001c0001t0006g0155 others(15): Show |
18 | HG01081.hp2 HG02280.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.122+10138delG | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157088281 | ||||||
| chr4:157088417 | C | A | 13 | a0001c0001t0003g0157 a0001c0001t0003g0160 a0001c0001t0006g0155 others(10): Show |
13 | HG01081.hp2 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.122+10271C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088417 | |||||||
| chr4:157088530 | G | T | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+10384G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088530 | |||||||
| chr4:157088644 | A | C | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+10498A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088644 | |||||||
| chr4:157088700 | A | G | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.122+10554A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088700 | |||||||
| chr4:157088704 | C | T | 13 | a0001c0001t0003g0157 a0001c0001t0003g0160 a0001c0001t0006g0155 others(10): Show |
13 | HG01081.hp2 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.122+10558C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088704 | |||||||
| chr4:157088850 | A | T | 2 | a0001c0001t0002g0211 a0001c0001t0009g0076 |
2 | NA19084.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.122+10704A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088850 | |||||||
| chr4:157088866 | A | G | 8 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(5): Show |
8 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.122+10720A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088866 | |||||||
| chr4:157088878 | T | A | 1 | a0001c0001t0004g0279 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.122+10732T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088878 | |||||||
| chr4:157088879 | A | T | 1 | a0001c0001t0004g0279 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.122+10733A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088879 | |||||||
| chr4:157088881 | T | A | 1 | a0001c0001t0004g0279 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.122+10735T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088881 | |||||||
| chr4:157089141 | A | G | 3 | a0001c0001t0002g0012 a0001c0001t0002g0208 a0001c0001t0019g0240 |
4 | HG02572.hp2 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+10995A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157089141 | |||||||
| chr4:157089162 | G | A | 2 | a0001c0003t0001g0115 a0001c0003t0001g0136 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.122+11016G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157089162 | |||||||
| chr4:157089318 | G | A | 13 | a0001c0001t0003g0157 a0001c0001t0003g0160 a0001c0001t0006g0155 others(10): Show |
13 | HG01081.hp2 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.122+11172G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157089318 | |||||||
| chr4:157089319 | A | G | 2 | a0001c0001t0004g0001 a0001c0001t0004g0275 |
5 | HG00558.hp1 NA18964.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+11173A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157089319 | |||||||
| chr4:157089501 | A | C | 1 | a0001c0001t0002g0216 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.122+11355A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157089501 | |||||||
| chr4:157089841 | C | T | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+11695C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157089841 | |||||||
| chr4:157089975 | G | T | 1 | a0001c0001t0003g0287 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122+11829G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157089975 | |||||||
| chr4:157089999 | C | T | 9 | a0001c0001t0005g0168 a0001c0001t0005g0181 a0001c0002t0006g0176 others(6): Show |
9 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+11853C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157089999 | |||||||
| chr4:157090301 | T | C | 4 | a0001c0003t0001g0057 a0001c0003t0001g0086 a0001c0003t0001g0115 others(1): Show |
4 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+12155T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157090301 | |||||||
| chr4:157090486 | G | T | 1 | a0001c0001t0005g0215 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.122+12340G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157090486 | |||||||
| chr4:157090506 | G | A | 5 | a0001c0001t0010g0255 a0001c0001t0010g0256 a0001c0001t0010g0257 others(2): Show |
5 | HG02647.hp1 HG03195.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+12360G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157090506 | |||||||
| chr4:157090603 | G | A | 1 | a0001c0001t0007g0192 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.122+12457G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157090603 | |||||||
| chr4:157090718 | A | T | 21 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(18): Show |
24 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.122+12572A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157090718 | |||||||
| chr4:157090912 | T | C | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+12766T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157090912 | |||||||
| chr4:157090985 | A | C | 79 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(76): Show |
86 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.122+12839A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157090985 | |||||||
| chr4:157091017 | A | C | 1 | a0001c0001t0007g0192 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.122+12871A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157091017 | |||||||
| chr4:157091164 | G | A | 185 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(182): Show |
198 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.122+13018G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157091164 | |||||||
| chr4:157091197 | C | T | 3 | a0001c0001t0003g0045 a0001c0002t0008g0024 a0001c0002t0008g0025 |
3 | HG02559.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.122+13051C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157091197 | |||||||
| chr4:157091205 | A | G | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+13059A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157091205 | |||||||
| chr4:157091530 | A | T | 1 | a0001c0001t0001g0056 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.122+13384A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157091530 | |||||||
| chr4:157091613 | T | C | 5 | a0001c0001t0003g0027 a0001c0001t0003g0072 a0001c0001t0003g0073 others(2): Show |
5 | HG02055.hp1 HG02145.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+13467T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157091613 | |||||||
| chr4:157091648 | G | C | 12 | a0001c0001t0003g0020 a0001c0001t0003g0028 a0001c0001t0003g0029 others(9): Show |
12 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.122+13502G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157091648 | |||||||
| chr4:157091689 | T | C | 12 | a0001c0001t0003g0020 a0001c0001t0003g0028 a0001c0001t0003g0029 others(9): Show |
12 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.122+13543T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157091689 | |||||||
| chr4:157091690 | G | C | 8 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0030 others(5): Show |
8 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.122+13544G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157091690 | |||||||
| chr4:157091749 | C | G | 13 | a0001c0001t0003g0027 a0001c0001t0003g0072 a0001c0001t0003g0073 others(10): Show |
13 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.122+13603C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157091749 | |||||||
| chr4:157091909 | G | T | 12 | a0001c0001t0003g0020 a0001c0001t0003g0028 a0001c0001t0003g0029 others(9): Show |
12 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.122+13763G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157091909 | |||||||
| chr4:157091924 | A | G | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+13778A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157091924 | |||||||
| chr4:157092056 | T | C | 185 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(182): Show |
198 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.122+13910T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092056 | |||||||
| chr4:157092071 | A | ACT | 185 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(182): Show |
198 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.122+13926_122+1392 others(6): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157092071 | ||||||
| chr4:157092160 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.122+14014C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092160 | |||||||
| chr4:157092291 | G | C | 185 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(182): Show |
198 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.122+14145G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092291 | |||||||
| chr4:157092414 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.122+14268A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092414 | |||||||
| chr4:157092416 | T | G | 185 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(182): Show |
198 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.122+14270T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092416 | |||||||
| chr4:157092433 | G | A | 2 | a0001c0001t0003g0048 a0001c0001t0005g0079 |
2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.122+14287G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092433 | |||||||
| chr4:157092439 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.122+14293G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092439 | |||||||
| chr4:157092529 | A | G | 13 | a0001c0001t0003g0157 a0001c0001t0003g0160 a0001c0001t0006g0155 others(10): Show |
13 | HG01081.hp2 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.122+14383A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092529 | |||||||
| chr4:157092740 | G | A | 4 | a0001c0001t0003g0027 a0001c0001t0003g0072 a0001c0001t0003g0073 others(1): Show |
4 | HG02145.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+14594G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092740 | |||||||
| chr4:157092793 | G | T | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+14647G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092793 | |||||||
| chr4:157092827 | T | C | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+14681T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092827 | |||||||
| chr4:157092910 | G | A | 13 | a0001c0001t0003g0157 a0001c0001t0003g0160 a0001c0001t0006g0155 others(10): Show |
13 | HG01081.hp2 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.122+14764G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092910 | |||||||
| chr4:157092954 | A | G | 2 | a0001c0001t0003g0027 a0001c0001t0003g0073 |
2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.122+14808A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092954 | |||||||
| chr4:157093062 | T | C | 1 | a0001c0001t0002g0194 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.122+14916T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157093062 | |||||||
| chr4:157093160 | T | TA | 79 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(76): Show |
86 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.122+15014_122+1501 others(5): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157093160 | |||||||
| chr4:157093369 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.122+15223C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157093369 | |||||||
| chr4:157093455 | T | C | 3 | a0001c0001t0003g0003 a0001c0001t0003g0022 a0001c0001t0003g0023 |
4 | HG01884.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+15309T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157093455 | |||||||
| chr4:157093460 | G | A | 6 | a0001c0001t0005g0251 a0001c0001t0007g0217 a0001c0001t0007g0218 others(3): Show |
6 | HG02622.hp2 HG02818.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+15314G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157093460 | |||||||
| chr4:157093479 | A | C | 1 | a0001c0001t0002g0238 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.122+15333A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157093479 | |||||||
| chr4:157093615 | C | T | 1 | a0001c0001t0003g0287 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122+15469C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157093615 | |||||||
| chr4:157093733 | C | T | 79 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(76): Show |
86 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.122+15587C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157093733 | |||||||
| chr4:157093754 | C | CA | 34 | a0001c0001t0002g0164 a0001c0001t0002g0183 a0001c0001t0002g0202 others(31): Show |
36 | HG01255.hp1 HG01884.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.122+15632dupA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157093754 | ||||||
| chr4:157093754 | C | CAA | 15 | a0001c0001t0002g0189 a0001c0001t0003g0005 a0001c0001t0003g0041 others(12): Show |
16 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.122+15631_122+1563 others(6): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157093754 | ||||||
| chr4:157093754 | CA | C | 84 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0016 others(81): Show |
87 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.122+15632delA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157093754 | ||||||
| chr4:157093754 | CAAAAAA | C | 23 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(20): Show |
26 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(23): Show |
intron_variant | MODIFIER | c.122+15627_122+1563 others(10): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157093754 | ||||||
| chr4:157093826 | G | C | 126 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(123): Show |
136 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.122+15680G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157093826 | |||||||
| chr4:157093889 | G | A | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+15743G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157093889 | |||||||
| chr4:157093906 | T | C | 7 | a0001c0001t0001g0116 a0001c0001t0001g0119 a0001c0001t0001g0121 others(4): Show |
7 | HG00280.hp2 HG01109.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+15760T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157093906 | |||||||
| chr4:157094123 | ACCAATCA others(21): Show |
A | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+15979_122+1600 others(32): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157094123 | ||||||
| chr4:157094169 | G | A | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+16023G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094169 | |||||||
| chr4:157094188 | G | A | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+16042G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094188 | |||||||
| chr4:157094227 | A | G | 1 | a0001c0001t0003g0287 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122+16081A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094227 | |||||||
| chr4:157094234 | A | G | 44 | a0001c0001t0003g0157 a0001c0001t0003g0160 a0001c0001t0004g0001 others(41): Show |
47 | HG00408.hp1 HG00558.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.122+16088A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094234 | |||||||
| chr4:157094343 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.122+16197T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094343 | |||||||
| chr4:157094367 | A | G | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+16221A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094367 | |||||||
| chr4:157094427 | GTTTA | G | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+16285_122+1628 others(8): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157094427 | ||||||
| chr4:157094456 | C | A | 71 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(68): Show |
78 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.122+16310C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094456 | |||||||
| chr4:157094499 | A | G | 4 | a0001c0001t0003g0027 a0001c0001t0003g0072 a0001c0001t0003g0073 others(1): Show |
4 | HG02145.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+16353A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094499 | |||||||
| chr4:157094652 | G | C | 9 | a0001c0001t0005g0168 a0001c0001t0005g0181 a0001c0002t0006g0176 others(6): Show |
9 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+16506G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094652 | |||||||
| chr4:157094669 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.122+16523A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094669 | |||||||
| chr4:157094715 | A | G | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+16569A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094715 | |||||||
| chr4:157094766 | A | G | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+16620A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094766 | |||||||
| chr4:157094871 | C | G | 1 | a0001c0001t0001g0017 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.122+16725C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094871 | |||||||
| chr4:157094883 | CAT | C | 9 | a0001c0001t0005g0168 a0001c0001t0005g0181 a0001c0002t0006g0176 others(6): Show |
9 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+16738_122+1673 others(6): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094883 | |||||||
| chr4:157094927 | T | G | 1 | a0001c0001t0003g0287 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122+16781T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094927 | |||||||
| chr4:157094936 | T | C | 1 | a0001c0001t0002g0195 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.122+16790T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094936 | |||||||
| chr4:157094948 | T | C | 9 | a0001c0001t0005g0168 a0001c0001t0005g0181 a0001c0002t0006g0176 others(6): Show |
9 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+16802T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094948 | |||||||
| chr4:157095045 | A | G | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+16899A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095045 | |||||||
| chr4:157095111 | G | A | 3 | a0001c0001t0004g0271 a0001c0001t0004g0273 a0001c0001t0023g0272 |
3 | NA18965.hp1 NA18998.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.122+16965G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095111 | |||||||
| chr4:157095180 | G | C | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+17034G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095180 | |||||||
| chr4:157095291 | GT | G | 12 | a0001c0001t0003g0020 a0001c0001t0003g0028 a0001c0001t0003g0029 others(9): Show |
12 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.122+17149delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157095291 | ||||||
| chr4:157095305 | C | CA | 36 | a0001c0001t0001g0053 a0001c0001t0001g0059 a0001c0001t0001g0088 others(33): Show |
40 | HG00280.hp1 HG00558.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.122+17175dupA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157095305 | ||||||
| chr4:157095305 | CA | C | 8 | a0001c0001t0001g0113 a0001c0001t0003g0027 a0001c0001t0003g0031 others(5): Show |
8 | HG01168.hp2 HG02145.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.122+17175delA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157095305 | ||||||
| chr4:157095305 | CAAA | C | 25 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(22): Show |
28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.122+17173_122+1717 others(7): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157095305 | ||||||
| chr4:157095363 | A | C | 25 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(22): Show |
28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.122+17217A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095363 | |||||||
| chr4:157095425 | C | T | 1 | a0001c0001t0005g0079 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.122+17279C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095425 | |||||||
| chr4:157095436 | A | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0148 |
3 | HG02080.hp1 NA18962.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.122+17290A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095436 | |||||||
| chr4:157095464 | C | T | 25 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(22): Show |
28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.122+17318C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095464 | |||||||
| chr4:157095514 | A | G | 1 | a0001c0002t0012g0107 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.122+17368A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095514 | |||||||
| chr4:157095646 | G | C | 2 | a0001c0001t0001g0059 a0001c0001t0001g0092 |
2 | NA18973.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.122+17500G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095646 | |||||||
| chr4:157095701 | G | T | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+17555G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095701 | |||||||
| chr4:157095871 | T | C | 11 | a0001c0001t0005g0168 a0001c0001t0005g0181 a0001c0001t0014g0253 others(8): Show |
11 | HG00544.hp2 HG01255.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.122+17725T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095871 | |||||||
| chr4:157095876 | C | T | 25 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(22): Show |
28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.122+17730C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095876 | |||||||
| chr4:157095995 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.122+17849G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095995 | |||||||
| chr4:157096069 | G | A | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+17923G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096069 | |||||||
| chr4:157096256 | C | A | 24 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(21): Show |
26 | HG00544.hp2 HG01255.hp1 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.122+18110C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096256 | |||||||
| chr4:157096404 | T | C | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+18258T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096404 | |||||||
| chr4:157096575 | A | G | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+18429A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096575 | |||||||
| chr4:157096716 | A | G | 1 | a0001c0001t0013g0019 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.122+18570A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096716 | |||||||
| chr4:157096726 | T | G | 3 | a0001c0001t0001g0116 a0001c0001t0001g0119 a0001c0001t0001g0151 |
3 | HG00280.hp2 HG01515.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.122+18580T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096726 | |||||||
| chr4:157096760 | A | G | 6 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0270 others(3): Show |
6 | NA18612.hp2 NA18951.hp2 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+18614A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096760 | |||||||
| chr4:157096811 | G | A | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+18665G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096811 | |||||||
| chr4:157096844 | C | A | 2 | a0001c0001t0002g0233 a0001c0001t0002g0247 |
2 | NA18961.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.122+18698C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096844 | |||||||
| chr4:157096866 | G | A | 1 | a0001c0001t0005g0168 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.122+18720G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096866 | |||||||
| chr4:157096882 | T | C | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+18736T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096882 | |||||||
| chr4:157096979 | T | A | 1 | a0001c0001t0017g0021 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.122+18833T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096979 | |||||||
| chr4:157096991 | A | G | 6 | a0001c0001t0003g0004 a0001c0001t0003g0038 a0001c0001t0003g0039 others(3): Show |
7 | HG02486.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.122+18845A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096991 | |||||||
| chr4:157097014 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.122+18868T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097014 | |||||||
| chr4:157097028 | A | G | 69 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(66): Show |
76 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.122+18882A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097028 | |||||||
| chr4:157097121 | T | C | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+18975T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097121 | |||||||
| chr4:157097241 | A | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0056 |
3 | NA18939.hp1 NA18952.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.122+19095A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097241 | |||||||
| chr4:157097326 | C | T | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+19180C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097326 | |||||||
| chr4:157097416 | T | G | 1 | a0001c0001t0002g0208 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.122+19270T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097416 | |||||||
| chr4:157097445 | A | G | 1 | a0001c0002t0012g0107 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.122+19299A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097445 | |||||||
| chr4:157097458 | G | C | 2 | a0001c0001t0002g0207 a0002c0005t0006g0204 |
2 | HG02683.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.122+19312G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097458 | |||||||
| chr4:157097459 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.122+19313C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097459 | |||||||
| chr4:157097524 | C | G | 27 | a0001c0001t0003g0287 a0001c0001t0004g0001 a0001c0001t0004g0262 others(24): Show |
30 | HG00408.hp1 HG00558.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.122+19378C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097524 | |||||||
| chr4:157097574 | C | T | 1 | a0001c0001t0003g0048 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.122+19428C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097574 | |||||||
| chr4:157097665 | C | A | 1 | a0001c0001t0010g0255 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.122+19519C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097665 | |||||||
| chr4:157097818 | C | T | 21 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(18): Show |
23 | HG01192.hp1 HG01884.hp1 HG01981.hp1 others(20): Show |
intron_variant | MODIFIER | c.122+19672C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097818 | |||||||
| chr4:157097849 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.122+19703C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097849 | |||||||
| chr4:157097936 | T | G | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+19790T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097936 | |||||||
| chr4:157097969 | C | T | 3 | a0001c0001t0003g0045 a0001c0002t0008g0024 a0001c0002t0008g0025 |
3 | HG02559.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.122+19823C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097969 | |||||||
| chr4:157097970 | G | A | 7 | a0001c0002t0006g0176 a0001c0002t0006g0177 a0001c0002t0006g0178 others(4): Show |
7 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+19824G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097970 | |||||||
| chr4:157097972 | G | T | 1 | a0001c0001t0005g0214 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.122+19826G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097972 | |||||||
| chr4:157097998 | G | C | 1 | a0001c0001t0017g0021 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.122+19852G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097998 | |||||||
| chr4:157098021 | C | CAA | 16 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(13): Show |
19 | HG00558.hp1 HG02074.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.122+19886_122+1988 others(6): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157098021 | ||||||
| chr4:157098021 | C | CAAA | 10 | a0001c0001t0004g0271 a0001c0001t0004g0273 a0001c0001t0004g0274 others(7): Show |
10 | HG00408.hp1 NA18965.hp1 NA18975.hp2 others(7): Show |
intron_variant | MODIFIER | c.122+19885_122+1988 others(7): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157098021 | ||||||
| chr4:157098473 | G | A | 2 | a0001c0001t0005g0168 a0001c0001t0005g0181 |
2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.122+20327G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157098473 | |||||||
| chr4:157098592 | C | T | 7 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(4): Show |
7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.122+20446C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157098592 | |||||||
| chr4:157098634 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.122+20488G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157098634 | |||||||
| chr4:157098634 | G | T | 1 | a0001c0001t0004g0285 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.122+20488G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157098634 | |||||||
| chr4:157098657 | G | C | 1 | a0001c0001t0017g0021 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.122+20511G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157098657 | |||||||
| chr4:157098677 | G | A | 1 | a0001c0001t0003g0068 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.122+20531G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157098677 | |||||||
| chr4:157098773 | T | A | 2 | a0001c0001t0002g0196 a0001c0001t0002g0228 |
2 | NA18971.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.122+20627T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157098773 | |||||||
| chr4:157098796 | C | T | 1 | a0001c0002t0006g0176 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.122+20650C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157098796 | |||||||
| chr4:157098965 | G | T | 1 | a0004c0004t0002g0244 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.122+20819G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157098965 | |||||||
| chr4:157099082 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.122+20936G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157099082 | |||||||
| chr4:157099145 | A | G | 281 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(278): Show |
298 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(295): Show |
intron_variant | MODIFIER | c.122+20999A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157099145 | |||||||
| chr4:157099147 | G | A | 2 | a0001c0001t0005g0026 a0001c0001t0005g0079 |
2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.122+21001G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157099147 | |||||||
| chr4:157099168 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.122+21022A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157099168 | |||||||
| chr4:157099340 | CT | C | 46 | a0001c0001t0001g0090 a0001c0001t0001g0141 a0001c0001t0003g0005 others(43): Show |
50 | HG00408.hp1 HG00558.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.123-21201delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157099340 | ||||||
| chr4:157099357 | G | A | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.123-21199G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157099357 | |||||||
| chr4:157099595 | C | A | 4 | a0001c0001t0003g0004 a0001c0001t0003g0038 a0001c0001t0003g0040 others(1): Show |
5 | HG02622.hp1 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-20961C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157099595 | |||||||
| chr4:157099834 | A | AATCATTT others(4): Show |
1 | a0001c0001t0005g0215 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.123-20721_123-2071 others(15): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157099834 | ||||||
| chr4:157099865 | TATA | T | 3 | a0001c0001t0002g0201 a0001c0001t0002g0226 a0001c0001t0002g0227 |
3 | HG02523.hp1 NA18956.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.123-20688_123-2068 others(7): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157099865 | ||||||
| chr4:157099872 | T | A | 183 | a0001c0001t0001g0044 a0001c0001t0001g0078 a0001c0001t0001g0080 others(180): Show |
196 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.123-20684T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157099872 | |||||||
| chr4:157099876 | C | G | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.123-20680C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157099876 | |||||||
| chr4:157099898 | T | C | 1 | a0001c0001t0003g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.123-20658T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157099898 | |||||||
| chr4:157099910 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.123-20646T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157099910 | |||||||
| chr4:157099961 | T | G | 73 | a0001c0001t0001g0044 a0001c0001t0001g0078 a0001c0001t0001g0080 others(70): Show |
80 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.123-20595T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157099961 | |||||||
| chr4:157099999 | T | A | 1 | a0001c0001t0002g0224 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.123-20557T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157099999 | |||||||
| chr4:157100015 | G | A | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.123-20541G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157100015 | |||||||
| chr4:157100117 | T | C | 1 | a0001c0001t0002g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.123-20439T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157100117 | |||||||
| chr4:157100240 | C | G | 1 | a0001c0001t0001g0016 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.123-20316C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157100240 | |||||||
| chr4:157100391 | A | G | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.123-20165A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157100391 | |||||||
| chr4:157100474 | C | T | 2 | a0001c0001t0004g0262 a0001c0001t0004g0263 |
2 | NA18995.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.123-20082C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157100474 | |||||||
| chr4:157100482 | C | G | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.123-20074C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157100482 | |||||||
| chr4:157100648 | G | A | 1 | a0001c0002t0012g0107 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.123-19908G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157100648 | |||||||
| chr4:157100731 | T | A | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.123-19825T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157100731 | |||||||
| chr4:157100811 | C | A | 3 | a0001c0001t0001g0017 a0001c0001t0005g0170 a0001c0001t0019g0240 |
3 | HG02895.hp1 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.123-19745C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157100811 | |||||||
| chr4:157100964 | T | A | 28 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0004g0001 others(25): Show |
31 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(28): Show |
intron_variant | MODIFIER | c.123-19592T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157100964 | |||||||
| chr4:157101039 | G | A | 1 | a0001c0001t0003g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.123-19517G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157101039 | |||||||
| chr4:157101130 | C | T | 69 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(66): Show |
76 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.123-19426C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157101130 | |||||||
| chr4:157101298 | T | C | 30 | a0001c0001t0003g0020 a0001c0001t0003g0028 a0001c0001t0003g0029 others(27): Show |
30 | HG00544.hp2 HG00639.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.123-19258T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157101298 | |||||||
| chr4:157101338 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.123-19218A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157101338 | |||||||
| chr4:157101395 | G | A | 1 | a0001c0001t0002g0184 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.123-19161G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157101395 | |||||||
| chr4:157101422 | G | A | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.123-19134G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157101422 | |||||||
| chr4:157101469 | T | A | 69 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(66): Show |
76 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.123-19087T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157101469 | |||||||
| chr4:157101609 | G | C | 1 | a0001c0001t0022g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.123-18947G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157101609 | |||||||
| chr4:157101797 | G | GT | 58 | a0001c0001t0001g0101 a0001c0001t0001g0130 a0001c0001t0001g0131 others(55): Show |
65 | HG00280.hp1 HG00558.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.123-18743dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157101797 | ||||||
| chr4:157101797 | GT | G | 29 | a0001c0001t0001g0044 a0001c0001t0001g0090 a0001c0001t0001g0137 others(26): Show |
32 | HG00408.hp1 HG00558.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.123-18743delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157101797 | ||||||
| chr4:157101819 | G | C | 1 | a0001c0001t0013g0037 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.123-18737G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157101819 | |||||||
| chr4:157101819 | G | T | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.123-18737G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157101819 | |||||||
| chr4:157101846 | C | T | 2 | a0001c0001t0002g0012 a0001c0001t0002g0208 |
3 | HG02572.hp2 HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.123-18710C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157101846 | |||||||
| chr4:157102065 | C | A | 7 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(4): Show |
7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-18491C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157102065 | |||||||
| chr4:157102275 | G | A | 2 | a0001c0001t0011g0264 a0001c0001t0011g0265 |
2 | NA18939.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.123-18281G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157102275 | |||||||
| chr4:157102443 | G | A | 1 | a0001c0001t0003g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.123-18113G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157102443 | |||||||
| chr4:157102622 | T | C | 1 | a0001c0001t0015g0186 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.123-17934T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157102622 | |||||||
| chr4:157102750 | A | C | 1 | a0001c0001t0001g0144 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.123-17806A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157102750 | |||||||
| chr4:157102825 | C | T | 18 | a0001c0001t0001g0112 a0001c0001t0003g0160 a0001c0001t0006g0155 others(15): Show |
18 | HG00544.hp2 HG01081.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.123-17731C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157102825 | |||||||
| chr4:157102849 | T | C | 1 | a0002c0005t0006g0204 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.123-17707T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157102849 | |||||||
| chr4:157102853 | A | G | 2 | a0001c0001t0003g0027 a0001c0001t0003g0073 |
2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.123-17703A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157102853 | |||||||
| chr4:157102981 | A | G | 26 | a0001c0001t0003g0287 a0001c0001t0004g0001 a0001c0001t0004g0262 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.123-17575A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157102981 | |||||||
| chr4:157102982 | T | C | 2 | a0001c0001t0003g0027 a0001c0001t0003g0073 |
2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.123-17574T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157102982 | |||||||
| chr4:157103145 | G | A | 5 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(2): Show |
5 | HG02486.hp2 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-17411G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157103145 | |||||||
| chr4:157103157 | C | CA | 75 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(72): Show |
82 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.123-17383dupA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157103157 | ||||||
| chr4:157103161 | A | C | 14 | a0001c0001t0001g0049 a0001c0001t0001g0061 a0001c0001t0001g0062 others(11): Show |
14 | HG01070.hp1 HG02071.hp1 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.123-17395A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157103161 | |||||||
| chr4:157103162 | A | C | 38 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0003g0287 others(35): Show |
41 | HG00408.hp1 HG00558.hp1 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.123-17394A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157103162 | |||||||
| chr4:157103769 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0143 |
2 | HG01123.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.123-16787G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157103769 | |||||||
| chr4:157103889 | C | T | 3 | a0001c0001t0003g0003 a0001c0001t0003g0022 a0001c0001t0003g0023 |
4 | HG01884.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-16667C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157103889 | |||||||
| chr4:157103939 | T | TTG | 47 | a0001c0001t0001g0008 a0001c0001t0001g0059 a0001c0001t0001g0060 others(44): Show |
51 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.123-16595_123-1659 others(6): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157103939 | ||||||
| chr4:157104396 | G | A | 69 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(66): Show |
76 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.123-16160G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157104396 | |||||||
| chr4:157104528 | G | GT | 34 | a0001c0001t0002g0002 a0001c0001t0002g0164 a0001c0001t0002g0165 others(31): Show |
36 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.123-16018dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157104528 | ||||||
| chr4:157104942 | A | G | 2 | a0001c0001t0004g0001 a0001c0001t0004g0275 |
5 | HG00558.hp1 NA18964.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-15614A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157104942 | |||||||
| chr4:157104979 | T | C | 1 | a0001c0001t0013g0037 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.123-15577T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157104979 | |||||||
| chr4:157105022 | T | A | 8 | a0001c0001t0005g0251 a0001c0001t0007g0192 a0001c0001t0007g0217 others(5): Show |
8 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-15534T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157105022 | |||||||
| chr4:157105038 | C | A | 7 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(4): Show |
7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-15518C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157105038 | |||||||
| chr4:157105065 | T | G | 2 | a0001c0002t0008g0156 a0001c0002t0008g0162 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.123-15491T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157105065 | |||||||
| chr4:157105075 | G | A | 1 | a0001c0001t0022g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.123-15481G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157105075 | |||||||
| chr4:157105204 | C | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0060 a0001c0001t0001g0148 others(1): Show |
5 | HG02080.hp1 HG02129.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-15352C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157105204 | |||||||
| chr4:157105595 | AT | A | 4 | a0001c0001t0002g0164 a0001c0001t0002g0165 a0001c0001t0002g0166 others(1): Show |
4 | HG01069.hp1 HG01993.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-14959delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157105595 | ||||||
| chr4:157105671 | T | C | 25 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(22): Show |
28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.123-14885T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157105671 | |||||||
| chr4:157105766 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.123-14790G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157105766 | |||||||
| chr4:157105993 | T | C | 7 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(4): Show |
7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-14563T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157105993 | |||||||
| chr4:157106830 | C | T | 69 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(66): Show |
76 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.123-13726C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157106830 | |||||||
| chr4:157106911 | C | T | 3 | a0001c0001t0003g0003 a0001c0001t0003g0022 a0001c0001t0003g0023 |
4 | HG01884.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-13645C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157106911 | |||||||
| chr4:157107092 | G | A | 9 | a0001c0001t0005g0251 a0001c0001t0007g0192 a0001c0001t0007g0217 others(6): Show |
9 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-13464G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107092 | |||||||
| chr4:157107148 | C | G | 2 | a0001c0001t0003g0027 a0001c0001t0003g0073 |
2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.123-13408C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107148 | |||||||
| chr4:157107187 | C | A | 1 | a0001c0001t0002g0012 | 2 | HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.123-13369C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107187 | |||||||
| chr4:157107201 | G | A | 9 | a0001c0001t0005g0251 a0001c0001t0007g0192 a0001c0001t0007g0217 others(6): Show |
9 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-13355G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107201 | |||||||
| chr4:157107226 | C | T | 1 | a0001c0001t0003g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.123-13330C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107226 | |||||||
| chr4:157107366 | T | C | 36 | a0001c0001t0003g0287 a0001c0001t0004g0001 a0001c0001t0004g0262 others(33): Show |
39 | HG00408.hp1 HG00558.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.123-13190T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107366 | |||||||
| chr4:157107420 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.123-13136T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107420 | |||||||
| chr4:157107480 | G | A | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | NA18967.hp2 NA18973.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.123-13076G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107480 | |||||||
| chr4:157107513 | C | A | 11 | a0001c0001t0003g0020 a0001c0001t0003g0028 a0001c0001t0003g0029 others(8): Show |
11 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.123-13043C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107513 | |||||||
| chr4:157107522 | C | T | 1 | a0001c0001t0012g0091 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.123-13034C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107522 | |||||||
| chr4:157107583 | A | G | 1 | a0001c0001t0009g0075 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.123-12973A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107583 | |||||||
| chr4:157107722 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.123-12834C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107722 | |||||||
| chr4:157107746 | C | T | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.123-12810C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107746 | |||||||
| chr4:157107848 | A | C | 1 | a0001c0001t0001g0110 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.123-12708A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107848 | |||||||
| chr4:157108136 | T | A | 1 | a0001c0001t0003g0182 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.123-12420T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157108136 | |||||||
| chr4:157108228 | G | C | 1 | a0001c0001t0011g0264 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.123-12328G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157108228 | |||||||
| chr4:157108411 | T | C | 3 | a0001c0001t0010g0255 a0001c0001t0010g0256 a0001c0001t0010g0257 |
3 | HG02647.hp1 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.123-12145T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157108411 | |||||||
| chr4:157108441 | A | AG | 69 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(66): Show |
76 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.123-12115_123-1211 others(5): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157108441 | |||||||
| chr4:157108627 | C | T | 7 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(4): Show |
7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-11929C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157108627 | |||||||
| chr4:157108642 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.123-11914A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157108642 | |||||||
| chr4:157108728 | C | T | 43 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0028 others(40): Show |
44 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.123-11828C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157108728 | |||||||
| chr4:157108782 | A | C | 3 | a0001c0001t0003g0020 a0001c0001t0003g0032 a0001c0001t0003g0047 |
3 | HG00639.hp1 HG02145.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.123-11774A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157108782 | |||||||
| chr4:157109236 | A | G | 1 | a0001c0001t0016g0175 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.123-11320A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157109236 | |||||||
| chr4:157109243 | T | G | 1 | a0001c0001t0003g0068 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.123-11313T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157109243 | |||||||
| chr4:157109273 | T | G | 2 | a0001c0002t0008g0156 a0001c0002t0008g0162 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.123-11283T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157109273 | |||||||
| chr4:157109358 | G | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0078 a0001c0001t0001g0080 others(1): Show |
4 | HG00733.hp2 HG01169.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-11198G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157109358 | |||||||
| chr4:157109470 | C | T | 1 | a0001c0001t0002g0194 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.123-11086C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157109470 | |||||||
| chr4:157109553 | A | G | 1 | a0001c0001t0003g0048 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.123-11003A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157109553 | |||||||
| chr4:157109733 | T | C | 1 | a0001c0002t0006g0180 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.123-10823T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157109733 | |||||||
| chr4:157109861 | C | A | 9 | a0001c0001t0005g0251 a0001c0001t0007g0192 a0001c0001t0007g0217 others(6): Show |
9 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-10695C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157109861 | |||||||
| chr4:157109936 | A | G | 9 | a0001c0001t0005g0251 a0001c0001t0007g0192 a0001c0001t0007g0217 others(6): Show |
9 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-10620A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157109936 | |||||||
| chr4:157110074 | G | A | 1 | a0001c0001t0013g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.123-10482G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157110074 | |||||||
| chr4:157110078 | C | T | 8 | a0001c0001t0005g0251 a0001c0001t0007g0192 a0001c0001t0007g0217 others(5): Show |
8 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-10478C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157110078 | |||||||
| chr4:157110079 | G | C | 1 | a0001c0001t0002g0221 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.123-10477G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157110079 | |||||||
| chr4:157110291 | T | A | 2 | a0001c0001t0003g0027 a0001c0001t0003g0073 |
2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.123-10265T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157110291 | |||||||
| chr4:157110323 | C | CTTAAG | 37 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0004g0001 others(34): Show |
40 | HG00408.hp1 HG00558.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.123-10231_123-1023 others(9): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157110323 | ||||||
| chr4:157110363 | T | C | 2 | a0001c0002t0008g0156 a0001c0002t0008g0162 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.123-10193T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157110363 | |||||||
| chr4:157110429 | T | A | 179 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(176): Show |
192 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.123-10127T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157110429 | |||||||
| chr4:157110444 | T | C | 11 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0251 others(8): Show |
11 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.123-10112T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157110444 | |||||||
| chr4:157110758 | C | T | 3 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0008t0024g0286 |
3 | HG02145.hp1 HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.123-9798C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157110758 | |||||||
| chr4:157110759 | G | T | 1 | a0001c0001t0003g0254 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.123-9797G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157110759 | |||||||
| chr4:157110805 | T | C | 37 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0004g0001 others(34): Show |
40 | HG00408.hp1 HG00558.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.123-9751T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157110805 | |||||||
| chr4:157111125 | G | A | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.123-9431G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157111125 | |||||||
| chr4:157111243 | G | C | 38 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0003g0287 others(35): Show |
41 | HG00408.hp1 HG00558.hp1 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.123-9313G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157111243 | |||||||
| chr4:157111420 | A | G | 179 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(176): Show |
192 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.123-9136A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157111420 | |||||||
| chr4:157111560 | G | C | 1 | a0001c0001t0003g0073 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.123-8996G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157111560 | |||||||
| chr4:157111717 | A | T | 1 | a0001c0001t0002g0184 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.123-8839A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157111717 | |||||||
| chr4:157111729 | G | C | 7 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(4): Show |
7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-8827G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157111729 | |||||||
| chr4:157111913 | C | T | 1 | a0002c0005t0006g0204 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.123-8643C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157111913 | |||||||
| chr4:157112034 | T | A | 3 | a0001c0001t0010g0255 a0001c0001t0010g0256 a0001c0001t0010g0257 |
3 | HG02647.hp1 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.123-8522T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112034 | |||||||
| chr4:157112076 | C | CT | 20 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0014 others(17): Show |
23 | HG00597.hp2 HG02055.hp2 HG02071.hp2 others(20): Show |
intron_variant | MODIFIER | c.123-8469dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157112076 | ||||||
| chr4:157112076 | CT | C | 41 | a0001c0001t0001g0063 a0001c0001t0001g0098 a0001c0001t0001g0140 others(38): Show |
45 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.123-8469delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157112076 | ||||||
| chr4:157112090 | C | G | 11 | a0001c0001t0003g0020 a0001c0001t0003g0028 a0001c0001t0003g0029 others(8): Show |
11 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.123-8466C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112090 | |||||||
| chr4:157112169 | G | A | 2 | a0001c0001t0010g0255 a0001c0001t0010g0256 |
2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.123-8387G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112169 | |||||||
| chr4:157112225 | A | C | 1 | a0001c0001t0001g0049 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.123-8331A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112225 | |||||||
| chr4:157112229 | T | G | 11 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0251 others(8): Show |
11 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.123-8327T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112229 | |||||||
| chr4:157112252 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.123-8304A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112252 | |||||||
| chr4:157112257 | G | A | 179 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(176): Show |
192 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.123-8299G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112257 | |||||||
| chr4:157112314 | AT | A | 47 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0003g0169 others(44): Show |
50 | HG00408.hp1 HG00558.hp1 HG01192.hp1 others(47): Show |
intron_variant | MODIFIER | c.123-8234delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157112314 | ||||||
| chr4:157112345 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.123-8211T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112345 | |||||||
| chr4:157112406 | G | A | 11 | a0001c0001t0003g0020 a0001c0001t0003g0028 a0001c0001t0003g0029 others(8): Show |
11 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.123-8150G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112406 | |||||||
| chr4:157112529 | T | A | 8 | a0001c0001t0003g0160 a0001c0001t0006g0155 a0001c0001t0006g0158 others(5): Show |
8 | HG01081.hp2 HG02615.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-8027T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112529 | |||||||
| chr4:157112610 | G | A | 2 | a0001c0002t0008g0156 a0001c0002t0008g0162 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.123-7946G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112610 | |||||||
| chr4:157112679 | A | T | 1 | a0001c0001t0002g0236 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.123-7877A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112679 | |||||||
| chr4:157112690 | C | T | 7 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(4): Show |
7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-7866C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112690 | |||||||
| chr4:157112773 | A | C | 1 | a0001c0001t0002g0235 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.123-7783A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112773 | |||||||
| chr4:157112873 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.123-7683G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112873 | |||||||
| chr4:157112999 | G | A | 2 | a0001c0001t0003g0027 a0001c0001t0003g0073 |
2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.123-7557G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112999 | |||||||
| chr4:157113131 | A | ATG | 4 | a0001c0001t0005g0168 a0001c0001t0005g0181 a0001c0001t0014g0253 others(1): Show |
4 | HG01255.hp1 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.123-7413_123-7412d others(4): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157113131 | ||||||
| chr4:157113235 | C | T | 2 | a0001c0002t0008g0024 a0001c0002t0008g0025 |
2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.123-7321C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157113235 | |||||||
| chr4:157113243 | GT | G | 3 | a0001c0001t0005g0251 a0001c0001t0007g0249 a0001c0001t0007g0250 |
3 | HG02622.hp2 HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.123-7311delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157113243 | ||||||
| chr4:157113260 | C | T | 2 | a0001c0001t0003g0287 a0001c0001t0020g0174 |
2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.123-7296C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157113260 | |||||||
| chr4:157113267 | A | G | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.123-7289A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157113267 | |||||||
| chr4:157113418 | T | A | 2 | a0001c0001t0003g0027 a0001c0001t0003g0073 |
2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.123-7138T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157113418 | |||||||
| chr4:157113445 | T | C | 25 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(22): Show |
28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.123-7111T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157113445 | |||||||
| chr4:157113575 | T | C | 38 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0003g0287 others(35): Show |
41 | HG00408.hp1 HG00558.hp1 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.123-6981T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157113575 | |||||||
| chr4:157113701 | A | G | 9 | a0001c0001t0005g0251 a0001c0001t0007g0192 a0001c0001t0007g0217 others(6): Show |
9 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-6855A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157113701 | |||||||
| chr4:157113705 | CA | C | 6 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0117 others(3): Show |
6 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.123-6850delA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157113705 | |||||||
| chr4:157113859 | G | C | 1 | a0001c0001t0009g0093 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.123-6697G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157113859 | |||||||
| chr4:157113914 | G | A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0092 |
2 | NA18973.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.123-6642G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157113914 | |||||||
| chr4:157113971 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.123-6585T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157113971 | |||||||
| chr4:157114209 | T | C | 179 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(176): Show |
192 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.123-6347T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157114209 | |||||||
| chr4:157114341 | C | CT | 30 | a0001c0001t0001g0077 a0001c0001t0001g0117 a0001c0001t0001g0121 others(27): Show |
33 | HG00408.hp1 HG00558.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.123-6203dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157114341 | ||||||
| chr4:157114648 | C | T | 8 | a0001c0001t0005g0251 a0001c0001t0007g0192 a0001c0001t0007g0217 others(5): Show |
8 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-5908C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157114648 | |||||||
| chr4:157114666 | A | G | 91 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(88): Show |
100 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.123-5890A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157114666 | |||||||
| chr4:157114750 | T | C | 2 | a0001c0001t0010g0255 a0001c0001t0010g0256 |
2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.123-5806T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157114750 | |||||||
| chr4:157114876 | A | ACT | 3 | a0001c0001t0003g0045 a0001c0002t0008g0024 a0001c0002t0008g0025 |
3 | HG02559.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.123-5679_123-5678d others(4): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157114876 | ||||||
| chr4:157114918 | C | A | 8 | a0001c0001t0003g0160 a0001c0001t0006g0155 a0001c0001t0006g0158 others(5): Show |
8 | HG01081.hp2 HG02615.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-5638C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157114918 | |||||||
| chr4:157114937 | G | A | 70 | a0001c0001t0001g0053 a0001c0001t0002g0002 a0001c0001t0002g0009 others(67): Show |
77 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.123-5619G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157114937 | |||||||
| chr4:157114943 | C | G | 26 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(23): Show |
29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.123-5613C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157114943 | |||||||
| chr4:157114958 | A | G | 69 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(66): Show |
76 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.123-5598A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157114958 | |||||||
| chr4:157115217 | C | T | 169 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(166): Show |
182 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.123-5339C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157115217 | |||||||
| chr4:157115251 | G | GT | 9 | a0001c0001t0001g0146 a0001c0001t0001g0154 a0001c0001t0002g0203 others(6): Show |
9 | HG01109.hp1 HG01175.hp2 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-5287dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157115251 | ||||||
| chr4:157115251 | GT | G | 53 | a0001c0001t0001g0035 a0001c0001t0001g0083 a0001c0001t0001g0117 others(50): Show |
55 | HG00408.hp1 HG01192.hp1 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.123-5287delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157115251 | ||||||
| chr4:157115255 | T | G | 1 | a0001c0001t0020g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.123-5301T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157115255 | |||||||
| chr4:157115315 | T | TA | 98 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(95): Show |
107 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.123-5232dupA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157115315 | ||||||
| chr4:157115345 | A | G | 9 | a0001c0001t0005g0251 a0001c0001t0007g0192 a0001c0001t0007g0217 others(6): Show |
9 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-5211A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157115345 | |||||||
| chr4:157115703 | T | C | 69 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0028 others(66): Show |
73 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.123-4853T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157115703 | |||||||
| chr4:157115730 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.123-4826T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157115730 | |||||||
| chr4:157115800 | C | T | 2 | a0001c0001t0004g0273 a0001c0001t0023g0272 |
2 | NA18965.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.123-4756C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157115800 | |||||||
| chr4:157115996 | C | G | 1 | a0001c0001t0001g0141 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.123-4560C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157115996 | |||||||
| chr4:157115996 | C | T | 13 | a0001c0001t0003g0005 a0001c0001t0003g0041 a0001c0001t0003g0042 others(10): Show |
14 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.123-4560C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157115996 | |||||||
| chr4:157116237 | T | C | 76 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(73): Show |
79 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.123-4319T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157116237 | |||||||
| chr4:157116411 | A | G | 1 | a0001c0001t0002g0164 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.123-4145A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157116411 | |||||||
| chr4:157116422 | C | T | 1 | a0001c0002t0006g0188 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.123-4134C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157116422 | |||||||
| chr4:157116437 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.123-4119T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157116437 | |||||||
| chr4:157116455 | G | A | 2 | a0001c0001t0003g0027 a0001c0001t0003g0073 |
2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.123-4101G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157116455 | |||||||
| chr4:157116574 | T | C | 4 | a0001c0001t0003g0160 a0001c0001t0006g0155 a0001c0001t0006g0158 others(1): Show |
4 | HG01081.hp2 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-3982T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157116574 | |||||||
| chr4:157116646 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.123-3910A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157116646 | |||||||
| chr4:157116844 | G | C | 69 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(66): Show |
76 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.123-3712G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157116844 | |||||||
| chr4:157116908 | A | G | 7 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(4): Show |
7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-3648A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157116908 | |||||||
| chr4:157117002 | G | T | 1 | a0001c0001t0017g0021 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.123-3554G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157117002 | |||||||
| chr4:157117106 | G | A | 22 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(19): Show |
24 | HG01255.hp1 HG01884.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.123-3450G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157117106 | |||||||
| chr4:157117213 | A | G | 7 | a0001c0001t0002g0002 a0001c0001t0002g0231 a0001c0001t0002g0232 others(4): Show |
9 | HG00408.hp2 HG00438.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-3343A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157117213 | |||||||
| chr4:157117331 | C | T | 3 | a0001c0001t0003g0045 a0001c0002t0008g0024 a0001c0002t0008g0025 |
3 | HG02559.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.123-3225C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157117331 | |||||||
| chr4:157117492 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.123-3064G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157117492 | |||||||
| chr4:157117579 | G | A | 43 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0028 others(40): Show |
44 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.123-2977G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157117579 | |||||||
| chr4:157117769 | A | G | 1 | a0003c0009t0009g0106 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.123-2787A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157117769 | |||||||
| chr4:157117805 | A | G | 7 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(4): Show |
7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-2751A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157117805 | |||||||
| chr4:157117862 | T | C | 179 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(176): Show |
192 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.123-2694T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157117862 | |||||||
| chr4:157118075 | G | T | 175 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(172): Show |
188 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.123-2481G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157118075 | |||||||
| chr4:157118183 | C | T | 7 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(4): Show |
7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-2373C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157118183 | |||||||
| chr4:157118311 | T | A | 25 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(22): Show |
28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.123-2245T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157118311 | |||||||
| chr4:157118344 | G | A | 1 | a0001c0001t0003g0034 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.123-2212G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157118344 | |||||||
| chr4:157118380 | C | T | 1 | a0001c0001t0011g0265 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.123-2176C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157118380 | |||||||
| chr4:157118483 | C | G | 1 | a0001c0001t0003g0254 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.123-2073C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157118483 | |||||||
| chr4:157118558 | A | C | 179 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(176): Show |
192 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.123-1998A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157118558 | |||||||
| chr4:157118587 | T | A | 1 | a0001c0001t0021g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.123-1969T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157118587 | |||||||
| chr4:157118922 | A | C | 1 | a0001c0001t0001g0101 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.123-1634A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157118922 | |||||||
| chr4:157118983 | G | A | 4 | a0001c0001t0005g0013 a0001c0001t0005g0212 a0001c0001t0005g0213 others(1): Show |
5 | NA18965.hp2 NA18975.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-1573G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157118983 | |||||||
| chr4:157119083 | G | T | 42 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0028 others(39): Show |
43 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.123-1473G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157119083 | |||||||
| chr4:157119087 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.123-1469C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157119087 | |||||||
| chr4:157119191 | T | C | 1 | a0001c0001t0002g0201 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.123-1365T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157119191 | |||||||
| chr4:157119237 | A | G | 7 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(4): Show |
7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-1319A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157119237 | |||||||
| chr4:157119315 | T | C | 22 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(19): Show |
24 | HG01255.hp1 HG01884.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.123-1241T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157119315 | |||||||
| chr4:157119328 | T | C | 29 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(26): Show |
31 | HG01255.hp1 HG01884.hp1 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.123-1228T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157119328 | |||||||
| chr4:157119687 | C | A | 3 | a0001c0001t0005g0168 a0001c0001t0005g0181 a0001c0001t0014g0253 |
3 | HG01255.hp1 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.123-869C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157119687 | |||||||
| chr4:157119854 | G | A | 286 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(283): Show |
303 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.123-702G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157119854 | |||||||
| chr4:157119882 | G | C | 1 | a0001c0001t0014g0253 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.123-674G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157119882 | |||||||
| chr4:157119895 | A | G | 2 | a0001c0001t0003g0043 a0001c0001t0003g0069 |
2 | HG02074.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.123-661A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157119895 | |||||||
| chr4:157120042 | G | A | 3 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0008t0024g0286 |
3 | HG02145.hp1 HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.123-514G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120042 | |||||||
| chr4:157120063 | G | A | 2 | a0001c0001t0010g0255 a0001c0001t0010g0256 |
2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.123-493G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120063 | |||||||
| chr4:157120089 | T | C | 1 | a0001c0001t0002g0225 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.123-467T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120089 | |||||||
| chr4:157120126 | C | T | 3 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0008t0024g0286 |
3 | HG02145.hp1 HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.123-430C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120126 | |||||||
| chr4:157120127 | G | A | 1 | a0001c0001t0002g0191 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.123-429G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120127 | |||||||
| chr4:157120152 | G | A | 1 | a0001c0002t0008g0163 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.123-404G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120152 | |||||||
| chr4:157120161 | T | C | 179 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(176): Show |
192 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.123-395T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120161 | |||||||
| chr4:157120193 | T | G | 8 | a0001c0001t0003g0160 a0001c0001t0006g0155 a0001c0001t0006g0158 others(5): Show |
8 | HG01081.hp2 HG02615.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-363T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120193 | |||||||
| chr4:157120253 | G | T | 3 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0008t0024g0286 |
3 | HG02145.hp1 HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.123-303G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120253 | |||||||
| chr4:157120257 | T | A | 43 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0028 others(40): Show |
44 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.123-299T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120257 | |||||||
| chr4:157120259 | G | A | 43 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0028 others(40): Show |
44 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.123-297G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120259 | |||||||
| chr4:157120383 | TAATAATA others(11): Show |
T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0110 a0001c0001t0001g0111 |
3 | NA18985.hp1 NA19012.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.123-153_123-136del others(18): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157120383 | ||||||
| chr4:157120386 | TAATAA | T | 25 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(22): Show |
28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.123-154_123-150del others(5): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157120386 | ||||||
| chr4:157120433 | G | GA | 29 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(26): Show |
31 | HG01255.hp1 HG01884.hp1 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.123-118dupA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157120433 | ||||||
| chr4:157120439 | G | A | 176 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(173): Show |
189 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.123-117G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120439 | |||||||
| chr4:157120454 | T | C | 2 | a0001c0001t0003g0027 a0001c0001t0003g0073 |
2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.123-102T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120454 | |||||||
| chr4:157120714 | A | T | 1 | a0001c0001t0014g0253 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.229+52A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157120714 | |||||||
| chr4:157120744 | G | A | 147 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(144): Show |
158 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.229+82G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157120744 | |||||||
| chr4:157120800 | T | C | 69 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(66): Show |
76 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.229+138T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157120800 | |||||||
| chr4:157120816 | A | G | 179 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(176): Show |
192 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.229+154A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157120816 | |||||||
| chr4:157120927 | C | T | 1 | a0001c0001t0002g0193 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.229+265C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157120927 | |||||||
| chr4:157120947 | A | C | 1 | a0001c0001t0005g0214 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.229+285A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157120947 | |||||||
| chr4:157121040 | A | T | 1 | a0001c0001t0001g0151 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.229+378A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157121040 | |||||||
| chr4:157121164 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.229+502G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157121164 | |||||||
| chr4:157121202 | G | A | 1 | a0001c0001t0002g0237 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.229+540G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157121202 | |||||||
| chr4:157121215 | C | A | 1 | a0001c0001t0001g0139 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.229+553C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157121215 | |||||||
| chr4:157121330 | C | T | 2 | a0001c0001t0003g0027 a0001c0001t0003g0073 |
2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.229+668C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157121330 | |||||||
| chr4:157121456 | A | AT | 16 | a0001c0001t0001g0060 a0001c0001t0003g0020 a0001c0001t0003g0029 others(13): Show |
16 | HG00639.hp1 HG01168.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.229+808dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | 157121456 | ||||||
| chr4:157121456 | A | ATT | 18 | a0001c0001t0003g0160 a0001c0001t0006g0155 a0001c0001t0006g0158 others(15): Show |
18 | HG00544.hp2 HG01081.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.229+807_229+808dup others(2): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | 157121456 | ||||||
| chr4:157121456 | AT | A | 33 | a0001c0001t0001g0088 a0001c0001t0002g0207 a0001c0001t0003g0003 others(30): Show |
35 | HG01255.hp1 HG01884.hp1 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.229+808delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | 157121456 | ||||||
| chr4:157121511 | C | G | 7 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(4): Show |
7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.230-819C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157121511 | |||||||
| chr4:157121585 | A | G | 2 | a0001c0001t0003g0027 a0001c0001t0003g0073 |
2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.230-745A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157121585 | |||||||
| chr4:157121605 | T | C | 22 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(19): Show |
24 | HG01255.hp1 HG01884.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.230-725T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157121605 | |||||||
| chr4:157121703 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.230-627C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157121703 | |||||||
| chr4:157121704 | G | C | 3 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0008t0024g0286 |
3 | HG02145.hp1 HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.230-626G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157121704 | |||||||
| chr4:157122007 | G | A | 6 | a0001c0001t0003g0004 a0001c0001t0003g0038 a0001c0001t0003g0039 others(3): Show |
7 | HG02486.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.230-323G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157122007 | |||||||
| chr4:157122080 | A | G | 9 | a0001c0001t0005g0251 a0001c0001t0007g0192 a0001c0001t0007g0217 others(6): Show |
9 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.230-250A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157122080 | |||||||
| chr4:157122092 | G | GA | 95 | a0001c0001t0001g0152 a0001c0001t0002g0002 a0001c0001t0002g0009 others(92): Show |
105 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.230-226dupA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | 157122092 | ||||||
| chr4:157122092 | GA | G | 6 | a0001c0001t0001g0147 a0001c0001t0003g0042 a0001c0001t0003g0043 others(3): Show |
6 | HG01891.hp2 HG02074.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.230-226delA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | 157122092 | ||||||
| chr4:157122130 | TG | T | 25 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(22): Show |
27 | HG01255.hp1 HG01884.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.230-199delG | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157122130 | |||||||
| chr4:157122132 | C | T | 25 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(22): Show |
27 | HG01255.hp1 HG01884.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.230-198C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157122132 | |||||||
| chr4:157122165 | C | T | 179 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(176): Show |
192 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.230-165C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157122165 | |||||||
| chr4:157122407 | C | T | 179 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(176): Show |
192 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.297+10C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157122407 | |||||||
| chr4:157122468 | T | C | 34 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(31): Show |
37 | HG00408.hp1 HG00558.hp1 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.297+71T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157122468 | |||||||
| chr4:157122483 | C | T | 11 | a0001c0001t0003g0020 a0001c0001t0003g0028 a0001c0001t0003g0029 others(8): Show |
11 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.297+86C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157122483 | |||||||
| chr4:157122486 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.297+89C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157122486 | |||||||
| chr4:157122902 | G | C | 22 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(19): Show |
24 | HG01255.hp1 HG01884.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.297+505G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157122902 | |||||||
| chr4:157122904 | T | A | 1 | a0001c0001t0002g0226 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.297+507T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157122904 | |||||||
| chr4:157123249 | A | G | 22 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(19): Show |
24 | HG01255.hp1 HG01884.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.297+852A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157123249 | |||||||
| chr4:157123289 | A | G | 2 | a0001c0001t0003g0027 a0001c0001t0003g0073 |
2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.297+892A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157123289 | |||||||
| chr4:157123651 | G | C | 1 | a0001c0001t0002g0198 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.297+1254G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157123651 | |||||||
| chr4:157123726 | T | G | 22 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(19): Show |
24 | HG01255.hp1 HG01884.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.297+1329T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157123726 | |||||||
| chr4:157124143 | C | T | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.297+1746C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157124143 | |||||||
| chr4:157124144 | A | G | 3 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0008t0024g0286 |
3 | HG02145.hp1 HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.297+1747A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157124144 | |||||||
| chr4:157124172 | C | T | 25 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(22): Show |
28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.297+1775C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157124172 | |||||||
| chr4:157124192 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.297+1795G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157124192 | |||||||
| chr4:157124211 | C | T | 9 | a0001c0001t0005g0251 a0001c0001t0007g0192 a0001c0001t0007g0217 others(6): Show |
9 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.297+1814C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157124211 | |||||||
| chr4:157124413 | C | T | 1 | a0001c0001t0003g0020 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.297+2016C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157124413 | |||||||
| chr4:157124470 | C | T | 110 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(107): Show |
116 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.297+2073C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157124470 | |||||||
| chr4:157124473 | A | AT | 3 | a0001c0001t0001g0087 a0001c0001t0001g0095 a0001c0001t0001g0114 |
3 | NA18984.hp2 NA19057.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.297+2081dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 157124473 | ||||||
| chr4:157124675 | G | A | 2 | a0001c0001t0017g0021 a0001c0002t0008g0024 |
2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.297+2278G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157124675 | |||||||
| chr4:157124804 | G | A | 3 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0008t0024g0286 |
3 | HG02145.hp1 HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.297+2407G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157124804 | |||||||
| chr4:157124856 | A | C | 9 | a0001c0001t0003g0005 a0001c0001t0003g0041 a0001c0001t0003g0042 others(6): Show |
10 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.297+2459A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157124856 | |||||||
| chr4:157124885 | G | A | 1 | a0001c0001t0002g0226 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.297+2488G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157124885 | |||||||
| chr4:157124900 | T | C | 1 | a0001c0001t0002g0232 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.297+2503T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157124900 | |||||||
| chr4:157125096 | C | T | 7 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(4): Show |
7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.297+2699C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157125096 | |||||||
| chr4:157125152 | AG | A | 7 | a0001c0001t0004g0274 a0001c0001t0004g0276 a0001c0001t0004g0277 others(4): Show |
7 | HG00408.hp1 NA18975.hp2 NA18989.hp1 others(4): Show |
intron_variant | MODIFIER | c.297+2756delG | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157125152 | |||||||
| chr4:157125751 | C | G | 13 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0003g0287 others(10): Show |
13 | HG01192.hp1 HG01981.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.297+3354C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157125751 | |||||||
| chr4:157125786 | A | G | 1 | a0001c0001t0010g0257 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.297+3389A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157125786 | |||||||
| chr4:157125814 | G | A | 5 | a0001c0001t0002g0010 a0001c0001t0002g0014 a0001c0001t0002g0195 others(2): Show |
7 | HG00597.hp2 HG02071.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.297+3417G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157125814 | |||||||
| chr4:157125830 | C | T | 69 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(66): Show |
76 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.297+3433C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157125830 | |||||||
| chr4:157125887 | G | T | 7 | a0001c0002t0006g0176 a0001c0002t0006g0177 a0001c0002t0006g0178 others(4): Show |
7 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.297+3490G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157125887 | |||||||
| chr4:157125968 | A | G | 1 | a0001c0001t0003g0287 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.297+3571A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157125968 | |||||||
| chr4:157126021 | C | T | 1 | a0001c0002t0006g0179 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.297+3624C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157126021 | |||||||
| chr4:157126121 | G | A | 43 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0028 others(40): Show |
44 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.297+3724G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157126121 | |||||||
| chr4:157126195 | A | G | 2 | a0001c0001t0003g0005 a0001c0001t0003g0070 |
3 | HG01256.hp2 HG01258.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.297+3798A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157126195 | |||||||
| chr4:157126544 | T | C | 12 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0251 others(9): Show |
12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.297+4147T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157126544 | |||||||
| chr4:157126746 | T | A | 25 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(22): Show |
28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.297+4349T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157126746 | |||||||
| chr4:157126799 | T | G | 3 | a0001c0001t0011g0264 a0001c0001t0011g0265 a0001c0001t0011g0278 |
3 | NA18939.hp2 NA18957.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.297+4402T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157126799 | |||||||
| chr4:157126802 | C | T | 12 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0251 others(9): Show |
12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.297+4405C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157126802 | |||||||
| chr4:157126932 | T | C | 1 | a0001c0001t0013g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.297+4535T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157126932 | |||||||
| chr4:157127177 | C | T | 1 | a0001c0001t0003g0287 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.297+4780C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157127177 | |||||||
| chr4:157127294 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.297+4897A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157127294 | |||||||
| chr4:157127300 | T | C | 2 | a0001c0001t0002g0220 a0005c0006t0002g0199 |
2 | NA19066.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.297+4903T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157127300 | |||||||
| chr4:157127345 | T | G | 50 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0028 others(47): Show |
51 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.297+4948T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157127345 | |||||||
| chr4:157127397 | G | A | 8 | a0001c0001t0005g0251 a0001c0001t0007g0192 a0001c0001t0007g0217 others(5): Show |
8 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.297+5000G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157127397 | |||||||
| chr4:157127431 | C | T | 1 | a0001c0001t0009g0093 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.297+5034C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157127431 | |||||||
| chr4:157127783 | G | T | 1 | a0001c0001t0001g0060 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.297+5386G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157127783 | |||||||
| chr4:157127793 | C | A | 3 | a0001c0001t0010g0255 a0001c0001t0010g0256 a0001c0001t0010g0257 |
3 | HG02647.hp1 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.297+5396C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157127793 | |||||||
| chr4:157127864 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.297+5467T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157127864 | |||||||
| chr4:157127984 | A | T | 108 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(105): Show |
114 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.297+5587A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157127984 | |||||||
| chr4:157127999 | A | C | 3 | a0001c0001t0003g0028 a0001c0001t0003g0030 a0001c0001t0003g0031 |
3 | HG01168.hp2 HG01169.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.297+5602A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157127999 | |||||||
| chr4:157128024 | G | A | 25 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(22): Show |
28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.297+5627G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157128024 | |||||||
| chr4:157128192 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.297+5795A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157128192 | |||||||
| chr4:157128506 | A | C | 13 | a0001c0001t0003g0005 a0001c0001t0003g0041 a0001c0001t0003g0042 others(10): Show |
14 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.297+6109A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157128506 | |||||||
| chr4:157128588 | C | T | 7 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(4): Show |
7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.297+6191C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157128588 | |||||||
| chr4:157128704 | A | C | 1 | a0001c0001t0002g0231 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.297+6307A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157128704 | |||||||
| chr4:157128986 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.297+6589A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157128986 | |||||||
| chr4:157129119 | G | A | 30 | a0001c0001t0003g0020 a0001c0001t0003g0028 a0001c0001t0003g0029 others(27): Show |
30 | HG00544.hp2 HG00639.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.297+6722G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157129119 | |||||||
| chr4:157129254 | A | G | 1 | a0001c0001t0003g0029 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.297+6857A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157129254 | |||||||
| chr4:157129548 | C | T | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.298-6921C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157129548 | |||||||
| chr4:157129558 | T | G | 1 | a0001c0001t0003g0287 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.298-6911T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157129558 | |||||||
| chr4:157129561 | T | C | 1 | a0001c0001t0004g0281 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.298-6908T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157129561 | |||||||
| chr4:157129614 | G | T | 1 | a0001c0001t0001g0094 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.298-6855G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157129614 | |||||||
| chr4:157129751 | G | A | 1 | a0003c0009t0009g0106 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.298-6718G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157129751 | |||||||
| chr4:157129754 | CT | C | 8 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0030 others(5): Show |
8 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.298-6706delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 157129754 | ||||||
| chr4:157129931 | T | A | 3 | a0001c0001t0003g0003 a0001c0001t0003g0022 a0001c0001t0003g0023 |
4 | HG01884.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-6538T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157129931 | |||||||
| chr4:157129960 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.298-6509C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157129960 | |||||||
| chr4:157130016 | C | T | 2 | a0001c0001t0002g0211 a0001c0001t0009g0076 |
2 | NA19084.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.298-6453C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157130016 | |||||||
| chr4:157130183 | C | T | 22 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(19): Show |
24 | HG01255.hp1 HG01884.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.298-6286C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157130183 | |||||||
| chr4:157130201 | T | G | 1 | a0001c0001t0003g0070 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.298-6268T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157130201 | |||||||
| chr4:157130233 | G | A | 109 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(106): Show |
115 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.298-6236G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157130233 | |||||||
| chr4:157130519 | A | T | 12 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0251 others(9): Show |
12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.298-5950A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157130519 | |||||||
| chr4:157130623 | A | T | 29 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(26): Show |
31 | HG01255.hp1 HG01884.hp1 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.298-5846A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157130623 | |||||||
| chr4:157130940 | C | T | 1 | a0001c0001t0017g0021 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.298-5529C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157130940 | |||||||
| chr4:157131030 | A | G | 34 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(31): Show |
36 | HG01192.hp1 HG01255.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.298-5439A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131030 | |||||||
| chr4:157131034 | A | AT | 43 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0028 others(40): Show |
44 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.298-5427dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 157131034 | ||||||
| chr4:157131071 | A | T | 25 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(22): Show |
28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.298-5398A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131071 | |||||||
| chr4:157131139 | A | G | 6 | a0001c0002t0006g0176 a0001c0002t0006g0177 a0001c0002t0006g0178 others(3): Show |
6 | HG01515.hp1 HG02015.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-5330A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131139 | |||||||
| chr4:157131162 | C | T | 12 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0251 others(9): Show |
12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.298-5307C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131162 | |||||||
| chr4:157131312 | G | A | 1 | a0001c0001t0003g0040 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.298-5157G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131312 | |||||||
| chr4:157131401 | A | G | 42 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(39): Show |
44 | HG01192.hp1 HG01255.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.298-5068A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131401 | |||||||
| chr4:157131429 | G | A | 3 | a0001c0001t0003g0072 a0001c0001t0013g0018 a0001c0001t0013g0019 |
3 | HG02896.hp1 HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.298-5040G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131429 | |||||||
| chr4:157131429 | G | C | 1 | a0001c0002t0008g0015 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.298-5040G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131429 | |||||||
| chr4:157131453 | A | G | 8 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(5): Show |
8 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.298-5016A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131453 | |||||||
| chr4:157131486 | A | G | 30 | a0001c0001t0003g0020 a0001c0001t0003g0028 a0001c0001t0003g0029 others(27): Show |
30 | HG00544.hp2 HG00639.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.298-4983A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131486 | |||||||
| chr4:157131561 | A | G | 25 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(22): Show |
28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.298-4908A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131561 | |||||||
| chr4:157131577 | C | G | 9 | a0001c0001t0005g0251 a0001c0001t0007g0192 a0001c0001t0007g0217 others(6): Show |
9 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.298-4892C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131577 | |||||||
| chr4:157131962 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.298-4507T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131962 | |||||||
| chr4:157131968 | G | A | 30 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(27): Show |
32 | HG01255.hp1 HG01884.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.298-4501G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131968 | |||||||
| chr4:157132062 | G | A | 11 | a0001c0001t0003g0020 a0001c0001t0003g0028 a0001c0001t0003g0029 others(8): Show |
11 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.298-4407G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157132062 | |||||||
| chr4:157132069 | T | A | 42 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(39): Show |
44 | HG01192.hp1 HG01255.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.298-4400T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157132069 | |||||||
| chr4:157132100 | A | G | 8 | a0001c0001t0005g0251 a0001c0001t0007g0192 a0001c0001t0007g0217 others(5): Show |
8 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.298-4369A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157132100 | |||||||
| chr4:157132196 | A | G | 4 | a0001c0001t0002g0164 a0001c0001t0002g0165 a0001c0001t0002g0166 others(1): Show |
4 | HG01069.hp1 HG01993.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.298-4273A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157132196 | |||||||
| chr4:157132198 | A | G | 1 | a0001c0001t0020g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298-4271A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157132198 | |||||||
| chr4:157132280 | A | G | 2 | a0001c0001t0001g0059 a0001c0001t0002g0236 |
2 | HG00408.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.298-4189A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157132280 | |||||||
| chr4:157132334 | T | C | 12 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0251 others(9): Show |
12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.298-4135T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157132334 | |||||||
| chr4:157132595 | C | T | 43 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0028 others(40): Show |
44 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.298-3874C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157132595 | |||||||
| chr4:157132700 | C | A | 2 | a0001c0001t0003g0034 a0001c0001t0003g0036 |
2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.298-3769C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157132700 | |||||||
| chr4:157132789 | G | A | 5 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(2): Show |
5 | HG02486.hp2 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.298-3680G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157132789 | |||||||
| chr4:157132973 | T | C | 1 | a0001c0001t0003g0048 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.298-3496T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157132973 | |||||||
| chr4:157133006 | T | C | 30 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(27): Show |
32 | HG01255.hp1 HG01884.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.298-3463T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157133006 | |||||||
| chr4:157133071 | A | C | 4 | a0001c0001t0005g0168 a0001c0001t0005g0181 a0001c0001t0014g0253 others(1): Show |
4 | HG01255.hp1 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.298-3398A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157133071 | |||||||
| chr4:157133106 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.298-3363A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157133106 | |||||||
| chr4:157133183 | A | T | 69 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(66): Show |
76 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.298-3286A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157133183 | |||||||
| chr4:157133212 | T | C | 1 | a0001c0001t0001g0016 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.298-3257T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157133212 | |||||||
| chr4:157133262 | C | T | 69 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(66): Show |
76 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.298-3207C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157133262 | |||||||
| chr4:157133522 | A | G | 12 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0251 others(9): Show |
12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.298-2947A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157133522 | |||||||
| chr4:157133534 | C | A | 1 | a0001c0001t0001g0128 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.298-2935C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157133534 | |||||||
| chr4:157133579 | C | A | 12 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0251 others(9): Show |
12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.298-2890C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157133579 | |||||||
| chr4:157133761 | G | A | 11 | a0001c0001t0003g0020 a0001c0001t0003g0028 a0001c0001t0003g0029 others(8): Show |
11 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.298-2708G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157133761 | |||||||
| chr4:157133881 | G | C | 3 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0008t0024g0286 |
3 | HG02145.hp1 HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.298-2588G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157133881 | |||||||
| chr4:157133888 | A | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0131 |
2 | HG01175.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.298-2581A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157133888 | |||||||
| chr4:157134003 | A | G | 2 | a0001c0001t0005g0168 a0001c0001t0005g0181 |
2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.298-2466A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157134003 | |||||||
| chr4:157134271 | G | A | 30 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(27): Show |
32 | HG01255.hp1 HG01884.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.298-2198G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157134271 | |||||||
| chr4:157134337 | G | T | 12 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0251 others(9): Show |
12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.298-2132G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157134337 | |||||||
| chr4:157134458 | C | T | 1 | a0001c0001t0003g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298-2011C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157134458 | |||||||
| chr4:157134860 | G | A | 1 | a0001c0001t0014g0253 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.298-1609G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157134860 | |||||||
| chr4:157134886 | GC | G | 30 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(27): Show |
32 | HG01255.hp1 HG01884.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.298-1582delC | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157134886 | |||||||
| chr4:157135070 | G | A | 1 | a0001c0001t0022g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.298-1399G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157135070 | |||||||
| chr4:157135179 | A | G | 7 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(4): Show |
7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.298-1290A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157135179 | |||||||
| chr4:157135311 | G | A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0092 |
2 | NA18973.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.298-1158G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157135311 | |||||||
| chr4:157135535 | T | C | 1 | a0001c0001t0014g0253 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.298-934T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157135535 | |||||||
| chr4:157135697 | A | G | 1 | a0001c0001t0013g0037 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.298-772A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157135697 | |||||||
| chr4:157135889 | C | T | 3 | a0001c0001t0001g0077 a0001c0001t0001g0117 a0001c0001t0005g0215 |
3 | HG01884.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.298-580C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157135889 | |||||||
| chr4:157135942 | G | A | 42 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(39): Show |
44 | HG01192.hp1 HG01255.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.298-527G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157135942 | |||||||
| chr4:157135996 | C | T | 1 | a0001c0002t0008g0163 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.298-473C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157135996 | |||||||
| chr4:157136094 | C | A | 1 | a0001c0001t0003g0034 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.298-375C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157136094 | |||||||
| chr4:157136447 | C | T | 1 | a0001c0001t0013g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.298-22C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157136447 | |||||||
| chr4:157137410 | A | G | 31 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(28): Show |
33 | HG01255.hp1 HG01884.hp1 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.610+524A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157137410 | |||||||
| chr4:157137418 | A | C | 2 | a0001c0001t0003g0027 a0001c0001t0003g0073 |
2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.610+532A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157137418 | |||||||
| chr4:157137483 | C | CA | 12 | a0001c0001t0003g0048 a0001c0001t0003g0072 a0001c0001t0005g0251 others(9): Show |
12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.610+608dupA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 157137483 | ||||||
| chr4:157137483 | CA | C | 6 | a0001c0001t0003g0004 a0001c0001t0003g0038 a0001c0001t0003g0039 others(3): Show |
7 | HG02486.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.610+608delA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 157137483 | ||||||
| chr4:157137490 | A | C | 1 | a0001c0002t0008g0025 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.610+604A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157137490 | |||||||
| chr4:157137499 | A | G | 1 | a0001c0001t0004g0267 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.610+613A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157137499 | |||||||
| chr4:157137518 | C | T | 1 | a0001c0001t0003g0287 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.610+632C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157137518 | |||||||
| chr4:157137589 | A | T | 25 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(22): Show |
28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.610+703A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157137589 | |||||||
| chr4:157137734 | A | G | 25 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(22): Show |
28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.610+848A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157137734 | |||||||
| chr4:157137754 | A | G | 1 | a0001c0001t0022g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.610+868A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157137754 | |||||||
| chr4:157138029 | G | A | 1 | a0001c0001t0002g0222 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.611-780G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157138029 | |||||||
| chr4:157138082 | T | G | 1 | a0001c0001t0003g0072 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.611-727T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157138082 | |||||||
| chr4:157138133 | G | A | 3 | a0001c0001t0002g0194 a0001c0001t0002g0197 a0001c0001t0002g0225 |
3 | HG01070.hp2 HG01109.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.611-676G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157138133 | |||||||
| chr4:157138160 | T | C | 42 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(39): Show |
44 | HG01192.hp1 HG01255.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.611-649T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157138160 | |||||||
| chr4:157138162 | T | C | 42 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(39): Show |
44 | HG01192.hp1 HG01255.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.611-647T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157138162 | |||||||
| chr4:157138206 | A | G | 179 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(176): Show |
192 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.611-603A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157138206 | |||||||
| chr4:157138470 | G | T | 1 | a0001c0001t0003g0029 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.611-339G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157138470 | |||||||
| chr4:157138743 | A | G | 7 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(4): Show |
7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.611-66A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157138743 | |||||||
| chr4:157138745 | G | T | 1 | a0001c0001t0021g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.611-64G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157138745 | |||||||
| chr4:157138795 | G | A | 6 | a0001c0001t0005g0251 a0001c0001t0007g0217 a0001c0001t0007g0218 others(3): Show |
6 | HG02622.hp2 HG02818.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.611-14G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157138795 | |||||||
| chr4:157139121 | GT | G | 42 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0028 others(39): Show |
43 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.751+178delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 157139121 | ||||||
| chr4:157139147 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.751+198A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157139147 | |||||||
| chr4:157139235 | C | T | 9 | a0001c0001t0005g0251 a0001c0001t0007g0192 a0001c0001t0007g0217 others(6): Show |
9 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.751+286C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157139235 | |||||||
| chr4:157139528 | A | T | 2 | a0001c0002t0008g0156 a0001c0002t0008g0162 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.751+579A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157139528 | |||||||
| chr4:157139650 | T | A | 31 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(28): Show |
33 | HG01255.hp1 HG01884.hp1 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.751+701T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157139650 | |||||||
| chr4:157139743 | C | T | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.751+794C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157139743 | |||||||
| chr4:157139761 | A | G | 1 | a0001c0001t0003g0029 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.751+812A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157139761 | |||||||
| chr4:157139981 | G | A | 4 | a0001c0001t0002g0203 a0001c0001t0002g0206 a0001c0001t0002g0245 others(1): Show |
4 | NA18980.hp2 NA19054.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.751+1032G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157139981 | |||||||
| chr4:157140085 | A | G | 1 | a0001c0001t0002g0196 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.751+1136A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157140085 | |||||||
| chr4:157140251 | A | G | 43 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(40): Show |
45 | HG01192.hp1 HG01255.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.751+1302A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157140251 | |||||||
| chr4:157140633 | A | G | 2 | a0001c0001t0003g0046 a0001c0001t0003g0254 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.751+1684A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157140633 | |||||||
| chr4:157140698 | T | A | 1 | a0001c0001t0017g0021 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.751+1749T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157140698 | |||||||
| chr4:157140712 | G | A | 31 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(28): Show |
33 | HG01255.hp1 HG01884.hp1 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.751+1763G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157140712 | |||||||
| chr4:157140724 | T | C | 1 | a0001c0001t0021g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.751+1775T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157140724 | |||||||
| chr4:157140931 | G | A | 42 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0028 others(39): Show |
43 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.751+1982G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157140931 | |||||||
| chr4:157140956 | G | T | 3 | a0001c0001t0003g0072 a0001c0001t0013g0018 a0001c0001t0013g0019 |
3 | HG02896.hp1 HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.751+2007G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157140956 | |||||||
| chr4:157140970 | A | G | 1 | a0001c0001t0022g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.751+2021A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157140970 | |||||||
| chr4:157141069 | T | G | 1 | a0001c0001t0003g0254 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.751+2120T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157141069 | |||||||
| chr4:157141088 | G | T | 3 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0008t0024g0286 |
3 | HG02145.hp1 HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.751+2139G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157141088 | |||||||
| chr4:157141255 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.751+2306C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157141255 | |||||||
| chr4:157141537 | G | C | 7 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(4): Show |
7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.752-2270G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157141537 | |||||||
| chr4:157141862 | T | C | 12 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0251 others(9): Show |
12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.752-1945T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157141862 | |||||||
| chr4:157141938 | T | C | 9 | a0001c0001t0001g0044 a0001c0001t0001g0049 a0001c0001t0001g0061 others(6): Show |
9 | HG00733.hp2 HG01070.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.752-1869T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157141938 | |||||||
| chr4:157141951 | G | A | 12 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0251 others(9): Show |
12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.752-1856G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157141951 | |||||||
| chr4:157142067 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0025g0120 |
2 | HG01109.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.752-1740A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157142067 | |||||||
| chr4:157142196 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.752-1611A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157142196 | |||||||
| chr4:157142218 | G | A | 9 | a0001c0001t0005g0251 a0001c0001t0007g0192 a0001c0001t0007g0217 others(6): Show |
9 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.752-1589G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157142218 | |||||||
| chr4:157142802 | A | G | 1 | a0001c0001t0002g0206 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.752-1005A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157142802 | |||||||
| chr4:157143067 | A | T | 42 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0028 others(39): Show |
43 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.752-740A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157143067 | |||||||
| chr4:157143332 | T | G | 179 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(176): Show |
192 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.752-475T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157143332 | |||||||
| chr4:157143444 | G | C | 1 | a0001c0001t0003g0172 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.752-363G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157143444 | |||||||
| chr4:157143508 | A | G | 1 | a0001c0001t0003g0287 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.752-299A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157143508 | |||||||
| chr4:157143634 | A | G | 3 | a0001c0001t0001g0049 a0001c0001t0001g0061 a0001c0001t0001g0062 |
3 | HG01070.hp1 HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.752-173A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157143634 | |||||||
| chr4:157143963 | A | T | 8 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(5): Show |
8 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.904+4A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157143963 | |||||||
| chr4:157144236 | G | A | 12 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0251 others(9): Show |
12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.904+277G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157144236 | |||||||
| chr4:157144351 | C | A | 110 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(107): Show |
116 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.904+392C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157144351 | |||||||
| chr4:157144387 | A | G | 286 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(283): Show |
303 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.904+428A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157144387 | |||||||
| chr4:157144438 | C | G | 12 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0251 others(9): Show |
12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.904+479C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157144438 | |||||||
| chr4:157144569 | C | T | 25 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0263 others(22): Show |
28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.904+610C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157144569 | |||||||
| chr4:157144797 | C | T | 1 | a0001c0001t0012g0091 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.904+838C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157144797 | |||||||
| chr4:157144803 | A | T | 1 | a0001c0001t0010g0257 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.904+844A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157144803 | |||||||
| chr4:157144828 | A | C | 1 | a0001c0001t0002g0194 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.904+869A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157144828 | |||||||
| chr4:157144936 | T | C | 176 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(173): Show |
189 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.904+977T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157144936 | |||||||
| chr4:157145073 | T | C | 3 | a0001c0001t0003g0045 a0001c0002t0008g0024 a0001c0002t0008g0025 |
3 | HG02559.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.904+1114T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157145073 | |||||||
| chr4:157145228 | C | A | 1 | a0001c0001t0002g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.904+1269C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157145228 | |||||||
| chr4:157145316 | A | T | 1 | a0001c0002t0012g0107 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.904+1357A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157145316 | |||||||
| chr4:157145432 | G | A | 66 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(63): Show |
73 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.904+1473G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157145432 | |||||||
| chr4:157145766 | C | T | 4 | a0001c0001t0010g0255 a0001c0001t0010g0256 a0001c0001t0010g0257 others(1): Show |
4 | HG02647.hp1 HG03195.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.904+1807C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157145766 | |||||||
| chr4:157146024 | C | CT | 7 | a0001c0002t0006g0176 a0001c0002t0006g0177 a0001c0002t0006g0178 others(4): Show |
7 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.904+2077dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 157146024 | ||||||
| chr4:157146040 | G | A | 1 | a0001c0001t0013g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.904+2081G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157146040 | |||||||
| chr4:157146144 | A | G | 14 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(11): Show |
14 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.904+2185A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157146144 | |||||||
| chr4:157146160 | G | C | 14 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(11): Show |
14 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.904+2201G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157146160 | |||||||
| chr4:157146236 | C | T | 1 | a0001c0002t0006g0180 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.904+2277C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157146236 | |||||||
| chr4:157146239 | A | G | 1 | a0001c0002t0006g0188 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.904+2280A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157146239 | |||||||
| chr4:157146428 | C | T | 66 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(63): Show |
73 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.904+2469C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157146428 | |||||||
| chr4:157146558 | C | G | 13 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(10): Show |
13 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.904+2599C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157146558 | |||||||
| chr4:157146558 | C | T | 3 | a0001c0001t0003g0003 a0001c0001t0003g0022 a0001c0001t0003g0023 |
4 | HG01884.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.904+2599C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157146558 | |||||||
| chr4:157146656 | C | CAAAAATG others(310): Show |
3 | a0001c0001t0003g0003 a0001c0001t0003g0022 a0001c0001t0003g0023 |
4 | HG01884.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.904+2713_904+2714i others(319): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 157146656 | ||||||
| chr4:157146834 | C | CA | 7 | a0001c0001t0001g0121 a0001c0001t0003g0004 a0001c0001t0003g0038 others(4): Show |
8 | HG02486.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.904+2886dupA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 157146834 | ||||||
| chr4:157146899 | G | A | 1 | a0001c0001t0003g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.904+2940G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157146899 | |||||||
| chr4:157146985 | G | A | 3 | a0001c0001t0011g0264 a0001c0001t0011g0265 a0001c0001t0011g0278 |
3 | NA18939.hp2 NA18957.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.904+3026G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157146985 | |||||||
| chr4:157147159 | C | T | 33 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(30): Show |
35 | HG01081.hp2 HG01884.hp1 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.904+3200C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157147159 | |||||||
| chr4:157147160 | T | A | 13 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(10): Show |
13 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.904+3201T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157147160 | |||||||
| chr4:157147298 | A | T | 13 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(10): Show |
13 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.904+3339A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157147298 | |||||||
| chr4:157147347 | T | C | 1 | a0001c0001t0004g0269 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.904+3388T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157147347 | |||||||
| chr4:157147362 | T | A | 1 | a0001c0001t0020g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.904+3403T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157147362 | |||||||
| chr4:157147406 | A | G | 70 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(67): Show |
77 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.904+3447A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157147406 | |||||||
| chr4:157147465 | GA | G | 33 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(30): Show |
35 | HG01081.hp2 HG01884.hp1 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.904+3507delA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157147465 | |||||||
| chr4:157147697 | G | A | 5 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(2): Show |
5 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.904+3738G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157147697 | |||||||
| chr4:157147859 | C | G | 174 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(171): Show |
187 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.904+3900C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157147859 | |||||||
| chr4:157147890 | C | T | 12 | a0001c0001t0003g0020 a0001c0001t0003g0028 a0001c0001t0003g0029 others(9): Show |
12 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.904+3931C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157147890 | |||||||
| chr4:157147906 | G | T | 1 | a0001c0001t0006g0261 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.904+3947G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157147906 | |||||||
| chr4:157147933 | G | A | 3 | a0001c0001t0003g0072 a0001c0001t0013g0018 a0001c0001t0013g0019 |
3 | HG02896.hp1 HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.904+3974G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157147933 | |||||||
| chr4:157148033 | G | C | 1 | a0001c0001t0021g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.904+4074G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157148033 | |||||||
| chr4:157148213 | T | C | 12 | a0001c0002t0006g0176 a0001c0002t0006g0177 a0001c0002t0006g0178 others(9): Show |
12 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.904+4254T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157148213 | |||||||
| chr4:157148239 | A | G | 5 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(2): Show |
5 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.904+4280A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157148239 | |||||||
| chr4:157148398 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG00544.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.905-4320C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157148398 | |||||||
| chr4:157148479 | C | T | 177 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(174): Show |
190 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.905-4239C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157148479 | |||||||
| chr4:157148815 | T | TTTG | 13 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(10): Show |
13 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.905-3898_905-3896d others(5): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 157148815 | ||||||
| chr4:157148906 | G | A | 1 | a0001c0001t0002g0241 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.905-3812G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157148906 | |||||||
| chr4:157148944 | C | T | 1 | a0001c0001t0003g0287 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.905-3774C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157148944 | |||||||
| chr4:157149102 | A | G | 12 | a0001c0001t0003g0020 a0001c0001t0003g0028 a0001c0001t0003g0029 others(9): Show |
12 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.905-3616A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157149102 | |||||||
| chr4:157149193 | G | A | 1 | a0001c0001t0005g0181 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.905-3525G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157149193 | |||||||
| chr4:157149337 | A | G | 2 | a0001c0002t0008g0024 a0001c0002t0008g0025 |
2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.905-3381A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157149337 | |||||||
| chr4:157149413 | G | A | 2 | a0001c0001t0002g0012 a0001c0001t0003g0027 |
3 | HG02572.hp2 HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.905-3305G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157149413 | |||||||
| chr4:157149478 | T | C | 1 | a0001c0001t0003g0287 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.905-3240T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157149478 | |||||||
| chr4:157149921 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.905-2797A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157149921 | |||||||
| chr4:157149959 | G | A | 70 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(67): Show |
77 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.905-2759G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157149959 | |||||||
| chr4:157150017 | T | C | 13 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(10): Show |
13 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.905-2701T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150017 | |||||||
| chr4:157150194 | G | A | 1 | a0001c0001t0003g0048 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.905-2524G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150194 | |||||||
| chr4:157150246 | C | A | 13 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(10): Show |
13 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.905-2472C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150246 | |||||||
| chr4:157150308 | G | A | 3 | a0001c0001t0002g0230 a0001c0001t0015g0186 a0001c0001t0015g0239 |
3 | HG01952.hp2 HG02293.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.905-2410G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150308 | |||||||
| chr4:157150518 | A | C | 1 | a0001c0001t0022g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.905-2200A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150518 | |||||||
| chr4:157150530 | C | A | 82 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(79): Show |
89 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.905-2188C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150530 | |||||||
| chr4:157150619 | G | A | 70 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(67): Show |
77 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.905-2099G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150619 | |||||||
| chr4:157150730 | G | A | 1 | a0001c0001t0020g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.905-1988G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150730 | |||||||
| chr4:157150799 | G | C | 45 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(42): Show |
47 | HG01081.hp2 HG01192.hp1 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.905-1919G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150799 | |||||||
| chr4:157150847 | G | T | 32 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(29): Show |
34 | HG01081.hp2 HG01884.hp1 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.905-1871G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150847 | |||||||
| chr4:157150864 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.905-1854T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150864 | |||||||
| chr4:157150921 | C | A | 1 | a0001c0001t0003g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.905-1797C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150921 | |||||||
| chr4:157150922 | C | A | 1 | a0001c0001t0003g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.905-1796C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150922 | |||||||
| chr4:157150923 | A | C | 15 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(12): Show |
15 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.905-1795A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150923 | |||||||
| chr4:157151019 | C | A | 1 | a0001c0001t0001g0154 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.905-1699C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157151019 | |||||||
| chr4:157151255 | T | C | 24 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(21): Show |
26 | HG01081.hp2 HG01884.hp1 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.905-1463T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157151255 | |||||||
| chr4:157151286 | A | G | 27 | a0001c0001t0003g0005 a0001c0001t0003g0041 a0001c0001t0003g0042 others(24): Show |
28 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.905-1432A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157151286 | |||||||
| chr4:157151379 | T | G | 1 | a0001c0002t0008g0163 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.905-1339T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157151379 | |||||||
| chr4:157151586 | C | A | 32 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(29): Show |
34 | HG01081.hp2 HG01884.hp1 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.905-1132C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157151586 | |||||||
| chr4:157151973 | C | G | 6 | a0001c0001t0003g0004 a0001c0001t0003g0038 a0001c0001t0003g0039 others(3): Show |
7 | HG02486.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.905-745C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157151973 | |||||||
| chr4:157152048 | A | T | 3 | a0001c0001t0001g0065 a0001c0001t0001g0081 a0001c0001t0001g0131 |
3 | HG01175.hp1 HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.905-670A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157152048 | |||||||
| chr4:157152256 | A | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0128 |
2 | NA18612.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.905-462A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157152256 | |||||||
| chr4:157152452 | C | A | 2 | a0001c0001t0010g0255 a0001c0001t0010g0256 |
2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.905-266C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157152452 | |||||||
| chr4:157152558 | G | A | 2 | a0001c0001t0010g0255 a0001c0001t0010g0256 |
2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.905-160G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157152558 | |||||||
| chr4:157153074 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1197+64C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153074 | |||||||
| chr4:157153153 | A | G | 1 | a0001c0001t0002g0246 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1197+143A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153153 | |||||||
| chr4:157153206 | G | A | 13 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(10): Show |
13 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.1197+196G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153206 | |||||||
| chr4:157153351 | T | C | 27 | a0001c0001t0003g0005 a0001c0001t0003g0041 a0001c0001t0003g0042 others(24): Show |
28 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1197+341T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153351 | |||||||
| chr4:157153512 | T | G | 1 | a0001c0003t0001g0150 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1197+502T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153512 | |||||||
| chr4:157153606 | C | A | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1197+596C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153606 | |||||||
| chr4:157153619 | C | T | 1 | a0001c0001t0003g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1197+609C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153619 | |||||||
| chr4:157153642 | A | G | 3 | a0001c0001t0003g0003 a0001c0001t0003g0022 a0001c0001t0003g0023 |
4 | HG01884.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1197+632A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153642 | |||||||
| chr4:157153664 | T | C | 45 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(42): Show |
47 | HG01081.hp2 HG01192.hp1 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.1197+654T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153664 | |||||||
| chr4:157153735 | C | T | 27 | a0001c0001t0003g0005 a0001c0001t0003g0041 a0001c0001t0003g0042 others(24): Show |
28 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1197+725C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153735 | |||||||
| chr4:157153790 | G | A | 27 | a0001c0001t0003g0005 a0001c0001t0003g0041 a0001c0001t0003g0042 others(24): Show |
28 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1197+780G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153790 | |||||||
| chr4:157153851 | C | T | 1 | a0001c0001t0018g0234 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1197+841C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153851 | |||||||
| chr4:157153921 | G | A | 1 | a0001c0001t0009g0093 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1197+911G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153921 | |||||||
| chr4:157154113 | G | A | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1197+1103G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154113 | |||||||
| chr4:157154423 | C | CT | 48 | a0001c0001t0001g0094 a0001c0001t0001g0100 a0001c0001t0001g0116 others(45): Show |
50 | HG00280.hp2 HG01081.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.1197+1434dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157154423 | ||||||
| chr4:157154423 | CT | C | 10 | a0001c0001t0001g0108 a0001c0001t0003g0005 a0001c0001t0003g0041 others(7): Show |
11 | HG00733.hp1 HG00738.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.1197+1434delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157154423 | ||||||
| chr4:157154423 | CTT | C | 6 | a0001c0001t0007g0217 a0001c0001t0007g0218 a0001c0001t0007g0242 others(3): Show |
6 | HG02109.hp2 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1197+1433_1197+143 others(6): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157154423 | ||||||
| chr4:157154479 | G | A | 3 | a0001c0002t0006g0178 a0001c0002t0006g0179 a0001c0002t0006g0180 |
3 | HG02015.hp1 HG02080.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1197+1469G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154479 | |||||||
| chr4:157154505 | G | A | 8 | a0001c0001t0007g0192 a0001c0001t0007g0217 a0001c0001t0007g0218 others(5): Show |
8 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1197+1495G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154505 | |||||||
| chr4:157154506 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1197+1496C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154506 | |||||||
| chr4:157154552 | C | T | 4 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(1): Show |
4 | HG01255.hp1 HG02145.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1197+1542C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154552 | |||||||
| chr4:157154578 | C | A | 1 | a0001c0001t0005g0248 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1197+1568C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154578 | |||||||
| chr4:157154586 | T | G | 1 | a0001c0001t0003g0182 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1197+1576T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154586 | |||||||
| chr4:157154625 | T | C | 13 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(10): Show |
13 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.1197+1615T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154625 | |||||||
| chr4:157154642 | G | C | 13 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(10): Show |
13 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.1197+1632G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154642 | |||||||
| chr4:157154867 | C | T | 1 | a0001c0001t0007g0242 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1197+1857C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154867 | |||||||
| chr4:157154911 | A | G | 4 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(1): Show |
4 | HG01255.hp1 HG02145.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1197+1901A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154911 | |||||||
| chr4:157154915 | G | A | 32 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(29): Show |
34 | HG01081.hp2 HG01884.hp1 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.1197+1905G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154915 | |||||||
| chr4:157154960 | A | G | 3 | a0001c0001t0003g0042 a0001c0001t0003g0043 a0001c0001t0003g0069 |
3 | HG02074.hp1 HG02132.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1197+1950A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154960 | |||||||
| chr4:157155144 | T | G | 1 | a0001c0001t0001g0062 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1197+2134T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157155144 | |||||||
| chr4:157155199 | A | C | 5 | a0001c0001t0007g0217 a0001c0001t0007g0218 a0001c0001t0007g0242 others(2): Show |
5 | HG02622.hp2 HG02818.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1197+2189A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157155199 | |||||||
| chr4:157155221 | T | G | 1 | a0001c0001t0002g0166 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1197+2211T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157155221 | |||||||
| chr4:157155272 | G | T | 1 | a0001c0001t0022g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1197+2262G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157155272 | |||||||
| chr4:157155431 | C | T | 14 | a0001c0002t0006g0176 a0001c0002t0006g0177 a0001c0002t0006g0178 others(11): Show |
14 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.1197+2421C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157155431 | |||||||
| chr4:157155535 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1197+2525T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157155535 | |||||||
| chr4:157155573 | A | G | 70 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(67): Show |
77 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1197+2563A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157155573 | |||||||
| chr4:157155675 | G | A | 1 | a0001c0001t0005g0181 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1197+2665G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157155675 | |||||||
| chr4:157155686 | C | T | 1 | a0001c0001t0004g0262 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1197+2676C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157155686 | |||||||
| chr4:157155690 | T | C | 13 | a0001c0001t0003g0005 a0001c0001t0003g0041 a0001c0001t0003g0042 others(10): Show |
14 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.1197+2680T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157155690 | |||||||
| chr4:157155775 | C | A | 12 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(9): Show |
12 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1197+2765C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157155775 | |||||||
| chr4:157155784 | G | C | 14 | a0001c0002t0006g0176 a0001c0002t0006g0177 a0001c0002t0006g0178 others(11): Show |
14 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.1197+2774G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157155784 | |||||||
| chr4:157156204 | C | T | 1 | a0001c0001t0007g0250 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1197+3194C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157156204 | |||||||
| chr4:157156394 | T | C | 13 | a0001c0001t0003g0005 a0001c0001t0003g0041 a0001c0001t0003g0042 others(10): Show |
14 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.1197+3384T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157156394 | |||||||
| chr4:157156406 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1197+3396C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157156406 | |||||||
| chr4:157156413 | C | T | 1 | a0001c0001t0007g0192 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1197+3403C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157156413 | |||||||
| chr4:157156414 | G | A | 12 | a0001c0001t0003g0020 a0001c0001t0003g0028 a0001c0001t0003g0029 others(9): Show |
12 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.1197+3404G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157156414 | |||||||
| chr4:157156526 | T | A | 1 | a0001c0001t0009g0093 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1197+3516T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157156526 | |||||||
| chr4:157156632 | G | A | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1197+3622G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157156632 | |||||||
| chr4:157156718 | T | C | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1197+3708T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157156718 | |||||||
| chr4:157157056 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1197+4046A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157157056 | |||||||
| chr4:157157093 | G | A | 1 | a0001c0002t0012g0153 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1197+4083G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157157093 | |||||||
| chr4:157157109 | C | A | 32 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0022 others(29): Show |
34 | HG01081.hp2 HG01884.hp1 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.1197+4099C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157157109 | |||||||
| chr4:157157224 | A | G | 1 | a0001c0001t0001g0054 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1197+4214A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157157224 | |||||||
| chr4:157157327 | G | A | 2 | a0001c0001t0003g0041 a0001c0001t0016g0175 |
2 | HG00738.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1197+4317G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157157327 | |||||||
| chr4:157157336 | C | T | 4 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(1): Show |
4 | HG01255.hp1 HG02145.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1197+4326C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157157336 | |||||||
| chr4:157157465 | G | T | 12 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(9): Show |
12 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1197+4455G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157157465 | |||||||
| chr4:157157488 | C | T | 5 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(2): Show |
5 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1197+4478C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157157488 | |||||||
| chr4:157157497 | C | A | 4 | a0001c0001t0003g0072 a0001c0001t0013g0018 a0001c0001t0013g0019 others(1): Show |
4 | HG02896.hp1 HG03195.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1197+4487C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157157497 | |||||||
| chr4:157157647 | G | A | 44 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0020 others(41): Show |
46 | HG00639.hp1 HG01081.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.1197+4637G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157157647 | |||||||
| chr4:157157717 | A | T | 6 | a0001c0001t0005g0168 a0001c0003t0001g0057 a0001c0003t0001g0086 others(3): Show |
6 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1197+4707A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157157717 | |||||||
| chr4:157157739 | T | C | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1197+4729T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157157739 | |||||||
| chr4:157158056 | T | G | 177 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(174): Show |
190 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.1197+5046T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157158056 | |||||||
| chr4:157158112 | T | C | 7 | a0001c0001t0007g0192 a0001c0001t0007g0217 a0001c0001t0007g0218 others(4): Show |
7 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1197+5102T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157158112 | |||||||
| chr4:157158173 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1197+5163T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157158173 | |||||||
| chr4:157158217 | G | C | 1 | a0001c0001t0004g0276 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1197+5207G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157158217 | |||||||
| chr4:157158382 | C | T | 4 | a0001c0002t0006g0178 a0001c0002t0006g0179 a0001c0002t0006g0180 others(1): Show |
4 | HG00544.hp2 HG02015.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1197+5372C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157158382 | |||||||
| chr4:157158456 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1197+5446T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157158456 | |||||||
| chr4:157158618 | G | C | 7 | a0001c0001t0007g0192 a0001c0001t0007g0217 a0001c0001t0007g0218 others(4): Show |
7 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1197+5608G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157158618 | |||||||
| chr4:157158790 | G | T | 12 | a0001c0002t0006g0176 a0001c0002t0006g0177 a0001c0002t0006g0178 others(9): Show |
12 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.1197+5780G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157158790 | |||||||
| chr4:157158809 | A | T | 1 | a0001c0001t0005g0026 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1197+5799A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157158809 | |||||||
| chr4:157158888 | T | TG | 56 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0020 others(53): Show |
58 | HG00639.hp1 HG01081.hp2 HG01168.hp2 others(55): Show |
intron_variant | MODIFIER | c.1197+5881dupG | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157158888 | ||||||
| chr4:157159050 | C | G | 1 | a0001c0002t0008g0156 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1197+6040C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159050 | |||||||
| chr4:157159063 | A | T | 44 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0020 others(41): Show |
46 | HG00639.hp1 HG01081.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.1197+6053A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159063 | |||||||
| chr4:157159110 | G | A | 7 | a0001c0001t0007g0192 a0001c0001t0007g0217 a0001c0001t0007g0218 others(4): Show |
7 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1197+6100G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159110 | |||||||
| chr4:157159261 | A | G | 5 | a0001c0001t0002g0183 a0001c0001t0002g0189 a0001c0001t0002g0190 others(2): Show |
5 | HG01123.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1197+6251A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159261 | |||||||
| chr4:157159375 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1197+6365A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159375 | |||||||
| chr4:157159399 | T | G | 2 | a0001c0002t0008g0156 a0001c0002t0008g0162 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1197+6389T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159399 | |||||||
| chr4:157159529 | G | C | 1 | a0001c0001t0020g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1197+6519G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159529 | |||||||
| chr4:157159530 | T | G | 7 | a0001c0001t0007g0192 a0001c0001t0007g0217 a0001c0001t0007g0218 others(4): Show |
7 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1197+6520T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159530 | |||||||
| chr4:157159553 | A | G | 1 | a0001c0001t0013g0037 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1197+6543A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159553 | |||||||
| chr4:157159592 | A | G | 1 | a0001c0001t0013g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1197+6582A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159592 | |||||||
| chr4:157159622 | G | T | 11 | a0001c0001t0003g0045 a0001c0001t0003g0048 a0001c0001t0003g0160 others(8): Show |
11 | HG01081.hp2 HG02559.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1197+6612G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159622 | |||||||
| chr4:157159624 | A | C | 11 | a0001c0001t0003g0045 a0001c0001t0003g0048 a0001c0001t0003g0160 others(8): Show |
11 | HG01081.hp2 HG02559.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1197+6614A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159624 | |||||||
| chr4:157159624 | A | G | 6 | a0001c0001t0002g0009 a0001c0001t0002g0184 a0001c0001t0004g0263 others(3): Show |
7 | HG00558.hp2 HG02040.hp1 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.1197+6614A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159624 | |||||||
| chr4:157159628 | G | A | 11 | a0001c0001t0003g0045 a0001c0001t0003g0048 a0001c0001t0003g0160 others(8): Show |
11 | HG01081.hp2 HG02559.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1197+6618G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159628 | |||||||
| chr4:157159694 | T | C | 1 | a0001c0002t0012g0153 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1197+6684T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159694 | |||||||
| chr4:157159699 | G | A | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1197+6689G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159699 | |||||||
| chr4:157159763 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1197+6753A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159763 | |||||||
| chr4:157159772 | C | T | 2 | a0001c0002t0008g0156 a0001c0002t0008g0162 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1197+6762C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159772 | |||||||
| chr4:157159816 | A | C | 1 | a0001c0002t0008g0163 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1197+6806A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159816 | |||||||
| chr4:157159860 | G | A | 4 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(1): Show |
4 | HG01255.hp1 HG02145.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1197+6850G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159860 | |||||||
| chr4:157159953 | C | T | 14 | a0001c0002t0006g0176 a0001c0002t0006g0177 a0001c0002t0006g0178 others(11): Show |
14 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.1197+6943C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159953 | |||||||
| chr4:157160043 | C | T | 14 | a0001c0002t0006g0176 a0001c0002t0006g0177 a0001c0002t0006g0178 others(11): Show |
14 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.1197+7033C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160043 | |||||||
| chr4:157160046 | T | C | 7 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0030 others(4): Show |
7 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1197+7036T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160046 | |||||||
| chr4:157160077 | G | A | 2 | a0001c0002t0008g0024 a0001c0002t0008g0025 |
2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1197+7067G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160077 | |||||||
| chr4:157160092 | T | G | 1 | a0001c0001t0002g0211 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1197+7082T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160092 | |||||||
| chr4:157160108 | A | T | 1 | a0001c0001t0002g0211 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1197+7098A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160108 | |||||||
| chr4:157160163 | C | T | 1 | a0001c0001t0005g0251 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1197+7153C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160163 | |||||||
| chr4:157160170 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0143 |
2 | HG01123.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1197+7160G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160170 | |||||||
| chr4:157160171 | G | T | 1 | a0001c0001t0003g0157 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1197+7161G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160171 | |||||||
| chr4:157160173 | G | A | 5 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(2): Show |
5 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1197+7163G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160173 | |||||||
| chr4:157160258 | A | AT | 44 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0020 others(41): Show |
46 | HG00639.hp1 HG01081.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.1197+7255dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157160258 | ||||||
| chr4:157160290 | A | T | 6 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(3): Show |
6 | HG02486.hp2 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1197+7280A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160290 | |||||||
| chr4:157160371 | C | A | 7 | a0001c0001t0007g0192 a0001c0001t0007g0217 a0001c0001t0007g0218 others(4): Show |
7 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1197+7361C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160371 | |||||||
| chr4:157160415 | C | T | 164 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(161): Show |
176 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.1197+7405C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160415 | |||||||
| chr4:157160530 | T | G | 9 | a0001c0001t0003g0048 a0001c0001t0003g0160 a0001c0001t0006g0155 others(6): Show |
9 | HG01081.hp2 HG02615.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1197+7520T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160530 | |||||||
| chr4:157160601 | C | T | 177 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(174): Show |
190 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.1197+7591C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160601 | |||||||
| chr4:157160610 | A | G | 6 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(3): Show |
6 | HG02486.hp2 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1197+7600A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160610 | |||||||
| chr4:157160623 | T | G | 44 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0020 others(41): Show |
46 | HG00639.hp1 HG01081.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.1197+7613T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160623 | |||||||
| chr4:157160638 | G | A | 2 | a0001c0001t0003g0027 a0001c0001t0003g0073 |
2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1197+7628G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160638 | |||||||
| chr4:157160675 | G | T | 3 | a0001c0001t0003g0003 a0001c0001t0003g0022 a0001c0001t0003g0023 |
4 | HG01884.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1197+7665G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160675 | |||||||
| chr4:157160716 | T | C | 1 | a0001c0001t0013g0037 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1197+7706T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160716 | |||||||
| chr4:157160772 | T | G | 1 | a0001c0001t0003g0072 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1197+7762T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160772 | |||||||
| chr4:157160776 | T | C | 44 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0020 others(41): Show |
46 | HG00639.hp1 HG01081.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.1197+7766T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160776 | |||||||
| chr4:157160892 | T | A | 1 | a0001c0001t0012g0091 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1197+7882T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160892 | |||||||
| chr4:157160904 | G | A | 1 | a0001c0001t0003g0171 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1197+7894G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160904 | |||||||
| chr4:157161022 | C | T | 12 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(9): Show |
12 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1197+8012C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161022 | |||||||
| chr4:157161043 | T | A | 1 | a0001c0001t0001g0104 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1197+8033T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161043 | |||||||
| chr4:157161223 | T | A | 44 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0020 others(41): Show |
46 | HG00639.hp1 HG01081.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.1197+8213T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161223 | |||||||
| chr4:157161284 | A | G | 1 | a0001c0001t0017g0021 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1197+8274A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161284 | |||||||
| chr4:157161301 | C | A | 1 | a0001c0001t0013g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1197+8291C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161301 | |||||||
| chr4:157161351 | G | A | 12 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(9): Show |
12 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1197+8341G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161351 | |||||||
| chr4:157161370 | A | G | 1 | a0001c0001t0002g0206 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1197+8360A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161370 | |||||||
| chr4:157161535 | A | C | 1 | a0001c0001t0002g0196 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1197+8525A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161535 | |||||||
| chr4:157161566 | A | T | 1 | a0001c0001t0023g0272 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1197+8556A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161566 | |||||||
| chr4:157161699 | C | T | 1 | a0001c0001t0003g0072 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1197+8689C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161699 | |||||||
| chr4:157161711 | G | A | 14 | a0001c0002t0006g0176 a0001c0002t0006g0177 a0001c0002t0006g0178 others(11): Show |
14 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.1197+8701G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161711 | |||||||
| chr4:157161718 | T | C | 70 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(67): Show |
77 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1197+8708T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161718 | |||||||
| chr4:157161727 | T | A | 7 | a0001c0001t0007g0192 a0001c0001t0007g0217 a0001c0001t0007g0218 others(4): Show |
7 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1198-8705T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161727 | |||||||
| chr4:157162123 | C | T | 14 | a0001c0002t0006g0176 a0001c0002t0006g0177 a0001c0002t0006g0178 others(11): Show |
14 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.1198-8309C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162123 | |||||||
| chr4:157162168 | G | T | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | NA18967.hp2 NA18973.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1198-8264G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162168 | |||||||
| chr4:157162217 | C | T | 1 | a0001c0001t0003g0160 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1198-8215C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162217 | |||||||
| chr4:157162234 | C | A | 163 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(160): Show |
175 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.1198-8198C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162234 | |||||||
| chr4:157162280 | C | A | 5 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(2): Show |
5 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1198-8152C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162280 | |||||||
| chr4:157162312 | A | C | 1 | a0003c0009t0009g0106 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1198-8120A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162312 | |||||||
| chr4:157162444 | C | A | 13 | a0001c0001t0003g0005 a0001c0001t0003g0041 a0001c0001t0003g0042 others(10): Show |
14 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.1198-7988C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162444 | |||||||
| chr4:157162460 | T | C | 1 | a0001c0001t0005g0209 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1198-7972T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162460 | |||||||
| chr4:157162511 | C | T | 23 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0266 others(20): Show |
26 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1198-7921C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162511 | |||||||
| chr4:157162518 | G | A | 1 | a0001c0001t0003g0287 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1198-7914G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162518 | |||||||
| chr4:157162580 | T | C | 6 | a0001c0001t0005g0168 a0001c0003t0001g0057 a0001c0003t0001g0086 others(3): Show |
6 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1198-7852T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162580 | |||||||
| chr4:157162603 | C | A | 1 | a0001c0001t0003g0073 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1198-7829C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162603 | |||||||
| chr4:157162667 | A | G | 1 | a0001c0001t0017g0021 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1198-7765A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162667 | |||||||
| chr4:157162682 | A | T | 1 | a0001c0001t0001g0143 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1198-7750A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162682 | |||||||
| chr4:157162684 | C | G | 1 | a0001c0001t0001g0064 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1198-7748C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162684 | |||||||
| chr4:157162701 | C | T | 8 | a0001c0002t0006g0176 a0001c0002t0006g0177 a0001c0002t0006g0178 others(5): Show |
8 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.1198-7731C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162701 | |||||||
| chr4:157162718 | C | T | 2 | a0001c0001t0002g0202 a0001c0001t0002g0229 |
2 | HG03017.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1198-7714C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162718 | |||||||
| chr4:157162724 | T | C | 70 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(67): Show |
77 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1198-7708T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162724 | |||||||
| chr4:157162729 | G | A | 1 | a0001c0001t0020g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1198-7703G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162729 | |||||||
| chr4:157162743 | C | G | 23 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0266 others(20): Show |
26 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1198-7689C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162743 | |||||||
| chr4:157163024 | C | T | 12 | a0001c0002t0006g0176 a0001c0002t0006g0177 a0001c0002t0006g0178 others(9): Show |
12 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.1198-7408C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163024 | |||||||
| chr4:157163137 | C | T | 5 | a0001c0001t0001g0071 a0001c0001t0002g0183 a0001c0001t0002g0189 others(2): Show |
5 | HG01123.hp2 HG01258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1198-7295C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163137 | |||||||
| chr4:157163178 | G | A | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1198-7254G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163178 | |||||||
| chr4:157163212 | C | G | 12 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(9): Show |
12 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1198-7220C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163212 | |||||||
| chr4:157163310 | C | T | 2 | a0001c0001t0004g0266 a0001c0001t0004g0267 |
2 | NA18973.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1198-7122C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163310 | |||||||
| chr4:157163311 | A | G | 177 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(174): Show |
190 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.1198-7121A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163311 | |||||||
| chr4:157163322 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1198-7110C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163322 | |||||||
| chr4:157163323 | G | A | 1 | a0001c0001t0002g0243 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1198-7109G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163323 | |||||||
| chr4:157163391 | C | T | 12 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(9): Show |
12 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1198-7041C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163391 | |||||||
| chr4:157163425 | C | G | 1 | a0001c0002t0008g0024 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1198-7007C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163425 | |||||||
| chr4:157163436 | T | C | 286 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(283): Show |
303 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.1198-6996T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163436 | |||||||
| chr4:157163437 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1198-6995G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163437 | |||||||
| chr4:157163521 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0005g0213 |
2 | NA18956.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1198-6911C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163521 | |||||||
| chr4:157163522 | G | A | 23 | a0001c0001t0004g0001 a0001c0001t0004g0262 a0001c0001t0004g0266 others(20): Show |
26 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1198-6910G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163522 | |||||||
| chr4:157163787 | C | T | 12 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(9): Show |
12 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1198-6645C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163787 | |||||||
| chr4:157163829 | A | AGT | 4 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0098 others(1): Show |
4 | HG00741.hp1 HG02080.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1198-6580_1198-657 others(6): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157163829 | ||||||
| chr4:157163829 | A | AGTGTGT | 7 | a0001c0001t0003g0020 a0001c0001t0003g0032 a0001c0001t0007g0217 others(4): Show |
7 | HG02145.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1198-6584_1198-657 others(10): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157163829 | ||||||
| chr4:157163829 | A | AGTGTGTG others(1): Show |
11 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0030 others(8): Show |
11 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.1198-6586_1198-657 others(12): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157163829 | ||||||
| chr4:157163829 | A | AGTGTGTG others(3): Show |
15 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0004g0001 others(12): Show |
18 | HG00544.hp2 HG00558.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.1198-6588_1198-657 others(14): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157163829 | ||||||
| chr4:157163829 | A | AGTGTGTG others(5): Show |
26 | a0001c0001t0004g0262 a0001c0001t0004g0267 a0001c0001t0004g0268 others(23): Show |
26 | HG00408.hp1 HG02015.hp1 HG02074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1198-6590_1198-657 others(16): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157163829 | ||||||
| chr4:157163829 | A | AGTGTGTG others(7): Show |
2 | a0001c0001t0003g0045 a0001c0002t0008g0024 |
2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1198-6592_1198-657 others(18): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157163829 | ||||||
| chr4:157163829 | A | AGTGTGTG others(9): Show |
12 | a0001c0001t0003g0038 a0001c0001t0003g0040 a0001c0001t0003g0048 others(9): Show |
12 | HG01081.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1198-6594_1198-657 others(20): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157163829 | ||||||
| chr4:157163829 | A | AGTGTGTG others(11): Show |
12 | a0001c0001t0003g0004 a0001c0001t0003g0022 a0001c0001t0003g0039 others(9): Show |
13 | HG01255.hp1 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1198-6596_1198-657 others(22): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157163829 | ||||||
| chr4:157163829 | A | AGTGTGTG others(13): Show |
2 | a0001c0001t0003g0003 a0001c0001t0003g0023 |
3 | HG01884.hp1 HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1198-6598_1198-657 others(24): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157163829 | ||||||
| chr4:157163829 | A | AGTGTGTG others(15): Show |
3 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0182 |
3 | HG02615.hp2 HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1198-6600_1198-657 others(26): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157163829 | ||||||
| chr4:157163829 | A | AGTGTGTG others(17): Show |
3 | a0001c0001t0003g0072 a0001c0001t0003g0173 a0001c0001t0016g0175 |
3 | HG02486.hp2 HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1198-6602_1198-657 others(28): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157163829 | ||||||
| chr4:157163874 | T | C | 1 | a0001c0001t0017g0021 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1198-6558T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163874 | |||||||
| chr4:157163880 | T | C | 2 | a0001c0001t0004g0001 a0001c0001t0004g0275 |
5 | HG00558.hp1 NA18964.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.1198-6552T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163880 | |||||||
| chr4:157164007 | T | C | 5 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(2): Show |
5 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1198-6425T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157164007 | |||||||
| chr4:157164025 | G | T | 12 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(9): Show |
12 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1198-6407G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157164025 | |||||||
| chr4:157164120 | G | A | 1 | a0001c0008t0024g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1198-6312G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157164120 | |||||||
| chr4:157164144 | A | AT | 32 | a0001c0001t0001g0108 a0001c0001t0001g0152 a0001c0001t0003g0027 others(29): Show |
35 | HG00408.hp1 HG00558.hp1 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.1198-6276dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157164144 | ||||||
| chr4:157164243 | G | T | 1 | a0001c0001t0002g0208 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1198-6189G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157164243 | |||||||
| chr4:157164394 | A | G | 1 | a0001c0001t0013g0019 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1198-6038A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157164394 | |||||||
| chr4:157164546 | C | T | 13 | a0001c0001t0003g0005 a0001c0001t0003g0041 a0001c0001t0003g0042 others(10): Show |
14 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.1198-5886C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157164546 | |||||||
| chr4:157164923 | T | C | 13 | a0001c0001t0003g0005 a0001c0001t0003g0041 a0001c0001t0003g0042 others(10): Show |
14 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.1198-5509T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157164923 | |||||||
| chr4:157164967 | A | G | 2 | a0001c0001t0003g0005 a0001c0001t0003g0070 |
3 | HG01256.hp2 HG01258.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1198-5465A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157164967 | |||||||
| chr4:157165023 | C | T | 5 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(2): Show |
5 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1198-5409C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157165023 | |||||||
| chr4:157165311 | G | A | 1 | a0001c0001t0002g0164 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1198-5121G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157165311 | |||||||
| chr4:157165447 | A | G | 3 | a0001c0002t0006g0178 a0001c0002t0006g0179 a0001c0002t0006g0180 |
3 | HG02015.hp1 HG02080.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1198-4985A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157165447 | |||||||
| chr4:157165671 | C | G | 20 | a0001c0001t0003g0160 a0001c0001t0006g0155 a0001c0001t0006g0158 others(17): Show |
20 | HG00544.hp2 HG01081.hp2 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.1198-4761C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157165671 | |||||||
| chr4:157165888 | C | G | 1 | a0001c0001t0002g0164 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1198-4544C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157165888 | |||||||
| chr4:157165997 | G | A | 2 | a0001c0001t0003g0046 a0001c0001t0003g0254 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1198-4435G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157165997 | |||||||
| chr4:157166036 | A | G | 1 | a0001c0001t0002g0210 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1198-4396A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166036 | |||||||
| chr4:157166094 | G | A | 3 | a0001c0001t0001g0116 a0001c0001t0001g0119 a0001c0001t0001g0151 |
3 | HG00280.hp2 HG01515.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1198-4338G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166094 | |||||||
| chr4:157166101 | G | T | 1 | a0001c0001t0002g0210 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1198-4331G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166101 | |||||||
| chr4:157166133 | GT | G | 93 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0020 others(90): Show |
98 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.1198-4292delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157166133 | ||||||
| chr4:157166172 | A | G | 2 | a0001c0002t0008g0024 a0001c0002t0008g0025 |
2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1198-4260A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166172 | |||||||
| chr4:157166420 | G | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0056 |
2 | NA18952.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1198-4012G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166420 | |||||||
| chr4:157166483 | A | T | 1 | a0001c0001t0003g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1198-3949A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166483 | |||||||
| chr4:157166486 | G | C | 3 | a0001c0001t0003g0003 a0001c0001t0003g0022 a0001c0001t0003g0023 |
4 | HG01884.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1198-3946G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166486 | |||||||
| chr4:157166521 | G | A | 70 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(67): Show |
77 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1198-3911G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166521 | |||||||
| chr4:157166569 | A | G | 12 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0005g0181 others(9): Show |
12 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1198-3863A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166569 | |||||||
| chr4:157166613 | A | G | 48 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0020 others(45): Show |
50 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(47): Show |
intron_variant | MODIFIER | c.1198-3819A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166613 | |||||||
| chr4:157166632 | C | T | 1 | a0001c0001t0013g0019 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1198-3800C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166632 | |||||||
| chr4:157166691 | C | T | 1 | a0001c0001t0002g0207 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1198-3741C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166691 | |||||||
| chr4:157166955 | G | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0060 a0001c0001t0001g0148 others(2): Show |
6 | HG02080.hp1 HG02129.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.1198-3477G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166955 | |||||||
| chr4:157167220 | C | T | 35 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0020 others(32): Show |
37 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.1198-3212C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157167220 | |||||||
| chr4:157167281 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1198-3151T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157167281 | |||||||
| chr4:157167312 | A | G | 35 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0020 others(32): Show |
37 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.1198-3120A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157167312 | |||||||
| chr4:157167893 | A | T | 2 | a0001c0001t0002g0196 a0001c0001t0002g0228 |
2 | NA18971.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.1198-2539A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157167893 | |||||||
| chr4:157167953 | G | A | 7 | a0001c0001t0007g0192 a0001c0001t0007g0217 a0001c0001t0007g0218 others(4): Show |
7 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1198-2479G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157167953 | |||||||
| chr4:157168016 | C | G | 7 | a0001c0001t0003g0169 a0001c0001t0003g0171 a0001c0001t0003g0172 others(4): Show |
7 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1198-2416C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157168016 | |||||||
| chr4:157168051 | G | A | 2 | a0001c0001t0003g0027 a0001c0001t0003g0073 |
2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1198-2381G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157168051 | |||||||
| chr4:157168115 | A | ATTT | 8 | a0001c0001t0007g0192 a0001c0001t0007g0217 a0001c0001t0007g0218 others(5): Show |
8 | HG01192.hp1 HG01981.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1198-2306_1198-230 others(7): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157168115 | ||||||
| chr4:157168115 | AT | A | 139 | a0001c0001t0001g0065 a0001c0001t0001g0081 a0001c0001t0001g0095 others(136): Show |
151 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.1198-2304delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157168115 | ||||||
| chr4:157168141 | G | C | 2 | a0001c0001t0003g0046 a0001c0001t0003g0254 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1198-2291G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157168141 | |||||||
| chr4:157168266 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0056 |
2 | NA18952.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1198-2166T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157168266 | |||||||
| chr4:157168375 | A | G | 10 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0007g0192 others(7): Show |
10 | HG01192.hp1 HG01981.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1198-2057A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157168375 | |||||||
| chr4:157168434 | C | T | 24 | a0001c0001t0001g0147 a0001c0001t0006g0155 a0001c0001t0006g0158 others(21): Show |
24 | HG00544.hp2 HG00639.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1198-1998C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157168434 | |||||||
| chr4:157168497 | A | T | 10 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0007g0192 others(7): Show |
10 | HG01192.hp1 HG01981.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1198-1935A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157168497 | |||||||
| chr4:157168508 | G | A | 26 | a0001c0001t0001g0147 a0001c0001t0005g0181 a0001c0001t0006g0155 others(23): Show |
26 | HG00544.hp2 HG00639.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.1198-1924G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157168508 | |||||||
| chr4:157168560 | C | G | 24 | a0001c0001t0001g0147 a0001c0001t0006g0155 a0001c0001t0006g0158 others(21): Show |
24 | HG00544.hp2 HG00639.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1198-1872C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157168560 | |||||||
| chr4:157168563 | T | A | 1 | a0003c0009t0009g0106 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1198-1869T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157168563 | |||||||
| chr4:157168646 | G | A | 10 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0007g0192 others(7): Show |
10 | HG01192.hp1 HG01981.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1198-1786G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157168646 | |||||||
| chr4:157169181 | G | A | 45 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(42): Show |
48 | HG00639.hp1 HG00733.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.1198-1251G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157169181 | |||||||
| chr4:157169213 | A | G | 2 | a0001c0001t0010g0257 a0001c0001t0016g0175 |
2 | HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1198-1219A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157169213 | |||||||
| chr4:157169714 | A | C | 1 | a0002c0005t0006g0204 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1198-718A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157169714 | |||||||
| chr4:157169729 | G | T | 2 | a0001c0001t0005g0181 a0001c0001t0014g0253 |
2 | HG01255.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1198-703G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157169729 | |||||||
| chr4:157169834 | G | A | 1 | a0001c0001t0002g0196 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1198-598G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157169834 | |||||||
| chr4:157169837 | A | T | 80 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(77): Show |
83 | HG00544.hp2 HG00639.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.1198-595A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157169837 | |||||||
| chr4:157169880 | T | G | 10 | a0001c0001t0003g0027 a0001c0001t0003g0073 a0001c0001t0007g0192 others(7): Show |
10 | HG01192.hp1 HG01981.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1198-552T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157169880 | |||||||
| chr4:157169910 | T | A | 2 | a0001c0001t0003g0027 a0001c0001t0003g0073 |
2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1198-522T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157169910 | |||||||
| chr4:157169941 | G | C | 1 | a0001c0002t0006g0176 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1198-491G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157169941 | |||||||
| chr4:157169990 | G | A | 1 | a0001c0003t0014g0258 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1198-442G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157169990 | |||||||
| chr4:157170416 | C | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0101 |
2 | NA19060.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1198-16C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157170416 |