Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 130589 |
| ensemblid | ENSG00000143891.17 |
| hgncid | 24063 |
| symbol | GALM |
| name | galactose mutarotase |
| refseq_nuc | NM_138801.3 |
| refseq_prot | NP_620156.1 |
| ensembl_nuc | ENST00000272252.10 |
| ensembl_prot | ENSP00000272252.5 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 38666114 |
| end | 38734765 |
| strand | + |
| ver | v1.2 |
| region | chr2:38666114-38734765 |
| region5000 | chr2:38661114-38739765 |
| regionname0 | GALM_chr2_38666114_38734765 |
| regionname5000 | GALM_chr2_38661114_38739765 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 342 | 245 | 62 | 50 | 97 | 7 | 27 | 64 | GALM_chr2_38661114_38739765 | GALM | MASVT others(337): Show |
chr2 | 38661114 | 38739765 |
| a0002 | 0/0 | 342 | 80 | 29 | 8 | 29 | 1 | 13 | 24 | GALM_chr2_38661114_38739765 | GALM | MASVT others(337): Show |
chr2 | 38661114 | 38739765 |
| a0003 | 0/0 | 342 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | MASVT others(337): Show |
chr2 | 38661114 | 38739765 |
| a0004 | 0/0 | 342 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | MASVT others(337): Show |
chr2 | 38661114 | 38739765 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1026 | 233 | 51 | 49 | 97 | 7 | 27 | GALM_chr2_38661114_38739765 | GALM | ATGGC others(1021): Show |
chr2 | 38661114 | 38739765 | ||
| a0001c0003 | 0/0 | 1026 | 12 | 11 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | ATGGC others(1021): Show |
chr2 | 38661114 | 38739765 | ||
| a0002c0002 | 0/0 | 1026 | 80 | 29 | 8 | 29 | 1 | 13 | GALM_chr2_38661114_38739765 | GALM | ATGGC others(1021): Show |
chr2 | 38661114 | 38739765 | ||
| a0003c0004 | 0/0 | 1026 | 2 | 2 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | ATGGC others(1021): Show |
chr2 | 38661114 | 38739765 | ||
| a0004c0005 | 0/0 | 1026 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | ATGGC others(1021): Show |
chr2 | 38661114 | 38739765 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2279 | 115 | 15 | 20 | 63 | 2 | 15 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0002 | 0/1 | 2279 | 43 | 9 | 12 | 14 | 1 | 6 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0003 | 0/0 | 2278 | 19 | 6 | 8 | 0 | 2 | 3 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2273): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0004 | 0/0 | 2279 | 11 | 0 | 0 | 10 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0005 | 0/0 | 2275 | 2 | 2 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2270): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0006 | 0/0 | 2279 | 7 | 6 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0007 | 0/0 | 2280 | 3 | 1 | 1 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2275): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0008 | 0/0 | 2278 | 4 | 2 | 1 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2273): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0010 | 0/0 | 2280 | 2 | 1 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2275): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0011 | 0/0 | 2279 | 4 | 0 | 0 | 4 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0013 | 0/0 | 2279 | 2 | 2 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0015 | 0/0 | 2279 | 3 | 2 | 0 | 0 | 1 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0016 | 0/0 | 2279 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0017 | 0/0 | 2279 | 2 | 0 | 0 | 0 | 1 | 1 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0019 | 0/0 | 2279 | 2 | 1 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0020 | 1/0 | 2277 | 2 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2272): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0022 | 0/0 | 2279 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0023 | 0/0 | 2279 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0024 | 0/0 | 2278 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2273): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0025 | 0/0 | 2279 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0026 | 0/0 | 2280 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2275): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0027 | 0/0 | 2278 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2273): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0028 | 0/0 | 2278 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2273): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0031 | 0/0 | 2280 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2275): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0032 | 0/0 | 2280 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2275): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0033 | 0/0 | 2275 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2270): Show |
chr2 | 38661114 | 38739765 |
| a0001c0001t0034 | 0/0 | 2274 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2269): Show |
chr2 | 38661114 | 38739765 |
| a0001c0003t0005 | 0/0 | 2275 | 11 | 10 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2270): Show |
chr2 | 38661114 | 38739765 |
| a0001c0003t0035 | 0/0 | 2279 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| a0002c0002t0001 | 0/0 | 2279 | 41 | 0 | 7 | 26 | 1 | 7 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| a0002c0002t0002 | 0/0 | 2279 | 3 | 3 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| a0002c0002t0003 | 0/0 | 2278 | 3 | 3 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2273): Show |
chr2 | 38661114 | 38739765 |
| a0002c0002t0004 | 0/0 | 2279 | 4 | 4 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| a0002c0002t0006 | 0/0 | 2279 | 5 | 2 | 0 | 0 | 0 | 3 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| a0002c0002t0007 | 0/0 | 2280 | 2 | 1 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2275): Show |
chr2 | 38661114 | 38739765 |
| a0002c0002t0008 | 0/0 | 2278 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2273): Show |
chr2 | 38661114 | 38739765 |
| a0002c0002t0009 | 0/0 | 2279 | 5 | 5 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| a0002c0002t0010 | 0/0 | 2280 | 2 | 0 | 0 | 2 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2275): Show |
chr2 | 38661114 | 38739765 |
| a0002c0002t0012 | 0/0 | 2279 | 4 | 4 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| a0002c0002t0013 | 0/0 | 2279 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| a0002c0002t0014 | 0/0 | 2280 | 3 | 3 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2275): Show |
chr2 | 38661114 | 38739765 |
| a0002c0002t0016 | 0/0 | 2279 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| a0002c0002t0018 | 0/0 | 2281 | 2 | 2 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2276): Show |
chr2 | 38661114 | 38739765 |
| a0002c0002t0021 | 0/0 | 2279 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | ACTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| a0002c0002t0029 | 0/0 | 2280 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2275): Show |
chr2 | 38661114 | 38739765 |
| a0002c0002t0030 | 0/0 | 2279 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| a0003c0004t0004 | 0/0 | 2279 | 2 | 2 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| a0004c0005t0002 | 0/0 | 2279 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | GCTGG others(2274): Show |
chr2 | 38661114 | 38739765 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0024 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0006g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0007g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0007g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0007g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0008g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0008g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0008g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0008g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0010g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0010g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0011g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0011g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0011g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0011g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0013g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0013g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0015g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0015g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0015g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0016g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0017g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0017g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0019g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0019g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0020g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0020g0111 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0022g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0023g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0024g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0025g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0026g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0027g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0028g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0031g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0032g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0033g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0034g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0003t0005g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0003t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0003t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0003t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0003t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0003t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0003t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0003t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0003t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0003t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0003t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0003t0035g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0006g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0006g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0006g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0007g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0007g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0008g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0009g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0009g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0009g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0009g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0010g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0010g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0012g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0012g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0012g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0012g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0013g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0014g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0014g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0014g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0016g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0018g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0018g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0021g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0029g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0030g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0003c0004t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0003c0004t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0004c0005t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0101 | EUR | FIN | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00280 | hp2 | a0001 | c0001 | t0017 | g0038 | EUR | FIN | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0264 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0124 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00597 | hp1 | a0001 | c0001 | t0024 | g0066 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00609 | hp1 | a0001 | c0001 | t0011 | g0172 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0063 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00673 | hp2 | a0001 | c0001 | t0011 | g0025 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00738 | hp1 | a0001 | c0001 | t0008 | g0228 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0100 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01070 | hp2 | a0001 | c0001 | t0020 | g0076 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0255 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0079 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01081 | hp2 | a0001 | c0001 | t0027 | g0031 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01106 | hp1 | a0001 | c0001 | t0019 | g0304 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01106 | hp2 | a0001 | c0001 | t0007 | g0096 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0133 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0075 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0054 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01243 | hp1 | a0001 | c0003 | t0005 | g0215 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01255 | hp1 | a0001 | c0001 | t0023 | g0322 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0285 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0283 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0057 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01361 | hp1 | a0001 | c0001 | t0033 | g0213 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0113 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0301 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01496 | hp2 | a0002 | c0002 | t0030 | g0139 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01515 | hp1 | a0001 | c0001 | t0015 | g0053 | EUR | IBS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0296 | EUR | IBS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0034 | EUR | IBS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0284 | EUR | IBS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01884 | hp2 | a0002 | c0002 | t0029 | g0001 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0305 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01891 | hp2 | a0001 | c0001 | t0010 | g0132 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0265 | AMR | PEL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PEL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0256 | AMR | PEL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01978 | hp1 | a0001 | c0001 | t0026 | g0045 | AMR | PEL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0201 | AMR | PEL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0267 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02055 | hp1 | a0002 | c0002 | t0006 | g0232 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02055 | hp2 | a0002 | c0002 | t0012 | g0236 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0293 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0279 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02145 | hp1 | a0002 | c0002 | t0009 | g0238 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0144 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0310 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0102 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0206 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02451 | hp1 | a0001 | c0001 | t0015 | g0309 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0161 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02523 | hp1 | a0001 | c0001 | t0011 | g0155 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02572 | hp1 | a0002 | c0002 | t0004 | g0316 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02572 | hp2 | a0001 | c0003 | t0005 | g0226 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02602 | hp1 | a0001 | c0001 | t0016 | g0176 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0052 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02615 | hp1 | a0004 | c0005 | t0002 | g0125 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02615 | hp2 | a0001 | c0003 | t0005 | g0220 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02622 | hp1 | a0002 | c0002 | t0002 | g0204 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02622 | hp2 | a0001 | c0003 | t0005 | g0224 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0312 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02630 | hp2 | a0002 | c0002 | t0014 | g0320 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0302 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0162 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0257 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02698 | hp1 | a0002 | c0002 | t0008 | g0286 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02698 | hp2 | a0001 | c0001 | t0017 | g0042 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02723 | hp1 | a0002 | c0002 | t0009 | g0001 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02723 | hp2 | a0001 | c0001 | t0032 | g0319 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02735 | hp2 | a0002 | c0002 | t0016 | g0195 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0194 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0205 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02809 | hp2 | a0002 | c0002 | t0002 | g0203 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02818 | hp1 | a0002 | c0002 | t0018 | g0237 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02818 | hp2 | a0001 | c0003 | t0035 | g0222 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02886 | hp1 | a0002 | c0002 | t0009 | g0235 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02886 | hp2 | a0001 | c0001 | t0019 | g0202 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0307 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02895 | hp2 | a0002 | c0002 | t0014 | g0152 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02896 | hp1 | a0002 | c0002 | t0003 | g0299 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02897 | hp1 | a0002 | c0002 | t0003 | g0300 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02897 | hp2 | a0002 | c0002 | t0014 | g0151 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02922 | hp1 | a0002 | c0002 | t0012 | g0321 | AFR | ESN | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02922 | hp2 | a0001 | c0001 | t0015 | g0308 | AFR | ESN | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02965 | hp1 | a0001 | c0001 | t0008 | g0136 | AFR | ESN | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0116 | AFR | ESN | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02976 | hp1 | a0002 | c0002 | t0012 | g0233 | AFR | ESN | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03041 | hp1 | a0001 | c0001 | t0013 | g0227 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03130 | hp1 | a0001 | c0003 | t0005 | g0218 | AFR | ESN | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03130 | hp2 | a0003 | c0004 | t0004 | g0211 | AFR | ESN | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0190 | AFR | ESN | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03195 | hp1 | a0001 | c0003 | t0005 | g0221 | AFR | ESN | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03195 | hp2 | a0001 | c0003 | t0005 | g0223 | AFR | ESN | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | MSL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03209 | hp2 | a0002 | c0002 | t0006 | g0059 | AFR | MSL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03225 | hp1 | a0002 | c0002 | t0004 | g0317 | AFR | MSL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0291 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0160 | AFR | MSL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03453 | hp2 | a0001 | c0001 | t0028 | g0303 | AFR | MSL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03486 | hp1 | a0002 | c0002 | t0007 | g0315 | AFR | MSL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0051 | AFR | MSL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03491 | hp1 | a0002 | c0002 | t0006 | g0272 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03492 | hp1 | a0002 | c0002 | t0006 | g0290 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0210 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03516 | hp1 | a0002 | c0002 | t0009 | g0001 | AFR | ESN | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03516 | hp2 | a0003 | c0004 | t0004 | g0214 | AFR | ESN | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03579 | hp1 | a0002 | c0002 | t0012 | g0234 | AFR | MSL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03579 | hp2 | a0001 | c0003 | t0005 | g0217 | AFR | MSL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03669 | hp2 | a0002 | c0002 | t0021 | g0185 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0200 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0292 | SAS | BEB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0281 | SAS | BEB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | BEB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0273 | SAS | BEB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0138 | SAS | BEB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG04199 | hp1 | a0002 | c0002 | t0006 | g0295 | SAS | STU | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | STU | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | STU | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0282 | SAS | STU | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18522 | hp1 | a0001 | c0001 | t0034 | g0212 | AFR | YRI | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | YRI | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18612 | hp1 | a0001 | c0001 | t0011 | g0248 | EAS | CHB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | CHB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18906 | hp1 | a0002 | c0002 | t0004 | g0314 | AFR | YRI | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | YRI | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18951 | hp2 | a0001 | c0001 | t0008 | g0091 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18968 | hp1 | a0001 | c0001 | t0025 | g0175 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0289 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0287 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18985 | hp1 | a0002 | c0002 | t0010 | g0277 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18985 | hp2 | a0001 | c0001 | t0010 | g0072 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18991 | hp1 | a0001 | c0001 | t0031 | g0253 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18991 | hp2 | a0002 | c0002 | t0007 | g0294 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19000 | hp1 | a0002 | c0002 | t0010 | g0187 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19030 | hp2 | a0002 | c0002 | t0003 | g0298 | AFR | LWK | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19043 | hp1 | a0001 | c0003 | t0005 | g0225 | AFR | LWK | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | LWK | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19075 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19075 | hp2 | a0001 | c0001 | t0007 | g0060 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19240 | hp1 | a0001 | c0003 | t0005 | g0216 | AFR | YRI | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19240 | hp2 | a0001 | c0001 | t0022 | g0050 | AFR | YRI | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | TSI | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0058 | EUR | TSI | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | GIH | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0056 | SAS | GIH | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02109 | hp1 | a0002 | c0002 | t0009 | g0231 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0164 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02559 | hp1 | a0002 | c0002 | t0004 | g0318 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02559 | hp2 | a0001 | c0001 | t0013 | g0073 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0311 | AFR | MSL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03471 | hp2 | a0002 | c0002 | t0013 | g0209 | AFR | MSL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0010 | AFR | USA | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG06807 | hp2 | a0002 | c0002 | t0018 | g0012 | AFR | USA | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA20300 | hp1 | a0001 | c0001 | t0007 | g0092 | AFR | USA | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA20300 | hp2 | a0001 | c0003 | t0005 | g0219 | AFR | USA | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0159 | AFR | LWK | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0024 | REF | REF | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0020 | g0111 | REF | REF | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:38681323 | C | T | 1 | a0004 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.389C>T | p.Ser130Leu | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/7 | 437/2277 | 389/1029 | 130/342 | chr2 | 38681323 | |||
| chr2:38681358 | G | A | 1 | a0003 | 2 | HG03130.hp2 HG03516.hp2 |
missense_variant | MODERATE | c.424G>A | p.Gly142Arg | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/7 | 472/2277 | 424/1029 | 142/342 | chr2 | 38681358 | |||
| chr2:38689828 | A | T | 1 | a0002 | 80 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(77): Show |
missense_variant | MODERATE | c.568A>T | p.Asn190Tyr | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/7 | 616/2277 | 568/1029 | 190/342 | chr2 | 38689828 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:38666308 | G | A | 1 | a0001c0003 | 12 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(9): Show |
synonymous_variant | LOW | c.147G>A | p.Gln49Gln | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/7 | 195/2277 | 147/1029 | 49/342 | chr2 | 38666308 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:38666114 | G | A | 1 | a0002c0002t0021 | 1 | HG03669.hp2 | 5_prime_UTR_variant | MODIFIER | c.-48G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/7 | 48 | chr2 | 38666114 | ||||||
| chr2:38733681 | A | G | 5 | a0001c0001t0005 a0001c0001t0033 a0001c0001t0034 others(2): Show |
16 | HG01243.hp1 HG01361.hp1 HG02572.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*116A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 7/7 | 116 | chr2 | 38733681 | ||||||
| chr2:38733785 | G | A | 20 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(17): Show |
207 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*220G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 7/7 | 220 | chr2 | 38733785 | ||||||
| chr2:38733825 | G | A | 9 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0017 others(6): Show |
56 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*260G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 7/7 | 260 | chr2 | 38733825 | ||||||
| chr2:38733869 | C | T | 2 | a0001c0001t0016 a0002c0002t0016 |
2 | HG02602.hp1 HG02735.hp2 |
3_prime_UTR_variant | MODIFIER | c.*304C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 7/7 | 304 | chr2 | 38733869 | ||||||
| chr2:38733879 | CTTTCT | C | 4 | a0001c0001t0005 a0001c0001t0033 a0001c0001t0034 others(1): Show |
15 | HG01243.hp1 HG01361.hp1 HG02572.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*319_*323delTTTTC | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 7/7 | 319 | INFO_REALIGN_3_PRIME | chr2 | 38733879 | |||||
| chr2:38734191 | G | A | 1 | a0001c0001t0028 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*626G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 7/7 | 626 | chr2 | 38734191 | ||||||
| chr2:38734226 | G | A | 2 | a0002c0002t0009 a0002c0002t0029 |
6 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*661G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 7/7 | 661 | chr2 | 38734226 | ||||||
| chr2:38734262 | G | A | 1 | a0001c0001t0022 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*697G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 7/7 | 697 | chr2 | 38734262 | ||||||
| chr2:38734267 | T | C | 15 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0008 others(12): Show |
177 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*702T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 7/7 | 702 | chr2 | 38734267 | ||||||
| chr2:38734267 | T | G | 3 | a0002c0002t0009 a0002c0002t0012 a0002c0002t0029 |
10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*702T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 7/7 | 702 | chr2 | 38734267 | ||||||
| chr2:38734273 | C | T | 17 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 others(14): Show |
193 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*708C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 7/7 | 708 | chr2 | 38734273 | ||||||
| chr2:38734360 | G | A | 4 | a0001c0001t0005 a0001c0001t0033 a0001c0001t0034 others(1): Show |
15 | HG01243.hp1 HG01361.hp1 HG02572.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*795G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 7/7 | 795 | chr2 | 38734360 | ||||||
| chr2:38734383 | C | CA | 32 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(29): Show |
284 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(281): Show |
3_prime_UTR_variant | MODIFIER | c.*838dupA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 7/7 | 839 | INFO_REALIGN_3_PRIME | chr2 | 38734383 | |||||
| chr2:38734383 | C | CAA | 7 | a0001c0001t0007 a0001c0001t0026 a0001c0001t0031 others(4): Show |
11 | HG01106.hp2 HG01361.hp1 HG01884.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*837_*838dupAA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 7/7 | 839 | INFO_REALIGN_3_PRIME | chr2 | 38734383 | |||||
| chr2:38734429 | G | A | 1 | a0001c0001t0017 | 2 | HG00280.hp2 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*864G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 7/7 | 864 | chr2 | 38734429 | ||||||
| chr2:38734483 | C | G | 1 | a0001c0001t0023 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*918C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 7/7 | 918 | chr2 | 38734483 | ||||||
| chr2:38734526 | C | T | 1 | a0001c0001t0032 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*961C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 7/7 | 961 | chr2 | 38734526 | ||||||
| chr2:38734690 | G | GA | 35 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(32): Show |
292 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(289): Show |
3_prime_UTR_variant | MODIFIER | c.*1141dupA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 7/7 | 1142 | INFO_REALIGN_3_PRIME | chr2 | 38734690 | |||||
| chr2:38734690 | G | GAA | 10 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0013 others(7): Show |
28 | HG01106.hp1 HG01243.hp1 HG01891.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1140_*1141dupAA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 7/7 | 1142 | INFO_REALIGN_3_PRIME | chr2 | 38734690 | |||||
| chr2:38734729 | G | C | 1 | a0001c0001t0011 | 4 | HG00609.hp1 HG00673.hp2 HG02523.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1164G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 7/7 | 1164 | chr2 | 38734729 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:38666426 | C | T | 1 | a0001c0001t0023g0322 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.190+75C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38666426 | |||||||
| chr2:38666518 | A | G | 125 | a0001c0001t0001g0004 a0001c0001t0001g0207 a0001c0001t0001g0208 others(122): Show |
128 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.190+167A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38666518 | |||||||
| chr2:38666523 | T | C | 1 | a0002c0002t0001g0201 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.190+172T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38666523 | |||||||
| chr2:38666535 | G | A | 122 | a0001c0001t0001g0004 a0001c0001t0001g0207 a0001c0001t0001g0208 others(119): Show |
125 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.190+184G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38666535 | |||||||
| chr2:38666566 | G | C | 1 | a0001c0001t0001g0006 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.190+215G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38666566 | |||||||
| chr2:38666625 | T | G | 1 | a0001c0001t0019g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.190+274T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38666625 | |||||||
| chr2:38666647 | T | G | 1 | a0001c0001t0001g0006 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.190+296T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38666647 | |||||||
| chr2:38666808 | C | T | 120 | a0001c0001t0001g0004 a0001c0001t0001g0207 a0001c0001t0001g0208 others(117): Show |
123 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.190+457C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38666808 | |||||||
| chr2:38666831 | C | G | 123 | a0001c0001t0001g0004 a0001c0001t0001g0207 a0001c0001t0001g0208 others(120): Show |
126 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.190+480C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38666831 | |||||||
| chr2:38666835 | G | T | 5 | a0002c0002t0004g0314 a0002c0002t0004g0316 a0002c0002t0004g0317 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+484G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38666835 | |||||||
| chr2:38666854 | C | A | 1 | a0001c0001t0004g0007 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.190+503C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38666854 | |||||||
| chr2:38666923 | G | A | 1 | a0001c0001t0032g0319 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.190+572G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38666923 | |||||||
| chr2:38666967 | C | T | 7 | a0001c0001t0001g0313 a0001c0001t0002g0307 a0001c0001t0002g0310 others(4): Show |
7 | HG02258.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.190+616C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38666967 | |||||||
| chr2:38667165 | T | C | 1 | a0001c0001t0005g0205 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.190+814T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38667165 | |||||||
| chr2:38667249 | G | A | 1 | a0001c0001t0006g0206 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.190+898G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38667249 | |||||||
| chr2:38667386 | G | A | 122 | a0001c0001t0001g0004 a0001c0001t0001g0207 a0001c0001t0001g0208 others(119): Show |
125 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.190+1035G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38667386 | |||||||
| chr2:38667445 | C | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.190+1094C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38667445 | |||||||
| chr2:38667468 | G | A | 1 | a0002c0002t0012g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.190+1117G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38667468 | |||||||
| chr2:38667650 | A | C | 1 | a0002c0002t0014g0320 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.190+1299A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38667650 | |||||||
| chr2:38667688 | G | A | 1 | a0002c0002t0012g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.190+1337G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38667688 | |||||||
| chr2:38667692 | G | C | 1 | a0001c0001t0004g0007 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.190+1341G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38667692 | |||||||
| chr2:38667694 | C | T | 1 | a0001c0001t0004g0007 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.190+1343C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38667694 | |||||||
| chr2:38667697 | G | C | 1 | a0001c0001t0004g0007 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.190+1346G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38667697 | |||||||
| chr2:38667716 | A | G | 1 | a0002c0002t0014g0320 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.190+1365A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38667716 | |||||||
| chr2:38667728 | T | C | 122 | a0001c0001t0001g0004 a0001c0001t0001g0207 a0001c0001t0001g0208 others(119): Show |
125 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.190+1377T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38667728 | |||||||
| chr2:38667802 | A | T | 3 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0001c0001t0002g0200 |
3 | HG00735.hp1 HG01168.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.190+1451A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38667802 | |||||||
| chr2:38667803 | C | T | 9 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0313 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.190+1452C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38667803 | |||||||
| chr2:38667813 | G | C | 1 | a0001c0001t0004g0007 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.190+1462G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38667813 | |||||||
| chr2:38667815 | C | A | 1 | a0001c0001t0004g0007 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.190+1464C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38667815 | |||||||
| chr2:38667816 | G | C | 1 | a0001c0001t0004g0007 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.190+1465G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38667816 | |||||||
| chr2:38667818 | C | T | 122 | a0001c0001t0001g0004 a0001c0001t0001g0207 a0001c0001t0001g0208 others(119): Show |
125 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.190+1467C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38667818 | |||||||
| chr2:38667844 | T | A | 1 | a0001c0001t0004g0007 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.190+1493T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38667844 | |||||||
| chr2:38667845 | A | T | 1 | a0001c0001t0004g0007 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.190+1494A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38667845 | |||||||
| chr2:38667931 | C | T | 1 | a0001c0001t0032g0319 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.190+1580C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38667931 | |||||||
| chr2:38667944 | G | A | 1 | a0001c0001t0004g0007 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.190+1593G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38667944 | |||||||
| chr2:38667949 | A | G | 122 | a0001c0001t0001g0004 a0001c0001t0001g0207 a0001c0001t0001g0208 others(119): Show |
125 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.190+1598A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38667949 | |||||||
| chr2:38668017 | T | A | 1 | a0001c0001t0004g0008 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.190+1666T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668017 | |||||||
| chr2:38668027 | T | G | 2 | a0001c0001t0032g0319 a0002c0002t0014g0320 |
2 | HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.190+1676T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668027 | |||||||
| chr2:38668038 | T | G | 1 | a0001c0001t0004g0007 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.190+1687T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668038 | |||||||
| chr2:38668040 | G | T | 1 | a0001c0001t0004g0007 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.190+1689G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668040 | |||||||
| chr2:38668044 | A | T | 1 | a0001c0001t0004g0007 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.190+1693A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668044 | |||||||
| chr2:38668050 | A | G | 1 | a0001c0001t0004g0007 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.190+1699A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668050 | |||||||
| chr2:38668051 | T | A | 1 | a0001c0001t0004g0007 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.190+1700T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668051 | |||||||
| chr2:38668057 | C | T | 1 | a0002c0002t0001g0306 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.190+1706C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668057 | |||||||
| chr2:38668076 | T | A | 1 | a0001c0001t0004g0007 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.190+1725T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668076 | |||||||
| chr2:38668096 | G | A | 6 | a0002c0002t0004g0314 a0002c0002t0004g0316 a0002c0002t0004g0317 others(3): Show |
6 | HG02559.hp1 HG02572.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.190+1745G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668096 | |||||||
| chr2:38668110 | G | T | 1 | a0002c0002t0012g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.190+1759G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668110 | |||||||
| chr2:38668124 | T | C | 1 | a0002c0002t0012g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.190+1773T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668124 | |||||||
| chr2:38668172 | G | C | 1 | a0002c0002t0001g0210 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.190+1821G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668172 | |||||||
| chr2:38668184 | T | A | 1 | a0001c0001t0032g0319 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.190+1833T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668184 | |||||||
| chr2:38668187 | G | A | 1 | a0001c0001t0004g0007 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.190+1836G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668187 | |||||||
| chr2:38668216 | C | T | 120 | a0001c0001t0001g0004 a0001c0001t0001g0207 a0001c0001t0001g0208 others(117): Show |
123 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.190+1865C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668216 | |||||||
| chr2:38668229 | A | T | 1 | a0001c0001t0004g0007 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.190+1878A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668229 | |||||||
| chr2:38668231 | G | T | 1 | a0001c0001t0004g0007 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.190+1880G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668231 | |||||||
| chr2:38668233 | T | C | 1 | a0001c0001t0004g0007 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.190+1882T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668233 | |||||||
| chr2:38668376 | G | A | 1 | a0001c0001t0032g0319 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.190+2025G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668376 | |||||||
| chr2:38668470 | T | C | 126 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0207 others(123): Show |
129 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.190+2119T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668470 | |||||||
| chr2:38668496 | A | C | 4 | a0001c0001t0003g0302 a0001c0001t0003g0305 a0001c0001t0019g0304 others(1): Show |
4 | HG01106.hp1 HG01891.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+2145A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668496 | |||||||
| chr2:38668532 | G | A | 124 | a0001c0001t0001g0004 a0001c0001t0001g0207 a0001c0001t0001g0208 others(121): Show |
127 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.190+2181G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668532 | |||||||
| chr2:38668576 | T | C | 4 | a0001c0001t0033g0213 a0001c0001t0034g0212 a0003c0004t0004g0211 others(1): Show |
4 | HG01361.hp1 HG03130.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.190+2225T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668576 | |||||||
| chr2:38668600 | G | A | 1 | a0001c0001t0019g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.190+2249G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668600 | |||||||
| chr2:38668652 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.190+2301C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668652 | |||||||
| chr2:38668679 | G | A | 1 | a0001c0001t0008g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.190+2328G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668679 | |||||||
| chr2:38668746 | T | C | 1 | a0002c0002t0012g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.190+2395T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668746 | |||||||
| chr2:38668776 | A | T | 124 | a0001c0001t0001g0004 a0001c0001t0001g0207 a0001c0001t0001g0208 others(121): Show |
127 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.190+2425A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668776 | |||||||
| chr2:38668778 | T | A | 124 | a0001c0001t0001g0004 a0001c0001t0001g0207 a0001c0001t0001g0208 others(121): Show |
127 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.190+2427T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668778 | |||||||
| chr2:38668806 | T | A | 2 | a0001c0001t0032g0319 a0002c0002t0014g0320 |
2 | HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.190+2455T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668806 | |||||||
| chr2:38668806 | T | TA | 12 | a0001c0003t0005g0215 a0001c0003t0005g0216 a0001c0003t0005g0217 others(9): Show |
12 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.190+2463dupA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38668806 | ||||||
| chr2:38668814 | A | T | 4 | a0001c0001t0005g0205 a0001c0001t0032g0319 a0002c0002t0001g0301 others(1): Show |
4 | HG01496.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.190+2463A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668814 | |||||||
| chr2:38668815 | T | A | 3 | a0001c0001t0001g0011 a0001c0001t0019g0202 a0002c0002t0012g0321 |
3 | HG02886.hp2 HG02922.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.190+2464T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668815 | |||||||
| chr2:38668821 | T | A | 44 | a0001c0001t0001g0004 a0001c0001t0001g0239 a0001c0001t0001g0240 others(41): Show |
46 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.190+2470T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38668821 | |||||||
| chr2:38669021 | G | A | 1 | a0001c0001t0013g0227 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.190+2670G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38669021 | |||||||
| chr2:38669048 | A | AT | 125 | a0001c0001t0001g0004 a0001c0001t0001g0207 a0001c0001t0001g0208 others(122): Show |
128 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.190+2704dupT | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38669048 | ||||||
| chr2:38669091 | T | A | 3 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0001c0001t0008g0228 |
3 | HG00738.hp1 HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.190+2740T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38669091 | |||||||
| chr2:38669124 | C | T | 1 | a0001c0001t0019g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.190+2773C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38669124 | |||||||
| chr2:38669230 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.190+2879A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38669230 | |||||||
| chr2:38669300 | T | C | 12 | a0001c0003t0005g0215 a0001c0003t0005g0216 a0001c0003t0005g0217 others(9): Show |
12 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.190+2949T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38669300 | |||||||
| chr2:38669400 | G | C | 4 | a0001c0001t0003g0302 a0001c0001t0003g0305 a0001c0001t0019g0304 others(1): Show |
4 | HG01106.hp1 HG01891.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+3049G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38669400 | |||||||
| chr2:38669401 | C | A | 1 | a0002c0002t0001g0254 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.190+3050C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38669401 | |||||||
| chr2:38669489 | C | T | 125 | a0001c0001t0001g0004 a0001c0001t0001g0207 a0001c0001t0001g0208 others(122): Show |
128 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.190+3138C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38669489 | |||||||
| chr2:38669498 | G | A | 1 | a0002c0002t0018g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.190+3147G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38669498 | |||||||
| chr2:38669528 | G | A | 2 | a0002c0002t0002g0203 a0002c0002t0002g0204 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.190+3177G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38669528 | |||||||
| chr2:38669607 | G | A | 5 | a0001c0001t0001g0174 a0001c0001t0003g0302 a0001c0001t0003g0305 others(2): Show |
5 | HG01106.hp1 HG01891.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.190+3256G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38669607 | |||||||
| chr2:38669641 | C | T | 124 | a0001c0001t0001g0004 a0001c0001t0001g0207 a0001c0001t0001g0208 others(121): Show |
127 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.190+3290C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38669641 | |||||||
| chr2:38669678 | A | G | 1 | a0001c0001t0003g0194 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.190+3327A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38669678 | |||||||
| chr2:38669895 | C | CT | 6 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0192 others(3): Show |
6 | HG01192.hp1 HG01192.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.190+3561dupT | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38669895 | ||||||
| chr2:38669895 | CTTT | C | 123 | a0001c0001t0001g0004 a0001c0001t0001g0207 a0001c0001t0001g0208 others(120): Show |
126 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.190+3559_190+3561d others(5): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38669895 | ||||||
| chr2:38669932 | G | A | 50 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0296 others(47): Show |
51 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(48): Show |
intron_variant | MODIFIER | c.190+3581G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38669932 | |||||||
| chr2:38670107 | A | G | 135 | a0001c0001t0001g0004 a0001c0001t0001g0145 a0001c0001t0001g0146 others(132): Show |
137 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.190+3756A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38670107 | |||||||
| chr2:38670117 | G | C | 1 | a0001c0001t0003g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.190+3766G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38670117 | |||||||
| chr2:38670157 | C | G | 6 | a0002c0002t0004g0314 a0002c0002t0004g0316 a0002c0002t0004g0317 others(3): Show |
6 | HG02559.hp1 HG02572.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.190+3806C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38670157 | |||||||
| chr2:38670161 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.190+3810G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38670161 | |||||||
| chr2:38670226 | C | G | 1 | a0001c0001t0019g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.190+3875C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38670226 | |||||||
| chr2:38670247 | C | T | 7 | a0001c0001t0001g0313 a0001c0001t0002g0307 a0001c0001t0002g0310 others(4): Show |
7 | HG02258.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.190+3896C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38670247 | |||||||
| chr2:38670275 | A | G | 1 | a0001c0001t0001g0143 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.190+3924A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38670275 | |||||||
| chr2:38670281 | G | C | 9 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0313 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.190+3930G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38670281 | |||||||
| chr2:38670324 | C | T | 1 | a0002c0002t0012g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.190+3973C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38670324 | |||||||
| chr2:38670465 | C | G | 9 | a0002c0002t0003g0298 a0002c0002t0003g0299 a0002c0002t0003g0300 others(6): Show |
9 | HG02559.hp1 HG02572.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.190+4114C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38670465 | |||||||
| chr2:38670501 | G | A | 1 | a0001c0001t0032g0319 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.190+4150G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38670501 | |||||||
| chr2:38670508 | G | T | 47 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(44): Show |
47 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.190+4157G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38670508 | |||||||
| chr2:38670535 | G | A | 1 | a0001c0001t0019g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.190+4184G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38670535 | |||||||
| chr2:38670540 | C | T | 47 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(44): Show |
47 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.190+4189C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38670540 | |||||||
| chr2:38670575 | T | G | 45 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(42): Show |
45 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.190+4224T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38670575 | |||||||
| chr2:38670585 | C | A | 1 | a0002c0002t0014g0320 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.190+4234C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38670585 | |||||||
| chr2:38670612 | C | T | 167 | a0001c0001t0001g0004 a0001c0001t0001g0146 a0001c0001t0001g0147 others(164): Show |
170 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.190+4261C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38670612 | |||||||
| chr2:38670639 | A | G | 118 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(115): Show |
119 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.190+4288A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38670639 | |||||||
| chr2:38670668 | T | C | 162 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(159): Show |
165 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.190+4317T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38670668 | |||||||
| chr2:38670681 | C | T | 71 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0268 others(68): Show |
72 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(69): Show |
intron_variant | MODIFIER | c.190+4330C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38670681 | |||||||
| chr2:38670726 | C | A | 1 | a0002c0002t0001g0257 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.190+4375C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38670726 | |||||||
| chr2:38670774 | A | T | 72 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0268 others(69): Show |
73 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(70): Show |
intron_variant | MODIFIER | c.190+4423A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38670774 | |||||||
| chr2:38671088 | G | GC | 135 | a0001c0001t0001g0004 a0001c0001t0001g0141 a0001c0001t0001g0142 others(132): Show |
137 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.190+4737_190+4738i others(3): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38671088 | |||||||
| chr2:38671093 | G | A | 69 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0268 others(66): Show |
70 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(67): Show |
intron_variant | MODIFIER | c.190+4742G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38671093 | |||||||
| chr2:38671188 | T | C | 2 | a0002c0002t0002g0203 a0002c0002t0002g0204 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.191-4724T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38671188 | |||||||
| chr2:38671367 | T | C | 2 | a0002c0002t0001g0186 a0002c0002t0010g0187 |
2 | NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.191-4545T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38671367 | |||||||
| chr2:38671444 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.191-4468A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38671444 | |||||||
| chr2:38671486 | C | A | 64 | a0001c0001t0001g0004 a0001c0001t0001g0141 a0001c0001t0001g0142 others(61): Show |
65 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.191-4426C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38671486 | |||||||
| chr2:38671539 | C | A | 124 | a0001c0001t0001g0004 a0001c0001t0001g0141 a0001c0001t0001g0142 others(121): Show |
126 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.191-4373C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38671539 | |||||||
| chr2:38671891 | C | A | 5 | a0001c0001t0001g0014 a0001c0001t0004g0007 a0001c0001t0004g0015 others(2): Show |
5 | NA18946.hp1 NA19002.hp1 NA19065.hp2 others(2): Show |
intron_variant | MODIFIER | c.191-4021C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38671891 | |||||||
| chr2:38671932 | G | A | 1 | a0002c0002t0012g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.191-3980G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38671932 | |||||||
| chr2:38671935 | G | A | 10 | a0002c0002t0006g0232 a0002c0002t0009g0001 a0002c0002t0009g0231 others(7): Show |
11 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.191-3977G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38671935 | |||||||
| chr2:38671938 | A | G | 114 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(111): Show |
117 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(114): Show |
intron_variant | MODIFIER | c.191-3974A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38671938 | |||||||
| chr2:38671951 | A | G | 5 | a0001c0001t0019g0202 a0001c0001t0033g0213 a0001c0001t0034g0212 others(2): Show |
5 | HG01361.hp1 HG02886.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.191-3961A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38671951 | |||||||
| chr2:38672005 | CA | C | 5 | a0001c0001t0019g0202 a0001c0001t0033g0213 a0001c0001t0034g0212 others(2): Show |
5 | HG01361.hp1 HG02886.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.191-3899delA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38672005 | ||||||
| chr2:38672013 | A | C | 213 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(210): Show |
218 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.191-3899A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38672013 | |||||||
| chr2:38672026 | TG | T | 9 | a0002c0002t0003g0298 a0002c0002t0003g0299 a0002c0002t0003g0300 others(6): Show |
9 | HG02559.hp1 HG02572.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.191-3882delG | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38672026 | ||||||
| chr2:38672030 | G | A | 2 | a0002c0002t0001g0186 a0002c0002t0010g0187 |
2 | NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.191-3882G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38672030 | |||||||
| chr2:38672045 | C | A | 1 | a0001c0001t0001g0006 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.191-3867C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38672045 | |||||||
| chr2:38672086 | A | T | 60 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0297 others(57): Show |
61 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(58): Show |
intron_variant | MODIFIER | c.191-3826A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38672086 | |||||||
| chr2:38672345 | C | T | 1 | a0001c0001t0013g0227 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.191-3567C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38672345 | |||||||
| chr2:38672363 | G | T | 64 | a0001c0001t0001g0004 a0001c0001t0001g0141 a0001c0001t0001g0142 others(61): Show |
65 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.191-3549G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38672363 | |||||||
| chr2:38672433 | A | G | 3 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0001c0001t0008g0228 |
3 | HG00738.hp1 HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.191-3479A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38672433 | |||||||
| chr2:38672531 | G | A | 64 | a0001c0001t0001g0004 a0001c0001t0001g0141 a0001c0001t0001g0142 others(61): Show |
65 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.191-3381G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38672531 | |||||||
| chr2:38672672 | A | G | 1 | a0002c0002t0014g0320 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.191-3240A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38672672 | |||||||
| chr2:38672743 | G | A | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.191-3169G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38672743 | |||||||
| chr2:38672825 | G | A | 2 | a0001c0001t0013g0227 a0001c0001t0032g0319 |
2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.191-3087G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38672825 | |||||||
| chr2:38672844 | TA | T | 6 | a0001c0001t0004g0049 a0001c0001t0033g0213 a0001c0001t0034g0212 others(3): Show |
6 | HG01361.hp1 HG02735.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.191-3053delA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38672844 | ||||||
| chr2:38672866 | T | C | 138 | a0001c0001t0001g0004 a0001c0001t0001g0141 a0001c0001t0001g0142 others(135): Show |
140 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.191-3046T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38672866 | |||||||
| chr2:38672878 | C | T | 13 | a0001c0001t0005g0205 a0001c0003t0005g0215 a0001c0003t0005g0216 others(10): Show |
13 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.191-3034C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38672878 | |||||||
| chr2:38672884 | C | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.191-3028C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38672884 | |||||||
| chr2:38672946 | G | A | 54 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0297 others(51): Show |
55 | HG00408.hp2 HG01070.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.191-2966G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38672946 | |||||||
| chr2:38673016 | A | C | 6 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(3): Show |
6 | HG00673.hp1 HG01192.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.191-2896A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38673016 | |||||||
| chr2:38673242 | A | G | 1 | a0002c0002t0014g0320 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.191-2670A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38673242 | |||||||
| chr2:38673265 | G | T | 3 | a0002c0002t0003g0298 a0002c0002t0003g0299 a0002c0002t0003g0300 |
3 | HG02896.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.191-2647G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38673265 | |||||||
| chr2:38673268 | C | G | 20 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(17): Show |
20 | HG00639.hp1 HG01099.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.191-2644C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38673268 | |||||||
| chr2:38673323 | G | A | 1 | a0003c0004t0004g0211 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.191-2589G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38673323 | |||||||
| chr2:38673427 | T | C | 7 | a0001c0001t0003g0052 a0001c0001t0003g0054 a0001c0001t0003g0055 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.191-2485T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38673427 | |||||||
| chr2:38673446 | A | G | 2 | a0002c0002t0001g0186 a0002c0002t0010g0187 |
2 | NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.191-2466A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38673446 | |||||||
| chr2:38673473 | G | A | 2 | a0001c0001t0002g0002 a0001c0001t0002g0020 |
3 | HG03654.hp1 HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.191-2439G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38673473 | |||||||
| chr2:38673533 | T | G | 1 | a0001c0001t0013g0227 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.191-2379T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38673533 | |||||||
| chr2:38673797 | G | A | 1 | a0002c0002t0013g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.191-2115G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38673797 | |||||||
| chr2:38673805 | G | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0239 a0001c0001t0001g0240 others(12): Show |
16 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(13): Show |
intron_variant | MODIFIER | c.191-2107G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38673805 | |||||||
| chr2:38673809 | C | CA | 68 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0268 others(65): Show |
69 | HG00408.hp2 HG01070.hp1 HG01071.hp1 others(66): Show |
intron_variant | MODIFIER | c.191-2088dupA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38673809 | ||||||
| chr2:38673809 | C | CAA | 59 | a0001c0001t0001g0004 a0001c0001t0001g0141 a0001c0001t0001g0142 others(56): Show |
60 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.191-2089_191-2088d others(4): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38673809 | ||||||
| chr2:38673809 | C | CAAA | 9 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(6): Show |
9 | HG02129.hp1 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.191-2090_191-2088d others(5): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38673809 | ||||||
| chr2:38673832 | C | CA | 61 | a0001c0001t0001g0004 a0001c0001t0001g0141 a0001c0001t0001g0142 others(58): Show |
62 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.191-2071dupA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38673832 | ||||||
| chr2:38673944 | G | A | 137 | a0001c0001t0001g0004 a0001c0001t0001g0141 a0001c0001t0001g0142 others(134): Show |
139 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.191-1968G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38673944 | |||||||
| chr2:38673967 | AAT | A | 137 | a0001c0001t0001g0004 a0001c0001t0001g0141 a0001c0001t0001g0142 others(134): Show |
139 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.191-1942_191-1941d others(4): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38673967 | ||||||
| chr2:38674003 | T | G | 137 | a0001c0001t0001g0004 a0001c0001t0001g0141 a0001c0001t0001g0142 others(134): Show |
139 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.191-1909T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38674003 | |||||||
| chr2:38674004 | G | A | 7 | a0001c0001t0001g0313 a0001c0001t0002g0307 a0001c0001t0002g0310 others(4): Show |
7 | HG02258.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.191-1908G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38674004 | |||||||
| chr2:38674048 | T | C | 64 | a0001c0001t0001g0004 a0001c0001t0001g0141 a0001c0001t0001g0142 others(61): Show |
65 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.191-1864T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38674048 | |||||||
| chr2:38674191 | C | CT | 10 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0191 others(7): Show |
10 | HG01192.hp1 HG01515.hp2 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.191-1702dupT | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38674191 | ||||||
| chr2:38674191 | CT | C | 66 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0268 others(63): Show |
67 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(64): Show |
intron_variant | MODIFIER | c.191-1702delT | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38674191 | ||||||
| chr2:38674335 | A | G | 135 | a0001c0001t0001g0004 a0001c0001t0001g0141 a0001c0001t0001g0142 others(132): Show |
137 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.191-1577A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38674335 | |||||||
| chr2:38674379 | G | A | 67 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0268 others(64): Show |
68 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(65): Show |
intron_variant | MODIFIER | c.191-1533G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38674379 | |||||||
| chr2:38674394 | T | C | 5 | a0001c0001t0019g0202 a0001c0001t0033g0213 a0001c0001t0034g0212 others(2): Show |
5 | HG01361.hp1 HG02886.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.191-1518T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38674394 | |||||||
| chr2:38674410 | A | G | 172 | a0001c0001t0001g0004 a0001c0001t0001g0141 a0001c0001t0001g0142 others(169): Show |
175 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.191-1502A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38674410 | |||||||
| chr2:38674480 | G | T | 1 | a0001c0001t0004g0124 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.191-1432G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38674480 | |||||||
| chr2:38674502 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.191-1410A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38674502 | |||||||
| chr2:38674578 | C | T | 1 | a0001c0001t0001g0009 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.191-1334C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38674578 | |||||||
| chr2:38674588 | A | G | 135 | a0001c0001t0001g0004 a0001c0001t0001g0141 a0001c0001t0001g0142 others(132): Show |
137 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.191-1324A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38674588 | |||||||
| chr2:38674598 | A | G | 1 | a0002c0002t0014g0320 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.191-1314A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38674598 | |||||||
| chr2:38674610 | A | G | 170 | a0001c0001t0001g0004 a0001c0001t0001g0141 a0001c0001t0001g0142 others(167): Show |
173 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.191-1302A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38674610 | |||||||
| chr2:38674648 | C | T | 168 | a0001c0001t0001g0004 a0001c0001t0001g0141 a0001c0001t0001g0142 others(165): Show |
171 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.191-1264C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38674648 | |||||||
| chr2:38674693 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.191-1219G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38674693 | |||||||
| chr2:38674712 | G | T | 66 | a0001c0001t0001g0004 a0001c0001t0001g0141 a0001c0001t0001g0142 others(63): Show |
67 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.191-1200G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38674712 | |||||||
| chr2:38674780 | T | C | 61 | a0001c0001t0001g0004 a0001c0001t0001g0141 a0001c0001t0001g0142 others(58): Show |
62 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.191-1132T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38674780 | |||||||
| chr2:38674966 | G | A | 13 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0001c0001t0008g0228 others(10): Show |
14 | HG00738.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.191-946G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38674966 | |||||||
| chr2:38675003 | C | T | 17 | a0001c0001t0001g0004 a0001c0001t0001g0239 a0001c0001t0001g0240 others(14): Show |
18 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.191-909C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675003 | |||||||
| chr2:38675044 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.191-868G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675044 | |||||||
| chr2:38675072 | G | T | 2 | a0002c0002t0001g0186 a0002c0002t0010g0187 |
2 | NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.191-840G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675072 | |||||||
| chr2:38675257 | G | T | 1 | a0002c0002t0014g0320 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.191-655G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675257 | |||||||
| chr2:38675329 | C | G | 3 | a0002c0002t0014g0151 a0002c0002t0014g0152 a0002c0002t0018g0012 |
3 | HG02895.hp2 HG02897.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.191-583C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675329 | |||||||
| chr2:38675330 | T | C | 1 | a0001c0001t0005g0205 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.191-582T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675330 | |||||||
| chr2:38675428 | G | A | 1 | a0004c0005t0002g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.191-484G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675428 | |||||||
| chr2:38675482 | A | G | 172 | a0001c0001t0001g0004 a0001c0001t0001g0122 a0001c0001t0001g0141 others(169): Show |
175 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.191-430A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675482 | |||||||
| chr2:38675518 | GTTTTTTT others(6): Show |
G | 2 | a0002c0002t0001g0186 a0002c0002t0010g0187 |
2 | NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.191-386_191-374del others(13): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675518 | ||||||
| chr2:38675518 | GTTTTTTT others(10): Show |
G | 1 | a0001c0001t0002g0251 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.191-386_191-370del others(17): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675518 | ||||||
| chr2:38675518 | GTTTTTTT others(11): Show |
G | 1 | a0001c0001t0001g0250 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.191-386_191-369del others(18): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675518 | ||||||
| chr2:38675518 | GTTTTTTT others(12): Show |
G | 13 | a0001c0001t0001g0004 a0001c0001t0001g0239 a0001c0001t0001g0240 others(10): Show |
14 | HG00544.hp1 HG00558.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.191-384_191-366del others(19): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675518 | ||||||
| chr2:38675519 | T | G | 72 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0268 others(69): Show |
73 | HG00408.hp2 HG01070.hp1 HG01071.hp1 others(70): Show |
intron_variant | MODIFIER | c.191-393T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675519 | |||||||
| chr2:38675524 | TTGTTTTT others(14): Show |
T | 1 | a0001c0001t0006g0206 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.191-384_191-364del others(21): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675524 | ||||||
| chr2:38675524 | TTGTTTTT others(20): Show |
T | 1 | a0001c0001t0001g0179 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.191-384_191-358del others(27): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675524 | ||||||
| chr2:38675524 | TTGTTTTT others(22): Show |
T | 33 | a0001c0001t0001g0122 a0001c0001t0001g0141 a0001c0001t0001g0142 others(30): Show |
33 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.191-384_191-356del others(29): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675524 | ||||||
| chr2:38675524 | TTGTTTTT others(24): Show |
T | 1 | a0001c0001t0003g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.191-384_191-354del others(31): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675524 | ||||||
| chr2:38675525 | TGTTTTTT others(21): Show |
T | 2 | a0001c0001t0001g0197 a0001c0001t0016g0176 |
2 | HG02602.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.191-386_191-359del others(28): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675525 | |||||||
| chr2:38675526 | G | T | 85 | a0001c0001t0001g0062 a0001c0001t0001g0177 a0001c0001t0001g0249 others(82): Show |
86 | HG00408.hp1 HG00408.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.191-386G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675526 | |||||||
| chr2:38675526 | GTT | G | 10 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0064 others(7): Show |
10 | HG00609.hp2 HG01243.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.191-369_191-368del others(2): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675526 | ||||||
| chr2:38675526 | GTTTT | G | 9 | a0001c0001t0002g0002 a0001c0001t0006g0051 a0001c0001t0022g0050 others(6): Show |
9 | HG02572.hp2 HG02622.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.191-371_191-368del others(4): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675526 | ||||||
| chr2:38675526 | GTTTTTTT others(10): Show |
G | 1 | a0001c0001t0001g0071 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.191-384_191-368del others(17): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675526 | ||||||
| chr2:38675527 | T | G | 1 | a0001c0001t0001g0061 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.191-385T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675527 | |||||||
| chr2:38675528 | TTTTTTTT others(12): Show |
T | 1 | a0001c0001t0001g0249 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.191-382_191-364del others(19): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675528 | ||||||
| chr2:38675528 | TTTTTTTT others(22): Show |
T | 7 | a0001c0001t0002g0156 a0001c0001t0002g0157 a0001c0001t0002g0158 others(4): Show |
7 | HG02451.hp2 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.191-382_191-354del others(29): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675528 | ||||||
| chr2:38675530 | TTTTTTTT others(22): Show |
T | 1 | a0001c0001t0001g0177 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.191-380_191-352del others(29): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675530 | ||||||
| chr2:38675531 | T | G | 4 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG02717.hp2 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-381T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675531 | |||||||
| chr2:38675532 | T | G | 3 | a0002c0002t0001g0186 a0002c0002t0010g0187 a0002c0002t0014g0320 |
3 | HG02630.hp2 NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.191-380T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675532 | |||||||
| chr2:38675533 | T | G | 1 | a0001c0001t0011g0025 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.191-379T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675533 | |||||||
| chr2:38675534 | TTTTTTTT others(6): Show |
T | 3 | a0002c0002t0014g0151 a0002c0002t0014g0152 a0002c0002t0018g0012 |
3 | HG02895.hp2 HG02897.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.191-376_191-364del others(13): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675534 | ||||||
| chr2:38675534 | TTTTTTTT others(10): Show |
T | 1 | a0001c0001t0013g0227 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.191-376_191-360del others(17): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675534 | ||||||
| chr2:38675537 | T | G | 2 | a0001c0001t0002g0021 a0001c0003t0005g0219 |
2 | HG00639.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.191-375T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675537 | |||||||
| chr2:38675539 | T | G | 13 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0002g0021 others(10): Show |
13 | HG00423.hp1 HG00639.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.191-373T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675539 | |||||||
| chr2:38675539 | T | TTG | 6 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0003g0054 others(3): Show |
6 | HG00642.hp2 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.191-372_191-371ins others(2): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675539 | ||||||
| chr2:38675539 | TTTTTTGT others(9): Show |
T | 1 | a0001c0001t0008g0228 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.191-371_191-356del others(16): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675539 | ||||||
| chr2:38675539 | TTTTTTGT others(13): Show |
T | 5 | a0001c0001t0001g0268 a0002c0002t0001g0264 a0002c0002t0001g0265 others(2): Show |
5 | HG00408.hp2 HG01928.hp2 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.191-371_191-352del others(20): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675539 | ||||||
| chr2:38675539 | TTTTTTGT others(15): Show |
T | 1 | a0002c0002t0009g0231 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.191-371_191-350del others(22): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675539 | ||||||
| chr2:38675539 | TTTTTTGT others(17): Show |
T | 4 | a0002c0002t0001g0260 a0002c0002t0001g0261 a0002c0002t0001g0262 others(1): Show |
4 | NA18943.hp2 NA18953.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.191-371_191-348del others(24): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675539 | ||||||
| chr2:38675540 | TTTTTGTG others(6): Show |
T | 1 | a0002c0002t0014g0320 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.191-370_191-358del others(13): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675540 | ||||||
| chr2:38675540 | TTTTTGTG others(8): Show |
T | 1 | a0001c0001t0002g0229 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.191-370_191-356del others(15): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675540 | ||||||
| chr2:38675540 | TTTTTGTG others(14): Show |
T | 7 | a0002c0002t0001g0270 a0002c0002t0001g0271 a0002c0002t0006g0232 others(4): Show |
7 | HG02055.hp1 HG02976.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.191-370_191-350del others(21): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675540 | ||||||
| chr2:38675540 | TTTTTGTG others(16): Show |
T | 1 | a0001c0001t0001g0269 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.191-370_191-348del others(23): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675540 | ||||||
| chr2:38675541 | T | G | 31 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0067 others(28): Show |
31 | HG00423.hp1 HG00639.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.191-371T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675541 | |||||||
| chr2:38675541 | T | TG | 7 | a0001c0001t0001g0009 a0001c0001t0001g0095 a0001c0001t0001g0145 others(4): Show |
7 | HG01192.hp1 HG02809.hp2 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.191-371_191-370ins others(1): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675541 | |||||||
| chr2:38675541 | T | TGTG | 3 | a0001c0001t0001g0014 a0001c0001t0001g0082 a0001c0001t0023g0322 |
3 | HG01255.hp1 HG01255.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.191-371_191-370ins others(3): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675541 | |||||||
| chr2:38675541 | T | TTG | 19 | a0001c0001t0001g0080 a0001c0001t0001g0106 a0001c0001t0001g0107 others(16): Show |
19 | HG00642.hp1 HG01070.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.191-370_191-369ins others(2): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675541 | ||||||
| chr2:38675541 | T | TTGTG | 7 | a0001c0001t0001g0115 a0001c0001t0002g0026 a0001c0001t0002g0083 others(4): Show |
7 | HG01943.hp1 NA18946.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.191-370_191-369ins others(4): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675541 | ||||||
| chr2:38675541 | TTTTG | T | 7 | a0001c0001t0002g0002 a0001c0001t0002g0040 a0001c0001t0002g0198 others(4): Show |
7 | HG00735.hp1 HG01106.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.191-369_191-366del others(4): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675541 | ||||||
| chr2:38675541 | TTTTGTGT others(9): Show |
T | 1 | a0001c0001t0002g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.191-369_191-354del others(16): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675541 | ||||||
| chr2:38675541 | TTTTGTGT others(11): Show |
T | 2 | a0002c0002t0001g0258 a0002c0002t0001g0289 |
2 | NA18945.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.191-369_191-352del others(18): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675541 | ||||||
| chr2:38675541 | TTTTGTGT others(13): Show |
T | 21 | a0001c0001t0001g0297 a0001c0001t0002g0018 a0001c0001t0002g0019 others(18): Show |
22 | HG01070.hp1 HG01071.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.191-369_191-350del others(20): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675541 | ||||||
| chr2:38675541 | TTTTGTGT others(15): Show |
T | 1 | a0001c0001t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.191-369_191-348del others(22): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675541 | ||||||
| chr2:38675542 | TTTGTGTG others(8): Show |
T | 1 | a0002c0002t0001g0256 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.191-368_191-354del others(15): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675542 | ||||||
| chr2:38675542 | TTTGTGTG others(12): Show |
T | 14 | a0002c0002t0001g0201 a0002c0002t0001g0210 a0002c0002t0001g0275 others(11): Show |
14 | HG01261.hp1 HG01346.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.191-368_191-350del others(19): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675542 | ||||||
| chr2:38675542 | TTTGTGTG others(14): Show |
T | 4 | a0002c0002t0009g0001 a0002c0002t0009g0238 a0002c0002t0018g0237 others(1): Show |
5 | HG01884.hp2 HG02145.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.191-368_191-348del others(21): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675542 | ||||||
| chr2:38675543 | T | G | 106 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(103): Show |
107 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.191-369T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675543 | |||||||
| chr2:38675543 | T | TG | 3 | a0001c0001t0001g0098 a0001c0001t0001g0137 a0001c0001t0001g0196 |
3 | HG02293.hp2 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.191-369_191-368ins others(1): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675543 | |||||||
| chr2:38675543 | T | TTG | 11 | a0001c0001t0001g0099 a0001c0001t0001g0120 a0001c0001t0001g0126 others(8): Show |
11 | HG01099.hp1 HG01099.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.191-324_191-323dup others(2): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675543 | ||||||
| chr2:38675543 | TTGTGTGT others(5): Show |
T | 1 | a0002c0002t0004g0314 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.191-334_191-323del others(12): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675543 | ||||||
| chr2:38675543 | TTGTGTGT others(7): Show |
T | 3 | a0002c0002t0004g0317 a0002c0002t0004g0318 a0002c0002t0007g0315 |
3 | HG02559.hp1 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.191-336_191-323del others(14): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675543 | ||||||
| chr2:38675543 | TTGTGTGT others(9): Show |
T | 7 | a0001c0001t0001g0313 a0001c0001t0002g0310 a0001c0001t0002g0311 others(4): Show |
7 | HG02258.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.191-338_191-323del others(16): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675543 | ||||||
| chr2:38675543 | TTGTGTGT others(11): Show |
T | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.191-340_191-323del others(18): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675543 | ||||||
| chr2:38675543 | TTGTGTGT others(13): Show |
T | 4 | a0002c0002t0003g0299 a0002c0002t0003g0300 a0002c0002t0009g0235 others(1): Show |
4 | HG02055.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.191-342_191-323del others(20): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 38675543 | ||||||
| chr2:38675544 | TGTGTGTG others(6): Show |
T | 1 | a0002c0002t0004g0316 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.191-367_191-355del others(13): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675544 | |||||||
| chr2:38675544 | TGTGTGTG others(8): Show |
T | 1 | a0002c0002t0013g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.191-367_191-353del others(15): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675544 | |||||||
| chr2:38675544 | TGTGTGTG others(10): Show |
T | 1 | a0001c0001t0002g0307 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.191-367_191-351del others(17): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675544 | |||||||
| chr2:38675544 | TGTGTGTG others(12): Show |
T | 1 | a0002c0002t0003g0298 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.191-367_191-349del others(19): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675544 | |||||||
| chr2:38675545 | G | T | 18 | a0001c0001t0001g0004 a0001c0001t0001g0128 a0001c0001t0001g0239 others(15): Show |
18 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.191-367G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675545 | |||||||
| chr2:38675547 | G | T | 2 | a0001c0001t0002g0035 a0004c0005t0002g0125 |
2 | HG02615.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.191-365G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675547 | |||||||
| chr2:38675553 | G | T | 1 | a0001c0001t0001g0179 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.191-359G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675553 | |||||||
| chr2:38675555 | G | T | 33 | a0001c0001t0001g0122 a0001c0001t0001g0141 a0001c0001t0001g0142 others(30): Show |
33 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.191-357G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675555 | |||||||
| chr2:38675557 | G | T | 1 | a0001c0001t0003g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.191-355G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675557 | |||||||
| chr2:38675561 | G | T | 7 | a0001c0001t0001g0313 a0001c0001t0002g0310 a0001c0001t0002g0311 others(4): Show |
7 | HG02258.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.191-351G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675561 | |||||||
| chr2:38675563 | G | T | 10 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0313 others(7): Show |
10 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.191-349G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675563 | |||||||
| chr2:38675565 | G | T | 4 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0002c0002t0003g0299 others(1): Show |
4 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.191-347G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675565 | |||||||
| chr2:38675586 | T | A | 1 | a0001c0001t0011g0025 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.191-326T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675586 | |||||||
| chr2:38675600 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0004g0124 |
2 | HG00423.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.191-312G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675600 | |||||||
| chr2:38675621 | T | C | 1 | a0001c0001t0032g0319 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.191-291T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675621 | |||||||
| chr2:38675646 | G | C | 1 | a0002c0002t0009g0235 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.191-266G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675646 | |||||||
| chr2:38675771 | G | A | 3 | a0001c0001t0001g0064 a0002c0002t0001g0260 a0002c0002t0001g0261 |
3 | HG00609.hp2 NA18953.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.191-141G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675771 | |||||||
| chr2:38675784 | T | C | 66 | a0001c0001t0001g0004 a0001c0001t0001g0122 a0001c0001t0001g0141 others(63): Show |
67 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.191-128T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675784 | |||||||
| chr2:38675791 | G | A | 1 | a0001c0001t0019g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.191-121G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675791 | |||||||
| chr2:38675812 | G | T | 3 | a0002c0002t0003g0298 a0002c0002t0003g0299 a0002c0002t0003g0300 |
3 | HG02896.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.191-100G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675812 | |||||||
| chr2:38675880 | T | A | 49 | a0001c0001t0001g0269 a0001c0001t0001g0297 a0002c0002t0001g0005 others(46): Show |
50 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(47): Show |
intron_variant | MODIFIER | c.191-32T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675880 | |||||||
| chr2:38675882 | T | C | 1 | a0002c0002t0014g0320 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.191-30T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38675882 | |||||||
| chr2:38676074 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02027.hp2 | splice_region_variant&intron_variant | LOW | c.345+8C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38676074 | |||||||
| chr2:38676099 | A | G | 1 | a0001c0003t0005g0220 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.345+33A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38676099 | |||||||
| chr2:38676247 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.345+181A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38676247 | |||||||
| chr2:38676262 | C | T | 2 | a0001c0001t0003g0305 a0001c0001t0019g0304 |
2 | HG01106.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.345+196C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38676262 | |||||||
| chr2:38676347 | C | T | 1 | a0001c0001t0001g0297 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.345+281C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38676347 | |||||||
| chr2:38676400 | A | G | 6 | a0002c0002t0004g0314 a0002c0002t0004g0316 a0002c0002t0004g0317 others(3): Show |
6 | HG02559.hp1 HG02572.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.345+334A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38676400 | |||||||
| chr2:38676540 | G | A | 5 | a0001c0001t0019g0202 a0001c0001t0033g0213 a0001c0001t0034g0212 others(2): Show |
5 | HG01361.hp1 HG02886.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.345+474G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38676540 | |||||||
| chr2:38676580 | T | C | 1 | a0001c0001t0003g0056 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.345+514T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38676580 | |||||||
| chr2:38676617 | G | A | 3 | a0002c0002t0003g0298 a0002c0002t0003g0299 a0002c0002t0003g0300 |
3 | HG02896.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.345+551G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38676617 | |||||||
| chr2:38676627 | G | C | 1 | a0001c0001t0001g0178 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.345+561G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38676627 | |||||||
| chr2:38676631 | C | T | 48 | a0001c0001t0001g0269 a0002c0002t0001g0005 a0002c0002t0001g0201 others(45): Show |
49 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(46): Show |
intron_variant | MODIFIER | c.345+565C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38676631 | |||||||
| chr2:38676632 | G | A | 2 | a0002c0002t0006g0232 a0002c0002t0012g0233 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.345+566G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38676632 | |||||||
| chr2:38676677 | C | T | 48 | a0001c0001t0001g0269 a0002c0002t0001g0005 a0002c0002t0001g0201 others(45): Show |
49 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(46): Show |
intron_variant | MODIFIER | c.345+611C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38676677 | |||||||
| chr2:38676705 | G | A | 70 | a0001c0001t0001g0004 a0001c0001t0001g0122 a0001c0001t0001g0141 others(67): Show |
71 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.345+639G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38676705 | |||||||
| chr2:38676723 | A | G | 66 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0269 others(63): Show |
67 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(64): Show |
intron_variant | MODIFIER | c.345+657A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38676723 | |||||||
| chr2:38676751 | A | G | 2 | a0002c0002t0001g0186 a0002c0002t0010g0187 |
2 | NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.345+685A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38676751 | |||||||
| chr2:38676757 | C | T | 65 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0269 others(62): Show |
66 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(63): Show |
intron_variant | MODIFIER | c.345+691C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38676757 | |||||||
| chr2:38676781 | T | A | 169 | a0001c0001t0001g0004 a0001c0001t0001g0122 a0001c0001t0001g0141 others(166): Show |
172 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.345+715T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38676781 | |||||||
| chr2:38676949 | C | T | 5 | a0001c0001t0019g0202 a0001c0001t0033g0213 a0001c0001t0034g0212 others(2): Show |
5 | HG01361.hp1 HG02886.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.345+883C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38676949 | |||||||
| chr2:38676953 | G | T | 9 | a0002c0002t0003g0298 a0002c0002t0003g0299 a0002c0002t0003g0300 others(6): Show |
9 | HG02559.hp1 HG02572.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.345+887G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38676953 | |||||||
| chr2:38677260 | TAGAGAAG others(4): Show |
T | 1 | a0001c0001t0006g0206 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.345+1214_345+1224d others(13): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 38677260 | ||||||
| chr2:38677341 | A | T | 3 | a0002c0002t0014g0151 a0002c0002t0014g0152 a0002c0002t0018g0012 |
3 | HG02895.hp2 HG02897.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.345+1275A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38677341 | |||||||
| chr2:38677367 | G | A | 1 | a0002c0002t0001g0210 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.345+1301G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38677367 | |||||||
| chr2:38677375 | G | A | 50 | a0001c0001t0001g0122 a0001c0001t0001g0141 a0001c0001t0001g0142 others(47): Show |
50 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.345+1309G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38677375 | |||||||
| chr2:38677401 | C | T | 1 | a0002c0002t0012g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.345+1335C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38677401 | |||||||
| chr2:38677481 | T | A | 1 | a0001c0001t0002g0307 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.345+1415T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38677481 | |||||||
| chr2:38677624 | C | T | 7 | a0002c0002t0009g0001 a0002c0002t0009g0231 a0002c0002t0009g0235 others(4): Show |
8 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+1558C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38677624 | |||||||
| chr2:38677632 | C | A | 2 | a0002c0002t0001g0186 a0002c0002t0010g0187 |
2 | NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.345+1566C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38677632 | |||||||
| chr2:38677654 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0024g0066 |
2 | HG00597.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.345+1588G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38677654 | |||||||
| chr2:38677683 | A | G | 3 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0001c0001t0008g0228 |
3 | HG00738.hp1 HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.345+1617A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38677683 | |||||||
| chr2:38677832 | C | G | 7 | a0001c0001t0001g0313 a0001c0001t0002g0307 a0001c0001t0002g0310 others(4): Show |
7 | HG02258.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.345+1766C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38677832 | |||||||
| chr2:38677850 | A | G | 42 | a0001c0001t0001g0122 a0001c0001t0001g0141 a0001c0001t0001g0142 others(39): Show |
42 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.345+1784A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38677850 | |||||||
| chr2:38677869 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.345+1803A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38677869 | |||||||
| chr2:38678017 | C | CT | 107 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0036 others(104): Show |
110 | HG00280.hp2 HG00558.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.345+1967dupT | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 38678017 | ||||||
| chr2:38678017 | C | CTTTT | 17 | a0001c0001t0001g0004 a0001c0001t0001g0239 a0001c0001t0001g0240 others(14): Show |
18 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.345+1964_345+1967d others(6): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 38678017 | ||||||
| chr2:38678017 | CT | C | 6 | a0002c0002t0001g0186 a0002c0002t0010g0187 a0002c0002t0014g0151 others(3): Show |
6 | HG02630.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.345+1967delT | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 38678017 | ||||||
| chr2:38678102 | C | T | 3 | a0001c0001t0001g0137 a0001c0001t0008g0010 a0001c0001t0008g0136 |
3 | HG02965.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.345+2036C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38678102 | |||||||
| chr2:38678157 | C | T | 13 | a0001c0001t0005g0205 a0001c0003t0005g0215 a0001c0003t0005g0216 others(10): Show |
13 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.345+2091C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38678157 | |||||||
| chr2:38678237 | C | T | 7 | a0001c0001t0001g0313 a0001c0001t0002g0307 a0001c0001t0002g0310 others(4): Show |
7 | HG02258.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.345+2171C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38678237 | |||||||
| chr2:38678337 | G | A | 1 | a0002c0002t0001g0274 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.345+2271G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38678337 | |||||||
| chr2:38678407 | G | T | 5 | a0001c0001t0019g0202 a0001c0001t0033g0213 a0001c0001t0034g0212 others(2): Show |
5 | HG01361.hp1 HG02886.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.345+2341G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38678407 | |||||||
| chr2:38678735 | G | A | 3 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0001c0001t0002g0200 |
3 | HG00735.hp1 HG01168.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.346-2545G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38678735 | |||||||
| chr2:38678756 | C | T | 1 | a0002c0002t0014g0320 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.346-2524C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38678756 | |||||||
| chr2:38678955 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0004g0017 |
2 | HG02257.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.346-2325C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38678955 | |||||||
| chr2:38678982 | C | CTTTA | 11 | a0002c0002t0006g0232 a0002c0002t0009g0001 a0002c0002t0009g0231 others(8): Show |
12 | HG01496.hp2 HG01884.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.346-2282_346-2279d others(6): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 38678982 | ||||||
| chr2:38679009 | CGGA | C | 3 | a0002c0002t0014g0151 a0002c0002t0014g0152 a0002c0002t0018g0012 |
3 | HG02895.hp2 HG02897.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.346-2269_346-2267d others(5): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 38679009 | ||||||
| chr2:38679071 | C | G | 17 | a0001c0001t0001g0004 a0001c0001t0001g0239 a0001c0001t0001g0240 others(14): Show |
18 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.346-2209C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38679071 | |||||||
| chr2:38679192 | G | T | 2 | a0002c0002t0002g0203 a0002c0002t0002g0204 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.346-2088G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38679192 | |||||||
| chr2:38679210 | C | T | 5 | a0002c0002t0001g0186 a0002c0002t0010g0187 a0002c0002t0014g0151 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.346-2070C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38679210 | |||||||
| chr2:38679283 | G | A | 9 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0313 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.346-1997G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38679283 | |||||||
| chr2:38679344 | G | A | 49 | a0001c0001t0001g0269 a0001c0001t0001g0297 a0002c0002t0001g0005 others(46): Show |
50 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(47): Show |
intron_variant | MODIFIER | c.346-1936G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38679344 | |||||||
| chr2:38679356 | CG | C | 63 | a0001c0001t0001g0269 a0002c0002t0001g0005 a0002c0002t0001g0186 others(60): Show |
64 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(61): Show |
intron_variant | MODIFIER | c.346-1923delG | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38679356 | |||||||
| chr2:38679357 | G | C | 103 | a0001c0001t0001g0004 a0001c0001t0001g0122 a0001c0001t0001g0141 others(100): Show |
105 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.346-1923G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38679357 | |||||||
| chr2:38679359 | C | G | 1 | a0001c0001t0003g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.346-1921C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38679359 | |||||||
| chr2:38679492 | T | C | 13 | a0001c0001t0005g0205 a0001c0003t0005g0215 a0001c0003t0005g0216 others(10): Show |
13 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.346-1788T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38679492 | |||||||
| chr2:38679565 | C | G | 1 | a0001c0001t0013g0227 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.346-1715C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38679565 | |||||||
| chr2:38679565 | C | T | 2 | a0002c0002t0002g0190 a0002c0002t0006g0059 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.346-1715C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38679565 | |||||||
| chr2:38679705 | A | G | 1 | a0001c0001t0002g0188 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.346-1575A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38679705 | |||||||
| chr2:38679757 | C | T | 7 | a0001c0001t0001g0313 a0001c0001t0002g0307 a0001c0001t0002g0310 others(4): Show |
7 | HG02258.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.346-1523C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38679757 | |||||||
| chr2:38679758 | G | A | 1 | a0002c0002t0004g0314 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.346-1522G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38679758 | |||||||
| chr2:38679854 | A | T | 1 | a0001c0001t0005g0116 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.346-1426A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38679854 | |||||||
| chr2:38679859 | G | C | 66 | a0001c0001t0001g0269 a0001c0001t0001g0297 a0002c0002t0001g0005 others(63): Show |
67 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(64): Show |
intron_variant | MODIFIER | c.346-1421G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38679859 | |||||||
| chr2:38679881 | A | C | 1 | a0002c0002t0014g0320 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.346-1399A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38679881 | |||||||
| chr2:38679951 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.346-1329G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38679951 | |||||||
| chr2:38680007 | C | T | 1 | a0002c0002t0009g0235 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.346-1273C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38680007 | |||||||
| chr2:38680087 | C | T | 1 | a0001c0001t0024g0066 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.346-1193C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38680087 | |||||||
| chr2:38680185 | AT | A | 166 | a0001c0001t0001g0004 a0001c0001t0001g0122 a0001c0001t0001g0141 others(163): Show |
169 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.346-1088delT | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 38680185 | ||||||
| chr2:38680271 | C | T | 1 | a0001c0001t0019g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.346-1009C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38680271 | |||||||
| chr2:38680395 | C | CAAGAAGA others(2610): Show |
1 | a0001c0001t0002g0251 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.346-869_346-868ins others(2617): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 38680395 | ||||||
| chr2:38680463 | C | T | 58 | a0001c0001t0001g0269 a0001c0001t0001g0297 a0002c0002t0001g0005 others(55): Show |
59 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(56): Show |
intron_variant | MODIFIER | c.346-817C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38680463 | |||||||
| chr2:38680530 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.346-750T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38680530 | |||||||
| chr2:38680712 | TA | T | 29 | a0001c0001t0005g0205 a0001c0003t0005g0215 a0001c0003t0005g0216 others(26): Show |
30 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.346-557delA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 38680712 | ||||||
| chr2:38680767 | A | G | 3 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0001c0001t0008g0228 |
3 | HG00738.hp1 HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.346-513A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38680767 | |||||||
| chr2:38680806 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.346-474T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38680806 | |||||||
| chr2:38680853 | G | A | 1 | a0002c0002t0001g0275 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.346-427G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38680853 | |||||||
| chr2:38680863 | C | T | 8 | a0001c0001t0001g0115 a0002c0002t0009g0001 a0002c0002t0009g0231 others(5): Show |
9 | HG01884.hp2 HG01943.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.346-417C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38680863 | |||||||
| chr2:38680901 | C | T | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.346-379C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38680901 | |||||||
| chr2:38681123 | C | G | 2 | a0002c0002t0006g0232 a0002c0002t0012g0233 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.346-157C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38681123 | |||||||
| chr2:38681127 | C | T | 1 | a0001c0001t0002g0029 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.346-153C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | chr2 | 38681127 | |||||||
| chr2:38681129 | CA | C | 77 | a0001c0001t0001g0004 a0001c0001t0001g0122 a0001c0001t0001g0141 others(74): Show |
78 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.346-137delA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 38681129 | ||||||
| chr2:38681129 | CAA | C | 13 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0313 others(10): Show |
13 | HG00738.hp1 HG02109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.346-138_346-137del others(2): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 38681129 | ||||||
| chr2:38681641 | A | G | 4 | a0001c0003t0005g0223 a0001c0003t0005g0224 a0001c0003t0005g0225 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+155A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38681641 | |||||||
| chr2:38681654 | A | G | 4 | a0001c0003t0005g0223 a0001c0003t0005g0224 a0001c0003t0005g0225 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+168A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38681654 | |||||||
| chr2:38681733 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.552+247G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38681733 | |||||||
| chr2:38681737 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0121 |
2 | HG02027.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.552+251C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38681737 | |||||||
| chr2:38681758 | T | C | 1 | a0002c0002t0021g0185 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.552+272T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38681758 | |||||||
| chr2:38681961 | G | A | 1 | a0001c0001t0005g0116 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.552+475G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38681961 | |||||||
| chr2:38682128 | G | A | 1 | a0002c0002t0012g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.552+642G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38682128 | |||||||
| chr2:38682247 | G | A | 2 | a0001c0001t0033g0213 a0001c0001t0034g0212 |
2 | HG01361.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.552+761G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38682247 | |||||||
| chr2:38682257 | T | G | 2 | a0002c0002t0014g0151 a0002c0002t0014g0152 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.552+771T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38682257 | |||||||
| chr2:38682564 | G | T | 61 | a0001c0001t0001g0269 a0002c0002t0001g0005 a0002c0002t0001g0201 others(58): Show |
62 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(59): Show |
intron_variant | MODIFIER | c.552+1078G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38682564 | |||||||
| chr2:38682647 | G | A | 1 | a0001c0001t0032g0319 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.552+1161G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38682647 | |||||||
| chr2:38682669 | A | G | 1 | a0001c0001t0011g0025 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.552+1183A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38682669 | |||||||
| chr2:38682715 | A | G | 62 | a0001c0001t0001g0269 a0001c0001t0001g0297 a0002c0002t0001g0005 others(59): Show |
63 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(60): Show |
intron_variant | MODIFIER | c.552+1229A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38682715 | |||||||
| chr2:38682735 | A | G | 12 | a0002c0002t0006g0232 a0002c0002t0009g0001 a0002c0002t0009g0231 others(9): Show |
13 | HG01496.hp2 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.552+1249A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38682735 | |||||||
| chr2:38682745 | C | A | 18 | a0002c0002t0001g0186 a0002c0002t0006g0232 a0002c0002t0009g0001 others(15): Show |
19 | HG01496.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.552+1259C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38682745 | |||||||
| chr2:38682779 | C | A | 2 | a0002c0002t0001g0186 a0002c0002t0010g0187 |
2 | NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.552+1293C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38682779 | |||||||
| chr2:38682802 | A | G | 9 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0313 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.552+1316A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38682802 | |||||||
| chr2:38682809 | T | G | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.552+1323T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38682809 | |||||||
| chr2:38682897 | T | TA | 11 | a0001c0001t0001g0014 a0001c0001t0001g0068 a0001c0001t0001g0069 others(8): Show |
11 | HG01258.hp1 HG01346.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.552+1427dupA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38682897 | ||||||
| chr2:38682897 | TA | T | 65 | a0001c0001t0001g0269 a0001c0001t0001g0297 a0001c0001t0002g0200 others(62): Show |
66 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(63): Show |
intron_variant | MODIFIER | c.552+1427delA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38682897 | ||||||
| chr2:38682989 | T | G | 62 | a0001c0001t0001g0269 a0001c0001t0001g0297 a0002c0002t0001g0005 others(59): Show |
63 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(60): Show |
intron_variant | MODIFIER | c.552+1503T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38682989 | |||||||
| chr2:38683031 | T | C | 1 | a0002c0002t0007g0294 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.552+1545T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683031 | |||||||
| chr2:38683066 | A | G | 2 | a0002c0002t0001g0186 a0002c0002t0010g0187 |
2 | NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.552+1580A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683066 | |||||||
| chr2:38683066 | A | T | 4 | a0002c0002t0012g0321 a0002c0002t0014g0151 a0002c0002t0014g0152 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+1580A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683066 | |||||||
| chr2:38683207 | A | C | 2 | a0002c0002t0002g0203 a0002c0002t0002g0204 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.552+1721A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683207 | |||||||
| chr2:38683227 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.552+1741C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683227 | |||||||
| chr2:38683260 | C | A | 62 | a0001c0001t0001g0269 a0001c0001t0001g0297 a0002c0002t0001g0005 others(59): Show |
63 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(60): Show |
intron_variant | MODIFIER | c.552+1774C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683260 | |||||||
| chr2:38683271 | G | C | 1 | a0001c0001t0001g0119 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.552+1785G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683271 | |||||||
| chr2:38683326 | G | A | 1 | a0001c0001t0003g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.552+1840G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683326 | |||||||
| chr2:38683333 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.552+1847A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683333 | |||||||
| chr2:38683338 | C | T | 2 | a0002c0002t0002g0190 a0002c0002t0006g0059 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.552+1852C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683338 | |||||||
| chr2:38683354 | A | G | 1 | a0001c0001t0023g0322 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.552+1868A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683354 | |||||||
| chr2:38683369 | C | T | 1 | a0001c0001t0023g0322 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.552+1883C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683369 | |||||||
| chr2:38683406 | T | G | 2 | a0002c0002t0002g0203 a0002c0002t0002g0204 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.552+1920T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683406 | |||||||
| chr2:38683437 | G | A | 1 | a0001c0001t0002g0030 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.552+1951G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683437 | |||||||
| chr2:38683453 | T | C | 203 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(200): Show |
208 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.552+1967T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683453 | |||||||
| chr2:38683480 | G | A | 1 | a0002c0002t0013g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.552+1994G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683480 | |||||||
| chr2:38683535 | CTCAGATT others(10): Show |
C | 13 | a0001c0001t0005g0205 a0001c0003t0005g0215 a0001c0003t0005g0216 others(10): Show |
13 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.552+2059_552+2075d others(19): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38683535 | ||||||
| chr2:38683606 | G | A | 1 | a0002c0002t0001g0275 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.552+2120G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683606 | |||||||
| chr2:38683636 | G | A | 1 | a0001c0003t0005g0221 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.552+2150G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683636 | |||||||
| chr2:38683693 | A | C | 62 | a0001c0001t0001g0269 a0001c0001t0001g0297 a0002c0002t0001g0005 others(59): Show |
63 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(60): Show |
intron_variant | MODIFIER | c.552+2207A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683693 | |||||||
| chr2:38683693 | A | G | 1 | a0001c0001t0016g0176 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.552+2207A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683693 | |||||||
| chr2:38683695 | T | C | 1 | a0001c0001t0004g0124 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.552+2209T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683695 | |||||||
| chr2:38683711 | C | T | 9 | a0002c0002t0003g0298 a0002c0002t0003g0299 a0002c0002t0003g0300 others(6): Show |
9 | HG02559.hp1 HG02572.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.552+2225C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683711 | |||||||
| chr2:38683727 | C | T | 51 | a0001c0001t0001g0269 a0001c0001t0001g0297 a0002c0002t0001g0005 others(48): Show |
52 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(49): Show |
intron_variant | MODIFIER | c.552+2241C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683727 | |||||||
| chr2:38683819 | A | G | 9 | a0002c0002t0003g0298 a0002c0002t0003g0299 a0002c0002t0003g0300 others(6): Show |
9 | HG02559.hp1 HG02572.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.552+2333A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683819 | |||||||
| chr2:38683837 | G | C | 1 | a0001c0001t0032g0319 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.552+2351G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683837 | |||||||
| chr2:38683888 | T | C | 4 | a0002c0002t0012g0321 a0002c0002t0014g0151 a0002c0002t0014g0152 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+2402T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683888 | |||||||
| chr2:38683895 | T | G | 218 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(215): Show |
223 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.552+2409T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683895 | |||||||
| chr2:38683918 | G | A | 13 | a0001c0001t0005g0205 a0001c0003t0005g0215 a0001c0003t0005g0216 others(10): Show |
13 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.552+2432G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683918 | |||||||
| chr2:38683988 | C | T | 8 | a0001c0001t0003g0052 a0001c0001t0003g0054 a0001c0001t0003g0055 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.552+2502C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683988 | |||||||
| chr2:38684099 | A | C | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.552+2613A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38684099 | |||||||
| chr2:38684243 | T | C | 18 | a0002c0002t0001g0186 a0002c0002t0006g0232 a0002c0002t0009g0001 others(15): Show |
19 | HG01496.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.552+2757T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38684243 | |||||||
| chr2:38684254 | G | A | 1 | a0001c0001t0013g0227 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.552+2768G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38684254 | |||||||
| chr2:38684382 | T | C | 2 | a0002c0002t0001g0186 a0002c0002t0010g0187 |
2 | NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.552+2896T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38684382 | |||||||
| chr2:38684449 | C | A | 3 | a0001c0001t0002g0156 a0001c0001t0002g0157 a0001c0001t0002g0158 |
3 | HG02717.hp1 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.552+2963C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38684449 | |||||||
| chr2:38684489 | A | G | 5 | a0001c0001t0019g0202 a0001c0001t0033g0213 a0001c0001t0034g0212 others(2): Show |
5 | HG01361.hp1 HG02886.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.552+3003A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38684489 | |||||||
| chr2:38684519 | C | A | 42 | a0001c0001t0001g0122 a0001c0001t0001g0141 a0001c0001t0001g0142 others(39): Show |
42 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.552+3033C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38684519 | |||||||
| chr2:38684545 | G | A | 16 | a0002c0002t0001g0186 a0002c0002t0006g0232 a0002c0002t0009g0001 others(13): Show |
17 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.552+3059G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38684545 | |||||||
| chr2:38684677 | G | C | 77 | a0001c0001t0001g0269 a0002c0002t0001g0005 a0002c0002t0001g0186 others(74): Show |
79 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(76): Show |
intron_variant | MODIFIER | c.552+3191G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38684677 | |||||||
| chr2:38684830 | C | CA | 9 | a0002c0002t0002g0190 a0002c0002t0003g0298 a0002c0002t0003g0299 others(6): Show |
9 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.552+3351dupA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38684830 | ||||||
| chr2:38684887 | G | A | 48 | a0001c0001t0001g0269 a0002c0002t0001g0005 a0002c0002t0001g0201 others(45): Show |
49 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(46): Show |
intron_variant | MODIFIER | c.552+3401G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38684887 | |||||||
| chr2:38685134 | A | C | 6 | a0002c0002t0004g0314 a0002c0002t0004g0316 a0002c0002t0004g0317 others(3): Show |
6 | HG02559.hp1 HG02572.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.552+3648A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38685134 | |||||||
| chr2:38685234 | C | G | 1 | a0002c0002t0012g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.552+3748C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38685234 | |||||||
| chr2:38685260 | G | T | 1 | a0002c0002t0016g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.552+3774G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38685260 | |||||||
| chr2:38685277 | C | T | 3 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0001c0001t0008g0228 |
3 | HG00738.hp1 HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.552+3791C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38685277 | |||||||
| chr2:38685464 | G | C | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.552+3978G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38685464 | |||||||
| chr2:38685644 | C | G | 11 | a0002c0002t0002g0190 a0002c0002t0003g0298 a0002c0002t0003g0299 others(8): Show |
11 | HG02559.hp1 HG02572.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.552+4158C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38685644 | |||||||
| chr2:38685708 | A | T | 1 | a0001c0001t0032g0319 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.553-4105A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38685708 | |||||||
| chr2:38685708 | ATTTTTAT | A | 75 | a0001c0001t0001g0269 a0002c0002t0001g0005 a0002c0002t0001g0186 others(72): Show |
77 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(74): Show |
intron_variant | MODIFIER | c.553-4085_553-4079d others(9): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38685708 | ||||||
| chr2:38685803 | C | T | 6 | a0002c0002t0004g0314 a0002c0002t0004g0316 a0002c0002t0004g0317 others(3): Show |
6 | HG02559.hp1 HG02572.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.553-4010C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38685803 | |||||||
| chr2:38685935 | A | C | 1 | a0001c0001t0002g0188 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.553-3878A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38685935 | |||||||
| chr2:38686051 | T | C | 11 | a0002c0002t0002g0190 a0002c0002t0003g0298 a0002c0002t0003g0299 others(8): Show |
11 | HG02559.hp1 HG02572.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.553-3762T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686051 | |||||||
| chr2:38686104 | T | C | 1 | a0002c0002t0007g0294 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.553-3709T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686104 | |||||||
| chr2:38686142 | A | G | 2 | a0001c0001t0013g0227 a0001c0001t0032g0319 |
2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.553-3671A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686142 | |||||||
| chr2:38686192 | T | TA | 12 | a0001c0003t0005g0215 a0001c0003t0005g0216 a0001c0003t0005g0217 others(9): Show |
12 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.553-3609dupA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686192 | ||||||
| chr2:38686220 | A | ATTTCTTT others(9): Show |
3 | a0001c0001t0019g0202 a0002c0002t0014g0151 a0002c0002t0014g0152 |
3 | HG02886.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.553-3550_553-3535d others(18): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686220 | ||||||
| chr2:38686220 | ATTTC | A | 6 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0135 others(3): Show |
6 | HG01099.hp2 HG02257.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.553-3538_553-3535d others(6): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686220 | ||||||
| chr2:38686220 | ATTTCTTT others(1): Show |
A | 24 | a0001c0001t0001g0062 a0001c0001t0001g0099 a0001c0001t0001g0103 others(21): Show |
24 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.553-3542_553-3535d others(10): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686220 | ||||||
| chr2:38686220 | ATTTCTTT others(5): Show |
A | 69 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0061 others(66): Show |
69 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.553-3546_553-3535d others(14): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686220 | ||||||
| chr2:38686220 | ATTTCTTT others(9): Show |
A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0127 a0001c0001t0003g0074 others(2): Show |
5 | HG01070.hp2 HG01109.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.553-3550_553-3535d others(18): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686220 | ||||||
| chr2:38686220 | ATTTCTTT others(13): Show |
A | 15 | a0002c0002t0001g0210 a0002c0002t0001g0266 a0002c0002t0001g0267 others(12): Show |
15 | HG02027.hp1 HG02040.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.553-3554_553-3535d others(22): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686220 | ||||||
| chr2:38686220 | ATTTCTTT others(17): Show |
A | 46 | a0001c0001t0001g0297 a0002c0002t0001g0005 a0002c0002t0001g0186 others(43): Show |
47 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(44): Show |
intron_variant | MODIFIER | c.553-3558_553-3535d others(26): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686220 | ||||||
| chr2:38686220 | ATTTCTTT others(21): Show |
A | 11 | a0002c0002t0006g0232 a0002c0002t0009g0001 a0002c0002t0009g0231 others(8): Show |
12 | HG01496.hp2 HG01884.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.553-3562_553-3535d others(30): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686220 | ||||||
| chr2:38686223 | T | TCCTTCCT others(38): Show |
1 | a0001c0001t0001g0192 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.553-3589_553-3588i others(47): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686223 | ||||||
| chr2:38686227 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.553-3586T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686227 | |||||||
| chr2:38686227 | T | TCCTTCCT others(18): Show |
2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | NA19000.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.553-3585_553-3584i others(27): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686227 | ||||||
| chr2:38686227 | T | TCCTTCCT others(26): Show |
4 | a0001c0001t0001g0147 a0001c0001t0001g0178 a0001c0001t0001g0197 others(1): Show |
4 | HG03831.hp1 HG04204.hp2 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-3585_553-3584i others(35): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686227 | ||||||
| chr2:38686227 | T | TCCTTCCT others(30): Show |
5 | a0001c0001t0001g0150 a0001c0001t0001g0168 a0001c0001t0001g0180 others(2): Show |
5 | HG00673.hp1 HG01934.hp2 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.553-3585_553-3584i others(39): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686227 | ||||||
| chr2:38686227 | T | TCCTTCCT others(34): Show |
14 | a0001c0001t0001g0122 a0001c0001t0001g0153 a0001c0001t0001g0154 others(11): Show |
14 | HG01192.hp2 HG01978.hp2 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.553-3585_553-3584i others(43): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686227 | ||||||
| chr2:38686227 | T | TCCTTCCT others(38): Show |
11 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0163 others(8): Show |
11 | HG01168.hp2 HG01169.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.553-3585_553-3584i others(47): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686227 | ||||||
| chr2:38686227 | T | TCCTTCCT others(42): Show |
3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0011g0172 |
3 | HG00609.hp1 HG00621.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.553-3585_553-3584i others(51): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686227 | ||||||
| chr2:38686227 | T | TCCTTCCT others(46): Show |
3 | a0001c0001t0001g0169 a0001c0001t0011g0155 a0001c0001t0025g0175 |
3 | HG00558.hp2 HG02523.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.553-3585_553-3584i others(55): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686227 | ||||||
| chr2:38686229 | T | C | 3 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0001c0001t0008g0228 |
3 | HG00738.hp1 HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.553-3584T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686229 | |||||||
| chr2:38686229 | T | TTTCTTTC others(49): Show |
2 | a0001c0001t0015g0308 a0001c0001t0015g0309 |
2 | HG02451.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.553-3535_553-3534i others(58): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686229 | ||||||
| chr2:38686231 | T | C | 43 | a0001c0001t0001g0122 a0001c0001t0001g0141 a0001c0001t0001g0142 others(40): Show |
43 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.553-3582T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686231 | |||||||
| chr2:38686231 | T | TCCTTCCT others(26): Show |
14 | a0001c0001t0001g0004 a0001c0001t0001g0239 a0001c0001t0001g0240 others(11): Show |
15 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(12): Show |
intron_variant | MODIFIER | c.553-3581_553-3580i others(35): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686231 | ||||||
| chr2:38686231 | T | TCCTTCCT others(30): Show |
3 | a0001c0001t0001g0244 a0001c0001t0001g0269 a0001c0001t0006g0206 |
3 | HG02074.hp1 HG02280.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.553-3581_553-3580i others(39): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686231 | ||||||
| chr2:38686231 | T | TCCTTCCT others(34): Show |
1 | a0001c0001t0001g0250 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.553-3581_553-3580i others(43): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686231 | ||||||
| chr2:38686233 | T | TTTCTTTC others(45): Show |
2 | a0001c0001t0002g0310 a0001c0001t0002g0311 |
2 | HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.553-3535_553-3534i others(54): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686233 | ||||||
| chr2:38686233 | T | TTTCTTTC others(49): Show |
1 | a0001c0001t0002g0307 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.553-3535_553-3534i others(58): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686233 | ||||||
| chr2:38686235 | T | C | 61 | a0001c0001t0001g0004 a0001c0001t0001g0122 a0001c0001t0001g0141 others(58): Show |
62 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.553-3578T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686235 | |||||||
| chr2:38686237 | T | TTTCTTTC others(49): Show |
2 | a0001c0001t0001g0313 a0001c0001t0002g0312 |
2 | HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.553-3535_553-3534i others(58): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686237 | ||||||
| chr2:38686239 | T | C | 61 | a0001c0001t0001g0004 a0001c0001t0001g0122 a0001c0001t0001g0141 others(58): Show |
62 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.553-3574T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686239 | |||||||
| chr2:38686241 | T | TTTCTTTC others(25): Show |
1 | a0001c0001t0001g0207 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.553-3541_553-3540i others(34): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686241 | ||||||
| chr2:38686241 | T | TTTCTTTC others(33): Show |
1 | a0001c0001t0001g0208 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.553-3535_553-3534i others(42): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686241 | ||||||
| chr2:38686243 | T | C | 60 | a0001c0001t0001g0004 a0001c0001t0001g0122 a0001c0001t0001g0141 others(57): Show |
61 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.553-3570T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686243 | |||||||
| chr2:38686243 | T | TTCTTCCT others(86): Show |
1 | a0001c0001t0002g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.553-3570_553-3569i others(95): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686243 | |||||||
| chr2:38686243 | T | TTCTTCCT others(94): Show |
1 | a0001c0001t0008g0228 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.553-3570_553-3569i others(103): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686243 | |||||||
| chr2:38686243 | T | TTCTTCCT others(98): Show |
1 | a0001c0001t0002g0229 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.553-3570_553-3569i others(107): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686243 | |||||||
| chr2:38686244 | C | CTTTCTTT others(26): Show |
1 | a0001c0001t0013g0227 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.553-3567_553-3535d others(35): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686244 | ||||||
| chr2:38686244 | C | CTTTCTTT others(35): Show |
1 | a0001c0001t0032g0319 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.553-3535_553-3534i others(44): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686244 | ||||||
| chr2:38686244 | CTTTCTTT others(18): Show |
C | 1 | a0002c0002t0007g0294 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.553-3566_553-3542d others(27): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686244 | ||||||
| chr2:38686247 | T | C | 54 | a0001c0001t0001g0004 a0001c0001t0001g0122 a0001c0001t0001g0141 others(51): Show |
55 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.553-3566T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686247 | |||||||
| chr2:38686251 | T | C | 5 | a0001c0001t0001g0148 a0001c0001t0002g0229 a0001c0001t0002g0230 others(2): Show |
5 | HG00738.hp1 HG02280.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.553-3562T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686251 | |||||||
| chr2:38686255 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.553-3558T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686255 | |||||||
| chr2:38686258 | T | TTCTTTCT others(33): Show |
2 | a0001c0001t0001g0006 a0001c0001t0011g0025 |
2 | HG00673.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.553-3540_553-3539i others(42): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686258 | ||||||
| chr2:38686258 | T | TTCTTTCT others(37): Show |
3 | a0001c0001t0001g0013 a0001c0001t0002g0188 a0001c0001t0027g0031 |
3 | HG01081.hp2 HG01192.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.553-3536_553-3535i others(46): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686258 | ||||||
| chr2:38686258 | T | TTCTTTCT others(41): Show |
9 | a0001c0001t0001g0036 a0001c0001t0002g0022 a0001c0001t0002g0027 others(6): Show |
9 | HG01099.hp1 HG01167.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.553-3535_553-3534i others(50): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686258 | ||||||
| chr2:38686258 | T | TTCTTTCT others(37): Show |
1 | a0001c0001t0002g0003 | 2 | NA18950.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.553-3535_553-3534i others(46): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686258 | ||||||
| chr2:38686258 | T | TTCTTTCT others(45): Show |
6 | a0001c0001t0002g0002 a0001c0001t0002g0023 a0001c0001t0002g0037 others(3): Show |
7 | HG01168.hp1 HG01358.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.553-3535_553-3534i others(54): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686258 | ||||||
| chr2:38686258 | T | TTCTTTCT others(49): Show |
14 | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0001g0128 others(11): Show |
14 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.553-3535_553-3534i others(58): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686258 | ||||||
| chr2:38686258 | T | TTCTTTCT others(52): Show |
1 | a0001c0001t0002g0030 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.553-3535_553-3534i others(61): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686258 | ||||||
| chr2:38686258 | T | TTCTTTCT others(53): Show |
7 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0043 others(4): Show |
7 | HG01928.hp1 HG01943.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.553-3535_553-3534i others(62): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686258 | ||||||
| chr2:38686258 | T | TTCTTTCT others(58): Show |
1 | a0001c0001t0004g0007 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.553-3535_553-3534i others(67): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686258 | ||||||
| chr2:38686258 | T | TTCTTTCT others(57): Show |
2 | a0001c0001t0004g0046 a0001c0001t0026g0045 |
2 | HG01978.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.553-3535_553-3534i others(66): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686258 | ||||||
| chr2:38686259 | T | C | 4 | a0001c0001t0001g0148 a0001c0001t0002g0229 a0001c0001t0002g0230 others(1): Show |
4 | HG00738.hp1 HG02280.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-3554T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686259 | |||||||
| chr2:38686261 | T | TTTCTTTC others(43): Show |
1 | a0001c0001t0002g0026 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.553-3535_553-3534i others(52): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686261 | ||||||
| chr2:38686264 | C | CTTCTTTC others(41): Show |
1 | a0001c0003t0005g0215 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.553-3547_553-3546i others(50): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686264 | ||||||
| chr2:38686264 | C | CTTCTTTC others(49): Show |
1 | a0001c0003t0035g0222 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.553-3547_553-3546i others(58): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686264 | ||||||
| chr2:38686264 | C | CTTCTTTC others(65): Show |
1 | a0001c0003t0005g0216 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.553-3547_553-3546i others(74): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686264 | ||||||
| chr2:38686264 | C | CTTCTTTC others(69): Show |
1 | a0001c0003t0005g0217 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.553-3547_553-3546i others(78): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686264 | ||||||
| chr2:38686267 | T | C | 4 | a0001c0003t0005g0215 a0001c0003t0005g0216 a0001c0003t0005g0217 others(1): Show |
4 | HG01243.hp1 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-3546T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686267 | |||||||
| chr2:38686267 | T | TCTTCTTT others(41): Show |
1 | a0001c0003t0005g0218 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.553-3543_553-3542i others(50): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686267 | ||||||
| chr2:38686267 | T | TCTTCTTT others(65): Show |
1 | a0001c0003t0005g0223 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.553-3543_553-3542i others(74): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686267 | ||||||
| chr2:38686267 | T | TCTTTCTT others(53): Show |
1 | a0001c0003t0005g0220 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.553-3539_553-3538i others(62): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686267 | ||||||
| chr2:38686267 | T | TCTTTCTT others(61): Show |
1 | a0001c0003t0005g0224 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.553-3539_553-3538i others(70): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686267 | ||||||
| chr2:38686267 | T | TCTTTCTT others(65): Show |
2 | a0001c0003t0005g0221 a0001c0003t0005g0225 |
2 | HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.553-3539_553-3538i others(74): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686267 | ||||||
| chr2:38686267 | T | TCTTTCTT others(71): Show |
1 | a0001c0001t0005g0205 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.553-3535_553-3534i others(80): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686267 | ||||||
| chr2:38686267 | T | TCTTTCTT others(69): Show |
1 | a0001c0003t0005g0226 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.553-3535_553-3534i others(78): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686267 | ||||||
| chr2:38686267 | T | TCTTTCTT others(65): Show |
1 | a0001c0003t0005g0219 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.553-3535_553-3534i others(74): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686267 | ||||||
| chr2:38686276 | C | CT | 3 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0001c0001t0008g0228 |
3 | HG00738.hp1 HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.553-3535dupT | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686276 | ||||||
| chr2:38686277 | TTA | T | 61 | a0001c0001t0001g0004 a0001c0001t0001g0122 a0001c0001t0001g0141 others(58): Show |
62 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.553-3534_553-3533d others(4): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38686277 | ||||||
| chr2:38686279 | A | C | 3 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0001c0001t0008g0228 |
3 | HG00738.hp1 HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.553-3534A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686279 | |||||||
| chr2:38686283 | T | C | 3 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0001c0001t0008g0228 |
3 | HG00738.hp1 HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.553-3530T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686283 | |||||||
| chr2:38686284 | G | T | 3 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0001c0001t0008g0228 |
3 | HG00738.hp1 HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.553-3529G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686284 | |||||||
| chr2:38686305 | T | G | 11 | a0002c0002t0002g0190 a0002c0002t0003g0298 a0002c0002t0003g0299 others(8): Show |
11 | HG02559.hp1 HG02572.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.553-3508T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686305 | |||||||
| chr2:38686410 | C | T | 4 | a0002c0002t0001g0291 a0002c0002t0006g0272 a0002c0002t0006g0290 others(1): Show |
4 | HG03239.hp2 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-3403C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686410 | |||||||
| chr2:38686422 | T | C | 5 | a0002c0002t0002g0190 a0002c0002t0003g0298 a0002c0002t0003g0299 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.553-3391T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686422 | |||||||
| chr2:38686427 | A | G | 5 | a0002c0002t0002g0190 a0002c0002t0003g0298 a0002c0002t0003g0299 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.553-3386A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686427 | |||||||
| chr2:38686429 | C | A | 2 | a0002c0002t0001g0186 a0002c0002t0010g0187 |
2 | NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.553-3384C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686429 | |||||||
| chr2:38686439 | G | A | 3 | a0001c0001t0001g0067 a0001c0001t0033g0213 a0001c0001t0034g0212 |
3 | HG01361.hp1 HG03017.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.553-3374G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686439 | |||||||
| chr2:38686477 | G | C | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.553-3336G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686477 | |||||||
| chr2:38686507 | A | G | 2 | a0003c0004t0004g0211 a0003c0004t0004g0214 |
2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.553-3306A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686507 | |||||||
| chr2:38686651 | C | A | 1 | a0002c0002t0001g0276 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.553-3162C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686651 | |||||||
| chr2:38686653 | A | T | 9 | a0002c0002t0003g0298 a0002c0002t0003g0299 a0002c0002t0003g0300 others(6): Show |
9 | HG02559.hp1 HG02572.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.553-3160A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686653 | |||||||
| chr2:38686709 | T | C | 5 | a0001c0001t0019g0202 a0001c0001t0033g0213 a0001c0001t0034g0212 others(2): Show |
5 | HG01361.hp1 HG02886.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.553-3104T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686709 | |||||||
| chr2:38686742 | A | G | 214 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(211): Show |
219 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.553-3071A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686742 | |||||||
| chr2:38686773 | A | G | 11 | a0002c0002t0002g0190 a0002c0002t0003g0298 a0002c0002t0003g0299 others(8): Show |
11 | HG02559.hp1 HG02572.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.553-3040A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686773 | |||||||
| chr2:38686944 | T | C | 11 | a0002c0002t0002g0190 a0002c0002t0003g0298 a0002c0002t0003g0299 others(8): Show |
11 | HG02559.hp1 HG02572.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.553-2869T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686944 | |||||||
| chr2:38686956 | G | T | 1 | a0001c0001t0032g0319 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.553-2857G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38686956 | |||||||
| chr2:38687054 | G | A | 31 | a0001c0001t0001g0013 a0001c0001t0002g0002 a0001c0001t0002g0003 others(28): Show |
33 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.553-2759G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38687054 | |||||||
| chr2:38687100 | G | C | 48 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(45): Show |
50 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.553-2713G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38687100 | |||||||
| chr2:38687109 | A | C | 76 | a0001c0001t0001g0122 a0001c0001t0001g0147 a0001c0001t0001g0148 others(73): Show |
77 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.553-2704A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38687109 | |||||||
| chr2:38687182 | C | T | 91 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(88): Show |
94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.553-2631C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38687182 | |||||||
| chr2:38687273 | C | T | 1 | a0002c0002t0012g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.553-2540C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38687273 | |||||||
| chr2:38687312 | A | G | 11 | a0002c0002t0002g0190 a0002c0002t0003g0298 a0002c0002t0003g0299 others(8): Show |
11 | HG02559.hp1 HG02572.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.553-2501A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38687312 | |||||||
| chr2:38687329 | G | A | 2 | a0002c0002t0001g0186 a0002c0002t0010g0187 |
2 | NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.553-2484G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38687329 | |||||||
| chr2:38687330 | C | T | 10 | a0002c0002t0006g0232 a0002c0002t0009g0001 a0002c0002t0009g0231 others(7): Show |
11 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.553-2483C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38687330 | |||||||
| chr2:38687336 | A | G | 11 | a0002c0002t0002g0190 a0002c0002t0003g0298 a0002c0002t0003g0299 others(8): Show |
11 | HG02559.hp1 HG02572.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.553-2477A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38687336 | |||||||
| chr2:38687486 | G | A | 2 | a0001c0001t0013g0227 a0001c0001t0032g0319 |
2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.553-2327G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38687486 | |||||||
| chr2:38687690 | G | A | 1 | a0001c0001t0032g0319 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.553-2123G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38687690 | |||||||
| chr2:38687785 | C | T | 9 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0313 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.553-2028C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38687785 | |||||||
| chr2:38687819 | T | C | 1 | a0002c0002t0002g0203 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.553-1994T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38687819 | |||||||
| chr2:38687924 | C | T | 11 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0004g0007 others(8): Show |
11 | HG02015.hp1 NA18943.hp1 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.553-1889C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38687924 | |||||||
| chr2:38688104 | C | A | 2 | a0002c0002t0001g0260 a0002c0002t0001g0261 |
2 | NA18953.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.553-1709C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38688104 | |||||||
| chr2:38688211 | C | CA | 7 | a0001c0001t0001g0268 a0002c0002t0001g0258 a0002c0002t0001g0306 others(4): Show |
7 | HG02055.hp1 HG02055.hp2 HG04199.hp2 others(4): Show |
intron_variant | MODIFIER | c.553-1588dupA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38688211 | ||||||
| chr2:38688225 | A | T | 11 | a0002c0002t0002g0190 a0002c0002t0003g0298 a0002c0002t0003g0299 others(8): Show |
11 | HG02559.hp1 HG02572.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.553-1588A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38688225 | |||||||
| chr2:38688237 | T | C | 11 | a0002c0002t0002g0190 a0002c0002t0003g0298 a0002c0002t0003g0299 others(8): Show |
11 | HG02559.hp1 HG02572.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.553-1576T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38688237 | |||||||
| chr2:38688302 | G | A | 1 | a0001c0001t0004g0124 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.553-1511G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38688302 | |||||||
| chr2:38688310 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.553-1503G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38688310 | |||||||
| chr2:38688467 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.553-1346C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38688467 | |||||||
| chr2:38688479 | C | T | 1 | a0003c0004t0004g0211 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.553-1334C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38688479 | |||||||
| chr2:38688498 | C | T | 9 | a0002c0002t0003g0298 a0002c0002t0003g0299 a0002c0002t0003g0300 others(6): Show |
9 | HG02559.hp1 HG02572.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.553-1315C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38688498 | |||||||
| chr2:38688513 | G | GA | 17 | a0001c0001t0001g0004 a0001c0001t0001g0077 a0001c0001t0001g0239 others(14): Show |
18 | HG00544.hp1 HG00558.hp1 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.553-1287dupA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38688513 | ||||||
| chr2:38688513 | GA | G | 14 | a0001c0001t0004g0008 a0001c0001t0005g0205 a0001c0003t0005g0215 others(11): Show |
14 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.553-1287delA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 38688513 | ||||||
| chr2:38688551 | A | G | 11 | a0002c0002t0002g0190 a0002c0002t0003g0298 a0002c0002t0003g0299 others(8): Show |
11 | HG02559.hp1 HG02572.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.553-1262A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38688551 | |||||||
| chr2:38688590 | C | T | 163 | a0001c0001t0001g0004 a0001c0001t0001g0122 a0001c0001t0001g0141 others(160): Show |
166 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.553-1223C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38688590 | |||||||
| chr2:38688638 | A | G | 167 | a0001c0001t0001g0004 a0001c0001t0001g0122 a0001c0001t0001g0141 others(164): Show |
170 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.553-1175A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38688638 | |||||||
| chr2:38688653 | A | G | 9 | a0002c0002t0003g0298 a0002c0002t0003g0299 a0002c0002t0003g0300 others(6): Show |
9 | HG02559.hp1 HG02572.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.553-1160A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38688653 | |||||||
| chr2:38688813 | T | G | 1 | a0001c0001t0001g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.553-1000T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38688813 | |||||||
| chr2:38688854 | A | T | 11 | a0002c0002t0002g0190 a0002c0002t0003g0298 a0002c0002t0003g0299 others(8): Show |
11 | HG02559.hp1 HG02572.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.553-959A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38688854 | |||||||
| chr2:38688897 | C | G | 1 | a0001c0001t0006g0206 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.553-916C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38688897 | |||||||
| chr2:38688898 | G | A | 3 | a0002c0002t0014g0151 a0002c0002t0014g0152 a0002c0002t0018g0012 |
3 | HG02895.hp2 HG02897.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.553-915G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38688898 | |||||||
| chr2:38688957 | A | T | 2 | a0002c0002t0004g0318 a0002c0002t0007g0315 |
2 | HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.553-856A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38688957 | |||||||
| chr2:38689005 | A | G | 2 | a0002c0002t0001g0186 a0002c0002t0010g0187 |
2 | NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.553-808A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38689005 | |||||||
| chr2:38689062 | C | T | 4 | a0001c0001t0006g0159 a0001c0001t0006g0160 a0001c0001t0006g0161 others(1): Show |
4 | HG02451.hp2 HG02647.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-751C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38689062 | |||||||
| chr2:38689115 | C | T | 3 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0001c0001t0008g0228 |
3 | HG00738.hp1 HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.553-698C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38689115 | |||||||
| chr2:38689286 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.553-527G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38689286 | |||||||
| chr2:38689332 | T | C | 9 | a0002c0002t0003g0298 a0002c0002t0003g0299 a0002c0002t0003g0300 others(6): Show |
9 | HG02559.hp1 HG02572.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.553-481T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38689332 | |||||||
| chr2:38689371 | C | A | 9 | a0002c0002t0003g0298 a0002c0002t0003g0299 a0002c0002t0003g0300 others(6): Show |
9 | HG02559.hp1 HG02572.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.553-442C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38689371 | |||||||
| chr2:38689537 | G | T | 1 | a0003c0004t0004g0214 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.553-276G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38689537 | |||||||
| chr2:38689729 | A | G | 1 | a0002c0002t0012g0234 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.553-84A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38689729 | |||||||
| chr2:38689764 | T | C | 48 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(45): Show |
50 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.553-49T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38689764 | |||||||
| chr2:38689791 | T | C | 2 | a0001c0001t0008g0010 a0001c0001t0008g0136 |
2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.553-22T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38689791 | |||||||
| chr2:38689975 | C | A | 1 | a0001c0001t0013g0227 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.634+81C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38689975 | |||||||
| chr2:38690021 | T | C | 21 | a0002c0002t0003g0298 a0002c0002t0003g0299 a0002c0002t0003g0300 others(18): Show |
22 | HG01496.hp2 HG01884.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.634+127T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38690021 | |||||||
| chr2:38690083 | A | C | 2 | a0002c0002t0003g0299 a0002c0002t0003g0300 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.634+189A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38690083 | |||||||
| chr2:38690102 | G | T | 1 | a0001c0001t0002g0307 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.634+208G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38690102 | |||||||
| chr2:38690138 | T | G | 1 | a0001c0001t0001g0078 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.634+244T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38690138 | |||||||
| chr2:38690196 | G | T | 1 | a0001c0001t0001g0249 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.634+302G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38690196 | |||||||
| chr2:38690223 | G | A | 3 | a0001c0001t0001g0137 a0001c0001t0008g0010 a0001c0001t0008g0136 |
3 | HG02965.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.634+329G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38690223 | |||||||
| chr2:38690242 | C | T | 2 | a0002c0002t0002g0190 a0002c0002t0006g0059 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.634+348C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38690242 | |||||||
| chr2:38690331 | T | A | 1 | a0001c0001t0001g0099 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.634+437T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38690331 | |||||||
| chr2:38690356 | G | A | 9 | a0002c0002t0003g0298 a0002c0002t0003g0299 a0002c0002t0003g0300 others(6): Show |
9 | HG02559.hp1 HG02572.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.634+462G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38690356 | |||||||
| chr2:38690445 | G | A | 2 | a0002c0002t0002g0190 a0002c0002t0006g0059 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.634+551G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38690445 | |||||||
| chr2:38690448 | G | A | 52 | a0002c0002t0001g0005 a0002c0002t0001g0201 a0002c0002t0001g0210 others(49): Show |
53 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(50): Show |
intron_variant | MODIFIER | c.634+554G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38690448 | |||||||
| chr2:38690532 | C | T | 3 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0007g0096 |
3 | HG01106.hp2 HG01952.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.634+638C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38690532 | |||||||
| chr2:38690623 | G | C | 1 | a0001c0001t0025g0175 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.634+729G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38690623 | |||||||
| chr2:38691083 | G | T | 5 | a0001c0003t0005g0215 a0001c0003t0005g0216 a0001c0003t0005g0217 others(2): Show |
5 | HG01243.hp1 HG02818.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.634+1189G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38691083 | |||||||
| chr2:38691113 | G | A | 10 | a0001c0001t0001g0014 a0001c0001t0004g0007 a0001c0001t0004g0008 others(7): Show |
10 | NA18943.hp1 NA18946.hp1 NA18961.hp2 others(7): Show |
intron_variant | MODIFIER | c.634+1219G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38691113 | |||||||
| chr2:38691393 | G | A | 2 | a0002c0002t0001g0273 a0002c0002t0016g0195 |
2 | HG02735.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.634+1499G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38691393 | |||||||
| chr2:38691452 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.634+1558G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38691452 | |||||||
| chr2:38691504 | A | G | 53 | a0001c0001t0001g0297 a0002c0002t0001g0005 a0002c0002t0001g0201 others(50): Show |
54 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(51): Show |
intron_variant | MODIFIER | c.634+1610A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38691504 | |||||||
| chr2:38691525 | G | GA | 14 | a0001c0001t0001g0123 a0001c0001t0005g0205 a0001c0003t0005g0215 others(11): Show |
14 | HG01243.hp1 HG01884.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.634+1641dupA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38691525 | ||||||
| chr2:38691558 | C | G | 1 | a0001c0001t0003g0052 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.634+1664C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38691558 | |||||||
| chr2:38691633 | G | A | 2 | a0002c0002t0002g0190 a0002c0002t0006g0059 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.634+1739G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38691633 | |||||||
| chr2:38691651 | T | C | 105 | a0001c0001t0001g0122 a0001c0001t0001g0147 a0001c0001t0001g0148 others(102): Show |
107 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.634+1757T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38691651 | |||||||
| chr2:38691719 | C | T | 1 | a0002c0002t0001g0210 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.634+1825C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38691719 | |||||||
| chr2:38691724 | G | GT | 64 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(61): Show |
67 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.634+1845dupT | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38691724 | ||||||
| chr2:38691739 | T | A | 1 | a0002c0002t0001g0256 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.634+1845T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38691739 | |||||||
| chr2:38691739 | T | TA | 10 | a0001c0001t0001g0069 a0002c0002t0003g0298 a0002c0002t0003g0299 others(7): Show |
10 | HG01346.hp1 HG02559.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.634+1851dupA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38691739 | ||||||
| chr2:38691740 | A | T | 43 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(40): Show |
45 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.634+1846A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38691740 | |||||||
| chr2:38691741 | A | T | 1 | a0001c0001t0004g0008 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.634+1847A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38691741 | |||||||
| chr2:38691985 | C | G | 2 | a0002c0002t0002g0190 a0002c0002t0006g0059 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.634+2091C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38691985 | |||||||
| chr2:38692127 | C | G | 1 | a0001c0001t0001g0094 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.634+2233C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38692127 | |||||||
| chr2:38692158 | C | T | 1 | a0002c0002t0012g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.634+2264C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38692158 | |||||||
| chr2:38692396 | G | A | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG00673.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.634+2502G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38692396 | |||||||
| chr2:38692417 | T | C | 18 | a0001c0001t0001g0004 a0001c0001t0001g0239 a0001c0001t0001g0240 others(15): Show |
19 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(16): Show |
intron_variant | MODIFIER | c.634+2523T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38692417 | |||||||
| chr2:38692542 | T | C | 115 | a0001c0001t0001g0122 a0001c0001t0001g0147 a0001c0001t0001g0148 others(112): Show |
117 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.634+2648T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38692542 | |||||||
| chr2:38692815 | A | G | 4 | a0002c0002t0001g0276 a0002c0002t0001g0287 a0002c0002t0001g0288 others(1): Show |
4 | NA18971.hp2 NA18972.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+2921A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38692815 | |||||||
| chr2:38692829 | A | T | 1 | a0001c0001t0019g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.634+2935A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38692829 | |||||||
| chr2:38692896 | G | A | 4 | a0001c0001t0003g0302 a0001c0001t0003g0305 a0001c0001t0019g0304 others(1): Show |
4 | HG01106.hp1 HG01891.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+3002G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38692896 | |||||||
| chr2:38693029 | T | G | 1 | a0001c0001t0001g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.634+3135T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38693029 | |||||||
| chr2:38693077 | C | T | 2 | a0002c0002t0002g0190 a0002c0002t0006g0059 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.634+3183C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38693077 | |||||||
| chr2:38693159 | A | T | 4 | a0001c0001t0033g0213 a0001c0001t0034g0212 a0003c0004t0004g0211 others(1): Show |
4 | HG01361.hp1 HG03130.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+3265A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38693159 | |||||||
| chr2:38693176 | C | T | 29 | a0001c0001t0001g0004 a0001c0001t0001g0141 a0001c0001t0001g0142 others(26): Show |
30 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.634+3282C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38693176 | |||||||
| chr2:38693191 | T | C | 22 | a0001c0001t0001g0146 a0001c0001t0003g0052 a0001c0001t0003g0054 others(19): Show |
22 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.634+3297T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38693191 | |||||||
| chr2:38693280 | C | T | 2 | a0001c0001t0013g0227 a0001c0001t0032g0319 |
2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.634+3386C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38693280 | |||||||
| chr2:38693308 | C | T | 10 | a0002c0002t0006g0232 a0002c0002t0009g0001 a0002c0002t0009g0231 others(7): Show |
11 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.634+3414C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38693308 | |||||||
| chr2:38693340 | G | C | 18 | a0001c0001t0003g0052 a0001c0001t0003g0054 a0001c0001t0003g0055 others(15): Show |
18 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.634+3446G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38693340 | |||||||
| chr2:38693429 | G | C | 1 | a0001c0001t0001g0117 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.634+3535G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38693429 | |||||||
| chr2:38693439 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0117 |
2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.634+3545C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38693439 | |||||||
| chr2:38693464 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.634+3570C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38693464 | |||||||
| chr2:38693479 | C | T | 170 | a0001c0001t0001g0004 a0001c0001t0001g0122 a0001c0001t0001g0141 others(167): Show |
173 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.634+3585C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38693479 | |||||||
| chr2:38693483 | CA | C | 141 | a0001c0001t0001g0004 a0001c0001t0001g0122 a0001c0001t0001g0141 others(138): Show |
143 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.634+3605delA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38693483 | ||||||
| chr2:38693483 | CAA | C | 14 | a0002c0002t0001g0186 a0002c0002t0001g0271 a0002c0002t0006g0232 others(11): Show |
15 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.634+3604_634+3605d others(4): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38693483 | ||||||
| chr2:38693530 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.634+3636C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38693530 | |||||||
| chr2:38693765 | A | T | 1 | a0001c0001t0001g0129 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.634+3871A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38693765 | |||||||
| chr2:38693805 | C | T | 10 | a0001c0001t0001g0014 a0001c0001t0004g0007 a0001c0001t0004g0008 others(7): Show |
10 | NA18943.hp1 NA18946.hp1 NA18961.hp2 others(7): Show |
intron_variant | MODIFIER | c.634+3911C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38693805 | |||||||
| chr2:38693815 | A | G | 3 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0001c0001t0008g0228 |
3 | HG00738.hp1 HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.634+3921A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38693815 | |||||||
| chr2:38693844 | C | G | 2 | a0002c0002t0001g0186 a0002c0002t0010g0187 |
2 | NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.634+3950C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38693844 | |||||||
| chr2:38693869 | G | C | 38 | a0001c0001t0001g0122 a0001c0001t0001g0141 a0001c0001t0001g0142 others(35): Show |
38 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.634+3975G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38693869 | |||||||
| chr2:38693879 | T | A | 1 | a0001c0001t0001g0099 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.634+3985T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38693879 | |||||||
| chr2:38693904 | G | A | 13 | a0001c0001t0005g0205 a0001c0003t0005g0215 a0001c0003t0005g0216 others(10): Show |
13 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.634+4010G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38693904 | |||||||
| chr2:38693920 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+4026C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38693920 | |||||||
| chr2:38694022 | A | G | 2 | a0002c0002t0001g0186 a0002c0002t0010g0187 |
2 | NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.634+4128A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38694022 | |||||||
| chr2:38694026 | T | C | 1 | a0001c0001t0002g0200 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.634+4132T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38694026 | |||||||
| chr2:38694061 | G | C | 3 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0001c0001t0008g0228 |
3 | HG00738.hp1 HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.634+4167G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38694061 | |||||||
| chr2:38694068 | G | C | 3 | a0001c0001t0001g0080 a0001c0001t0001g0094 a0001c0001t0001g0103 |
3 | HG02683.hp1 HG02738.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.634+4174G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38694068 | |||||||
| chr2:38694122 | C | T | 1 | a0002c0002t0012g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.634+4228C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38694122 | |||||||
| chr2:38694210 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.634+4316G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38694210 | |||||||
| chr2:38694293 | T | C | 9 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0313 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.634+4399T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38694293 | |||||||
| chr2:38694356 | C | T | 13 | a0001c0001t0001g0062 a0001c0001t0003g0052 a0001c0001t0003g0054 others(10): Show |
13 | HG01167.hp2 HG01169.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.634+4462C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38694356 | |||||||
| chr2:38694381 | A | G | 3 | a0001c0001t0001g0137 a0001c0001t0008g0010 a0001c0001t0008g0136 |
3 | HG02965.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.634+4487A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38694381 | |||||||
| chr2:38694402 | G | C | 1 | a0001c0001t0005g0116 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.634+4508G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38694402 | |||||||
| chr2:38694519 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.634+4625G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38694519 | |||||||
| chr2:38694623 | G | A | 11 | a0002c0002t0006g0232 a0002c0002t0009g0001 a0002c0002t0009g0231 others(8): Show |
12 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.634+4729G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38694623 | |||||||
| chr2:38694792 | C | G | 213 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(210): Show |
218 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.634+4898C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38694792 | |||||||
| chr2:38694852 | G | A | 1 | a0002c0002t0001g0256 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.634+4958G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38694852 | |||||||
| chr2:38694854 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.634+4960G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38694854 | |||||||
| chr2:38694883 | C | G | 2 | a0002c0002t0001g0186 a0002c0002t0010g0187 |
2 | NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.634+4989C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38694883 | |||||||
| chr2:38694896 | C | CA | 135 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(132): Show |
138 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.634+5018dupA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38694896 | ||||||
| chr2:38694896 | C | CAA | 20 | a0001c0001t0001g0062 a0001c0001t0001g0149 a0001c0001t0001g0166 others(17): Show |
20 | HG00735.hp1 HG01261.hp2 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.634+5017_634+5018d others(4): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38694896 | ||||||
| chr2:38694912 | AC | A | 15 | a0001c0001t0033g0213 a0002c0002t0001g0186 a0002c0002t0002g0190 others(12): Show |
16 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.634+5019delC | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38694912 | |||||||
| chr2:38694913 | C | A | 197 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(194): Show |
201 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.634+5019C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38694913 | |||||||
| chr2:38694914 | A | G | 9 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0313 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.634+5020A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38694914 | |||||||
| chr2:38694917 | A | G | 1 | a0002c0002t0009g0238 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.634+5023A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38694917 | |||||||
| chr2:38694996 | T | C | 1 | a0001c0001t0006g0160 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.634+5102T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38694996 | |||||||
| chr2:38695098 | G | C | 1 | a0002c0002t0001g0005 | 2 | NA19065.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.634+5204G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38695098 | |||||||
| chr2:38695144 | C | T | 1 | a0001c0001t0023g0322 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.634+5250C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38695144 | |||||||
| chr2:38695359 | A | T | 4 | a0001c0001t0019g0202 a0001c0001t0033g0213 a0003c0004t0004g0211 others(1): Show |
4 | HG01361.hp1 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+5465A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38695359 | |||||||
| chr2:38695362 | C | T | 315 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(312): Show |
320 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(317): Show |
intron_variant | MODIFIER | c.634+5468C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38695362 | |||||||
| chr2:38695442 | C | T | 2 | a0002c0002t0002g0190 a0002c0002t0006g0059 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.634+5548C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38695442 | |||||||
| chr2:38695464 | A | G | 9 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0313 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.634+5570A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38695464 | |||||||
| chr2:38695615 | T | G | 17 | a0001c0001t0001g0004 a0001c0001t0001g0239 a0001c0001t0001g0240 others(14): Show |
18 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.634+5721T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38695615 | |||||||
| chr2:38695658 | T | G | 2 | a0001c0001t0002g0040 a0001c0001t0026g0045 |
2 | HG01943.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.634+5764T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38695658 | |||||||
| chr2:38695674 | TTTGTTTG others(5): Show |
T | 2 | a0002c0002t0002g0190 a0002c0002t0006g0059 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.634+5803_634+5814d others(14): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38695674 | ||||||
| chr2:38695789 | C | T | 1 | a0001c0001t0003g0052 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.634+5895C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38695789 | |||||||
| chr2:38695800 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.634+5906G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38695800 | |||||||
| chr2:38695859 | C | T | 2 | a0002c0002t0001g0266 a0002c0002t0001g0267 |
2 | HG02027.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.634+5965C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38695859 | |||||||
| chr2:38695996 | G | A | 2 | a0001c0001t0006g0051 a0001c0001t0022g0050 |
2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.634+6102G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38695996 | |||||||
| chr2:38696001 | C | T | 14 | a0001c0001t0003g0052 a0001c0001t0003g0054 a0001c0001t0003g0055 others(11): Show |
14 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.634+6107C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38696001 | |||||||
| chr2:38696150 | G | A | 2 | a0002c0002t0002g0190 a0002c0002t0006g0059 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.634+6256G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38696150 | |||||||
| chr2:38696381 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.634+6487A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38696381 | |||||||
| chr2:38696433 | C | CT | 37 | a0001c0001t0001g0036 a0001c0001t0001g0141 a0001c0001t0001g0142 others(34): Show |
38 | HG01168.hp2 HG01169.hp2 HG01361.hp1 others(35): Show |
intron_variant | MODIFIER | c.634+6556dupT | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38696433 | ||||||
| chr2:38696433 | C | CTT | 40 | a0001c0001t0001g0297 a0002c0002t0001g0005 a0002c0002t0001g0201 others(37): Show |
41 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(38): Show |
intron_variant | MODIFIER | c.634+6555_634+6556d others(4): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38696433 | ||||||
| chr2:38696433 | CT | C | 17 | a0001c0001t0001g0095 a0001c0001t0001g0174 a0001c0001t0001g0182 others(14): Show |
17 | HG01169.hp1 HG01361.hp2 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.634+6556delT | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38696433 | ||||||
| chr2:38696549 | C | T | 1 | a0002c0002t0001g0265 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.634+6655C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38696549 | |||||||
| chr2:38696580 | C | G | 2 | a0001c0001t0013g0227 a0001c0001t0032g0319 |
2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.634+6686C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38696580 | |||||||
| chr2:38696580 | C | T | 50 | a0001c0001t0001g0297 a0002c0002t0001g0005 a0002c0002t0001g0201 others(47): Show |
51 | HG00408.hp2 HG01071.hp2 HG01261.hp1 others(48): Show |
intron_variant | MODIFIER | c.634+6686C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38696580 | |||||||
| chr2:38696699 | C | G | 1 | a0001c0001t0006g0206 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.634+6805C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38696699 | |||||||
| chr2:38696747 | C | G | 2 | a0002c0002t0002g0203 a0002c0002t0002g0204 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.634+6853C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38696747 | |||||||
| chr2:38696781 | C | CT | 101 | a0001c0001t0001g0061 a0001c0001t0001g0069 a0001c0001t0001g0077 others(98): Show |
102 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.634+6913dupT | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38696781 | ||||||
| chr2:38696781 | C | CTT | 35 | a0001c0001t0001g0011 a0001c0001t0001g0148 a0001c0001t0001g0168 others(32): Show |
35 | HG00609.hp1 HG00621.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.634+6912_634+6913d others(4): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38696781 | ||||||
| chr2:38696781 | C | CTTTT | 8 | a0001c0001t0005g0205 a0001c0003t0005g0218 a0001c0003t0005g0221 others(5): Show |
8 | HG02809.hp1 HG02818.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.634+6910_634+6913d others(6): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38696781 | ||||||
| chr2:38696781 | C | CTTTTT | 6 | a0001c0003t0005g0215 a0001c0003t0005g0217 a0001c0003t0005g0219 others(3): Show |
6 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.634+6909_634+6913d others(7): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38696781 | ||||||
| chr2:38696781 | CT | C | 8 | a0001c0001t0001g0014 a0001c0001t0002g0229 a0001c0001t0003g0144 others(5): Show |
8 | HG00738.hp1 HG01496.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.634+6913delT | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38696781 | ||||||
| chr2:38696850 | C | T | 1 | a0001c0001t0013g0227 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.634+6956C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38696850 | |||||||
| chr2:38696851 | G | A | 4 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0245 others(1): Show |
4 | HG00544.hp1 HG02074.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+6957G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38696851 | |||||||
| chr2:38696852 | C | T | 13 | a0001c0001t0003g0052 a0001c0001t0003g0054 a0001c0001t0003g0055 others(10): Show |
13 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.634+6958C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38696852 | |||||||
| chr2:38696961 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.634+7067T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38696961 | |||||||
| chr2:38697039 | T | C | 2 | a0002c0002t0002g0190 a0002c0002t0006g0059 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.634+7145T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38697039 | |||||||
| chr2:38697163 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.634+7269T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38697163 | |||||||
| chr2:38697180 | G | T | 18 | a0001c0001t0001g0004 a0001c0001t0001g0239 a0001c0001t0001g0240 others(15): Show |
19 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(16): Show |
intron_variant | MODIFIER | c.634+7286G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38697180 | |||||||
| chr2:38697456 | T | G | 4 | a0001c0001t0003g0302 a0001c0001t0003g0305 a0001c0001t0019g0304 others(1): Show |
4 | HG01106.hp1 HG01891.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+7562T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38697456 | |||||||
| chr2:38697546 | C | G | 3 | a0001c0001t0033g0213 a0003c0004t0004g0211 a0003c0004t0004g0214 |
3 | HG01361.hp1 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.634+7652C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38697546 | |||||||
| chr2:38697642 | A | C | 20 | a0001c0001t0001g0062 a0001c0001t0003g0052 a0001c0001t0003g0054 others(17): Show |
20 | HG01167.hp2 HG01169.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.634+7748A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38697642 | |||||||
| chr2:38697771 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.634+7877A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38697771 | |||||||
| chr2:38697831 | G | A | 22 | a0001c0001t0001g0004 a0001c0001t0001g0239 a0001c0001t0001g0240 others(19): Show |
23 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(20): Show |
intron_variant | MODIFIER | c.634+7937G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38697831 | |||||||
| chr2:38697856 | G | A | 1 | a0001c0001t0006g0206 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.634+7962G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38697856 | |||||||
| chr2:38697870 | G | A | 2 | a0001c0001t0013g0227 a0001c0001t0032g0319 |
2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.634+7976G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38697870 | |||||||
| chr2:38697886 | T | A | 3 | a0002c0002t0014g0151 a0002c0002t0014g0152 a0002c0002t0018g0012 |
3 | HG02895.hp2 HG02897.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.634+7992T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38697886 | |||||||
| chr2:38697950 | G | GT | 12 | a0001c0001t0001g0110 a0001c0001t0001g0153 a0001c0001t0001g0154 others(9): Show |
12 | HG01358.hp1 HG01978.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.634+8068dupT | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38697950 | ||||||
| chr2:38698013 | G | C | 173 | a0001c0001t0001g0004 a0001c0001t0001g0062 a0001c0001t0001g0122 others(170): Show |
176 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.634+8119G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38698013 | |||||||
| chr2:38698029 | C | T | 4 | a0001c0001t0019g0202 a0001c0001t0033g0213 a0003c0004t0004g0211 others(1): Show |
4 | HG01361.hp1 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+8135C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38698029 | |||||||
| chr2:38698101 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.634+8207G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38698101 | |||||||
| chr2:38698135 | G | A | 3 | a0001c0001t0033g0213 a0003c0004t0004g0211 a0003c0004t0004g0214 |
3 | HG01361.hp1 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.634+8241G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38698135 | |||||||
| chr2:38698161 | C | T | 7 | a0001c0001t0001g0313 a0001c0001t0002g0307 a0001c0001t0002g0310 others(4): Show |
7 | HG02258.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.634+8267C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38698161 | |||||||
| chr2:38698172 | G | C | 6 | a0002c0002t0004g0314 a0002c0002t0004g0316 a0002c0002t0004g0317 others(3): Show |
6 | HG02559.hp1 HG02572.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.634+8278G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38698172 | |||||||
| chr2:38698357 | C | G | 1 | a0002c0002t0001g0264 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.634+8463C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38698357 | |||||||
| chr2:38698449 | G | T | 1 | a0002c0002t0001g0259 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.634+8555G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38698449 | |||||||
| chr2:38698461 | T | A | 2 | a0002c0002t0001g0186 a0002c0002t0010g0187 |
2 | NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.634+8567T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38698461 | |||||||
| chr2:38698468 | A | G | 8 | a0001c0001t0001g0146 a0001c0001t0003g0074 a0001c0001t0003g0075 others(5): Show |
8 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.634+8574A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38698468 | |||||||
| chr2:38698566 | G | T | 76 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0061 others(73): Show |
76 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.634+8672G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38698566 | |||||||
| chr2:38698621 | A | G | 1 | a0002c0002t0001g0273 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.634+8727A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38698621 | |||||||
| chr2:38698736 | C | T | 1 | a0001c0001t0003g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.634+8842C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38698736 | |||||||
| chr2:38698982 | C | G | 1 | a0002c0002t0001g0257 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.634+9088C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38698982 | |||||||
| chr2:38699058 | C | T | 3 | a0001c0001t0033g0213 a0003c0004t0004g0211 a0003c0004t0004g0214 |
3 | HG01361.hp1 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.634+9164C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38699058 | |||||||
| chr2:38699103 | G | A | 2 | a0002c0002t0001g0186 a0002c0002t0010g0187 |
2 | NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.634+9209G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38699103 | |||||||
| chr2:38699134 | G | A | 10 | a0002c0002t0006g0232 a0002c0002t0009g0001 a0002c0002t0009g0231 others(7): Show |
11 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.634+9240G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38699134 | |||||||
| chr2:38699183 | G | A | 1 | a0001c0001t0019g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.634+9289G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38699183 | |||||||
| chr2:38699203 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.634+9309C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38699203 | |||||||
| chr2:38699217 | G | A | 1 | a0001c0001t0032g0319 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.634+9323G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38699217 | |||||||
| chr2:38699578 | G | T | 7 | a0001c0001t0001g0313 a0001c0001t0002g0307 a0001c0001t0002g0310 others(4): Show |
7 | HG02258.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.634+9684G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38699578 | |||||||
| chr2:38699662 | G | C | 3 | a0002c0002t0014g0151 a0002c0002t0014g0152 a0002c0002t0018g0012 |
3 | HG02895.hp2 HG02897.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.634+9768G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38699662 | |||||||
| chr2:38699720 | G | A | 1 | a0002c0002t0012g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.634+9826G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38699720 | |||||||
| chr2:38699776 | C | T | 216 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(213): Show |
221 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.634+9882C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38699776 | |||||||
| chr2:38699848 | A | T | 13 | a0001c0001t0005g0205 a0001c0003t0005g0215 a0001c0003t0005g0216 others(10): Show |
13 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.634+9954A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38699848 | |||||||
| chr2:38699865 | A | G | 317 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(314): Show |
322 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(319): Show |
intron_variant | MODIFIER | c.634+9971A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38699865 | |||||||
| chr2:38700195 | G | A | 5 | a0001c0001t0001g0014 a0001c0001t0004g0007 a0001c0001t0004g0015 others(2): Show |
5 | NA18946.hp1 NA19002.hp1 NA19065.hp2 others(2): Show |
intron_variant | MODIFIER | c.634+10301G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38700195 | |||||||
| chr2:38700218 | C | G | 1 | a0001c0001t0006g0206 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.634+10324C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38700218 | |||||||
| chr2:38700352 | G | A | 7 | a0001c0001t0019g0304 a0002c0002t0004g0314 a0002c0002t0004g0316 others(4): Show |
7 | HG01106.hp1 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.634+10458G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38700352 | |||||||
| chr2:38700407 | C | T | 24 | a0001c0001t0002g0156 a0001c0001t0002g0157 a0001c0001t0002g0158 others(21): Show |
24 | HG01106.hp1 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.634+10513C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38700407 | |||||||
| chr2:38700441 | G | T | 1 | a0002c0002t0012g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.634+10547G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38700441 | |||||||
| chr2:38700501 | T | TA | 78 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0047 others(75): Show |
78 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.634+10609dupA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38700501 | ||||||
| chr2:38700519 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.634+10625C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38700519 | |||||||
| chr2:38700553 | G | C | 1 | a0002c0002t0007g0315 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.634+10659G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38700553 | |||||||
| chr2:38700602 | G | A | 4 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0002c0002t0002g0190 others(1): Show |
4 | HG02523.hp2 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+10708G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38700602 | |||||||
| chr2:38700743 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.634+10849G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38700743 | |||||||
| chr2:38700786 | T | A | 1 | a0001c0001t0013g0227 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.634+10892T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38700786 | |||||||
| chr2:38700882 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.634+10988G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38700882 | |||||||
| chr2:38700962 | C | T | 2 | a0002c0002t0002g0190 a0002c0002t0006g0059 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.634+11068C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38700962 | |||||||
| chr2:38701109 | C | T | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG02523.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.634+11215C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38701109 | |||||||
| chr2:38701574 | C | G | 220 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(217): Show |
225 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.634+11680C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38701574 | |||||||
| chr2:38701591 | G | A | 18 | a0001c0001t0001g0004 a0001c0001t0001g0239 a0001c0001t0001g0240 others(15): Show |
19 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(16): Show |
intron_variant | MODIFIER | c.634+11697G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38701591 | |||||||
| chr2:38701625 | A | G | 7 | a0001c0001t0001g0313 a0001c0001t0002g0307 a0001c0001t0002g0310 others(4): Show |
7 | HG02258.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.634+11731A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38701625 | |||||||
| chr2:38701680 | C | T | 1 | a0001c0001t0003g0305 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.634+11786C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38701680 | |||||||
| chr2:38701797 | G | A | 2 | a0001c0001t0013g0227 a0001c0001t0032g0319 |
2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.634+11903G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38701797 | |||||||
| chr2:38701832 | G | A | 3 | a0002c0002t0014g0151 a0002c0002t0014g0152 a0002c0002t0018g0012 |
3 | HG02895.hp2 HG02897.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.634+11938G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38701832 | |||||||
| chr2:38701839 | T | C | 48 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0036 others(45): Show |
50 | HG00280.hp2 HG00558.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.634+11945T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38701839 | |||||||
| chr2:38701841 | T | C | 1 | a0001c0001t0001g0014 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.634+11947T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38701841 | |||||||
| chr2:38701945 | T | C | 4 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0002c0002t0002g0190 others(1): Show |
4 | HG02523.hp2 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+12051T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38701945 | |||||||
| chr2:38702124 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.634+12230A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38702124 | |||||||
| chr2:38702148 | G | A | 1 | a0001c0001t0003g0100 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.634+12254G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38702148 | |||||||
| chr2:38702187 | G | GA | 14 | a0001c0001t0005g0205 a0001c0001t0013g0227 a0001c0003t0005g0215 others(11): Show |
14 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.634+12304dupA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38702187 | ||||||
| chr2:38702187 | GA | G | 7 | a0001c0001t0019g0304 a0002c0002t0004g0314 a0002c0002t0004g0316 others(4): Show |
7 | HG01106.hp1 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.634+12304delA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38702187 | ||||||
| chr2:38702284 | C | T | 1 | a0002c0002t0012g0234 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.634+12390C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38702284 | |||||||
| chr2:38702295 | C | A | 46 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0036 others(43): Show |
48 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.634+12401C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38702295 | |||||||
| chr2:38702343 | A | T | 3 | a0002c0002t0014g0151 a0002c0002t0014g0152 a0002c0002t0018g0012 |
3 | HG02895.hp2 HG02897.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.634+12449A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38702343 | |||||||
| chr2:38702384 | G | A | 11 | a0002c0002t0006g0232 a0002c0002t0009g0001 a0002c0002t0009g0231 others(8): Show |
12 | HG01496.hp2 HG01884.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.634+12490G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38702384 | |||||||
| chr2:38702593 | T | C | 2 | a0001c0001t0003g0302 a0001c0001t0028g0303 |
2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.634+12699T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38702593 | |||||||
| chr2:38702915 | TTA | T | 79 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0147 others(76): Show |
80 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.634+13032_634+1303 others(6): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38702915 | ||||||
| chr2:38702926 | T | C | 3 | a0001c0001t0002g0156 a0001c0001t0002g0157 a0001c0001t0002g0158 |
3 | HG02717.hp1 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.634+13032T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38702926 | |||||||
| chr2:38702930 | T | C | 2 | a0002c0002t0002g0203 a0002c0002t0002g0204 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.634+13036T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38702930 | |||||||
| chr2:38702932 | T | A | 3 | a0001c0001t0003g0305 a0001c0001t0019g0202 a0003c0004t0004g0211 |
3 | HG01891.hp1 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.634+13038T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38702932 | |||||||
| chr2:38702932 | T | TTA | 51 | a0001c0001t0001g0004 a0001c0001t0001g0062 a0001c0001t0001g0153 others(48): Show |
52 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.634+13055_634+1305 others(6): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38702932 | ||||||
| chr2:38702932 | T | TTATATAT others(19): Show |
2 | a0002c0002t0002g0190 a0002c0002t0006g0059 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.634+13056_634+1305 others(30): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38702932 | ||||||
| chr2:38702932 | TTA | T | 78 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0147 others(75): Show |
79 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.634+13055_634+1305 others(6): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38702932 | ||||||
| chr2:38703014 | C | T | 1 | a0001c0001t0004g0138 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.634+13120C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703014 | |||||||
| chr2:38703049 | G | A | 1 | a0001c0001t0005g0116 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.634+13155G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703049 | |||||||
| chr2:38703049 | G | C | 2 | a0002c0002t0002g0190 a0002c0002t0006g0059 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.634+13155G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703049 | |||||||
| chr2:38703052 | T | TTATATAT others(9): Show |
2 | a0001c0003t0005g0221 a0001c0003t0005g0223 |
2 | HG03195.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.634+13159_634+1316 others(20): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703052 | ||||||
| chr2:38703054 | T | A | 6 | a0001c0003t0005g0221 a0001c0003t0005g0223 a0001c0003t0005g0224 others(3): Show |
6 | HG02572.hp2 HG02622.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.634+13160T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703054 | |||||||
| chr2:38703054 | T | TTA | 4 | a0001c0001t0001g0128 a0001c0001t0002g0311 a0001c0001t0006g0162 others(1): Show |
4 | HG00639.hp1 HG02647.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+13198_634+1319 others(6): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703054 | ||||||
| chr2:38703054 | T | TTATA | 7 | a0001c0001t0001g0011 a0001c0001t0005g0116 a0001c0001t0006g0159 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.634+13196_634+1319 others(8): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703054 | ||||||
| chr2:38703054 | T | TTATATAT others(3): Show |
7 | a0001c0001t0001g0071 a0001c0001t0001g0089 a0001c0001t0001g0098 others(4): Show |
7 | HG02293.hp2 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.634+13190_634+1319 others(14): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703054 | ||||||
| chr2:38703054 | T | TTATATAT others(5): Show |
9 | a0001c0001t0001g0064 a0001c0001t0001g0118 a0001c0001t0001g0197 others(6): Show |
9 | HG00609.hp2 HG01109.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.634+13188_634+1319 others(16): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703054 | ||||||
| chr2:38703054 | T | TTATATAT others(7): Show |
5 | a0001c0001t0001g0099 a0001c0001t0008g0010 a0002c0002t0006g0272 others(2): Show |
5 | HG02698.hp1 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.634+13186_634+1319 others(18): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703054 | ||||||
| chr2:38703054 | T | TTATATAT others(9): Show |
4 | a0001c0001t0001g0296 a0001c0001t0010g0072 a0001c0003t0005g0218 others(1): Show |
4 | HG01515.hp2 HG03130.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+13184_634+1319 others(20): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703054 | ||||||
| chr2:38703054 | T | TTATATAT others(11): Show |
4 | a0001c0001t0001g0297 a0001c0001t0003g0063 a0001c0001t0024g0066 others(1): Show |
4 | HG00597.hp1 HG00642.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+13182_634+1319 others(22): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703054 | ||||||
| chr2:38703054 | T | TTATATAT others(13): Show |
2 | a0001c0003t0005g0220 a0002c0002t0007g0294 |
2 | HG02615.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.634+13180_634+1319 others(24): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703054 | ||||||
| chr2:38703054 | T | TTATATAT others(15): Show |
2 | a0001c0001t0001g0080 a0002c0002t0001g0281 |
2 | HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.634+13178_634+1319 others(26): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703054 | ||||||
| chr2:38703054 | T | TTATATAT others(19): Show |
1 | a0002c0002t0001g0306 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.634+13174_634+1319 others(30): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703054 | ||||||
| chr2:38703054 | TTATATAT others(3): Show |
T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0177 a0002c0002t0001g0291 |
3 | HG01261.hp2 HG03239.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.634+13190_634+1319 others(14): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703054 | ||||||
| chr2:38703054 | TTATATAT others(5): Show |
T | 2 | a0003c0004t0004g0211 a0003c0004t0004g0214 |
2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.634+13188_634+1319 others(16): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703054 | ||||||
| chr2:38703054 | TTATATAT others(21): Show |
T | 1 | a0001c0001t0032g0319 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.634+13172_634+1319 others(32): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703054 | ||||||
| chr2:38703056 | A | T | 2 | a0002c0002t0002g0190 a0002c0002t0006g0059 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.634+13162A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703056 | |||||||
| chr2:38703065 | TATATATA others(20): Show |
T | 1 | a0001c0001t0013g0227 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.634+13172_634+1319 others(31): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703065 | |||||||
| chr2:38703066 | ATATATAT others(22): Show |
A | 1 | a0001c0001t0001g0107 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.634+13174_634+1320 others(33): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703066 | ||||||
| chr2:38703067 | T | A | 1 | a0001c0001t0001g0061 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.634+13173T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703067 | |||||||
| chr2:38703068 | ATATATAT others(18): Show |
A | 1 | a0001c0001t0001g0249 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.634+13176_634+1320 others(29): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703068 | ||||||
| chr2:38703068 | ATATATAT others(19): Show |
A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0241 a0001c0001t0001g0242 others(8): Show |
12 | HG00423.hp2 HG00544.hp1 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.634+13176_634+1320 others(30): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703068 | ||||||
| chr2:38703068 | ATATATAT others(20): Show |
A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0243 |
2 | HG00558.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.634+13176_634+1320 others(31): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703068 | ||||||
| chr2:38703070 | ATATATAT others(18): Show |
A | 4 | a0001c0001t0003g0302 a0001c0001t0003g0305 a0001c0001t0006g0206 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+13178_634+1320 others(29): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703070 | ||||||
| chr2:38703070 | ATATATAT others(19): Show |
A | 3 | a0001c0001t0001g0239 a0001c0001t0028g0303 a0001c0001t0031g0253 |
3 | HG03453.hp2 NA18991.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.634+13178_634+1320 others(30): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703070 | ||||||
| chr2:38703070 | ATATATAT others(20): Show |
A | 2 | a0002c0002t0006g0232 a0002c0002t0012g0236 |
2 | HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.634+13178_634+1320 others(31): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703070 | ||||||
| chr2:38703070 | ATATATAT others(21): Show |
A | 8 | a0002c0002t0009g0001 a0002c0002t0009g0231 a0002c0002t0009g0235 others(5): Show |
8 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.634+13178_634+1320 others(32): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703070 | ||||||
| chr2:38703072 | ATATATAT others(20): Show |
A | 1 | a0002c0002t0009g0001 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.634+13180_634+1320 others(31): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703072 | ||||||
| chr2:38703079 | TATATATA others(6): Show |
T | 1 | a0002c0002t0001g0259 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.634+13186_634+1319 others(17): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703079 | |||||||
| chr2:38703080 | ATATATAT others(8): Show |
A | 1 | a0001c0001t0002g0030 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.634+13188_634+1320 others(19): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703080 | ||||||
| chr2:38703080 | ATATATAT others(11): Show |
A | 1 | a0002c0002t0018g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.634+13188_634+1320 others(22): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703080 | ||||||
| chr2:38703081 | TATATATA others(4): Show |
T | 1 | a0001c0001t0001g0163 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.634+13188_634+1319 others(15): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703081 | |||||||
| chr2:38703082 | ATATATAT others(5): Show |
A | 2 | a0002c0002t0002g0190 a0002c0002t0006g0059 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.634+13190_634+1320 others(16): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703082 | ||||||
| chr2:38703084 | ATATATAT others(3): Show |
A | 8 | a0001c0001t0001g0122 a0001c0001t0001g0165 a0001c0001t0001g0170 others(5): Show |
8 | HG00621.hp2 HG00673.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.634+13192_634+1320 others(14): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703084 | ||||||
| chr2:38703084 | ATATATAT others(4): Show |
A | 3 | a0001c0001t0001g0140 a0001c0001t0011g0155 a0001c0001t0011g0172 |
3 | HG00609.hp1 HG01099.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.634+13192_634+1320 others(15): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703084 | ||||||
| chr2:38703084 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0036 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.634+13192_634+1320 others(17): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703084 | ||||||
| chr2:38703084 | ATATATAT others(7): Show |
A | 3 | a0001c0001t0004g0008 a0001c0001t0004g0046 a0001c0001t0004g0049 |
3 | NA18963.hp1 NA19010.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.634+13192_634+1320 others(18): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703084 | ||||||
| chr2:38703084 | ATATATAT others(8): Show |
A | 4 | a0001c0001t0001g0013 a0001c0001t0002g0034 a0001c0001t0002g0037 others(1): Show |
4 | HG01192.hp1 HG01258.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+13192_634+1320 others(19): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703084 | ||||||
| chr2:38703084 | ATATATAT others(9): Show |
A | 1 | a0001c0001t0017g0038 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.634+13192_634+1320 others(20): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703084 | ||||||
| chr2:38703086 | ATATATAT others(3): Show |
A | 9 | a0001c0001t0001g0166 a0001c0001t0001g0174 a0001c0001t0003g0054 others(6): Show |
9 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.634+13194_634+1320 others(14): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703086 | ||||||
| chr2:38703086 | ATATATAT others(4): Show |
A | 6 | a0001c0001t0001g0014 a0001c0001t0001g0147 a0001c0001t0001g0150 others(3): Show |
6 | HG02074.hp2 HG02129.hp1 NA19062.hp2 others(3): Show |
intron_variant | MODIFIER | c.634+13194_634+1320 others(15): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703086 | ||||||
| chr2:38703086 | ATATATAT others(6): Show |
A | 17 | a0001c0001t0001g0047 a0001c0001t0002g0002 a0001c0001t0002g0018 others(14): Show |
17 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.634+13194_634+1320 others(17): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703086 | ||||||
| chr2:38703086 | ATATATAT others(7): Show |
A | 3 | a0001c0001t0002g0027 a0001c0001t0002g0229 a0001c0001t0004g0015 |
3 | HG02280.hp1 NA18946.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.634+13194_634+1320 others(18): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703086 | ||||||
| chr2:38703086 | ATATATAT others(8): Show |
A | 6 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0022 others(3): Show |
7 | HG00639.hp2 HG01081.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.634+13194_634+1320 others(19): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703086 | ||||||
| chr2:38703086 | ATATATAT others(9): Show |
A | 3 | a0001c0001t0002g0023 a0001c0001t0002g0032 a0001c0001t0002g0041 |
3 | HG01358.hp2 HG01928.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.634+13194_634+1320 others(20): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703086 | ||||||
| chr2:38703088 | ATATAT | A | 6 | a0001c0001t0001g0081 a0001c0001t0001g0135 a0001c0001t0033g0213 others(3): Show |
6 | HG01071.hp2 HG01261.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.634+13196_634+1320 others(9): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703088 | ||||||
| chr2:38703088 | ATATATTT others(3): Show |
A | 1 | a0001c0001t0002g0200 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.634+13196_634+1320 others(14): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703088 | ||||||
| chr2:38703088 | ATATATTT others(4): Show |
A | 4 | a0001c0001t0001g0148 a0001c0001t0002g0002 a0001c0001t0002g0040 others(1): Show |
4 | HG00673.hp2 HG01943.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+13196_634+1320 others(15): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703088 | ||||||
| chr2:38703088 | ATATATTT others(5): Show |
A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0230 |
2 | HG03654.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.634+13196_634+1320 others(16): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703088 | ||||||
| chr2:38703090 | A | T | 1 | a0002c0002t0001g0279 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.634+13196A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703090 | |||||||
| chr2:38703092 | A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0145 a0002c0002t0001g0288 |
2 | NA18953.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.634+13199_634+1320 others(15): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(6): Show |
1 | a0001c0003t0005g0215 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.634+13199_634+1320 others(17): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(8): Show |
3 | a0001c0001t0001g0067 a0002c0002t0001g0264 a0002c0002t0001g0270 |
3 | HG00408.hp2 HG03017.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.634+13199_634+1320 others(19): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0112 a0002c0002t0001g0276 |
2 | HG00735.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.634+13199_634+1320 others(21): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0103 a0002c0002t0001g0292 |
2 | HG03239.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.634+13199_634+1320 others(23): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(26): Show |
1 | a0002c0002t0001g0005 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.634+13199_634+1320 others(37): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(32): Show |
1 | a0001c0001t0001g0178 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.634+13199_634+1320 others(43): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(24): Show |
1 | a0002c0002t0001g0005 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.634+13199_634+1320 others(35): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(17): Show |
1 | a0002c0002t0001g0210 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.634+13199_634+1320 others(28): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(18): Show |
1 | a0001c0003t0005g0217 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.634+13199_634+1320 others(29): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(14): Show |
2 | a0001c0001t0005g0205 a0001c0003t0005g0216 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.634+13199_634+1320 others(25): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(15): Show |
1 | a0002c0002t0001g0258 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.634+13199_634+1320 others(26): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(16): Show |
1 | a0001c0003t0005g0219 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.634+13199_634+1320 others(27): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0068 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.634+13199_634+1320 others(25): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(20): Show |
1 | a0001c0001t0019g0304 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.634+13199_634+1320 others(31): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(9): Show |
3 | a0002c0002t0001g0262 a0002c0002t0001g0263 a0002c0002t0001g0273 |
3 | HG03927.hp1 NA18943.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.634+13199_634+1320 others(20): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0065 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.634+13199_634+1320 others(21): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0094 a0001c0003t0005g0224 |
2 | HG02622.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.634+13199_634+1320 others(22): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(15): Show |
1 | a0002c0002t0001g0266 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.634+13199_634+1320 others(26): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(7): Show |
3 | a0001c0001t0001g0117 a0002c0002t0001g0271 a0002c0002t0006g0295 |
3 | HG02257.hp1 HG04199.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.634+13199_634+1320 others(18): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(8): Show |
3 | a0001c0001t0001g0077 a0002c0002t0001g0260 a0002c0002t0010g0187 |
3 | NA18953.hp1 NA18972.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.634+13199_634+1320 others(19): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(10): Show |
1 | a0002c0002t0001g0282 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.634+13199_634+1320 others(21): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(5): Show |
2 | a0001c0001t0007g0092 a0002c0002t0001g0267 |
2 | HG02040.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.634+13199_634+1320 others(16): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0110 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.634+13199_634+1320 others(17): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0078 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.634+13199_634+1320 others(18): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(8): Show |
1 | a0002c0002t0001g0261 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.634+13199_634+1320 others(19): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(3): Show |
3 | a0001c0001t0001g0069 a0001c0001t0001g0137 a0002c0002t0016g0195 |
3 | HG01346.hp1 HG02735.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.634+13199_634+1320 others(14): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(4): Show |
3 | a0001c0001t0001g0061 a0001c0001t0001g0142 a0001c0001t0007g0060 |
3 | HG01168.hp2 NA18945.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.634+13199_634+1320 others(15): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0141 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.634+13199_634+1320 others(16): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(6): Show |
1 | a0001c0003t0005g0225 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.634+13199_634+1320 others(17): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | ATATATAT others(3): Show |
1 | a0001c0001t0004g0124 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.634+13199_634+1320 others(14): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703092 | ||||||
| chr2:38703092 | A | T | 4 | a0001c0001t0002g0307 a0001c0001t0006g0051 a0002c0002t0001g0279 others(1): Show |
4 | HG02135.hp2 HG02895.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+13198A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703092 | |||||||
| chr2:38703093 | T | G | 1 | a0001c0001t0013g0227 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.634+13199T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703093 | |||||||
| chr2:38703093 | T | TA | 6 | a0001c0001t0001g0123 a0001c0001t0001g0208 a0001c0001t0013g0073 others(3): Show |
6 | HG01884.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.634+13199_634+1320 others(5): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703093 | |||||||
| chr2:38703093 | T | TATATATA | 4 | a0001c0001t0001g0115 a0001c0001t0001g0120 a0001c0001t0002g0088 others(1): Show |
4 | HG01943.hp1 HG01981.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+13199_634+1320 others(11): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703093 | |||||||
| chr2:38703093 | T | TATATATA others(2): Show |
6 | a0001c0001t0001g0070 a0001c0001t0002g0109 a0001c0001t0003g0079 others(3): Show |
6 | HG00280.hp1 HG01081.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.634+13199_634+1320 others(13): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703093 | |||||||
| chr2:38703093 | T | TATATATA others(4): Show |
4 | a0001c0001t0001g0087 a0001c0001t0001g0105 a0001c0001t0001g0191 others(1): Show |
4 | HG02015.hp2 HG02083.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+13199_634+1320 others(15): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703093 | |||||||
| chr2:38703093 | T | TATATATA others(6): Show |
5 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0097 others(2): Show |
5 | HG00642.hp1 HG01243.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.634+13199_634+1320 others(17): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703093 | |||||||
| chr2:38703093 | T | TATATATA others(8): Show |
8 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0104 others(5): Show |
8 | HG00544.hp2 HG00597.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.634+13199_634+1320 others(19): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703093 | |||||||
| chr2:38703093 | T | TATATATA others(10): Show |
2 | a0001c0001t0001g0009 a0001c0001t0001g0095 |
2 | NA18961.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.634+13199_634+1320 others(21): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703093 | |||||||
| chr2:38703093 | T | TATATATA others(16): Show |
1 | a0001c0001t0001g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.634+13199_634+1320 others(27): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703093 | |||||||
| chr2:38703093 | T | TATATATA others(20): Show |
1 | a0002c0002t0010g0277 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.634+13199_634+1320 others(31): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703093 | |||||||
| chr2:38703094 | T | A | 33 | a0001c0001t0001g0011 a0001c0001t0001g0071 a0001c0001t0001g0089 others(30): Show |
33 | HG00639.hp1 HG01106.hp2 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.634+13200T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703094 | |||||||
| chr2:38703094 | T | G | 1 | a0001c0001t0032g0319 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.634+13200T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703094 | |||||||
| chr2:38703095 | T | A | 18 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0095 others(15): Show |
18 | HG00642.hp1 HG00735.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.634+13201T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703095 | |||||||
| chr2:38703096 | T | A | 15 | a0001c0001t0001g0089 a0001c0001t0001g0098 a0001c0001t0001g0128 others(12): Show |
15 | HG00639.hp1 HG01928.hp2 HG02293.hp2 others(12): Show |
intron_variant | MODIFIER | c.634+13202T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703096 | |||||||
| chr2:38703097 | T | A | 6 | a0001c0001t0002g0083 a0001c0001t0002g0199 a0001c0001t0002g0312 others(3): Show |
6 | HG00735.hp1 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.634+13203T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703097 | |||||||
| chr2:38703098 | T | A | 14 | a0001c0001t0001g0089 a0001c0001t0001g0098 a0001c0001t0001g0128 others(11): Show |
14 | HG00639.hp1 HG02293.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.634+13204T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703098 | |||||||
| chr2:38703099 | T | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0196 |
2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.634+13205T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703099 | |||||||
| chr2:38703100 | T | A | 5 | a0001c0001t0010g0132 a0002c0002t0004g0314 a0002c0002t0013g0209 others(2): Show |
5 | HG01891.hp2 HG02615.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.634+13206T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703100 | |||||||
| chr2:38703100 | T | G | 1 | a0001c0001t0013g0227 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.634+13206T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703100 | |||||||
| chr2:38703102 | T | A | 1 | a0002c0002t0013g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.634+13208T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703102 | |||||||
| chr2:38703184 | C | T | 2 | a0002c0002t0002g0190 a0002c0002t0006g0059 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.634+13290C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703184 | |||||||
| chr2:38703205 | T | C | 2 | a0002c0002t0001g0186 a0002c0002t0010g0187 |
2 | NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.634+13311T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703205 | |||||||
| chr2:38703298 | G | A | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 |
3 | HG01258.hp1 HG01346.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.634+13404G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703298 | |||||||
| chr2:38703396 | G | A | 1 | a0001c0003t0005g0226 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.634+13502G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703396 | |||||||
| chr2:38703493 | A | G | 13 | a0001c0001t0001g0062 a0001c0001t0003g0052 a0001c0001t0003g0054 others(10): Show |
13 | HG01167.hp2 HG01169.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.634+13599A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703493 | |||||||
| chr2:38703664 | T | C | 24 | a0001c0001t0001g0062 a0001c0001t0002g0156 a0001c0001t0002g0157 others(21): Show |
24 | HG01106.hp1 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.634+13770T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703664 | |||||||
| chr2:38703681 | A | G | 1 | a0001c0001t0032g0319 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.634+13787A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703681 | |||||||
| chr2:38703744 | G | GGCTCATC others(22): Show |
1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13855_634+1385 others(33): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38703744 | ||||||
| chr2:38703773 | G | T | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13879G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703773 | |||||||
| chr2:38703774 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.634+13880A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703774 | |||||||
| chr2:38703775 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.634+13881G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703775 | |||||||
| chr2:38703799 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13905G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703799 | |||||||
| chr2:38703802 | C | G | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13908C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703802 | |||||||
| chr2:38703805 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13911G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703805 | |||||||
| chr2:38703806 | A | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13912A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703806 | |||||||
| chr2:38703807 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13913G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703807 | |||||||
| chr2:38703808 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13914T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703808 | |||||||
| chr2:38703809 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13915T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703809 | |||||||
| chr2:38703811 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13917G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703811 | |||||||
| chr2:38703812 | A | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13918A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703812 | |||||||
| chr2:38703813 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13919G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703813 | |||||||
| chr2:38703814 | A | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13920A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703814 | |||||||
| chr2:38703817 | A | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13923A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703817 | |||||||
| chr2:38703818 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13924G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703818 | |||||||
| chr2:38703821 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13927T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703821 | |||||||
| chr2:38703822 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13928G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703822 | |||||||
| chr2:38703826 | A | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13932A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703826 | |||||||
| chr2:38703827 | A | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13933A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703827 | |||||||
| chr2:38703829 | A | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13935A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703829 | |||||||
| chr2:38703830 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13936T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703830 | |||||||
| chr2:38703831 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13937G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703831 | |||||||
| chr2:38703832 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13938T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703832 | |||||||
| chr2:38703833 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13939T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703833 | |||||||
| chr2:38703834 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13940G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703834 | |||||||
| chr2:38703835 | A | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13941A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703835 | |||||||
| chr2:38703836 | A | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13942A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703836 | |||||||
| chr2:38703837 | A | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13943A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703837 | |||||||
| chr2:38703843 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13949T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703843 | |||||||
| chr2:38703845 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13951T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703845 | |||||||
| chr2:38703847 | T | G | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13953T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703847 | |||||||
| chr2:38703858 | A | C | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.634+13964A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703858 | |||||||
| chr2:38703884 | A | G | 7 | a0001c0001t0001g0313 a0001c0001t0002g0307 a0001c0001t0002g0310 others(4): Show |
7 | HG02258.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.634+13990A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703884 | |||||||
| chr2:38703982 | C | T | 2 | a0001c0001t0006g0051 a0001c0001t0022g0050 |
2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.634+14088C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38703982 | |||||||
| chr2:38704011 | G | A | 71 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0061 others(68): Show |
71 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.634+14117G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38704011 | |||||||
| chr2:38704042 | T | TAAATA | 105 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0122 others(102): Show |
106 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.634+14171_634+1417 others(9): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38704042 | ||||||
| chr2:38704103 | C | G | 3 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0001c0001t0008g0228 |
3 | HG00738.hp1 HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.634+14209C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38704103 | |||||||
| chr2:38704135 | T | G | 1 | a0001c0001t0019g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.634+14241T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38704135 | |||||||
| chr2:38704140 | C | T | 9 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0313 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.634+14246C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38704140 | |||||||
| chr2:38704171 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0007g0060 |
2 | NA18979.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.634+14277C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38704171 | |||||||
| chr2:38704185 | C | T | 1 | a0001c0001t0031g0253 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.634+14291C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38704185 | |||||||
| chr2:38704204 | A | AT | 24 | a0001c0001t0001g0004 a0001c0001t0001g0169 a0001c0001t0001g0173 others(21): Show |
25 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.634+14321dupT | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38704204 | ||||||
| chr2:38704302 | G | A | 16 | a0001c0001t0002g0156 a0001c0001t0002g0157 a0001c0001t0002g0158 others(13): Show |
16 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.634+14408G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38704302 | |||||||
| chr2:38704414 | A | G | 1 | a0001c0001t0032g0319 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.634+14520A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38704414 | |||||||
| chr2:38704541 | T | C | 44 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0036 others(41): Show |
46 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.634+14647T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38704541 | |||||||
| chr2:38704611 | G | T | 5 | a0001c0001t0019g0202 a0001c0001t0033g0213 a0001c0001t0034g0212 others(2): Show |
5 | HG01361.hp1 HG02886.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.634+14717G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38704611 | |||||||
| chr2:38704651 | G | A | 2 | a0001c0001t0008g0010 a0001c0001t0008g0136 |
2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.634+14757G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38704651 | |||||||
| chr2:38704662 | ACT | A | 10 | a0002c0002t0006g0232 a0002c0002t0009g0001 a0002c0002t0009g0231 others(7): Show |
11 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.634+14771_634+1477 others(6): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38704662 | ||||||
| chr2:38704754 | T | C | 1 | a0002c0002t0012g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.634+14860T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38704754 | |||||||
| chr2:38704805 | G | C | 1 | a0001c0001t0019g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.634+14911G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38704805 | |||||||
| chr2:38704872 | C | T | 2 | a0002c0002t0002g0190 a0002c0002t0006g0059 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.634+14978C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38704872 | |||||||
| chr2:38704914 | A | G | 13 | a0001c0001t0005g0205 a0001c0003t0005g0215 a0001c0003t0005g0216 others(10): Show |
13 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.634+15020A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38704914 | |||||||
| chr2:38704940 | C | G | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0163 |
3 | HG02523.hp2 NA19063.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.634+15046C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38704940 | |||||||
| chr2:38705318 | G | A | 13 | a0001c0001t0005g0205 a0001c0003t0005g0215 a0001c0003t0005g0216 others(10): Show |
13 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.634+15424G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38705318 | |||||||
| chr2:38705635 | T | G | 221 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(218): Show |
226 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.634+15741T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38705635 | |||||||
| chr2:38705898 | C | T | 77 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0147 others(74): Show |
78 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.634+16004C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38705898 | |||||||
| chr2:38705914 | G | A | 4 | a0002c0002t0001g0291 a0002c0002t0006g0272 a0002c0002t0006g0290 others(1): Show |
4 | HG03239.hp2 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+16020G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38705914 | |||||||
| chr2:38706040 | C | T | 1 | a0001c0001t0002g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.634+16146C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38706040 | |||||||
| chr2:38706069 | G | A | 17 | a0001c0001t0002g0156 a0001c0001t0002g0157 a0001c0001t0002g0158 others(14): Show |
17 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.634+16175G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38706069 | |||||||
| chr2:38706473 | G | A | 34 | a0001c0001t0001g0013 a0001c0001t0002g0002 a0001c0001t0002g0003 others(31): Show |
36 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.634+16579G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38706473 | |||||||
| chr2:38706511 | C | CA | 19 | a0001c0001t0001g0095 a0001c0001t0001g0121 a0001c0001t0001g0189 others(16): Show |
20 | HG00609.hp1 HG01167.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.634+16636dupA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38706511 | ||||||
| chr2:38706511 | CA | C | 81 | a0001c0001t0001g0014 a0001c0001t0001g0077 a0001c0001t0001g0122 others(78): Show |
82 | HG00408.hp2 HG00673.hp1 HG01071.hp2 others(79): Show |
intron_variant | MODIFIER | c.634+16636delA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38706511 | ||||||
| chr2:38706573 | G | A | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0163 |
3 | HG02523.hp2 NA19063.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.634+16679G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38706573 | |||||||
| chr2:38706623 | T | G | 4 | a0002c0002t0012g0321 a0002c0002t0014g0151 a0002c0002t0014g0152 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+16729T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38706623 | |||||||
| chr2:38706693 | C | G | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | HG00408.hp1 HG00423.hp2 |
intron_variant | MODIFIER | c.634+16799C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38706693 | |||||||
| chr2:38706826 | C | T | 68 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0147 others(65): Show |
69 | HG00408.hp2 HG00673.hp1 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.634+16932C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38706826 | |||||||
| chr2:38706875 | A | AG | 34 | a0001c0001t0001g0004 a0001c0001t0001g0169 a0001c0001t0001g0173 others(31): Show |
35 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.634+16987dupG | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38706875 | ||||||
| chr2:38706875 | A | G | 1 | a0001c0001t0025g0175 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.634+16981A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38706875 | |||||||
| chr2:38706882 | C | CG | 11 | a0001c0001t0001g0193 a0001c0001t0002g0156 a0001c0001t0002g0229 others(8): Show |
11 | HG00738.hp1 HG01109.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.634+16995dupG | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38706882 | ||||||
| chr2:38706882 | C | G | 1 | a0001c0001t0031g0253 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.634+16988C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38706882 | |||||||
| chr2:38706889 | G | A | 2 | a0002c0002t0006g0059 a0002c0002t0013g0209 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.634+16995G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38706889 | |||||||
| chr2:38707033 | C | A | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0171 |
3 | NA18986.hp1 NA18990.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.634+17139C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38707033 | |||||||
| chr2:38707036 | C | T | 4 | a0001c0001t0003g0302 a0001c0001t0003g0305 a0001c0001t0019g0304 others(1): Show |
4 | HG01106.hp1 HG01891.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+17142C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38707036 | |||||||
| chr2:38707046 | G | C | 3 | a0002c0002t0006g0272 a0002c0002t0006g0290 a0002c0002t0006g0295 |
3 | HG03491.hp1 HG03492.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.634+17152G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38707046 | |||||||
| chr2:38707160 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.634+17266G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38707160 | |||||||
| chr2:38707370 | A | C | 11 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0004g0007 others(8): Show |
11 | HG02015.hp1 HG04115.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.634+17476A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38707370 | |||||||
| chr2:38707481 | C | G | 4 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG01496.hp2 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+17587C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38707481 | |||||||
| chr2:38707544 | G | C | 2 | a0001c0001t0002g0229 a0001c0001t0002g0230 |
2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.634+17650G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38707544 | |||||||
| chr2:38707561 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.634+17667C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38707561 | |||||||
| chr2:38707696 | C | G | 1 | a0001c0001t0001g0089 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.634+17802C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38707696 | |||||||
| chr2:38707719 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.634+17825G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38707719 | |||||||
| chr2:38707815 | T | C | 1 | a0002c0002t0001g0270 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.634+17921T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38707815 | |||||||
| chr2:38707897 | C | T | 1 | a0002c0002t0012g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.634+18003C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38707897 | |||||||
| chr2:38707958 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.634+18064T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38707958 | |||||||
| chr2:38707968 | G | A | 69 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0147 others(66): Show |
70 | HG00408.hp2 HG00673.hp1 HG01071.hp2 others(67): Show |
intron_variant | MODIFIER | c.634+18074G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38707968 | |||||||
| chr2:38708078 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.634+18184G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38708078 | |||||||
| chr2:38708094 | G | A | 69 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0147 others(66): Show |
70 | HG00408.hp2 HG00673.hp1 HG01071.hp2 others(67): Show |
intron_variant | MODIFIER | c.634+18200G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38708094 | |||||||
| chr2:38708107 | A | AAAAAT | 37 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0002g0002 others(34): Show |
39 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.634+18216_634+1821 others(9): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38708107 | ||||||
| chr2:38708107 | A | AAAAATAA others(3): Show |
22 | a0001c0001t0001g0179 a0001c0001t0002g0312 a0001c0001t0004g0007 others(19): Show |
23 | HG01884.hp2 HG01928.hp2 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.634+18216_634+1821 others(14): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38708107 | ||||||
| chr2:38708107 | A | AAAAATAA others(8): Show |
52 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0122 others(49): Show |
53 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(50): Show |
intron_variant | MODIFIER | c.634+18216_634+1821 others(19): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38708107 | ||||||
| chr2:38708107 | A | AAAAATAA others(13): Show |
14 | a0001c0001t0001g0170 a0002c0002t0001g0201 a0002c0002t0001g0255 others(11): Show |
14 | HG01071.hp2 HG01261.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.634+18216_634+1821 others(24): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38708107 | ||||||
| chr2:38708107 | A | AAAAATAA others(18): Show |
1 | a0001c0001t0001g0149 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.634+18216_634+1821 others(29): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38708107 | ||||||
| chr2:38708107 | AAAATT | A | 24 | a0001c0001t0005g0205 a0001c0001t0007g0092 a0001c0001t0019g0202 others(21): Show |
24 | HG01243.hp1 HG02559.hp1 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.634+18217_634+1822 others(9): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38708107 | ||||||
| chr2:38708107 | AAAATTAA others(3): Show |
A | 29 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0163 others(26): Show |
29 | HG01106.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.634+18217_634+1822 others(14): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38708107 | ||||||
| chr2:38708107 | AAAATTAA others(8): Show |
A | 3 | a0002c0002t0014g0151 a0002c0002t0014g0152 a0002c0002t0018g0012 |
3 | HG02895.hp2 HG02897.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.634+18217_634+1823 others(19): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38708107 | ||||||
| chr2:38708111 | T | A | 137 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(134): Show |
141 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(138): Show |
intron_variant | MODIFIER | c.634+18217T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38708111 | |||||||
| chr2:38708111 | TTAAAA | T | 119 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(116): Show |
120 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.634+18253_634+1825 others(9): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38708111 | ||||||
| chr2:38708166 | G | A | 69 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0147 others(66): Show |
70 | HG00408.hp2 HG00673.hp1 HG01071.hp2 others(67): Show |
intron_variant | MODIFIER | c.634+18272G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38708166 | |||||||
| chr2:38708226 | G | A | 1 | a0002c0002t0001g0279 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.634+18332G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38708226 | |||||||
| chr2:38708257 | C | T | 2 | a0003c0004t0004g0211 a0003c0004t0004g0214 |
2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.634+18363C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38708257 | |||||||
| chr2:38708441 | T | G | 11 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0004g0007 others(8): Show |
11 | HG02015.hp1 HG04115.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.634+18547T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38708441 | |||||||
| chr2:38708601 | T | G | 11 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0004g0007 others(8): Show |
11 | HG02015.hp1 HG04115.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.634+18707T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38708601 | |||||||
| chr2:38708609 | C | T | 1 | a0001c0001t0011g0025 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.634+18715C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38708609 | |||||||
| chr2:38708715 | C | T | 33 | a0001c0001t0001g0013 a0001c0001t0002g0002 a0001c0001t0002g0003 others(30): Show |
35 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.634+18821C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38708715 | |||||||
| chr2:38708731 | G | GA | 7 | a0001c0001t0003g0302 a0001c0001t0003g0305 a0001c0001t0006g0206 others(4): Show |
7 | HG00609.hp1 HG01106.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.634+18855dupA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38708731 | ||||||
| chr2:38708731 | G | GAA | 24 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0163 others(21): Show |
24 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.634+18854_634+1885 others(6): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38708731 | ||||||
| chr2:38708731 | GA | G | 114 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0036 others(111): Show |
116 | HG00408.hp2 HG00673.hp1 HG01071.hp2 others(113): Show |
intron_variant | MODIFIER | c.634+18855delA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38708731 | ||||||
| chr2:38708774 | C | A | 1 | a0002c0002t0001g0301 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.634+18880C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38708774 | |||||||
| chr2:38708821 | G | GT | 9 | a0002c0002t0006g0232 a0002c0002t0009g0001 a0002c0002t0009g0231 others(6): Show |
10 | HG01496.hp2 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.634+18935dupT | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38708821 | ||||||
| chr2:38708830 | G | T | 2 | a0001c0001t0006g0206 a0001c0001t0031g0253 |
2 | HG02280.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.634+18936G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38708830 | |||||||
| chr2:38708922 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.634+19028C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38708922 | |||||||
| chr2:38708956 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.634+19062T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38708956 | |||||||
| chr2:38708976 | C | T | 2 | a0001c0001t0002g0018 a0001c0001t0002g0019 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.634+19082C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38708976 | |||||||
| chr2:38708981 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.634+19087G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38708981 | |||||||
| chr2:38709080 | G | A | 1 | a0002c0002t0001g0280 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.634+19186G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38709080 | |||||||
| chr2:38709147 | GGACAGGG others(2): Show |
G | 24 | a0001c0001t0005g0205 a0001c0003t0005g0215 a0001c0003t0005g0216 others(21): Show |
25 | HG01243.hp1 HG01496.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.634+19257_634+1926 others(13): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38709147 | ||||||
| chr2:38709159 | C | T | 1 | a0001c0001t0006g0206 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.634+19265C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38709159 | |||||||
| chr2:38709367 | T | C | 1 | a0001c0001t0019g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.634+19473T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38709367 | |||||||
| chr2:38709397 | C | T | 70 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0147 others(67): Show |
71 | HG00408.hp2 HG00673.hp1 HG01071.hp2 others(68): Show |
intron_variant | MODIFIER | c.634+19503C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38709397 | |||||||
| chr2:38709486 | A | G | 4 | a0001c0001t0001g0126 a0001c0001t0001g0134 a0001c0001t0001g0140 others(1): Show |
4 | HG01099.hp2 HG01109.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+19592A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38709486 | |||||||
| chr2:38709543 | C | T | 1 | a0002c0002t0013g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.634+19649C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38709543 | |||||||
| chr2:38709545 | G | C | 1 | a0001c0001t0019g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.634+19651G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38709545 | |||||||
| chr2:38709559 | A | C | 3 | a0001c0001t0033g0213 a0003c0004t0004g0211 a0003c0004t0004g0214 |
3 | HG01361.hp1 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.634+19665A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38709559 | |||||||
| chr2:38709564 | A | C | 1 | a0001c0001t0002g0200 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.634+19670A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38709564 | |||||||
| chr2:38709567 | A | C | 10 | a0001c0001t0001g0036 a0001c0001t0004g0007 a0001c0001t0004g0008 others(7): Show |
10 | HG02015.hp1 NA18943.hp1 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.634+19673A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38709567 | |||||||
| chr2:38709640 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.634+19746T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38709640 | |||||||
| chr2:38709699 | T | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0089 a0001c0001t0001g0095 others(2): Show |
5 | NA18939.hp1 NA18961.hp1 NA19068.hp2 others(2): Show |
intron_variant | MODIFIER | c.634+19805T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38709699 | |||||||
| chr2:38709735 | C | T | 9 | a0001c0001t0002g0307 a0001c0001t0002g0310 a0001c0001t0002g0311 others(6): Show |
9 | HG02258.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.635-19821C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38709735 | |||||||
| chr2:38709819 | C | A | 9 | a0001c0001t0002g0307 a0001c0001t0002g0310 a0001c0001t0002g0311 others(6): Show |
9 | HG02258.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.635-19737C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38709819 | |||||||
| chr2:38709876 | C | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0296 |
2 | HG01261.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.635-19680C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38709876 | |||||||
| chr2:38709879 | T | C | 11 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0004g0007 others(8): Show |
11 | HG02015.hp1 HG04115.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.635-19677T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38709879 | |||||||
| chr2:38710111 | A | T | 1 | a0002c0002t0012g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.635-19445A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38710111 | |||||||
| chr2:38710289 | C | T | 1 | a0001c0001t0002g0032 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.635-19267C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38710289 | |||||||
| chr2:38710297 | T | C | 9 | a0001c0001t0002g0307 a0001c0001t0002g0310 a0001c0001t0002g0311 others(6): Show |
9 | HG02258.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.635-19259T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38710297 | |||||||
| chr2:38710481 | C | G | 11 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0004g0007 others(8): Show |
11 | HG02015.hp1 HG04115.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.635-19075C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38710481 | |||||||
| chr2:38710567 | A | G | 1 | a0001c0001t0031g0253 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.635-18989A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38710567 | |||||||
| chr2:38710753 | C | CT | 12 | a0001c0001t0001g0180 a0001c0001t0001g0249 a0001c0001t0002g0029 others(9): Show |
12 | HG00408.hp1 HG01099.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.635-18785dupT | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38710753 | ||||||
| chr2:38710753 | CT | C | 20 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0118 others(17): Show |
20 | HG01167.hp2 HG01169.hp2 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.635-18785delT | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38710753 | ||||||
| chr2:38710775 | C | T | 1 | a0002c0002t0006g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.635-18781C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38710775 | |||||||
| chr2:38710783 | C | T | 11 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0004g0007 others(8): Show |
11 | HG02015.hp1 HG04115.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.635-18773C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38710783 | |||||||
| chr2:38710914 | C | A | 70 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0147 others(67): Show |
71 | HG00408.hp2 HG00673.hp1 HG01071.hp2 others(68): Show |
intron_variant | MODIFIER | c.635-18642C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38710914 | |||||||
| chr2:38710946 | G | A | 10 | a0002c0002t0006g0232 a0002c0002t0009g0001 a0002c0002t0009g0231 others(7): Show |
11 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.635-18610G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38710946 | |||||||
| chr2:38710964 | G | A | 9 | a0001c0001t0002g0307 a0001c0001t0002g0310 a0001c0001t0002g0311 others(6): Show |
9 | HG02258.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.635-18592G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38710964 | |||||||
| chr2:38711000 | C | T | 36 | a0001c0001t0001g0013 a0001c0001t0002g0002 a0001c0001t0002g0003 others(33): Show |
38 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.635-18556C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38711000 | |||||||
| chr2:38711114 | A | G | 11 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0004g0007 others(8): Show |
11 | HG02015.hp1 HG04115.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.635-18442A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38711114 | |||||||
| chr2:38711162 | C | CT | 114 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(111): Show |
115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.635-18379dupT | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711162 | ||||||
| chr2:38711221 | G | A | 40 | a0001c0001t0001g0013 a0001c0001t0001g0047 a0001c0001t0002g0002 others(37): Show |
42 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.635-18335G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38711221 | |||||||
| chr2:38711404 | G | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0004g0007 others(8): Show |
11 | HG02015.hp1 HG04115.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.635-18152G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38711404 | |||||||
| chr2:38711596 | T | C | 13 | a0001c0001t0005g0205 a0001c0003t0005g0215 a0001c0003t0005g0216 others(10): Show |
13 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.635-17960T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38711596 | |||||||
| chr2:38711743 | A | ACATCACC others(1336): Show |
3 | a0002c0002t0014g0151 a0002c0002t0014g0152 a0002c0002t0018g0012 |
3 | HG02895.hp2 HG02897.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.635-17778_635-1777 others(1347): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711743 | ||||||
| chr2:38711757 | A | G | 10 | a0002c0002t0006g0232 a0002c0002t0009g0001 a0002c0002t0009g0231 others(7): Show |
11 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.635-17799A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38711757 | |||||||
| chr2:38711781 | G | A | 3 | a0002c0002t0014g0151 a0002c0002t0014g0152 a0002c0002t0018g0012 |
3 | HG02895.hp2 HG02897.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.635-17775G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38711781 | |||||||
| chr2:38711794 | C | T | 3 | a0002c0002t0014g0151 a0002c0002t0014g0152 a0002c0002t0018g0012 |
3 | HG02895.hp2 HG02897.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.635-17762C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38711794 | |||||||
| chr2:38711801 | C | CATCATCA others(1829): Show |
1 | a0001c0001t0017g0038 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.635-17751_635-1775 others(1840): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711801 | ||||||
| chr2:38711801 | C | CATCATCA others(1856): Show |
1 | a0001c0001t0002g0037 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.635-17751_635-1775 others(1867): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711801 | ||||||
| chr2:38711801 | C | CATCATCA others(1883): Show |
32 | a0001c0001t0001g0013 a0001c0001t0001g0047 a0001c0001t0002g0002 others(29): Show |
34 | HG00639.hp2 HG00673.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.635-17751_635-1775 others(1894): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711801 | ||||||
| chr2:38711801 | C | CATCATCA others(1883): Show |
1 | a0001c0001t0027g0031 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.635-17751_635-1775 others(1894): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711801 | ||||||
| chr2:38711801 | C | CATCATCA others(1844): Show |
1 | a0001c0001t0002g0229 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.635-17751_635-1775 others(1855): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711801 | ||||||
| chr2:38711801 | C | CATCATCA others(1856): Show |
1 | a0001c0001t0002g0035 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.635-17751_635-1775 others(1867): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711801 | ||||||
| chr2:38711801 | C | T | 3 | a0002c0002t0014g0151 a0002c0002t0014g0152 a0002c0002t0018g0012 |
3 | HG02895.hp2 HG02897.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.635-17755C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38711801 | |||||||
| chr2:38711815 | T | C | 40 | a0001c0001t0001g0013 a0001c0001t0001g0047 a0001c0001t0002g0002 others(37): Show |
42 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.635-17741T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38711815 | |||||||
| chr2:38711815 | T | TCATACCA others(1861): Show |
1 | a0001c0001t0001g0242 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.635-17738_635-1773 others(1872): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1904): Show |
1 | a0001c0001t0033g0213 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.635-17738_635-1773 others(1915): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1886): Show |
2 | a0003c0004t0004g0211 a0003c0004t0004g0214 |
2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.635-17738_635-1773 others(1897): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1952): Show |
1 | a0001c0001t0001g0247 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.635-17738_635-1773 others(1963): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1862): Show |
8 | a0001c0001t0002g0307 a0001c0001t0002g0310 a0001c0001t0002g0311 others(5): Show |
8 | HG02258.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.635-17738_635-1773 others(1873): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1904): Show |
4 | a0001c0001t0002g0156 a0001c0001t0002g0157 a0001c0001t0002g0158 others(1): Show |
4 | HG02717.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.635-17738_635-1773 others(1915): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1889): Show |
1 | a0001c0001t0032g0319 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.635-17738_635-1773 others(1900): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1904): Show |
3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0002c0002t0001g0186 |
3 | HG02523.hp2 NA19012.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.635-17738_635-1773 others(1915): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1889): Show |
4 | a0001c0001t0003g0302 a0001c0001t0003g0305 a0001c0001t0019g0304 others(1): Show |
4 | HG01106.hp1 HG01891.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.635-17738_635-1773 others(1900): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1904): Show |
8 | a0001c0001t0003g0052 a0001c0001t0003g0054 a0001c0001t0003g0055 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.635-17738_635-1773 others(1915): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1907): Show |
7 | a0001c0001t0001g0163 a0001c0001t0003g0144 a0001c0001t0003g0164 others(4): Show |
7 | HG02145.hp2 HG02486.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.635-17738_635-1773 others(1918): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1889): Show |
1 | a0001c0001t0001g0062 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.635-17738_635-1773 others(1900): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1901): Show |
1 | a0001c0001t0003g0057 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.635-17738_635-1773 others(1912): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1829): Show |
1 | a0002c0002t0006g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.635-17738_635-1773 others(1840): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1877): Show |
1 | a0001c0001t0019g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.635-17738_635-1773 others(1888): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1890): Show |
1 | a0001c0001t0001g0077 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.635-17738_635-1773 others(1901): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1886): Show |
1 | a0001c0001t0001g0070 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.635-17738_635-1773 others(1897): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1886): Show |
1 | a0001c0001t0016g0176 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.635-17738_635-1773 others(1897): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1889): Show |
1 | a0001c0001t0001g0130 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.635-17738_635-1773 others(1900): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1886): Show |
1 | a0001c0001t0001g0129 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.635-17738_635-1773 others(1897): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1889): Show |
1 | a0001c0001t0001g0107 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.635-17738_635-1773 others(1900): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1889): Show |
111 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(108): Show |
112 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.635-17738_635-1773 others(1900): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1889): Show |
3 | a0002c0002t0004g0314 a0002c0002t0004g0316 a0002c0002t0004g0317 |
3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.635-17738_635-1773 others(1900): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(2500): Show |
1 | a0001c0001t0001g0036 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.635-17738_635-1773 others(2511): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(2458): Show |
8 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0015 others(5): Show |
8 | NA18943.hp1 NA18946.hp1 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.635-17738_635-1773 others(2469): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(2500): Show |
2 | a0001c0001t0001g0006 a0001c0001t0004g0044 |
2 | HG04115.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.635-17738_635-1773 others(2511): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1886): Show |
1 | a0001c0001t0013g0227 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.635-17738_635-1773 others(1897): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1904): Show |
1 | a0002c0002t0013g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.635-17738_635-1773 others(1915): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1886): Show |
2 | a0001c0001t0001g0145 a0001c0001t0001g0191 |
2 | NA18953.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.635-17738_635-1773 others(1897): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1913): Show |
1 | a0001c0001t0006g0206 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.635-17738_635-1773 others(1924): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1910): Show |
1 | a0001c0001t0031g0253 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.635-17738_635-1773 others(1921): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1874): Show |
1 | a0002c0002t0012g0233 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.635-17738_635-1773 others(1885): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1889): Show |
10 | a0002c0002t0006g0232 a0002c0002t0009g0001 a0002c0002t0009g0231 others(7): Show |
11 | HG01496.hp2 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.635-17738_635-1773 others(1900): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1877): Show |
13 | a0001c0001t0005g0205 a0001c0003t0005g0215 a0001c0003t0005g0216 others(10): Show |
13 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.635-17738_635-1773 others(1888): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711815 | T | TCATACCA others(1886): Show |
1 | a0001c0001t0001g0137 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.635-17738_635-1773 others(1897): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711815 | ||||||
| chr2:38711818 | T | TACCAC | 75 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0147 others(72): Show |
76 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.635-17738_635-1773 others(9): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38711818 | |||||||
| chr2:38711822 | T | C | 75 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0147 others(72): Show |
76 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.635-17734T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38711822 | |||||||
| chr2:38711823 | A | G | 1 | a0002c0002t0030g0139 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.635-17733A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38711823 | |||||||
| chr2:38711827 | C | T | 75 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0147 others(72): Show |
76 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.635-17729C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38711827 | |||||||
| chr2:38711831 | C | CATCCCTA others(2309): Show |
1 | a0002c0002t0001g0271 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.635-17722_635-1772 others(2320): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711831 | ||||||
| chr2:38711831 | C | CATCCCTA others(2312): Show |
1 | a0002c0002t0001g0270 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.635-17722_635-1772 others(2323): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711831 | ||||||
| chr2:38711831 | C | CATCCCTA others(1806): Show |
1 | a0002c0002t0016g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.635-17722_635-1772 others(1817): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711831 | ||||||
| chr2:38711831 | C | CATCCCTA others(1006): Show |
1 | a0002c0002t0001g0258 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.635-17722_635-1772 others(1017): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711831 | ||||||
| chr2:38711831 | C | CATCCCTA others(1845): Show |
1 | a0001c0001t0001g0183 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.635-17722_635-1772 others(1856): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711831 | ||||||
| chr2:38711831 | C | CATCCCTA others(1842): Show |
1 | a0002c0002t0001g0293 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.635-17722_635-1772 others(1853): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711831 | ||||||
| chr2:38711831 | C | CATCCCTA others(2726): Show |
1 | a0002c0002t0001g0005 | 2 | NA19065.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.635-17722_635-1772 others(2737): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711831 | ||||||
| chr2:38711831 | C | CATCCCTA others(1818): Show |
1 | a0001c0001t0001g0171 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.635-17722_635-1772 others(1829): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711831 | ||||||
| chr2:38711831 | C | CATCCCTA others(1845): Show |
50 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0147 others(47): Show |
50 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(47): Show |
intron_variant | MODIFIER | c.635-17722_635-1772 others(1856): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711831 | ||||||
| chr2:38711831 | C | CATCCCTA others(2466): Show |
1 | a0001c0001t0001g0179 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.635-17722_635-1772 others(2477): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711831 | ||||||
| chr2:38711831 | C | CATCCCTA others(1842): Show |
5 | a0002c0002t0001g0281 a0002c0002t0001g0291 a0002c0002t0006g0272 others(2): Show |
5 | HG03239.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.635-17722_635-1772 others(1853): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711831 | ||||||
| chr2:38711831 | C | CATCCCTA others(1821): Show |
1 | a0002c0002t0001g0255 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.635-17722_635-1772 others(1832): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711831 | ||||||
| chr2:38711831 | C | CATCCCTA others(1842): Show |
1 | a0002c0002t0021g0185 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.635-17722_635-1772 others(1853): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711831 | ||||||
| chr2:38711831 | C | CATCCCTA others(1842): Show |
1 | a0002c0002t0001g0288 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.635-17722_635-1772 others(1853): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711831 | ||||||
| chr2:38711831 | C | CATCCCTA others(1252): Show |
1 | a0002c0002t0001g0280 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.635-17722_635-1772 others(1263): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711831 | ||||||
| chr2:38711831 | C | CATCCCTA others(1875): Show |
4 | a0001c0001t0001g0174 a0001c0001t0011g0155 a0001c0001t0011g0172 others(1): Show |
4 | HG00609.hp1 HG02040.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.635-17722_635-1772 others(1886): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711831 | ||||||
| chr2:38711831 | C | CATCCCTA others(1875): Show |
2 | a0001c0001t0001g0169 a0001c0001t0001g0173 |
2 | HG00558.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.635-17722_635-1772 others(1886): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711831 | ||||||
| chr2:38711831 | C | CATCCCTA others(1846): Show |
1 | a0001c0001t0001g0170 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.635-17722_635-1772 others(1857): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38711831 | ||||||
| chr2:38711866 | T | G | 1 | a0001c0001t0001g0154 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.635-17690T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38711866 | |||||||
| chr2:38711869 | T | A | 9 | a0001c0001t0002g0307 a0001c0001t0002g0310 a0001c0001t0002g0311 others(6): Show |
9 | HG02258.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.635-17687T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38711869 | |||||||
| chr2:38711891 | T | C | 2 | a0001c0001t0033g0213 a0001c0001t0034g0212 |
2 | HG01361.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.635-17665T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38711891 | |||||||
| chr2:38712045 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.635-17511T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38712045 | |||||||
| chr2:38712151 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.635-17405A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38712151 | |||||||
| chr2:38712179 | T | C | 78 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0122 others(75): Show |
79 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.635-17377T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38712179 | |||||||
| chr2:38712401 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.635-17155A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38712401 | |||||||
| chr2:38712417 | G | T | 1 | a0001c0001t0003g0194 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.635-17139G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38712417 | |||||||
| chr2:38712707 | G | A | 1 | a0001c0003t0005g0223 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.635-16849G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38712707 | |||||||
| chr2:38712735 | G | A | 1 | a0001c0001t0006g0206 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.635-16821G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38712735 | |||||||
| chr2:38712902 | C | T | 4 | a0001c0001t0001g0181 a0001c0001t0003g0144 a0001c0001t0031g0253 others(1): Show |
4 | HG00673.hp1 HG02145.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.635-16654C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38712902 | |||||||
| chr2:38713026 | C | A | 1 | a0002c0002t0018g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.635-16530C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38713026 | |||||||
| chr2:38713044 | G | A | 253 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(250): Show |
257 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.635-16512G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38713044 | |||||||
| chr2:38713150 | A | T | 1 | a0001c0001t0032g0319 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.635-16406A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38713150 | |||||||
| chr2:38713166 | C | G | 3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0114 |
3 | HG02015.hp2 HG02080.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.635-16390C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38713166 | |||||||
| chr2:38713169 | A | G | 1 | a0002c0002t0001g0257 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.635-16387A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38713169 | |||||||
| chr2:38713174 | A | G | 281 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(278): Show |
286 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.635-16382A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38713174 | |||||||
| chr2:38713290 | G | A | 2 | a0001c0001t0003g0302 a0001c0001t0028g0303 |
2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.635-16266G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38713290 | |||||||
| chr2:38713334 | G | C | 1 | a0002c0002t0013g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.635-16222G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38713334 | |||||||
| chr2:38713440 | GC | G | 300 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(297): Show |
305 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.635-16110delC | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38713440 | ||||||
| chr2:38713496 | G | A | 2 | a0001c0001t0032g0319 a0002c0002t0006g0059 |
2 | HG02723.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.635-16060G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38713496 | |||||||
| chr2:38713534 | G | A | 5 | a0001c0001t0001g0126 a0001c0001t0001g0134 a0001c0001t0001g0140 others(2): Show |
5 | HG01099.hp2 HG01109.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.635-16022G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38713534 | |||||||
| chr2:38713545 | G | C | 1 | a0001c0001t0032g0319 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.635-16011G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38713545 | |||||||
| chr2:38713626 | A | G | 4 | a0001c0001t0003g0302 a0001c0001t0003g0305 a0001c0001t0019g0304 others(1): Show |
4 | HG01106.hp1 HG01891.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.635-15930A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38713626 | |||||||
| chr2:38713636 | G | C | 7 | a0001c0001t0031g0253 a0002c0002t0004g0314 a0002c0002t0004g0316 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.635-15920G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38713636 | |||||||
| chr2:38713904 | CA | C | 216 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(213): Show |
220 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.635-15635delA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38713904 | ||||||
| chr2:38713904 | CAA | C | 68 | a0001c0001t0001g0014 a0001c0001t0001g0064 a0001c0001t0001g0094 others(65): Show |
69 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.635-15636_635-1563 others(6): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38713904 | ||||||
| chr2:38713906 | A | C | 4 | a0001c0001t0003g0302 a0001c0001t0003g0305 a0001c0001t0019g0304 others(1): Show |
4 | HG01106.hp1 HG01891.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.635-15650A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38713906 | |||||||
| chr2:38714018 | T | TA | 7 | a0001c0001t0002g0307 a0001c0001t0002g0310 a0001c0001t0002g0311 others(4): Show |
7 | HG02258.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.635-15528dupA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38714018 | ||||||
| chr2:38714069 | G | C | 1 | a0001c0001t0001g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.635-15487G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38714069 | |||||||
| chr2:38714239 | G | A | 2 | a0001c0001t0032g0319 a0002c0002t0006g0059 |
2 | HG02723.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.635-15317G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38714239 | |||||||
| chr2:38714262 | G | A | 1 | a0001c0001t0020g0076 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.635-15294G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38714262 | |||||||
| chr2:38714406 | G | C | 1 | a0001c0001t0007g0096 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.635-15150G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38714406 | |||||||
| chr2:38714504 | C | T | 3 | a0001c0001t0003g0302 a0001c0001t0003g0305 a0001c0001t0028g0303 |
3 | HG01891.hp1 HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.635-15052C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38714504 | |||||||
| chr2:38714694 | A | C | 1 | a0001c0003t0005g0218 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.635-14862A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38714694 | |||||||
| chr2:38714794 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.635-14762C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38714794 | |||||||
| chr2:38714922 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.635-14634G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38714922 | |||||||
| chr2:38715444 | T | C | 5 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0131 others(2): Show |
5 | HG01496.hp2 HG02717.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.635-14112T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38715444 | |||||||
| chr2:38715530 | T | C | 2 | a0002c0002t0001g0276 a0002c0002t0001g0287 |
2 | NA18972.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.635-14026T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38715530 | |||||||
| chr2:38715713 | G | A | 1 | a0001c0003t0005g0218 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.635-13843G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38715713 | |||||||
| chr2:38715787 | T | A | 48 | a0001c0001t0001g0047 a0001c0001t0002g0002 a0001c0001t0002g0003 others(45): Show |
50 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.635-13769T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38715787 | |||||||
| chr2:38715882 | G | C | 206 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(203): Show |
208 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.635-13674G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38715882 | |||||||
| chr2:38715987 | T | C | 1 | a0002c0002t0001g0301 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.635-13569T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38715987 | |||||||
| chr2:38716139 | A | T | 11 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0004g0007 others(8): Show |
11 | HG02015.hp1 HG04115.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.635-13417A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38716139 | |||||||
| chr2:38716208 | C | A | 1 | a0001c0001t0002g0200 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.635-13348C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38716208 | |||||||
| chr2:38716257 | CGT | C | 3 | a0002c0002t0014g0151 a0002c0002t0014g0152 a0002c0002t0018g0012 |
3 | HG02895.hp2 HG02897.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.635-13296_635-1329 others(6): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38716257 | ||||||
| chr2:38716434 | G | A | 1 | a0002c0002t0001g0293 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.635-13122G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38716434 | |||||||
| chr2:38716443 | G | A | 3 | a0001c0001t0008g0010 a0001c0001t0008g0136 a0001c0001t0008g0228 |
3 | HG00738.hp1 HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.635-13113G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38716443 | |||||||
| chr2:38716462 | T | G | 1 | a0001c0001t0001g0128 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.635-13094T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38716462 | |||||||
| chr2:38716467 | G | A | 310 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(307): Show |
315 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.635-13089G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38716467 | |||||||
| chr2:38716664 | T | C | 1 | a0002c0002t0012g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.635-12892T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38716664 | |||||||
| chr2:38716800 | C | T | 11 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0004g0007 others(8): Show |
11 | HG02015.hp1 HG04115.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.635-12756C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38716800 | |||||||
| chr2:38716921 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0106 |
2 | HG03704.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.635-12635G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38716921 | |||||||
| chr2:38717064 | A | C | 1 | a0001c0001t0001g0082 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.635-12492A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38717064 | |||||||
| chr2:38717111 | G | A | 15 | a0001c0001t0005g0116 a0001c0001t0005g0205 a0001c0001t0033g0213 others(12): Show |
15 | HG01243.hp1 HG01361.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.635-12445G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38717111 | |||||||
| chr2:38717122 | T | G | 1 | a0001c0001t0019g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.635-12434T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38717122 | |||||||
| chr2:38717133 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.635-12423C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38717133 | |||||||
| chr2:38717185 | G | A | 1 | a0002c0002t0021g0185 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.635-12371G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38717185 | |||||||
| chr2:38717253 | GA | G | 15 | a0001c0001t0003g0302 a0001c0001t0003g0305 a0001c0001t0028g0303 others(12): Show |
16 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.635-12290delA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38717253 | ||||||
| chr2:38717306 | A | AGT | 36 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0084 others(33): Show |
36 | HG00280.hp1 HG00597.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.635-12211_635-1221 others(6): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38717306 | ||||||
| chr2:38717306 | A | AGTGT | 13 | a0001c0001t0001g0103 a0001c0001t0001g0153 a0001c0001t0001g0154 others(10): Show |
13 | HG01243.hp1 HG02523.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.635-12213_635-1221 others(8): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38717306 | ||||||
| chr2:38717306 | AGT | A | 60 | a0001c0001t0001g0013 a0001c0001t0001g0067 a0001c0001t0001g0071 others(57): Show |
61 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.635-12211_635-1221 others(6): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38717306 | ||||||
| chr2:38717306 | AGTGT | A | 15 | a0001c0001t0001g0135 a0001c0001t0001g0141 a0001c0001t0001g0142 others(12): Show |
15 | HG00558.hp1 HG01071.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.635-12213_635-1221 others(8): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38717306 | ||||||
| chr2:38717306 | AGTGTGT | A | 29 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0126 others(26): Show |
29 | HG01099.hp2 HG01109.hp1 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.635-12215_635-1221 others(10): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38717306 | ||||||
| chr2:38717306 | AGTGTGTG others(1): Show |
A | 47 | a0001c0001t0001g0128 a0001c0001t0002g0002 a0001c0001t0002g0003 others(44): Show |
49 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.635-12217_635-1221 others(12): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38717306 | ||||||
| chr2:38717306 | AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0001g0249 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.635-12219_635-1221 others(14): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38717306 | ||||||
| chr2:38717306 | AGTGTGTG others(5): Show |
A | 3 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0034 |
3 | HG01099.hp1 HG01516.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.635-12221_635-1221 others(16): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38717306 | ||||||
| chr2:38717306 | AGTGTGTG others(7): Show |
A | 1 | a0004c0005t0002g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.635-12223_635-1221 others(18): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38717306 | ||||||
| chr2:38717306 | AGTGTGTG others(19): Show |
A | 1 | a0001c0001t0003g0194 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.635-12235_635-1221 others(30): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38717306 | ||||||
| chr2:38717310 | T | A | 2 | a0001c0001t0019g0304 a0002c0002t0013g0209 |
2 | HG01106.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.635-12246T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38717310 | |||||||
| chr2:38717363 | G | A | 194 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(191): Show |
196 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.635-12193G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38717363 | |||||||
| chr2:38717377 | T | C | 195 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(192): Show |
197 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.635-12179T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38717377 | |||||||
| chr2:38717572 | G | A | 194 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(191): Show |
196 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.635-11984G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38717572 | |||||||
| chr2:38717641 | C | G | 3 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0004c0005t0002g0125 |
3 | HG02280.hp1 HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.635-11915C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38717641 | |||||||
| chr2:38717677 | A | G | 1 | a0002c0002t0012g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.635-11879A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38717677 | |||||||
| chr2:38717695 | CTGGCCTT others(2226): Show |
C | 11 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0004g0007 others(8): Show |
11 | HG02015.hp1 HG04115.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.635-11855_635-9623 others(3): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38717695 | ||||||
| chr2:38717715 | T | G | 1 | a0002c0002t0001g0259 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.635-11841T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38717715 | |||||||
| chr2:38717811 | G | C | 1 | a0002c0002t0001g0293 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.635-11745G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38717811 | |||||||
| chr2:38717866 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.635-11690G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38717866 | |||||||
| chr2:38717914 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.635-11642A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38717914 | |||||||
| chr2:38718057 | G | T | 1 | a0002c0002t0001g0275 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.635-11499G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38718057 | |||||||
| chr2:38718087 | T | C | 3 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0004c0005t0002g0125 |
3 | HG02280.hp1 HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.635-11469T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38718087 | |||||||
| chr2:38718196 | C | CT | 9 | a0001c0001t0001g0122 a0001c0001t0003g0074 a0001c0001t0003g0075 others(6): Show |
9 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.635-11345dupT | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38718196 | ||||||
| chr2:38718196 | C | CTT | 184 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(181): Show |
186 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.635-11346_635-1134 others(6): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38718196 | ||||||
| chr2:38718196 | CT | C | 14 | a0001c0001t0005g0116 a0001c0001t0005g0205 a0001c0003t0005g0215 others(11): Show |
14 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.635-11345delT | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38718196 | ||||||
| chr2:38718241 | C | G | 1 | a0002c0002t0006g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.635-11315C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38718241 | |||||||
| chr2:38718321 | T | A | 196 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(193): Show |
198 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.635-11235T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38718321 | |||||||
| chr2:38718327 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.635-11229G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38718327 | |||||||
| chr2:38718559 | C | A | 193 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(190): Show |
195 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.635-10997C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38718559 | |||||||
| chr2:38718736 | T | C | 8 | a0001c0001t0013g0227 a0002c0002t0004g0314 a0002c0002t0004g0316 others(5): Show |
8 | HG02559.hp1 HG02572.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.635-10820T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38718736 | |||||||
| chr2:38718831 | A | C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG02523.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.635-10725A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38718831 | |||||||
| chr2:38718902 | T | C | 310 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(307): Show |
315 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.635-10654T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38718902 | |||||||
| chr2:38719116 | C | T | 1 | a0002c0002t0013g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.635-10440C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38719116 | |||||||
| chr2:38719146 | C | T | 1 | a0001c0001t0013g0073 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.635-10410C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38719146 | |||||||
| chr2:38719237 | C | T | 7 | a0002c0002t0006g0232 a0002c0002t0009g0001 a0002c0002t0009g0231 others(4): Show |
8 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.635-10319C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38719237 | |||||||
| chr2:38719253 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.635-10303C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38719253 | |||||||
| chr2:38719254 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0118 |
2 | HG00597.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.635-10302G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38719254 | |||||||
| chr2:38719309 | A | C | 6 | a0001c0001t0005g0205 a0001c0003t0005g0219 a0001c0003t0005g0223 others(3): Show |
6 | HG02572.hp2 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.635-10247A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38719309 | |||||||
| chr2:38719375 | C | G | 10 | a0002c0002t0006g0232 a0002c0002t0009g0001 a0002c0002t0009g0231 others(7): Show |
11 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.635-10181C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38719375 | |||||||
| chr2:38719400 | T | A | 1 | a0002c0002t0013g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.635-10156T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38719400 | |||||||
| chr2:38719462 | T | G | 2 | a0001c0001t0007g0092 a0001c0001t0013g0073 |
2 | HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.635-10094T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38719462 | |||||||
| chr2:38719468 | CA | C | 267 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(264): Show |
271 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.635-10074delA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38719468 | ||||||
| chr2:38719693 | C | T | 1 | a0001c0001t0003g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.635-9863C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38719693 | |||||||
| chr2:38719735 | T | C | 1 | a0001c0001t0013g0227 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.635-9821T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38719735 | |||||||
| chr2:38719774 | C | CA | 11 | a0001c0001t0001g0013 a0001c0001t0001g0047 a0001c0001t0001g0067 others(8): Show |
11 | HG01258.hp2 HG02738.hp2 HG03017.hp1 others(8): Show |
intron_variant | MODIFIER | c.635-9765dupA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38719774 | ||||||
| chr2:38719774 | C | CAA | 183 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(180): Show |
185 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.635-9766_635-9765d others(4): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38719774 | ||||||
| chr2:38719774 | C | CAAA | 9 | a0001c0001t0001g0135 a0001c0001t0001g0170 a0001c0001t0001g0179 others(6): Show |
9 | HG01978.hp2 HG02280.hp2 HG03239.hp2 others(6): Show |
intron_variant | MODIFIER | c.635-9767_635-9765d others(5): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38719774 | ||||||
| chr2:38719831 | C | T | 1 | a0002c0002t0001g0291 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.635-9725C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38719831 | |||||||
| chr2:38719867 | A | G | 1 | a0001c0001t0032g0319 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.635-9689A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38719867 | |||||||
| chr2:38719927 | T | G | 1 | a0001c0001t0001g0250 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.635-9629T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38719927 | |||||||
| chr2:38719939 | C | T | 1 | a0001c0001t0031g0253 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.635-9617C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38719939 | |||||||
| chr2:38720010 | TG | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0106 a0001c0001t0001g0108 others(1): Show |
4 | HG00597.hp2 HG03704.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.635-9543delG | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38720010 | ||||||
| chr2:38720045 | A | T | 17 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0036 others(14): Show |
17 | HG02015.hp1 HG02647.hp1 HG03453.hp2 others(14): Show |
intron_variant | MODIFIER | c.635-9511A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38720045 | |||||||
| chr2:38720414 | TA | T | 162 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 others(159): Show |
163 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.635-9117delA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38720414 | ||||||
| chr2:38720414 | TAA | T | 97 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(94): Show |
100 | HG00639.hp2 HG00673.hp2 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.635-9118_635-9117d others(4): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38720414 | ||||||
| chr2:38720414 | TAAA | T | 11 | a0001c0001t0002g0034 a0001c0001t0004g0007 a0001c0001t0004g0008 others(8): Show |
11 | HG00280.hp2 HG01516.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.635-9119_635-9117d others(5): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38720414 | ||||||
| chr2:38720415 | A | T | 29 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0067 others(26): Show |
30 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.635-9141A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38720415 | |||||||
| chr2:38720416 | A | T | 151 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 others(148): Show |
152 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.635-9140A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38720416 | |||||||
| chr2:38720417 | A | T | 15 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(12): Show |
15 | HG01258.hp1 HG01346.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.635-9139A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38720417 | |||||||
| chr2:38720536 | G | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0004g0007 others(8): Show |
11 | HG02015.hp1 HG04115.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.635-9020G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38720536 | |||||||
| chr2:38720880 | G | A | 44 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0018 others(41): Show |
46 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.635-8676G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38720880 | |||||||
| chr2:38720925 | T | C | 5 | a0001c0003t0005g0215 a0001c0003t0005g0216 a0001c0003t0005g0217 others(2): Show |
5 | HG01243.hp1 HG02818.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.635-8631T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38720925 | |||||||
| chr2:38721028 | T | C | 1 | a0001c0001t0006g0162 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.635-8528T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38721028 | |||||||
| chr2:38721291 | A | C | 1 | a0001c0001t0002g0022 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.635-8265A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38721291 | |||||||
| chr2:38721297 | G | C | 2 | a0002c0002t0006g0059 a0002c0002t0013g0209 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.635-8259G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38721297 | |||||||
| chr2:38721551 | T | A | 52 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0018 others(49): Show |
54 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.635-8005T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38721551 | |||||||
| chr2:38721588 | C | T | 284 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(281): Show |
289 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.635-7968C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38721588 | |||||||
| chr2:38721644 | G | C | 2 | a0001c0001t0003g0302 a0001c0001t0028g0303 |
2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.635-7912G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38721644 | |||||||
| chr2:38721718 | G | T | 98 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(95): Show |
99 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.635-7838G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38721718 | |||||||
| chr2:38721807 | C | T | 193 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(190): Show |
195 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.635-7749C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38721807 | |||||||
| chr2:38721946 | A | G | 4 | a0001c0001t0003g0302 a0001c0001t0003g0305 a0001c0001t0019g0304 others(1): Show |
4 | HG01106.hp1 HG01891.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.635-7610A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38721946 | |||||||
| chr2:38722030 | T | TC | 17 | a0001c0001t0001g0064 a0001c0001t0001g0086 a0001c0001t0001g0115 others(14): Show |
17 | HG00609.hp2 HG01516.hp2 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.635-7517dupC | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38722030 | ||||||
| chr2:38722030 | TCCCCCCC others(5): Show |
T | 1 | a0001c0001t0001g0069 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.635-7516_635-7505d others(14): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38722030 | ||||||
| chr2:38722038 | C | CCCA | 27 | a0001c0001t0001g0011 a0001c0001t0001g0061 a0001c0001t0001g0077 others(24): Show |
27 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.635-7517_635-7516i others(5): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38722038 | ||||||
| chr2:38722038 | C | CCCCA | 18 | a0001c0001t0001g0062 a0001c0001t0001g0082 a0001c0001t0001g0093 others(15): Show |
18 | HG00642.hp1 HG01081.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.635-7517_635-7516i others(6): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38722038 | ||||||
| chr2:38722038 | CCA | C | 38 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0018 others(35): Show |
40 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.635-7516_635-7515d others(4): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38722038 | ||||||
| chr2:38722039 | C | CCA | 78 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0013 others(75): Show |
80 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.635-7517_635-7516i others(4): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38722039 | |||||||
| chr2:38722039 | C | CCCA | 36 | a0001c0001t0001g0067 a0001c0001t0001g0078 a0001c0001t0001g0080 others(33): Show |
36 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.635-7517_635-7516i others(5): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38722039 | |||||||
| chr2:38722039 | CA | C | 11 | a0001c0001t0001g0006 a0001c0001t0002g0026 a0001c0001t0002g0029 others(8): Show |
11 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.635-7516delA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38722039 | |||||||
| chr2:38722040 | A | AC | 14 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0003g0052 others(11): Show |
14 | HG01167.hp2 HG01169.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.635-7504dupC | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38722040 | ||||||
| chr2:38722040 | A | C | 175 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(172): Show |
177 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.635-7516A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38722040 | |||||||
| chr2:38722040 | ACC | A | 15 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0004g0007 others(12): Show |
15 | HG02055.hp2 HG02145.hp1 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.635-7505_635-7504d others(4): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38722040 | ||||||
| chr2:38722040 | ACCC | A | 20 | a0001c0001t0001g0036 a0001c0001t0004g0015 a0001c0001t0004g0016 others(17): Show |
21 | HG01884.hp2 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.635-7506_635-7504d others(5): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38722040 | ||||||
| chr2:38722041 | C | A | 3 | a0001c0001t0006g0159 a0001c0001t0008g0091 a0001c0001t0008g0228 |
3 | HG00738.hp1 NA18951.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.635-7515C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38722041 | |||||||
| chr2:38722042 | C | A | 8 | a0001c0001t0001g0006 a0001c0001t0002g0029 a0001c0001t0002g0041 others(5): Show |
8 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.635-7514C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38722042 | |||||||
| chr2:38722043 | C | A | 45 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0018 others(42): Show |
47 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.635-7513C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38722043 | |||||||
| chr2:38722049 | C | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG02523.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.635-7507C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38722049 | |||||||
| chr2:38722054 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.635-7502C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38722054 | |||||||
| chr2:38722090 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0150 |
2 | HG02129.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.635-7466C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38722090 | |||||||
| chr2:38722116 | T | G | 1 | a0002c0002t0001g0264 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.635-7440T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38722116 | |||||||
| chr2:38722123 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.635-7433G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38722123 | |||||||
| chr2:38722133 | C | G | 206 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(203): Show |
208 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.635-7423C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38722133 | |||||||
| chr2:38722204 | T | C | 11 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0004g0007 others(8): Show |
11 | HG02015.hp1 HG04115.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.635-7352T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38722204 | |||||||
| chr2:38722353 | G | C | 1 | a0002c0002t0012g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.635-7203G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38722353 | |||||||
| chr2:38722412 | G | A | 1 | a0001c0001t0019g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.635-7144G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38722412 | |||||||
| chr2:38722639 | T | G | 1 | a0002c0002t0012g0234 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.635-6917T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38722639 | |||||||
| chr2:38722642 | C | T | 1 | a0002c0002t0001g0266 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.635-6914C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38722642 | |||||||
| chr2:38722839 | A | T | 11 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0004g0007 others(8): Show |
11 | HG02015.hp1 HG04115.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.635-6717A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38722839 | |||||||
| chr2:38722866 | T | A | 10 | a0002c0002t0006g0232 a0002c0002t0009g0001 a0002c0002t0009g0231 others(7): Show |
11 | HG01496.hp2 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.635-6690T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38722866 | |||||||
| chr2:38722925 | G | A | 1 | a0002c0002t0006g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.635-6631G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38722925 | |||||||
| chr2:38723006 | G | A | 2 | a0002c0002t0006g0059 a0002c0002t0013g0209 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.635-6550G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38723006 | |||||||
| chr2:38723118 | C | T | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 |
3 | HG01258.hp1 HG01346.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.635-6438C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38723118 | |||||||
| chr2:38723152 | G | T | 2 | a0002c0002t0006g0059 a0002c0002t0013g0209 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.635-6404G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38723152 | |||||||
| chr2:38723380 | C | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0004g0007 others(8): Show |
11 | HG02015.hp1 HG04115.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.635-6176C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38723380 | |||||||
| chr2:38723498 | A | C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG02523.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.635-6058A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38723498 | |||||||
| chr2:38723524 | C | G | 1 | a0001c0001t0031g0253 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.635-6032C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38723524 | |||||||
| chr2:38723527 | G | A | 3 | a0001c0001t0004g0008 a0001c0001t0004g0046 a0001c0001t0004g0049 |
3 | NA18963.hp1 NA19010.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.635-6029G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38723527 | |||||||
| chr2:38723531 | G | C | 27 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0153 others(24): Show |
27 | HG01243.hp1 HG02015.hp1 HG02523.hp2 others(24): Show |
intron_variant | MODIFIER | c.635-6025G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38723531 | |||||||
| chr2:38723537 | G | A | 2 | a0002c0002t0001g0258 a0002c0002t0010g0187 |
2 | NA18945.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.635-6019G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38723537 | |||||||
| chr2:38723558 | G | A | 4 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0006g0051 others(1): Show |
4 | HG02109.hp2 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.635-5998G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38723558 | |||||||
| chr2:38723802 | CA | C | 299 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(296): Show |
304 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.635-5744delA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38723802 | ||||||
| chr2:38723882 | A | G | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG02523.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.635-5674A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38723882 | |||||||
| chr2:38723932 | T | G | 195 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(192): Show |
197 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.635-5624T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38723932 | |||||||
| chr2:38723938 | G | A | 3 | a0002c0002t0004g0314 a0002c0002t0004g0316 a0002c0002t0004g0317 |
3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.635-5618G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38723938 | |||||||
| chr2:38724396 | A | G | 14 | a0001c0001t0005g0116 a0001c0001t0005g0205 a0001c0003t0005g0215 others(11): Show |
14 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.635-5160A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38724396 | |||||||
| chr2:38724524 | T | C | 207 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(204): Show |
210 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.635-5032T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38724524 | |||||||
| chr2:38724691 | AG | A | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 |
3 | HG01258.hp1 HG01346.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.635-4862delG | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38724691 | ||||||
| chr2:38724795 | G | C | 7 | a0001c0001t0013g0227 a0002c0002t0004g0314 a0002c0002t0004g0316 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.635-4761G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38724795 | |||||||
| chr2:38724906 | G | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0067 |
2 | HG01258.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.635-4650G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38724906 | |||||||
| chr2:38724932 | T | C | 12 | a0001c0001t0001g0036 a0001c0001t0004g0007 a0001c0001t0004g0008 others(9): Show |
12 | HG00423.hp1 HG02015.hp1 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.635-4624T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38724932 | |||||||
| chr2:38724939 | T | C | 4 | a0001c0003t0005g0223 a0001c0003t0005g0224 a0001c0003t0005g0225 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.635-4617T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38724939 | |||||||
| chr2:38725097 | G | A | 1 | a0002c0002t0001g0210 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.635-4459G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38725097 | |||||||
| chr2:38725525 | G | T | 2 | a0002c0002t0003g0299 a0002c0002t0003g0300 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.635-4031G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38725525 | |||||||
| chr2:38725531 | C | T | 3 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0001c0001t0002g0200 |
3 | HG00735.hp1 HG01168.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.635-4025C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38725531 | |||||||
| chr2:38725547 | C | CAT | 52 | a0001c0001t0001g0047 a0001c0001t0002g0002 a0001c0001t0002g0003 others(49): Show |
54 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.635-4007_635-4006d others(4): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38725547 | ||||||
| chr2:38725549 | T | TAC | 55 | a0001c0001t0003g0052 a0001c0001t0003g0054 a0001c0001t0003g0055 others(52): Show |
55 | HG00423.hp1 HG01106.hp1 HG01167.hp2 others(52): Show |
intron_variant | MODIFIER | c.635-3992_635-3991d others(4): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38725549 | ||||||
| chr2:38725565 | C | T | 1 | a0002c0002t0001g0265 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.635-3991C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38725565 | |||||||
| chr2:38725566 | G | A | 1 | a0002c0002t0012g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.635-3990G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38725566 | |||||||
| chr2:38725648 | C | G | 1 | a0002c0002t0013g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.635-3908C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38725648 | |||||||
| chr2:38725788 | C | T | 1 | a0004c0005t0002g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.635-3768C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38725788 | |||||||
| chr2:38726154 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.635-3402T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38726154 | |||||||
| chr2:38726212 | CTTTATTT others(7): Show |
C | 93 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0018 others(90): Show |
95 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.635-3326_635-3313d others(16): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38726212 | ||||||
| chr2:38726217 | TTTTTTTT others(6): Show |
T | 3 | a0001c0001t0002g0188 a0001c0003t0005g0226 a0002c0002t0012g0321 |
3 | HG01192.hp1 HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.635-3326_635-3314d others(15): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38726217 | ||||||
| chr2:38726223 | T | A | 209 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(206): Show |
212 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.635-3333T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38726223 | |||||||
| chr2:38726224 | T | A | 4 | a0001c0001t0001g0085 a0001c0001t0001g0119 a0002c0002t0001g0301 others(1): Show |
4 | HG00544.hp2 HG01496.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.635-3332T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38726224 | |||||||
| chr2:38726228 | TTA | T | 209 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(206): Show |
212 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.635-3326_635-3325d others(4): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38726228 | ||||||
| chr2:38726230 | A | T | 1 | a0001c0001t0019g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.635-3326A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38726230 | |||||||
| chr2:38726231 | T | A | 208 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(205): Show |
211 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.635-3325T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38726231 | |||||||
| chr2:38726236 | T | A | 1 | a0001c0001t0001g0093 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.635-3320T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38726236 | |||||||
| chr2:38726268 | C | A | 1 | a0002c0002t0012g0234 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.635-3288C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38726268 | |||||||
| chr2:38726417 | G | A | 14 | a0001c0001t0005g0116 a0001c0001t0005g0205 a0001c0003t0005g0215 others(11): Show |
14 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.635-3139G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38726417 | |||||||
| chr2:38726473 | G | A | 11 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0015 others(8): Show |
11 | HG00423.hp1 HG03927.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.635-3083G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38726473 | |||||||
| chr2:38726478 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.635-3078G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38726478 | |||||||
| chr2:38726545 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0106 |
2 | HG03704.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.635-3011C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38726545 | |||||||
| chr2:38726632 | G | A | 1 | a0001c0001t0011g0248 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.635-2924G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38726632 | |||||||
| chr2:38726696 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.635-2860G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38726696 | |||||||
| chr2:38726790 | G | C | 1 | a0001c0001t0013g0227 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.635-2766G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38726790 | |||||||
| chr2:38726811 | G | A | 1 | a0001c0001t0003g0164 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.635-2745G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38726811 | |||||||
| chr2:38726850 | C | G | 1 | a0002c0002t0001g0281 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.635-2706C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38726850 | |||||||
| chr2:38726867 | G | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0166 |
2 | NA18986.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.635-2689G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38726867 | |||||||
| chr2:38726877 | C | A | 51 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0018 others(48): Show |
53 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.635-2679C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38726877 | |||||||
| chr2:38726983 | A | AGGT | 4 | a0001c0001t0032g0319 a0002c0002t0006g0059 a0002c0002t0012g0321 others(1): Show |
4 | HG02723.hp2 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.635-2570_635-2568d others(5): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38726983 | ||||||
| chr2:38726990 | T | G | 1 | a0001c0001t0031g0253 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.635-2566T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38726990 | |||||||
| chr2:38727027 | C | A | 1 | a0001c0001t0031g0253 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.635-2529C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38727027 | |||||||
| chr2:38727043 | C | T | 14 | a0001c0001t0005g0116 a0001c0001t0005g0205 a0001c0003t0005g0215 others(11): Show |
14 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.635-2513C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38727043 | |||||||
| chr2:38727151 | G | T | 1 | a0001c0001t0001g0242 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.635-2405G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38727151 | |||||||
| chr2:38727176 | A | C | 66 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0018 others(63): Show |
68 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.635-2380A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38727176 | |||||||
| chr2:38727210 | C | T | 1 | a0001c0001t0031g0253 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.635-2346C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38727210 | |||||||
| chr2:38727218 | GA | G | 95 | a0001c0001t0001g0036 a0001c0001t0002g0002 a0001c0001t0002g0003 others(92): Show |
97 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.635-2321delA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38727218 | ||||||
| chr2:38727277 | A | G | 213 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(210): Show |
216 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.635-2279A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38727277 | |||||||
| chr2:38727458 | G | A | 7 | a0001c0001t0013g0227 a0002c0002t0004g0314 a0002c0002t0004g0316 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.635-2098G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38727458 | |||||||
| chr2:38727477 | C | T | 14 | a0001c0001t0005g0116 a0001c0001t0005g0205 a0001c0003t0005g0215 others(11): Show |
14 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.635-2079C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38727477 | |||||||
| chr2:38727620 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.635-1936G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38727620 | |||||||
| chr2:38727723 | T | G | 51 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0018 others(48): Show |
53 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.635-1833T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38727723 | |||||||
| chr2:38727724 | C | CA | 21 | a0001c0001t0001g0118 a0001c0001t0003g0052 a0001c0001t0004g0007 others(18): Show |
21 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.635-1816dupA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38727724 | ||||||
| chr2:38727724 | CA | C | 7 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0296 others(4): Show |
7 | HG01168.hp2 HG01515.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.635-1816delA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38727724 | ||||||
| chr2:38727816 | C | T | 2 | a0001c0001t0032g0319 a0002c0002t0012g0321 |
2 | HG02723.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.635-1740C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38727816 | |||||||
| chr2:38727902 | T | C | 4 | a0002c0002t0014g0151 a0002c0002t0014g0152 a0002c0002t0018g0012 others(1): Show |
4 | HG02818.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.635-1654T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38727902 | |||||||
| chr2:38727973 | G | A | 4 | a0002c0002t0001g0260 a0002c0002t0001g0261 a0002c0002t0001g0262 others(1): Show |
4 | NA18943.hp2 NA18953.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.635-1583G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38727973 | |||||||
| chr2:38727987 | A | G | 196 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(193): Show |
199 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.635-1569A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38727987 | |||||||
| chr2:38728011 | G | T | 14 | a0001c0001t0005g0116 a0001c0001t0005g0205 a0001c0003t0005g0215 others(11): Show |
14 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.635-1545G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38728011 | |||||||
| chr2:38728026 | C | T | 3 | a0001c0001t0001g0081 a0001c0001t0001g0143 a0001c0001t0008g0091 |
3 | NA18951.hp2 NA18965.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.635-1530C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38728026 | |||||||
| chr2:38728116 | A | G | 196 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(193): Show |
199 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.635-1440A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38728116 | |||||||
| chr2:38728119 | A | C | 292 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(289): Show |
297 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(294): Show |
intron_variant | MODIFIER | c.635-1437A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38728119 | |||||||
| chr2:38728297 | G | A | 1 | a0001c0001t0005g0116 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.635-1259G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38728297 | |||||||
| chr2:38728308 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.635-1248C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38728308 | |||||||
| chr2:38728309 | A | G | 195 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(192): Show |
198 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.635-1247A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38728309 | |||||||
| chr2:38728326 | A | G | 196 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(193): Show |
199 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.635-1230A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38728326 | |||||||
| chr2:38728385 | T | C | 5 | a0001c0001t0001g0117 a0001c0001t0001g0126 a0001c0001t0001g0134 others(2): Show |
5 | HG01099.hp2 HG01109.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.635-1171T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38728385 | |||||||
| chr2:38728392 | C | CA | 193 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(190): Show |
196 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.635-1152dupA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38728392 | ||||||
| chr2:38728402 | A | AC | 4 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0006g0051 others(1): Show |
4 | HG02109.hp2 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.635-1154_635-1153i others(3): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38728402 | |||||||
| chr2:38728405 | C | A | 1 | a0001c0001t0001g0165 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.635-1151C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38728405 | |||||||
| chr2:38728405 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.635-1151C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38728405 | |||||||
| chr2:38728406 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.635-1150T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38728406 | |||||||
| chr2:38728523 | G | C | 72 | a0001c0001t0001g0047 a0001c0001t0002g0002 a0001c0001t0002g0003 others(69): Show |
74 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.635-1033G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38728523 | |||||||
| chr2:38728620 | G | A | 25 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0015 others(22): Show |
25 | HG00423.hp1 HG01243.hp1 HG02572.hp2 others(22): Show |
intron_variant | MODIFIER | c.635-936G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38728620 | |||||||
| chr2:38728635 | A | T | 1 | a0001c0001t0031g0253 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.635-921A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38728635 | |||||||
| chr2:38728642 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0106 |
2 | HG03704.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.635-914G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38728642 | |||||||
| chr2:38728686 | A | AAAAACAA others(3): Show |
188 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(185): Show |
191 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.635-850_635-841dup others(10): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38728686 | ||||||
| chr2:38728686 | A | AAAAACAA others(8): Show |
6 | a0001c0001t0001g0071 a0001c0001t0001g0103 a0001c0001t0001g0243 others(3): Show |
6 | HG02451.hp2 HG02647.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.635-855_635-841dup others(15): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38728686 | ||||||
| chr2:38728723 | C | T | 1 | a0001c0001t0017g0042 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.635-833C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38728723 | |||||||
| chr2:38728724 | G | A | 196 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(193): Show |
199 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.635-832G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38728724 | |||||||
| chr2:38728835 | A | G | 196 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(193): Show |
199 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.635-721A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38728835 | |||||||
| chr2:38728860 | C | CT | 196 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(193): Show |
199 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.635-695dupT | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38728860 | ||||||
| chr2:38728934 | C | T | 195 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(192): Show |
198 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.635-622C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38728934 | |||||||
| chr2:38729078 | C | T | 195 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(192): Show |
198 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.635-478C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38729078 | |||||||
| chr2:38729177 | C | T | 1 | a0001c0001t0006g0051 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.635-379C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38729177 | |||||||
| chr2:38729257 | G | T | 196 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(193): Show |
199 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.635-299G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38729257 | |||||||
| chr2:38729321 | G | A | 51 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0018 others(48): Show |
53 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.635-235G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38729321 | |||||||
| chr2:38729325 | C | A | 4 | a0002c0002t0001g0260 a0002c0002t0001g0261 a0002c0002t0001g0262 others(1): Show |
4 | NA18943.hp2 NA18953.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.635-231C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38729325 | |||||||
| chr2:38729362 | C | CATTT | 196 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(193): Show |
199 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.635-177_635-174dup others(4): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38729362 | ||||||
| chr2:38729805 | A | G | 195 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(192): Show |
198 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.776+108A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 5/6 | chr2 | 38729805 | |||||||
| chr2:38729852 | AG | A | 4 | a0002c0002t0014g0151 a0002c0002t0014g0152 a0002c0002t0018g0012 others(1): Show |
4 | HG02818.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.776+157delG | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 38729852 | ||||||
| chr2:38729890 | C | T | 4 | a0001c0001t0032g0319 a0002c0002t0006g0059 a0002c0002t0012g0321 others(1): Show |
4 | HG02723.hp2 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.776+193C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 5/6 | chr2 | 38729890 | |||||||
| chr2:38729899 | CT | C | 4 | a0002c0002t0014g0151 a0002c0002t0014g0152 a0002c0002t0018g0012 others(1): Show |
4 | HG02818.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.776+203delT | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 5/6 | chr2 | 38729899 | |||||||
| chr2:38729921 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.776+224G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 5/6 | chr2 | 38729921 | |||||||
| chr2:38729993 | C | G | 1 | a0002c0002t0001g0282 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.776+296C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 5/6 | chr2 | 38729993 | |||||||
| chr2:38730289 | C | T | 1 | a0001c0001t0006g0206 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.776+592C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 5/6 | chr2 | 38730289 | |||||||
| chr2:38730308 | C | T | 195 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(192): Show |
198 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.776+611C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 5/6 | chr2 | 38730308 | |||||||
| chr2:38730404 | T | A | 1 | a0001c0001t0024g0066 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.776+707T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 5/6 | chr2 | 38730404 | |||||||
| chr2:38730517 | G | A | 6 | a0002c0002t0004g0314 a0002c0002t0004g0316 a0002c0002t0004g0317 others(3): Show |
6 | HG02559.hp1 HG02572.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.776+820G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 5/6 | chr2 | 38730517 | |||||||
| chr2:38730558 | C | T | 195 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(192): Show |
198 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.776+861C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 5/6 | chr2 | 38730558 | |||||||
| chr2:38730877 | C | T | 2 | a0001c0001t0003g0057 a0004c0005t0002g0125 |
2 | HG01358.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.777-858C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 5/6 | chr2 | 38730877 | |||||||
| chr2:38730907 | C | A | 1 | a0001c0001t0001g0163 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.777-828C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 5/6 | chr2 | 38730907 | |||||||
| chr2:38730920 | C | CA | 7 | a0001c0001t0003g0302 a0001c0001t0013g0227 a0001c0001t0028g0303 others(4): Show |
7 | HG02647.hp1 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.777-802dupA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 38730920 | ||||||
| chr2:38730920 | C | CAA | 62 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0018 others(59): Show |
64 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.777-803_777-802dup others(2): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 38730920 | ||||||
| chr2:38731032 | T | C | 16 | a0001c0001t0005g0116 a0001c0001t0005g0205 a0001c0001t0033g0213 others(13): Show |
16 | HG01243.hp1 HG01361.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.777-703T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 5/6 | chr2 | 38731032 | |||||||
| chr2:38731034 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.777-701G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 5/6 | chr2 | 38731034 | |||||||
| chr2:38731146 | T | G | 295 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(292): Show |
300 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(297): Show |
intron_variant | MODIFIER | c.777-589T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 5/6 | chr2 | 38731146 | |||||||
| chr2:38731396 | CAA | C | 33 | a0001c0001t0001g0112 a0001c0001t0001g0249 a0001c0001t0004g0007 others(30): Show |
33 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.777-317_777-316del others(2): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 38731396 | ||||||
| chr2:38731396 | CAAA | C | 184 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(181): Show |
187 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(184): Show |
intron_variant | MODIFIER | c.777-318_777-316del others(3): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 38731396 | ||||||
| chr2:38731396 | CAAAA | C | 6 | a0001c0001t0001g0153 a0001c0001t0001g0196 a0001c0001t0001g0243 others(3): Show |
6 | HG01515.hp2 HG01891.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.777-319_777-316del others(4): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 38731396 | ||||||
| chr2:38731396 | CAAAAAAA others(3): Show |
C | 65 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0018 others(62): Show |
67 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.777-325_777-316del others(10): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 38731396 | ||||||
| chr2:38731539 | G | C | 1 | a0002c0002t0018g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.777-196G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 5/6 | chr2 | 38731539 | |||||||
| chr2:38731588 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0067 |
2 | HG01258.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.777-147C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 5/6 | chr2 | 38731588 | |||||||
| chr2:38731970 | A | C | 1 | a0002c0002t0010g0187 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.951+61A>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | chr2 | 38731970 | |||||||
| chr2:38732040 | G | A | 2 | a0002c0002t0012g0233 a0002c0002t0012g0236 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.951+131G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | chr2 | 38732040 | |||||||
| chr2:38732098 | G | T | 1 | a0001c0001t0011g0248 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.951+189G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | chr2 | 38732098 | |||||||
| chr2:38732107 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.951+198G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | chr2 | 38732107 | |||||||
| chr2:38732125 | C | G | 1 | a0001c0001t0006g0051 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.951+216C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | chr2 | 38732125 | |||||||
| chr2:38732181 | C | A | 1 | a0001c0001t0002g0312 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.951+272C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | chr2 | 38732181 | |||||||
| chr2:38732285 | T | C | 197 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(194): Show |
200 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.951+376T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | chr2 | 38732285 | |||||||
| chr2:38732397 | A | T | 1 | a0001c0001t0001g0130 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.951+488A>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | chr2 | 38732397 | |||||||
| chr2:38732444 | C | G | 2 | a0001c0001t0001g0243 a0002c0002t0001g0274 |
2 | NA18948.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.951+535C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | chr2 | 38732444 | |||||||
| chr2:38732446 | G | T | 1 | a0001c0001t0001g0086 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.951+537G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | chr2 | 38732446 | |||||||
| chr2:38732477 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.951+568T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | chr2 | 38732477 | |||||||
| chr2:38732481 | T | C | 1 | a0001c0001t0031g0253 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.951+572T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | chr2 | 38732481 | |||||||
| chr2:38732888 | C | T | 1 | a0002c0002t0012g0234 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.952-600C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | chr2 | 38732888 | |||||||
| chr2:38732914 | G | A | 1 | a0004c0005t0002g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.952-574G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | chr2 | 38732914 | |||||||
| chr2:38732919 | T | TA | 12 | a0001c0001t0001g0122 a0001c0001t0001g0168 a0001c0001t0001g0170 others(9): Show |
12 | HG02074.hp1 HG02074.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.952-551dupA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 38732919 | ||||||
| chr2:38732919 | T | TAA | 17 | a0001c0001t0003g0305 a0001c0001t0005g0116 a0001c0001t0005g0205 others(14): Show |
17 | HG01106.hp1 HG01243.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.952-552_952-551dup others(2): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 38732919 | ||||||
| chr2:38733019 | G | A | 185 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(182): Show |
187 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.952-469G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | chr2 | 38733019 | |||||||
| chr2:38733029 | C | T | 13 | a0001c0001t0005g0205 a0001c0003t0005g0215 a0001c0003t0005g0216 others(10): Show |
13 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.952-459C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | chr2 | 38733029 | |||||||
| chr2:38733169 | T | C | 5 | a0001c0001t0003g0302 a0001c0001t0019g0304 a0001c0001t0028g0303 others(2): Show |
5 | HG01106.hp1 HG02647.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.952-319T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | chr2 | 38733169 | |||||||
| chr2:38733220 | CA | C | 198 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(195): Show |
201 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.952-251delA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 38733220 | ||||||
| chr2:38733220 | CAA | C | 67 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0018 others(64): Show |
69 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.952-252_952-251del others(2): Show |
GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 38733220 | ||||||
| chr2:38733237 | A | G | 1 | a0001c0001t0003g0164 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.952-251A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | chr2 | 38733237 | |||||||
| chr2:38733303 | A | G | 14 | a0001c0001t0003g0302 a0001c0001t0003g0305 a0001c0001t0019g0304 others(11): Show |
15 | HG01106.hp1 HG01496.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.952-185A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | chr2 | 38733303 | |||||||
| chr2:38733349 | A | G | 52 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0018 others(49): Show |
54 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.952-139A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | chr2 | 38733349 | |||||||
| chr2:38733371 | C | T | 1 | a0001c0001t0003g0052 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.952-117C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | chr2 | 38733371 | |||||||
| chr2:38733375 | A | G | 3 | a0001c0001t0032g0319 a0002c0002t0012g0234 a0002c0002t0012g0321 |
3 | HG02723.hp2 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.952-113A>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | chr2 | 38733375 | |||||||
| chr2:38733476 | T | TC | 6 | a0001c0001t0003g0305 a0001c0001t0019g0202 a0001c0001t0019g0304 others(3): Show |
6 | HG01106.hp1 HG01891.hp1 HG02723.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.952-8dupC | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 38733476 |