Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 342 | 245 | 62 | 50 | 97 | 7 | 27 | 64 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0002 | 0/0 | 342 | 80 | 29 | 8 | 29 | 1 | 13 | 24 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0003 | 0/0 | 342 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0004 | 0/0 | 342 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1029 | 233 | 51 | 49 | 97 | 7 | 27 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| c0002 | 0/0 | 1029 | 80 | 29 | 8 | 29 | 1 | 13 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| c0003 | 0/0 | 1029 | 12 | 11 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| c0004 | 0/0 | 1029 | 2 | 2 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| c0005 | 0/0 | 1029 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1251 | 156 | 15 | 27 | 89 | 3 | 22 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0002 | 0/1 | 1251 | 47 | 13 | 12 | 14 | 1 | 6 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0003 | 0/0 | 1250 | 22 | 9 | 8 | 0 | 2 | 3 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0004 | 0/0 | 1251 | 17 | 6 | 0 | 10 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0005 | 0/0 | 1247 | 13 | 12 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0006 | 0/0 | 1251 | 12 | 8 | 1 | 0 | 0 | 3 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0007 | 0/0 | 1252 | 5 | 2 | 1 | 2 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0008 | 0/0 | 1250 | 5 | 2 | 1 | 1 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0009 | 0/0 | 1251 | 5 | 5 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0010 | 0/0 | 1252 | 4 | 1 | 0 | 3 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0011 | 0/0 | 1251 | 4 | 0 | 0 | 4 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0012 | 0/0 | 1251 | 4 | 4 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0013 | 0/0 | 1251 | 3 | 3 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0014 | 0/0 | 1252 | 3 | 3 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0015 | 0/0 | 1251 | 3 | 2 | 0 | 0 | 1 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0016 | 0/0 | 1251 | 2 | 0 | 0 | 0 | 0 | 2 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0017 | 0/0 | 1251 | 2 | 0 | 0 | 0 | 1 | 1 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0018 | 0/0 | 1253 | 2 | 2 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0019 | 0/0 | 1251 | 2 | 1 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0020 | 1/0 | 1249 | 2 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0021 | 0/0 | 1251 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0022 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0023 | 0/0 | 1251 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0024 | 0/0 | 1250 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0025 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0026 | 0/0 | 1252 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0027 | 0/0 | 1250 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0028 | 0/0 | 1250 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0029 | 0/0 | 1252 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0030 | 0/0 | 1251 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0031 | 0/0 | 1252 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0032 | 0/0 | 1252 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0033 | 0/0 | 1247 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0034 | 0/0 | 1246 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| t0035 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0028 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0112 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1029 | 233 | 51 | 49 | 97 | 7 | 27 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0003 | 0/0 | 1029 | 12 | 11 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0002c0002 | 0/0 | 1029 | 80 | 29 | 8 | 29 | 1 | 13 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0003c0004 | 0/0 | 1029 | 2 | 2 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0004c0005 | 0/0 | 1029 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | 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 | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0002 | 0/1 | 2279 | 43 | 9 | 12 | 14 | 1 | 6 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0003 | 0/0 | 2278 | 19 | 6 | 8 | 0 | 2 | 3 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0004 | 0/0 | 2279 | 11 | 0 | 0 | 10 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0005 | 0/0 | 2275 | 2 | 2 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0006 | 0/0 | 2279 | 7 | 6 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0007 | 0/0 | 2280 | 3 | 1 | 1 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0008 | 0/0 | 2278 | 4 | 2 | 1 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0010 | 0/0 | 2280 | 2 | 1 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0011 | 0/0 | 2279 | 4 | 0 | 0 | 4 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0013 | 0/0 | 2279 | 2 | 2 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0015 | 0/0 | 2279 | 3 | 2 | 0 | 0 | 1 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0016 | 0/0 | 2279 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0017 | 0/0 | 2279 | 2 | 0 | 0 | 0 | 1 | 1 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0019 | 0/0 | 2279 | 2 | 1 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0020 | 1/0 | 2277 | 2 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0022 | 0/0 | 2279 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0023 | 0/0 | 2279 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0024 | 0/0 | 2278 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0025 | 0/0 | 2279 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0026 | 0/0 | 2280 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0027 | 0/0 | 2278 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0028 | 0/0 | 2278 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0031 | 0/0 | 2280 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0032 | 0/0 | 2280 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0033 | 0/0 | 2275 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0001t0034 | 0/0 | 2274 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0003t0005 | 0/0 | 2275 | 11 | 10 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0001c0003t0035 | 0/0 | 2279 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0002c0002t0001 | 0/0 | 2279 | 41 | 0 | 7 | 26 | 1 | 7 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0002c0002t0002 | 0/0 | 2279 | 3 | 3 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0002c0002t0003 | 0/0 | 2278 | 3 | 3 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0002c0002t0004 | 0/0 | 2279 | 4 | 4 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0002c0002t0006 | 0/0 | 2279 | 5 | 2 | 0 | 0 | 0 | 3 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0002c0002t0007 | 0/0 | 2280 | 2 | 1 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0002c0002t0008 | 0/0 | 2278 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0002c0002t0009 | 0/0 | 2279 | 5 | 5 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0002c0002t0010 | 0/0 | 2280 | 2 | 0 | 0 | 2 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0002c0002t0012 | 0/0 | 2279 | 4 | 4 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0002c0002t0013 | 0/0 | 2279 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0002c0002t0014 | 0/0 | 2280 | 3 | 3 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0002c0002t0016 | 0/0 | 2279 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0002c0002t0018 | 0/0 | 2281 | 2 | 2 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0002c0002t0021 | 0/0 | 2279 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0002c0002t0029 | 0/0 | 2280 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0002c0002t0030 | 0/0 | 2279 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0003c0004t0004 | 0/0 | 2279 | 2 | 2 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| a0004c0005t0002 | 0/0 | 2279 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | copy fasta | chr2 | 38661114 | 38739765 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0124 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0138 | 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 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0151 | 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 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| 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 |
| 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 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| 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 |
| a0001c0001t0001g0248 | 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 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0019 | 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 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0028 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0172 | 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 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0166 | 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 |
| a0001c0001t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0004g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0004g0038 | 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 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0004g0139 | 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 |
| a0001c0001t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0006g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0006g0176 | 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 |
| a0001c0001t0007g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0007g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0007g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0008g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0008g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0008g0137 | 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 |
| a0001c0001t0010g0094 | 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 |
| a0001c0001t0011g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0011g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0011g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0011g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0013g0117 | 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 |
| a0001c0001t0015g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0015g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0015g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0016g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0017g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0017g0032 | 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 |
| a0001c0001t0019g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0020g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0020g0112 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0022g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0023g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0024g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0025g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0026g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0027g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0028g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0031g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0032g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0033g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0001t0034g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0003t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0001c0003t0005g0216 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0003t0005g0222 | 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 |
| a0001c0003t0035g0221 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 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 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0269 | 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 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0277 | 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 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0002c0002t0001g0290 | 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 | 1 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0001g0311 | 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 |
| a0002c0002t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0004g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0004g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0006g0060 | 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 |
| a0002c0002t0006g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0006g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0006g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0007g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0007g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0008g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0009g0001 | 0/0 | 1 | 1 | 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 |
| a0002c0002t0009g0237 | 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 |
| a0002c0002t0010g0279 | 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 |
| a0002c0002t0012g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0012g0326 | 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 |
| a0002c0002t0014g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0014g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0014g0325 | 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 |
| a0002c0002t0018g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0002c0002t0018g0236 | 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 |
| a0002c0002t0030g0140 | 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 |
| a0003c0004t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| a0004c0005t0002g0126 | 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 | g0090 | EUR | FIN | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00280 | hp2 | a0001 | c0001 | t0017 | g0031 | EUR | FIN | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0267 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0125 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00597 | hp1 | a0001 | c0001 | t0024 | g0120 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00609 | hp1 | a0001 | c0001 | t0011 | g0160 | 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 | g0079 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0138 | 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 | g0147 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0067 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG00673 | hp2 | a0001 | c0001 | t0011 | g0020 | 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 | g0114 | 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 | g0089 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01070 | hp2 | a0001 | c0001 | t0020 | g0095 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0258 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01081 | hp2 | a0001 | c0001 | t0027 | g0035 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01106 | hp1 | a0001 | c0001 | t0019 | g0309 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01106 | hp2 | a0001 | c0001 | t0007 | g0087 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0136 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0077 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0058 | 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 | g0057 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0143 | 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 | g0216 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01255 | hp1 | a0001 | c0001 | t0023 | g0327 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0294 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0293 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0059 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01361 | hp1 | a0001 | c0001 | t0033 | g0214 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0122 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0306 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01496 | hp2 | a0002 | c0002 | t0030 | g0140 | AMR | CLM | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01515 | hp1 | a0001 | c0001 | t0015 | g0054 | EUR | IBS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0301 | EUR | IBS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0046 | EUR | IBS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0292 | EUR | IBS | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0124 | 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 | g0310 | 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 | g0022 | AMR | PEL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0268 | AMR | PEL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PEL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0259 | AMR | PEL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG01978 | hp1 | a0001 | c0001 | t0026 | g0027 | 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 | g0119 | 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 | g0026 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0270 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0009 | 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 | g0239 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0272 | 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 | g0073 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0286 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0289 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02145 | hp1 | a0002 | c0002 | t0009 | g0237 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0313 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0091 | 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 | g0181 | AMR | PEL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02451 | hp1 | a0001 | c0001 | t0015 | g0316 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0175 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02523 | hp1 | a0001 | c0001 | t0011 | g0156 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02572 | hp1 | a0002 | c0002 | t0004 | g0322 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02572 | hp2 | a0001 | c0003 | t0005 | g0215 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02602 | hp1 | a0001 | c0001 | t0016 | g0169 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0053 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02615 | hp1 | a0004 | c0005 | t0002 | g0126 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02615 | hp2 | a0001 | c0003 | t0005 | g0226 | 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 | g0223 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0317 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02630 | hp2 | a0002 | c0002 | t0014 | g0325 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0308 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0173 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0260 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02698 | hp1 | a0002 | c0002 | t0008 | g0284 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02698 | hp2 | a0001 | c0001 | t0017 | g0032 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02723 | hp1 | a0002 | c0002 | t0009 | g0235 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02723 | hp2 | a0001 | c0001 | t0032 | g0324 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0083 | 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 | g0096 | 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 | g0236 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02818 | hp2 | a0001 | c0003 | t0035 | g0221 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02886 | hp1 | a0002 | c0002 | t0009 | g0238 | 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 | g0312 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02895 | hp2 | a0002 | c0002 | t0014 | g0153 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02896 | hp1 | a0002 | c0002 | t0003 | g0304 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02897 | hp1 | a0002 | c0002 | t0003 | g0305 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02897 | hp2 | a0002 | c0002 | t0014 | g0152 | AFR | GWD | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02922 | hp1 | a0002 | c0002 | t0012 | g0326 | AFR | ESN | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02922 | hp2 | a0001 | c0001 | t0015 | g0315 | AFR | ESN | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02965 | hp1 | a0001 | c0001 | t0008 | g0137 | 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 | g0135 | AFR | ESN | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0029 | 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 | g0225 | 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 | g0128 | AFR | ESN | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03195 | hp1 | a0001 | c0003 | t0005 | g0220 | AFR | ESN | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03195 | hp2 | a0001 | c0003 | t0005 | g0222 | AFR | ESN | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | MSL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03209 | hp2 | a0002 | c0002 | t0006 | g0060 | AFR | MSL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03225 | hp1 | a0002 | c0002 | t0004 | g0320 | AFR | MSL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0297 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0174 | AFR | MSL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03453 | hp2 | a0001 | c0001 | t0028 | g0307 | AFR | MSL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03486 | hp1 | a0002 | c0002 | t0007 | g0319 | AFR | MSL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0052 | AFR | MSL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03491 | hp1 | a0002 | c0002 | t0006 | g0275 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03492 | hp1 | a0002 | c0002 | t0006 | g0296 | 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 | g0212 | AFR | ESN | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0075 | 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 | g0218 | AFR | MSL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0017 | 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 | g0098 | 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 | g0298 | SAS | BEB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0283 | SAS | BEB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | BEB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0276 | SAS | BEB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0139 | SAS | BEB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | STU | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG04199 | hp1 | a0002 | c0002 | t0006 | g0299 | SAS | STU | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | STU | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0099 | 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 | g0134 | SAS | STU | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0291 | SAS | STU | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18522 | hp1 | a0001 | c0001 | t0034 | g0213 | 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 | g0252 | EAS | CHB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | CHB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18906 | hp1 | a0002 | c0002 | t0004 | g0321 | 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 | g0082 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0311 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18951 | hp2 | a0001 | c0001 | t0008 | g0068 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18968 | hp1 | a0001 | c0001 | t0025 | g0161 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0287 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0102 | 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 | g0279 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18985 | hp2 | a0001 | c0001 | t0010 | g0094 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18991 | hp1 | a0001 | c0001 | t0031 | g0256 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18991 | hp2 | a0002 | c0002 | t0007 | g0300 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0164 | 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 | g0151 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0249 | 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 | g0100 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0040 | 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 | g0273 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | LWK | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19030 | hp2 | a0002 | c0002 | t0003 | g0303 | AFR | LWK | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19043 | hp1 | a0001 | c0003 | t0005 | g0224 | AFR | LWK | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | LWK | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0251 | 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 | g0049 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0265 | 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 | g0004 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19075 | hp2 | a0001 | c0001 | t0007 | g0061 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0011 | 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 | g0278 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19240 | hp1 | a0001 | c0003 | t0005 | g0217 | AFR | YRI | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA19240 | hp2 | a0001 | c0001 | t0022 | g0051 | AFR | YRI | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | TSI | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0056 | EUR | TSI | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | GIH | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0055 | 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 | g0166 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0108 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02559 | hp1 | a0002 | c0002 | t0004 | g0323 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG02559 | hp2 | a0001 | c0001 | t0013 | g0117 | AFR | ACB | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0314 | 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 | g0006 | AFR | USA | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| HG06807 | hp2 | a0002 | c0002 | t0018 | g0008 | AFR | USA | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA20300 | hp1 | a0001 | c0001 | t0007 | g0097 | 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 | g0176 | AFR | LWK | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0028 | REF | REF | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0020 | g0112 | REF | REF | GALM_chr2_38661114_38739765 | GALM | chr2 | 38661114 | 38739765 |
| 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 |
| 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 |
| 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 | a0001c0001t0005a0001c0001t0033a0001c0001t0034others(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 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(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 | a0001c0001t0002a0001c0001t0011a0001c0001t0017others(6): Show | 57 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(54): 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 | a0001c0001t0016a0002c0002t0016 | 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 | a0001c0001t0005a0001c0001t0033a0001c0001t0034others(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 | a0002c0002t0009a0002c0002t0029 | 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 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(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 | a0002c0002t0009a0002c0002t0012a0002c0002t0029 | 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 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(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 | a0001c0001t0005a0001c0001t0033a0001c0001t0034others(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 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(29): Show | 285 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(282): 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 | a0001c0001t0007a0001c0001t0026a0001c0001t0031others(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 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(32): Show | 293 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(290): 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 | a0001c0001t0005a0001c0001t0010a0001c0001t0013others(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 |
| 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 | a0001c0001t0023g0327 | 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 | 128 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0240others(125): 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 | 125 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0240others(122): 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 | a0001c0001t0001g0002 | 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 | a0001c0001t0001g0002 | 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 | 123 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0240others(120): 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 | 126 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0240others(123): 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 | a0002c0002t0004g0320a0002c0002t0004g0321a0002c0002t0004g0322others(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 | a0001c0001t0004g0003 | 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 | a0001c0001t0032g0324 | 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 | a0001c0001t0001g0318a0001c0001t0002g0312a0001c0001t0002g0313others(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 | 125 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0240others(122): 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 | a0001c0001t0001g0207a0001c0001t0001g0208 | 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 | a0002c0002t0012g0326 | 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 | a0002c0002t0014g0325 | 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 | a0002c0002t0012g0326 | 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 | a0001c0001t0004g0003 | 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 | a0001c0001t0004g0003 | 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 | a0001c0001t0004g0003 | 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 | a0002c0002t0014g0325 | 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 | 125 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0240others(122): 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 | a0001c0001t0002g0198a0001c0001t0002g0199a0001c0001t0002g0200 | 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 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0318others(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 | a0001c0001t0004g0003 | 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 | a0001c0001t0004g0003 | 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 | a0001c0001t0004g0003 | 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 | 125 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0240others(122): 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 | a0001c0001t0004g0003 | 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 | a0001c0001t0004g0003 | 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 | a0001c0001t0032g0324 | 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 | a0001c0001t0004g0003 | 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 | 125 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0240others(122): 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 | a0001c0001t0004g0004 | 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 | a0001c0001t0032g0324a0002c0002t0014g0325 | 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 | a0001c0001t0004g0003 | 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 | a0001c0001t0004g0003 | 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 | a0001c0001t0004g0003 | 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 | a0001c0001t0004g0003 | 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 | a0001c0001t0004g0003 | 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 | a0002c0002t0001g0311 | 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 | a0001c0001t0004g0003 | 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 | a0002c0002t0004g0320a0002c0002t0004g0321a0002c0002t0004g0322others(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 | a0002c0002t0012g0326 | 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 | a0002c0002t0012g0326 | 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 | a0001c0001t0032g0324 | 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 | a0001c0001t0004g0003 | 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 | 123 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0240others(120): 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 | a0001c0001t0004g0003 | 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 | a0001c0001t0004g0003 | 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 | a0001c0001t0004g0003 | 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 | a0001c0001t0032g0324 | 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 | 129 | a0001c0001t0001g0005a0001c0001t0001g0207a0001c0001t0001g0208others(126): 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 | a0001c0001t0003g0308a0001c0001t0003g0310a0001c0001t0019g0309others(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 | 127 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0240others(124): 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 | a0001c0001t0033g0214a0001c0001t0034g0213a0003c0004t0004g0211others(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 | a0001c0001t0008g0006 | 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 | a0002c0002t0012g0326 | 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 | 127 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0240others(124): 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 | 127 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0240others(124): 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 | a0001c0001t0032g0324a0002c0002t0014g0325 | 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 | a0001c0003t0005g0215a0001c0003t0005g0216a0001c0003t0005g0217others(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 | a0001c0001t0005g0205a0001c0001t0032g0324a0002c0002t0001g0306others(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 | a0001c0001t0001g0007a0001c0001t0019g0202a0002c0002t0012g0326 | 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 | 46 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(43): 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 | 128 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0240others(125): 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 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0008g0228 | 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 | a0001c0003t0005g0215a0001c0003t0005g0216a0001c0003t0005g0217others(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 | a0001c0001t0003g0308a0001c0001t0003g0310a0001c0001t0019g0309others(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 | a0002c0002t0001g0257 | 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 | 128 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0240others(125): 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 | a0002c0002t0018g0008 | 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 | a0002c0002t0002g0203a0002c0002t0002g0204 | 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 | a0001c0001t0001g0009a0001c0001t0003g0308a0001c0001t0003g0310others(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 | 127 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0240others(124): 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 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0192others(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 | 126 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0240others(123): 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 | 51 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0301others(48): 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 | 137 | a0001c0001t0001g0009a0001c0001t0001g0146a0001c0001t0001g0147others(134): 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 | a0001c0001t0003g0145 | 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 | a0002c0002t0004g0320a0002c0002t0004g0321a0002c0002t0004g0322others(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 | a0001c0001t0001g0010 | 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 | a0001c0001t0001g0318a0001c0001t0002g0312a0001c0001t0002g0313others(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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0318others(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 | a0002c0002t0012g0326 | 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 | a0002c0002t0003g0303a0002c0002t0003g0304a0002c0002t0003g0305others(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 | a0001c0001t0032g0324 | 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 | a0001c0001t0001g0009a0001c0001t0001g0147a0001c0001t0001g0148others(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 | a0001c0001t0001g0009a0001c0001t0001g0147a0001c0001t0001g0148others(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 | a0001c0001t0001g0009a0001c0001t0001g0147a0001c0001t0001g0148others(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 | a0002c0002t0014g0325 | 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 | 170 | a0001c0001t0001g0009a0001c0001t0001g0147a0001c0001t0001g0148others(167): 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 | 119 | a0001c0001t0001g0009a0001c0001t0001g0147a0001c0001t0001g0148others(116): 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 | 166 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(163): Show | 166 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.190+4317T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 1/6 | chr2 | 38670668 | ||||||
| chr2:38670681
|
C | T | 72 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0271others(69): 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 | a0002c0002t0001g0260 | 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 | 73 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0271others(70): 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 | 137 | a0001c0001t0001g0009a0001c0001t0001g0142a0001c0001t0001g0143others(134): 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 | 70 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0271others(67): 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 | a0002c0002t0002g0203a0002c0002t0002g0204 | 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 | a0002c0002t0001g0186a0002c0002t0010g0187 | 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 | a0001c0001t0001g0141 | 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 | 65 | a0001c0001t0001g0009a0001c0001t0001g0142a0001c0001t0001g0143others(62): 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 | 126 | a0001c0001t0001g0009a0001c0001t0001g0142a0001c0001t0001g0143others(123): 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 | a0001c0001t0001g0011a0001c0001t0004g0003a0001c0001t0004g0012others(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 | a0002c0002t0012g0326 | 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 | 11 | a0002c0002t0006g0232a0002c0002t0009g0001a0002c0002t0009g0231others(8): 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 | 118 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(115): Show | 118 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(115): 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 | a0001c0001t0019g0202a0001c0001t0033g0214a0001c0001t0034g0213others(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 | a0001c0001t0019g0202a0001c0001t0033g0214a0001c0001t0034g0213others(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 | 219 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(216): Show | 219 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(216): 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 | a0002c0002t0003g0303a0002c0002t0003g0304a0002c0002t0003g0305others(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 | a0002c0002t0001g0186a0002c0002t0010g0187 | 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 | a0001c0001t0001g0002 | 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 | 61 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0302others(58): 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 | 65 | a0001c0001t0001g0009a0001c0001t0001g0142a0001c0001t0001g0143others(62): 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 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0008g0228 | 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 | 65 | a0001c0001t0001g0009a0001c0001t0001g0142a0001c0001t0001g0143others(62): 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 | a0002c0002t0014g0325 | 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 | a0001c0001t0001g0142a0001c0001t0001g0143 | 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 | a0001c0001t0013g0227a0001c0001t0032g0324 | 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 | a0001c0001t0004g0050a0001c0001t0033g0214a0001c0001t0034g0213others(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 | 140 | a0001c0001t0001g0009a0001c0001t0001g0142a0001c0001t0001g0143others(137): 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 | a0001c0001t0005g0205a0001c0003t0005g0215a0001c0003t0005g0216others(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 | a0001c0001t0001g0207a0001c0001t0001g0208 | 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 | 55 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0302others(52): 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0002c0002t0014g0325 | 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 | a0002c0002t0003g0303a0002c0002t0003g0304a0002c0002t0003g0305 | 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 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(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 | a0001c0001t0003g0053a0001c0001t0003g0055a0001c0001t0003g0056others(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 | a0002c0002t0001g0186a0002c0002t0010g0187 | 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 | 3 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0019 | 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 | 16 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(13): 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 | 69 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0271others(66): 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 | 60 | a0001c0001t0001g0009a0001c0001t0001g0142a0001c0001t0001g0143others(57): 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 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(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 | 62 | a0001c0001t0001g0009a0001c0001t0001g0142a0001c0001t0001g0143others(59): 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 | 139 | a0001c0001t0001g0009a0001c0001t0001g0142a0001c0001t0001g0143others(136): 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 | 139 | a0001c0001t0001g0009a0001c0001t0001g0142a0001c0001t0001g0143others(136): 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 | 139 | a0001c0001t0001g0009a0001c0001t0001g0142a0001c0001t0001g0143others(136): 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 | a0001c0001t0001g0318a0001c0001t0002g0312a0001c0001t0002g0313others(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 | 65 | a0001c0001t0001g0009a0001c0001t0001g0142a0001c0001t0001g0143others(62): 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 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0191others(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 | 67 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0271others(64): 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 | 137 | a0001c0001t0001g0009a0001c0001t0001g0142a0001c0001t0001g0143others(134): 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 | 68 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0271others(65): 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 | a0001c0001t0019g0202a0001c0001t0033g0214a0001c0001t0034g0213others(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 | 175 | a0001c0001t0001g0009a0001c0001t0001g0142a0001c0001t0001g0143others(172): 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 | a0001c0001t0004g0125 | 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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0005 | 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 | 137 | a0001c0001t0001g0009a0001c0001t0001g0142a0001c0001t0001g0143others(134): 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 | a0002c0002t0014g0325 | 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 | 173 | a0001c0001t0001g0009a0001c0001t0001g0142a0001c0001t0001g0143others(170): 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 | 171 | a0001c0001t0001g0009a0001c0001t0001g0142a0001c0001t0001g0143others(168): 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 | a0001c0001t0001g0010 | 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 | 67 | a0001c0001t0001g0009a0001c0001t0001g0142a0001c0001t0001g0143others(64): 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 | 62 | a0001c0001t0001g0009a0001c0001t0001g0142a0001c0001t0001g0143others(59): 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 | 14 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0008g0228others(11): 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 | 18 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(15): 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 | a0001c0001t0001g0154 | 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 | a0002c0002t0001g0186a0002c0002t0010g0187 | 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 | a0002c0002t0014g0325 | 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 | a0002c0002t0014g0152a0002c0002t0014g0153a0002c0002t0018g0008 | 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 | a0004c0005t0002g0126 | 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 | 175 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0142others(172): 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 | a0002c0002t0001g0186a0002c0002t0010g0187 | 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 | a0001c0001t0002g0253 | 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 | a0001c0001t0001g0241 | 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 | 14 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(11): 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 | 73 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0271others(70): 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 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0142others(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 | a0001c0001t0003g0145 | 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 | a0001c0001t0001g0197a0001c0001t0016g0169 | 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 | 86 | a0001c0001t0001g0121a0001c0001t0001g0177a0001c0001t0001g0254others(83): 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 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0064others(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 | a0001c0001t0002g0017a0001c0001t0006g0052a0001c0001t0022g0051others(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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0062 | 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 | a0001c0001t0001g0254 | 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 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172others(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 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(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 | a0002c0002t0001g0186a0002c0002t0010g0187a0002c0002t0014g0325 | 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 | a0001c0001t0011g0020 | 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 | a0002c0002t0014g0152a0002c0002t0014g0153a0002c0002t0018g0008 | 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 | a0001c0001t0002g0021a0001c0003t0005g0219 | 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 | a0001c0001t0001g0062a0001c0001t0001g0121a0001c0001t0002g0021others(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 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0003g0057others(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 | a0001c0001t0001g0271a0002c0002t0001g0267a0002c0002t0001g0268others(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 | a0002c0002t0001g0263a0002c0002t0001g0264a0002c0002t0001g0265others(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 | a0002c0002t0014g0325 | 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 | a0002c0002t0001g0273a0002c0002t0001g0274a0002c0002t0006g0232others(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 | a0001c0001t0001g0272 | 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 | a0001c0001t0001g0062a0001c0001t0001g0065a0001c0001t0001g0121others(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 | a0001c0001t0001g0005a0001c0001t0001g0069a0001c0001t0001g0146others(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 | a0001c0001t0001g0011a0001c0001t0001g0070a0001c0001t0023g0327 | 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 | a0001c0001t0001g0096a0001c0001t0001g0098a0001c0001t0001g0099others(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 | a0001c0001t0001g0104a0001c0001t0002g0041a0001c0001t0002g0102others(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 | a0001c0001t0002g0018a0001c0001t0002g0025a0001c0001t0002g0198others(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 | a0002c0002t0001g0262a0002c0002t0001g0287 | 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 | 22 | a0001c0001t0001g0302a0001c0001t0002g0015a0001c0001t0002g0016others(19): 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 | a0001c0001t0001g0071 | 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 | a0002c0002t0001g0259 | 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 | a0002c0002t0001g0201a0002c0002t0001g0210a0002c0002t0001g0288others(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 | 5 | a0002c0002t0009g0001a0002c0002t0009g0235a0002c0002t0009g0237others(2): 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 | 108 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(105): Show | 108 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(105): 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 | a0001c0001t0001g0105a0001c0001t0001g0131a0001c0001t0001g0196 | 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 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0135others(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 | a0002c0002t0004g0321 | 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 | a0002c0002t0004g0320a0002c0002t0004g0323a0002c0002t0007g0319 | 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 | a0001c0001t0001g0318a0001c0001t0002g0313a0001c0001t0002g0314others(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 | a0001c0001t0001g0207a0001c0001t0001g0208 | 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 | a0002c0002t0003g0304a0002c0002t0003g0305a0002c0002t0009g0238others(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 | a0002c0002t0004g0322 | 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 | a0001c0001t0002g0312 | 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 | a0002c0002t0003g0303 | 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 | a0001c0001t0001g0138a0001c0001t0001g0240a0001c0001t0001g0243others(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 | a0001c0001t0002g0048a0004c0005t0002g0126 | 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 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0142others(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 | a0001c0001t0003g0145 | 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 | a0001c0001t0001g0318a0001c0001t0002g0313a0001c0001t0002g0314others(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 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0318others(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 | a0001c0001t0001g0207a0001c0001t0001g0208a0002c0002t0003g0304others(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 | a0001c0001t0011g0020 | 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 | a0001c0001t0001g0062a0001c0001t0004g0125 | 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 | a0001c0001t0032g0324 | 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 | a0002c0002t0009g0238 | 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 | a0001c0001t0001g0064a0002c0002t0001g0263a0002c0002t0001g0264 | 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 | 67 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0142others(64): 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 | a0002c0002t0003g0303a0002c0002t0003g0304a0002c0002t0003g0305 | 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 | 50 | a0001c0001t0001g0272a0001c0001t0001g0302a0002c0002t0001g0201others(47): 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 | a0002c0002t0014g0325 | 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 | a0001c0001t0001g0101 | 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 | a0001c0003t0005g0226 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0003g0310a0001c0001t0019g0309 | 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 | a0001c0001t0001g0302 | 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 | a0002c0002t0004g0320a0002c0002t0004g0321a0002c0002t0004g0322others(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 | a0001c0001t0019g0202a0001c0001t0033g0214a0001c0001t0034g0213others(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 | a0001c0001t0003g0055 | 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 | a0002c0002t0003g0303a0002c0002t0003g0304a0002c0002t0003g0305 | 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 | 49 | a0001c0001t0001g0272a0002c0002t0001g0201a0002c0002t0001g0210others(46): 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 | a0002c0002t0006g0232a0002c0002t0012g0233 | 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 | 49 | a0001c0001t0001g0272a0002c0002t0001g0201a0002c0002t0001g0210others(46): 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 | 71 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0142others(68): 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 | 67 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0272others(64): 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 | a0002c0002t0001g0186a0002c0002t0010g0187 | 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 | 66 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0272others(63): 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 | 172 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0142others(169): 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 | a0001c0001t0019g0202a0001c0001t0033g0214a0001c0001t0034g0213others(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 | a0002c0002t0003g0303a0002c0002t0003g0304a0002c0002t0003g0305others(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 | a0002c0002t0014g0152a0002c0002t0014g0153a0002c0002t0018g0008 | 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 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0142others(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 | a0002c0002t0012g0326 | 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 | a0001c0001t0002g0312 | 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 | 8 | a0002c0002t0009g0001a0002c0002t0009g0231a0002c0002t0009g0235others(5): 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 | a0002c0002t0001g0186a0002c0002t0010g0187 | 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 | a0001c0001t0001g0106a0001c0001t0024g0120 | 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 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0008g0228 | 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 | a0001c0001t0001g0318a0001c0001t0002g0312a0001c0001t0002g0313others(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 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0142others(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 | a0001c0001t0001g0074 | 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 | 111 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(108): Show | 111 | HG00280.hp2 HG00558.hp2 HG00609.hp1 others(108): 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 | 18 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(15): 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 | a0002c0002t0001g0186a0002c0002t0010g0187a0002c0002t0014g0152others(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 | a0001c0001t0001g0131a0001c0001t0008g0006a0001c0001t0008g0137 | 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 | a0001c0001t0005g0205a0001c0003t0005g0215a0001c0003t0005g0216others(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 | a0001c0001t0001g0318a0001c0001t0002g0312a0001c0001t0002g0313others(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 | a0002c0002t0001g0277 | 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 | a0001c0001t0019g0202a0001c0001t0033g0214a0001c0001t0034g0213others(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 | a0001c0001t0002g0198a0001c0001t0002g0199a0001c0001t0002g0200 | 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 | a0002c0002t0014g0325 | 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 | a0001c0001t0001g0093a0001c0001t0004g0014 | 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 | 12 | a0002c0002t0006g0232a0002c0002t0009g0001a0002c0002t0009g0231others(9): 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 | a0002c0002t0014g0152a0002c0002t0014g0153a0002c0002t0018g0008 | 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 | 18 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(15): 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 | a0002c0002t0002g0203a0002c0002t0002g0204 | 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 | a0002c0002t0001g0186a0002c0002t0010g0187a0002c0002t0014g0152others(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 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0318others(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 | 50 | a0001c0001t0001g0272a0001c0001t0001g0302a0002c0002t0001g0201others(47): 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 | 64 | a0001c0001t0001g0272a0002c0002t0001g0186a0002c0002t0001g0201others(61): 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 | 105 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0142others(102): 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 | a0001c0001t0003g0145 | 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 | a0001c0001t0005g0205a0001c0003t0005g0215a0001c0003t0005g0216others(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 | a0002c0002t0002g0190a0002c0002t0006g0060 | 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 | a0001c0001t0001g0318a0001c0001t0002g0312a0001c0001t0002g0313others(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 | a0002c0002t0004g0321 | 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 | 67 | a0001c0001t0001g0272a0001c0001t0001g0302a0002c0002t0001g0186others(64): 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 | a0002c0002t0014g0325 | 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 | a0001c0001t0001g0135 | 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 | a0002c0002t0009g0238 | 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 | a0001c0001t0024g0120 | 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 | 169 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0142others(166): 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 | a0001c0001t0002g0253 | 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 | 59 | a0001c0001t0001g0272a0001c0001t0001g0302a0002c0002t0001g0201others(56): 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 | a0001c0001t0001g0065 | 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 | 30 | a0001c0001t0005g0205a0001c0003t0005g0215a0001c0003t0005g0216others(27): 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 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0008g0228 | 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 | a0001c0001t0001g0124 | 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 | a0002c0002t0001g0288 | 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 | 9 | a0001c0001t0001g0104a0002c0002t0009g0001a0002c0002t0009g0231others(6): 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 | a0001c0001t0001g0207a0001c0001t0001g0208 | 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 | a0002c0002t0006g0232a0002c0002t0012g0233 | 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 | a0001c0001t0002g0045 | 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 | 78 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0142others(75): 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 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0318others(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 | a0001c0003t0005g0215a0001c0003t0005g0222a0001c0003t0005g0223others(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 | a0001c0003t0005g0215a0001c0003t0005g0222a0001c0003t0005g0223others(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 | a0001c0001t0001g0065 | 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 | a0001c0001t0001g0101a0001c0001t0001g0115 | 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 | a0002c0002t0012g0326 | 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 | a0001c0001t0033g0214a0001c0001t0034g0213 | 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 | a0002c0002t0014g0152a0002c0002t0014g0153 | 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 | 62 | a0001c0001t0001g0272a0002c0002t0001g0201a0002c0002t0001g0210others(59): 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 | a0001c0001t0032g0324 | 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 | a0001c0001t0011g0020 | 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 | 63 | a0001c0001t0001g0272a0001c0001t0001g0302a0002c0002t0001g0201others(60): 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 | 13 | a0002c0002t0006g0232a0002c0002t0009g0001a0002c0002t0009g0231others(10): 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 | 19 | a0002c0002t0001g0186a0002c0002t0006g0232a0002c0002t0009g0001others(16): 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 | a0002c0002t0001g0186a0002c0002t0010g0187 | 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 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0318others(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 | a0001c0001t0001g0207a0001c0001t0001g0208 | 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 | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0075others(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 | 66 | a0001c0001t0001g0272a0001c0001t0001g0302a0001c0001t0002g0200others(63): 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 | 63 | a0001c0001t0001g0272a0001c0001t0001g0302a0002c0002t0001g0201others(60): 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 | a0002c0002t0007g0300 | 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 | a0002c0002t0001g0186a0002c0002t0010g0187 | 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 | a0002c0002t0012g0326a0002c0002t0014g0152a0002c0002t0014g0153others(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 | a0002c0002t0002g0203a0002c0002t0002g0204 | 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 | a0001c0001t0001g0271 | 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 | 63 | a0001c0001t0001g0272a0001c0001t0001g0302a0002c0002t0001g0201others(60): 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 | a0001c0001t0001g0074 | 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 | a0001c0001t0003g0145 | 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 | a0002c0002t0002g0190a0002c0002t0006g0060 | 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 | a0001c0001t0023g0327 | 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 | a0001c0001t0023g0327 | 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 | a0002c0002t0002g0203a0002c0002t0002g0204 | 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 | 2 | a0001c0001t0002g0028a0001c0001t0002g0029 | 2 | HG03017.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.552+1951G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38683437 | ||||||
| chr2:38683453
|
T | C | 209 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(206): Show | 209 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(206): 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 | a0001c0001t0005g0205a0001c0003t0005g0215a0001c0003t0005g0216others(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 | a0002c0002t0001g0288 | 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 | a0001c0003t0005g0220 | 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 | 63 | a0001c0001t0001g0272a0001c0001t0001g0302a0002c0002t0001g0201others(60): 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 | a0001c0001t0016g0169 | 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 | a0001c0001t0004g0125 | 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 | a0002c0002t0003g0303a0002c0002t0003g0304a0002c0002t0003g0305others(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 | 52 | a0001c0001t0001g0272a0001c0001t0001g0302a0002c0002t0001g0201others(49): 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 | a0002c0002t0003g0303a0002c0002t0003g0304a0002c0002t0003g0305others(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 | a0001c0001t0032g0324 | 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 | a0002c0002t0012g0326a0002c0002t0014g0152a0002c0002t0014g0153others(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 | 224 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(221): Show | 224 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(221): 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 | a0001c0001t0005g0205a0001c0003t0005g0215a0001c0003t0005g0216others(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 | a0001c0001t0003g0053a0001c0001t0003g0055a0001c0001t0003g0056others(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 | a0001c0001t0001g0207a0001c0001t0001g0208 | 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 | 19 | a0002c0002t0001g0186a0002c0002t0006g0232a0002c0002t0009g0001others(16): 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 | a0002c0002t0001g0186a0002c0002t0010g0187 | 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 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 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 | a0001c0001t0019g0202a0001c0001t0033g0214a0001c0001t0034g0213others(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 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0142others(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 | 17 | a0002c0002t0001g0186a0002c0002t0006g0232a0002c0002t0009g0001others(14): 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 | 79 | a0001c0001t0001g0272a0002c0002t0001g0186a0002c0002t0001g0201others(76): 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 | a0002c0002t0002g0190a0002c0002t0003g0303a0002c0002t0003g0304others(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 | 49 | a0001c0001t0001g0272a0002c0002t0001g0201a0002c0002t0001g0210others(46): 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 | a0002c0002t0004g0320a0002c0002t0004g0321a0002c0002t0004g0322others(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 | a0002c0002t0012g0326 | 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 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0008g0228 | 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 | a0001c0001t0001g0207a0001c0001t0001g0208 | 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 | a0002c0002t0002g0190a0002c0002t0003g0303a0002c0002t0003g0304others(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 | a0001c0001t0032g0324 | 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 | 77 | a0001c0001t0001g0272a0002c0002t0001g0186a0002c0002t0001g0201others(74): 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 | a0002c0002t0004g0320a0002c0002t0004g0321a0002c0002t0004g0322others(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 | a0002c0002t0002g0190a0002c0002t0003g0303a0002c0002t0003g0304others(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 | a0002c0002t0007g0300 | 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 | a0001c0001t0013g0227a0001c0001t0032g0324 | 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 | a0001c0003t0005g0215a0001c0003t0005g0216a0001c0003t0005g0217others(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 | a0001c0001t0019g0202a0002c0002t0014g0152a0002c0002t0014g0153 | 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 | a0001c0001t0001g0093a0001c0001t0001g0133a0001c0001t0001g0134others(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 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(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 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0062others(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 | a0001c0001t0001g0075a0001c0001t0001g0127a0001c0001t0003g0077others(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 | a0002c0002t0001g0210a0002c0002t0001g0269a0002c0002t0001g0270others(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 | 47 | a0001c0001t0001g0302a0002c0002t0001g0186a0002c0002t0001g0201others(44): 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 | 12 | a0002c0002t0006g0232a0002c0002t0009g0001a0002c0002t0009g0231others(9): 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 | a0001c0001t0001g0150a0001c0001t0001g0151 | 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 | a0001c0001t0001g0148a0001c0001t0001g0178a0001c0001t0001g0197others(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 | a0001c0001t0001g0149a0001c0001t0001g0168a0001c0001t0001g0182others(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 | a0001c0001t0001g0123a0001c0001t0001g0154a0001c0001t0001g0157others(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 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0155others(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 | a0001c0001t0001g0009a0001c0001t0001g0159a0001c0001t0011g0160 | 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 | a0001c0001t0001g0158a0001c0001t0011g0156a0001c0001t0025g0161 | 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 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0008g0228 | 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 | a0001c0001t0015g0315a0001c0001t0015g0316 | 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 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0142others(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 |
15 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0244others(12): 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 | a0001c0001t0001g0243a0001c0001t0001g0272a0001c0001t0006g0206 | 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 | a0001c0001t0001g0241 | 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 | a0001c0001t0002g0313a0001c0001t0002g0314 | 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 | a0001c0001t0002g0312 | 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 | 62 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0142others(59): 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 | a0001c0001t0001g0318a0001c0001t0002g0317 | 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 | 62 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0142others(59): 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 | 61 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0142others(58): 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 | a0001c0001t0032g0324 | 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 | a0002c0002t0007g0300 | 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 | 55 | a0001c0001t0001g0123a0001c0001t0001g0142a0001c0001t0001g0143others(52): 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 | a0001c0001t0001g0150a0001c0001t0002g0229a0001c0001t0002g0230others(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 | a0001c0001t0001g0150 | 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 | a0001c0001t0001g0002a0001c0001t0011g0020 | 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 | a0001c0001t0001g0010a0001c0001t0002g0188a0001c0001t0027g0035 | 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 | a0001c0001t0001g0026a0001c0001t0002g0023a0001c0001t0002g0036others(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 |
2 | a0001c0001t0002g0030a0001c0001t0002g0037 | 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 |
8 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0024others(5): Show | 8 | HG01168.hp1 HG01358.hp2 HG02615.hp1 others(5): 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 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0138others(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 | a0001c0001t0002g0029 | 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 | a0001c0001t0002g0022a0001c0001t0002g0025a0001c0001t0002g0033others(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 | a0001c0001t0004g0003 | 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 | a0001c0001t0004g0040a0001c0001t0026g0027 | 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 | a0001c0001t0001g0150a0001c0001t0002g0229a0001c0001t0002g0230others(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 | a0001c0001t0002g0041 | 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 | a0001c0003t0005g0216 | 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 | a0001c0003t0035g0221 | 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 | a0001c0003t0005g0217 | 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 | a0001c0003t0005g0218 | 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 | a0001c0003t0005g0216a0001c0003t0005g0217a0001c0003t0005g0218others(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 | a0001c0003t0005g0225 | 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 | a0001c0003t0005g0222 | 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 | a0001c0003t0005g0226 | 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 | a0001c0003t0005g0223 | 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 | a0001c0003t0005g0220a0001c0003t0005g0224 | 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 | a0001c0003t0005g0215 | 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 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0008g0228 | 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 | 62 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0142others(59): 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 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0008g0228 | 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 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0008g0228 | 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 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0008g0228 | 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 | a0002c0002t0002g0190a0002c0002t0003g0303a0002c0002t0003g0304others(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 | a0002c0002t0001g0297a0002c0002t0006g0275a0002c0002t0006g0296others(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 | a0002c0002t0002g0190a0002c0002t0003g0303a0002c0002t0003g0304others(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 | a0002c0002t0002g0190a0002c0002t0003g0303a0002c0002t0003g0304others(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 | a0002c0002t0001g0186a0002c0002t0010g0187 | 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 | a0001c0001t0001g0065a0001c0001t0033g0214a0001c0001t0034g0213 | 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 | a0001c0001t0001g0207a0001c0001t0001g0208 | 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 | a0003c0004t0004g0211a0003c0004t0004g0212 | 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 | a0002c0002t0001g0278 | 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 | a0002c0002t0003g0303a0002c0002t0003g0304a0002c0002t0003g0305others(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 | a0001c0001t0019g0202a0001c0001t0033g0214a0001c0001t0034g0213others(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 | 220 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(217): Show | 220 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(217): 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 | a0002c0002t0002g0190a0002c0002t0003g0303a0002c0002t0003g0304others(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 | a0002c0002t0002g0190a0002c0002t0003g0303a0002c0002t0003g0304others(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 | a0001c0001t0032g0324 | 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 | 34 | a0001c0001t0001g0010a0001c0001t0002g0015a0001c0001t0002g0016others(31): Show | 34 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.553-2759G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38687054 | ||||||
| chr2:38687100
|
G | C | 51 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(48): Show | 51 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.553-2713G>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38687100 | ||||||
| chr2:38687109
|
A | C | 77 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0148others(74): 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 | 95 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(92): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): 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 | a0002c0002t0012g0326 | 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 | a0002c0002t0002g0190a0002c0002t0003g0303a0002c0002t0003g0304others(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 | a0002c0002t0001g0186a0002c0002t0010g0187 | 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 | 11 | a0002c0002t0006g0232a0002c0002t0009g0001a0002c0002t0009g0231others(8): 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 | a0002c0002t0002g0190a0002c0002t0003g0303a0002c0002t0003g0304others(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 | a0001c0001t0013g0227a0001c0001t0032g0324 | 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 | a0001c0001t0032g0324 | 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 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0318others(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 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0004g0003others(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 | a0002c0002t0001g0263a0002c0002t0001g0264 | 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 | a0001c0001t0001g0271a0002c0002t0001g0262a0002c0002t0001g0311others(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 | a0002c0002t0002g0190a0002c0002t0003g0303a0002c0002t0003g0304others(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 | a0002c0002t0002g0190a0002c0002t0003g0303a0002c0002t0003g0304others(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 | a0001c0001t0004g0125 | 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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0181 | 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 | a0002c0002t0003g0303a0002c0002t0003g0304a0002c0002t0003g0305others(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 | 18 | a0001c0001t0001g0078a0001c0001t0001g0240a0001c0001t0001g0242others(15): 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 | a0001c0001t0004g0004a0001c0001t0005g0205a0001c0003t0005g0215others(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 | a0002c0002t0002g0190a0002c0002t0003g0303a0002c0002t0003g0304others(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 | 166 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0142others(163): 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 | 170 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0142others(167): 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 | a0002c0002t0003g0303a0002c0002t0003g0304a0002c0002t0003g0305others(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 | a0002c0002t0002g0190a0002c0002t0003g0303a0002c0002t0003g0304others(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 | a0002c0002t0014g0152a0002c0002t0014g0153a0002c0002t0018g0008 | 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 | a0002c0002t0004g0323a0002c0002t0007g0319 | 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 | a0002c0002t0001g0186a0002c0002t0010g0187 | 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 | a0001c0001t0006g0173a0001c0001t0006g0174a0001c0001t0006g0175others(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 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0008g0228 | 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 | ||||||
| chr2:38689206
|
C | G | 327 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(324): Show | 327 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.553-607C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 3/6 | chr2 | 38689206 | ||||||
| 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 | a0002c0002t0003g0303a0002c0002t0003g0304a0002c0002t0003g0305others(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 | a0002c0002t0003g0303a0002c0002t0003g0304a0002c0002t0003g0305others(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 | a0003c0004t0004g0212 | 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 | 51 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(48): Show | 51 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(48): 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 | a0001c0001t0008g0006a0001c0001t0008g0137 | 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 | 22 | a0002c0002t0003g0303a0002c0002t0003g0304a0002c0002t0003g0305others(19): 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 | a0002c0002t0003g0304a0002c0002t0003g0305 | 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 | a0001c0001t0002g0312 | 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0254 | 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 | a0001c0001t0001g0131a0001c0001t0008g0006a0001c0001t0008g0137 | 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 | a0002c0002t0002g0190a0002c0002t0006g0060 | 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 | a0001c0001t0001g0118 | 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 | a0002c0002t0003g0303a0002c0002t0003g0304a0002c0002t0003g0305others(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 | a0002c0002t0002g0190a0002c0002t0006g0060 | 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 | 53 | a0002c0002t0001g0201a0002c0002t0001g0210a0002c0002t0001g0257others(50): 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 | a0001c0001t0001g0088a0001c0001t0001g0105a0001c0001t0007g0087 | 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 | a0001c0001t0025g0161 | 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 | a0001c0003t0005g0216a0001c0003t0005g0217a0001c0003t0005g0218others(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 | a0001c0001t0001g0011a0001c0001t0004g0003a0001c0001t0004g0004others(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 | a0002c0002t0001g0276a0002c0002t0016g0195 | 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 | a0001c0001t0001g0271 | 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 | 54 | a0001c0001t0001g0302a0002c0002t0001g0201a0002c0002t0001g0210others(51): 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 | a0001c0001t0001g0124a0001c0001t0005g0205a0001c0003t0005g0215others(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 | a0001c0001t0003g0053 | 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 | a0002c0002t0002g0190a0002c0002t0006g0060 | 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 | 107 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0148others(104): 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 | 68 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(65): Show | 68 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(65): 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 | a0002c0002t0001g0259 | 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 | a0001c0001t0001g0107a0002c0002t0003g0303a0002c0002t0003g0304others(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 | 46 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(43): Show | 46 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(43): 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 | a0001c0001t0004g0004 | 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 | a0002c0002t0002g0190a0002c0002t0006g0060 | 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 | a0001c0001t0001g0086 | 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 | a0002c0002t0012g0326 | 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 | a0001c0001t0001g0182a0001c0001t0001g0183 | 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 | 19 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(16): 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 | 117 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0148others(114): 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 | a0002c0002t0001g0278a0002c0002t0001g0285a0002c0002t0001g0287others(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 | a0001c0001t0003g0308a0001c0001t0003g0310a0001c0001t0019g0309others(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 | a0001c0001t0001g0101 | 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 | a0002c0002t0002g0190a0002c0002t0006g0060 | 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 | a0001c0001t0033g0214a0001c0001t0034g0213a0003c0004t0004g0211others(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 | 30 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0154others(27): 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 | a0001c0001t0001g0147a0001c0001t0003g0053a0001c0001t0003g0055others(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 | a0001c0001t0013g0227a0001c0001t0032g0324 | 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 | 11 | a0002c0002t0006g0232a0002c0002t0009g0001a0002c0002t0009g0231others(8): 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 | a0001c0001t0003g0053a0001c0001t0003g0055a0001c0001t0003g0056others(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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0075a0001c0001t0001g0093 | 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 | a0001c0001t0001g0065 | 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 | 173 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0142others(170): 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 | 143 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0142others(140): 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 | 15 | a0002c0002t0001g0186a0002c0002t0001g0274a0002c0002t0006g0232others(12): 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0128 | 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 | a0001c0001t0001g0011a0001c0001t0004g0003a0001c0001t0004g0004others(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 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0008g0228 | 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 | a0002c0002t0001g0186a0002c0002t0010g0187 | 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 | a0001c0001t0001g0009a0001c0001t0001g0123a0001c0001t0001g0142others(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 | a0001c0001t0001g0118 | 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 | a0001c0001t0005g0205a0001c0003t0005g0215a0001c0003t0005g0216others(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 | a0001c0001t0001g0105 | 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 | a0002c0002t0001g0186a0002c0002t0010g0187 | 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 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0008g0228 | 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 | a0001c0001t0001g0072a0001c0001t0001g0086a0001c0001t0001g0096 | 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 | a0002c0002t0012g0326 | 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 | a0001c0001t0001g0244 | 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 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0318others(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 | a0001c0001t0001g0121a0001c0001t0003g0053a0001c0001t0003g0055others(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 | a0001c0001t0001g0131a0001c0001t0008g0006a0001c0001t0008g0137 | 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 | a0001c0001t0001g0119 | 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 | 12 | a0002c0002t0006g0232a0002c0002t0009g0001a0002c0002t0009g0231others(9): 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 | 219 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(216): Show | 219 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(216): 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 | a0002c0002t0001g0259 | 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 | a0001c0001t0001g0207a0001c0001t0001g0208 | 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 | a0002c0002t0001g0186a0002c0002t0010g0187 | 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 | 139 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(136): Show | 139 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(136): 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 | a0001c0001t0001g0121a0001c0001t0001g0151a0001c0001t0001g0163others(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 | 16 | a0001c0001t0033g0214a0002c0002t0001g0186a0002c0002t0002g0190others(13): 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 | 202 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(199): Show | 202 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(199): 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 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0318others(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 | a0002c0002t0009g0237 | 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 | a0001c0001t0006g0174 | 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 | 2 | a0002c0002t0001g0280a0002c0002t0001g0281 | 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 | a0001c0001t0023g0327 | 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 | a0001c0001t0019g0202a0001c0001t0033g0214a0003c0004t0004g0211others(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 | 321 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(318): Show | 321 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(318): 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 | a0002c0002t0002g0190a0002c0002t0006g0060 | 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 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0318others(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 | 18 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(15): 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 | a0001c0001t0002g0025a0001c0001t0026g0027 | 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 | a0002c0002t0002g0190a0002c0002t0006g0060 | 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 | a0001c0001t0003g0053 | 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 | a0001c0001t0001g0034 | 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 | a0002c0002t0001g0269a0002c0002t0001g0270 | 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 | a0001c0001t0006g0052a0001c0001t0022g0051 | 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 | a0001c0001t0003g0053a0001c0001t0003g0055a0001c0001t0003g0056others(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 | a0002c0002t0002g0190a0002c0002t0006g0060 | 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 | a0001c0001t0001g0092 | 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 | 38 | a0001c0001t0001g0026a0001c0001t0001g0142a0001c0001t0001g0143others(35): 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 | 41 | a0001c0001t0001g0302a0002c0002t0001g0201a0002c0002t0001g0210others(38): 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 | a0001c0001t0001g0009a0001c0001t0001g0069a0001c0001t0001g0184others(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 | a0002c0002t0001g0268 | 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 | a0001c0001t0013g0227a0001c0001t0032g0324 | 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 | 51 | a0001c0001t0001g0302a0002c0002t0001g0201a0002c0002t0001g0210others(48): 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 | ||||||
| chr2:38696708
|
G | T | 1 | a0001c0001t0002g0028 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.634+6814G>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38696708 | ||||||
| chr2:38696747
|
C | G | 2 | a0002c0002t0002g0203a0002c0002t0002g0204 | 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 | 103 | a0001c0001t0001g0062a0001c0001t0001g0070a0001c0001t0001g0078others(100): Show | 103 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(100): 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 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0150others(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 | a0001c0001t0005g0205a0001c0003t0005g0220a0001c0003t0005g0222others(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 | a0001c0003t0005g0215a0001c0003t0005g0216a0001c0003t0005g0218others(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 | a0001c0001t0001g0011a0001c0001t0002g0229a0001c0001t0003g0145others(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 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0249others(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 | a0001c0001t0003g0053a0001c0001t0003g0055a0001c0001t0003g0056others(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 | a0001c0001t0001g0162 | 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 | a0002c0002t0002g0190a0002c0002t0006g0060 | 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 | a0001c0001t0001g0138 | 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 | 19 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(16): 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 | a0001c0001t0003g0308a0001c0001t0003g0310a0001c0001t0019g0309others(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 | a0001c0001t0033g0214a0003c0004t0004g0211a0003c0004t0004g0212 | 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 | a0001c0001t0001g0121a0001c0001t0003g0053a0001c0001t0003g0055others(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 | a0001c0001t0001g0101 | 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 | 23 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(20): 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 | a0001c0001t0013g0227a0001c0001t0032g0324 | 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 | a0002c0002t0014g0152a0002c0002t0014g0153a0002c0002t0018g0008 | 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 | a0001c0001t0001g0113a0001c0001t0001g0154a0001c0001t0001g0157others(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 | 176 | a0001c0001t0001g0009a0001c0001t0001g0121a0001c0001t0001g0123others(173): 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 | a0001c0001t0019g0202a0001c0001t0033g0214a0003c0004t0004g0211others(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 | a0001c0001t0001g0129 | 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 | a0001c0001t0033g0214a0003c0004t0004g0211a0003c0004t0004g0212 | 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 | a0001c0001t0001g0318a0001c0001t0002g0312a0001c0001t0002g0313others(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 | a0002c0002t0004g0320a0002c0002t0004g0321a0002c0002t0004g0322others(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 | a0002c0002t0001g0267 | 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 | a0002c0002t0001g0261 | 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 | a0002c0002t0001g0186a0002c0002t0010g0187 | 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 | a0001c0001t0001g0147a0001c0001t0003g0077a0001c0001t0003g0080others(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 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0062others(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 | a0002c0002t0001g0276 | 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 | a0001c0001t0003g0145 | 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 | a0002c0002t0001g0260 | 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 | a0001c0001t0033g0214a0003c0004t0004g0211a0003c0004t0004g0212 | 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 | a0002c0002t0001g0186a0002c0002t0010g0187 | 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 | 11 | a0002c0002t0006g0232a0002c0002t0009g0001a0002c0002t0009g0231others(8): 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 | a0001c0001t0032g0324 | 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 | a0001c0001t0001g0318a0001c0001t0002g0312a0001c0001t0002g0313others(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 | a0002c0002t0014g0152a0002c0002t0014g0153a0002c0002t0018g0008 | 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 | a0002c0002t0012g0326 | 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 | 222 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(219): Show | 222 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(219): 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 | a0001c0001t0005g0205a0001c0003t0005g0215a0001c0003t0005g0216others(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 | 323 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(320): Show | 323 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(320): 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 | a0001c0001t0001g0011a0001c0001t0004g0003a0001c0001t0004g0012others(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 | a0001c0001t0019g0309a0002c0002t0004g0320a0002c0002t0004g0321others(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 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172others(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 | a0002c0002t0012g0326 | 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 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0034others(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 | a0001c0001t0001g0124 | 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 | a0002c0002t0007g0319 | 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 | a0001c0001t0001g0154a0001c0001t0001g0157a0002c0002t0002g0190others(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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0162 | 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 | a0002c0002t0002g0190a0002c0002t0006g0060 | 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 | a0001c0001t0001g0154a0001c0001t0001g0157 | 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 | 226 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(223): Show | 226 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.634+11680C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38701574 | ||||||
| chr2:38701591
|
G | A | 19 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(16): 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 | a0001c0001t0001g0318a0001c0001t0002g0312a0001c0001t0002g0313others(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 | a0001c0001t0003g0310 | 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 | a0001c0001t0013g0227a0001c0001t0032g0324 | 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 | a0002c0002t0014g0152a0002c0002t0014g0153a0002c0002t0018g0008 | 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 | 51 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0026others(48): Show | 51 | HG00280.hp2 HG00558.hp2 HG00621.hp2 others(48): 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 | a0001c0001t0001g0011 | 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 | a0001c0001t0001g0154a0001c0001t0001g0157a0002c0002t0002g0190others(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 | a0001c0001t0001g0124 | 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 | a0001c0001t0003g0089 | 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 | a0001c0001t0005g0205a0001c0001t0013g0227a0001c0003t0005g0215others(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 | a0001c0001t0019g0309a0002c0002t0004g0320a0002c0002t0004g0321others(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 | 49 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0026others(46): Show | 49 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(46): 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 | a0002c0002t0014g0152a0002c0002t0014g0153a0002c0002t0018g0008 | 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 | 12 | a0002c0002t0006g0232a0002c0002t0009g0001a0002c0002t0009g0231others(9): 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 | a0001c0001t0003g0308a0001c0001t0028g0307 | 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 | 80 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0123others(77): 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 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172 | 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 | a0002c0002t0002g0203a0002c0002t0002g0204 | 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 | a0001c0001t0003g0310a0001c0001t0019g0202a0003c0004t0004g0211 | 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 | 52 | a0001c0001t0001g0121a0001c0001t0001g0154a0001c0001t0001g0157others(49): 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 | a0002c0002t0002g0190a0002c0002t0006g0060 | 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 | 79 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0123others(76): 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 | a0001c0001t0004g0139 | 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 | a0002c0002t0002g0190a0002c0002t0006g0060 | 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 | a0001c0003t0005g0220a0001c0003t0005g0222 | 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 | a0001c0003t0005g0215a0001c0003t0005g0220a0001c0003t0005g0222others(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 | a0001c0001t0001g0138a0001c0001t0002g0314a0001c0001t0006g0173others(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 | a0001c0001t0001g0007a0001c0001t0005g0116a0001c0001t0006g0176others(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 | a0001c0001t0001g0063a0001c0001t0001g0074a0001c0001t0001g0082others(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 | a0001c0001t0001g0064a0001c0001t0001g0100a0001c0001t0001g0197others(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 | a0001c0001t0001g0118a0001c0001t0008g0006a0002c0002t0006g0275others(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 | a0001c0001t0001g0301a0001c0001t0010g0094a0001c0003t0005g0225others(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 | a0001c0001t0001g0302a0001c0001t0003g0067a0001c0001t0024g0120others(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 | a0001c0003t0005g0226a0002c0002t0007g0300 | 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 | a0001c0001t0001g0096a0002c0002t0001g0283 | 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 | a0002c0002t0001g0311 | 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 | a0001c0001t0001g0121a0001c0001t0001g0177a0002c0002t0001g0297 | 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 | a0003c0004t0004g0211a0003c0004t0004g0212 | 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 | a0001c0001t0032g0324 | 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 | a0002c0002t0002g0190a0002c0002t0006g0060 | 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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0062 | 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 | a0001c0001t0001g0254 | 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 | 12 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(9): 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 | a0001c0001t0001g0244a0001c0001t0001g0247 | 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 | a0001c0001t0003g0308a0001c0001t0003g0310a0001c0001t0006g0206others(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 | a0001c0001t0001g0240a0001c0001t0028g0307a0001c0001t0031g0256 | 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 | a0002c0002t0006g0232a0002c0002t0012g0239 | 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 | a0002c0002t0009g0001a0002c0002t0009g0231a0002c0002t0009g0237others(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 | a0002c0002t0009g0235 | 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 | a0002c0002t0001g0261 | 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 | a0001c0001t0002g0029 | 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 | a0002c0002t0018g0008 | 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 | a0001c0001t0001g0162 | 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 | a0002c0002t0002g0190a0002c0002t0006g0060 | 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 | |||||
| chr2:38703082
|
ATATATAT others(6): Show |
A | 1 | a0001c0001t0002g0028 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.634+13190_634+1320 others(17): 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 | a0001c0001t0001g0123a0001c0001t0001g0155a0001c0001t0001g0159others(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 | a0001c0001t0001g0141a0001c0001t0011g0156a0001c0001t0011g0160 | 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 | a0001c0001t0001g0026 | 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 | a0001c0001t0004g0004a0001c0001t0004g0040a0001c0001t0004g0050 | 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 | a0001c0001t0001g0010a0001c0001t0002g0046a0001c0001t0002g0047others(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 | a0001c0001t0017g0031 | 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 | a0001c0001t0001g0009a0001c0001t0001g0163a0001c0001t0003g0057others(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 | a0001c0001t0001g0011a0001c0001t0001g0148a0001c0001t0001g0149others(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 | a0001c0001t0001g0034a0001c0001t0002g0015a0001c0001t0002g0016others(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 | a0001c0001t0002g0042a0001c0001t0002g0229a0001c0001t0004g0012 | 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 | 7 | a0001c0001t0002g0021a0001c0001t0002g0023a0001c0001t0002g0030others(4): 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 | a0001c0001t0002g0022a0001c0001t0002g0024a0001c0001t0002g0044 | 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 | a0001c0001t0001g0081a0001c0001t0001g0134a0001c0001t0033g0214others(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 | a0001c0001t0001g0150a0001c0001t0002g0018a0001c0001t0002g0025others(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 | a0001c0001t0002g0019a0001c0001t0002g0230 | 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 | a0002c0002t0001g0289 | 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 | a0001c0001t0001g0146a0002c0002t0001g0295 | 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 | a0001c0003t0005g0216 | 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 | a0001c0001t0001g0065a0002c0002t0001g0267a0002c0002t0001g0273 | 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 | a0001c0001t0001g0114a0002c0002t0001g0278 | 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 | a0001c0001t0001g0072a0002c0002t0001g0298 | 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 | a0002c0002t0001g0280 | 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 | a0002c0002t0001g0281 | 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 | a0001c0003t0005g0218 | 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 | a0001c0001t0005g0205a0001c0003t0005g0217 | 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 | a0002c0002t0001g0262 | 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 | a0001c0001t0001g0075 | 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 | a0001c0001t0019g0309 | 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 | a0002c0002t0001g0265a0002c0002t0001g0266a0002c0002t0001g0276 | 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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0086a0001c0003t0005g0223 | 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 | a0002c0002t0001g0269 | 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 | a0001c0001t0001g0093a0002c0002t0001g0274a0002c0002t0006g0299 | 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 | a0001c0001t0001g0078a0002c0002t0001g0263a0002c0002t0010g0187 | 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 | a0002c0002t0001g0291 | 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 | a0001c0001t0007g0097a0002c0002t0001g0270 | 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0079 | 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 | a0002c0002t0001g0264 | 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 | a0001c0001t0001g0107a0001c0001t0001g0131a0002c0002t0016g0195 | 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 | a0001c0001t0001g0062a0001c0001t0001g0142a0001c0001t0007g0061 | 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 | a0001c0001t0001g0143 | 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 | a0001c0003t0005g0224 | 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 | a0001c0001t0004g0125 | 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 | a0001c0001t0002g0312a0001c0001t0006g0052a0002c0002t0001g0289others(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 | a0001c0001t0001g0124a0001c0001t0001g0208a0001c0001t0013g0117others(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 | a0001c0001t0001g0104a0001c0001t0001g0119a0001c0001t0002g0103others(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 | a0001c0001t0001g0076a0001c0001t0002g0111a0001c0001t0003g0080others(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 | a0001c0001t0001g0071a0001c0001t0001g0085a0001c0001t0001g0191others(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 | a0001c0001t0001g0070a0001c0001t0001g0088a0001c0001t0001g0098others(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 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0084others(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 | a0001c0001t0001g0005a0001c0001t0001g0069 | 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 | a0001c0001t0001g0101 | 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 | a0002c0002t0010g0279 | 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 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0082others(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 | a0001c0001t0032g0324 | 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 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(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 | a0001c0001t0001g0082a0001c0001t0001g0105a0001c0001t0001g0138others(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 | a0001c0001t0002g0102a0001c0001t0002g0199a0001c0001t0002g0317others(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 | a0001c0001t0001g0082a0001c0001t0001g0105a0001c0001t0001g0128others(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 | a0001c0001t0001g0127a0001c0001t0001g0196 | 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 | a0001c0001t0010g0132a0002c0002t0004g0321a0002c0002t0013g0209others(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 | a0002c0002t0002g0190a0002c0002t0006g0060 | 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 | a0002c0002t0001g0186a0002c0002t0010g0187 | 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 | a0001c0001t0001g0063a0001c0001t0001g0076a0001c0001t0001g0107 | 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 | a0001c0003t0005g0215 | 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 | a0001c0001t0001g0121a0001c0001t0003g0053a0001c0001t0003g0055others(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 | a0001c0001t0001g0121a0001c0001t0002g0170a0001c0001t0002g0171others(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 | a0001c0001t0032g0324 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0318a0001c0001t0002g0312a0001c0001t0002g0313others(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 | a0001c0001t0006g0052a0001c0001t0022g0051 | 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 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0062others(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 | 106 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0026others(103): 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 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0008g0228 | 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 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0318others(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 | a0001c0001t0001g0113a0001c0001t0007g0061 | 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 | a0001c0001t0031g0256 | 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 | 25 | a0001c0001t0001g0009a0001c0001t0001g0158a0001c0001t0001g0159others(22): 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 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172others(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 | a0001c0001t0032g0324 | 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 | 47 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0026others(44): Show | 47 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(44): 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 | a0001c0001t0019g0202a0001c0001t0033g0214a0001c0001t0034g0213others(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 | a0001c0001t0008g0006a0001c0001t0008g0137 | 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 | 11 | a0002c0002t0006g0232a0002c0002t0009g0001a0002c0002t0009g0231others(8): 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 | a0002c0002t0012g0326 | 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 | a0002c0002t0002g0190a0002c0002t0006g0060 | 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 | a0001c0001t0005g0205a0001c0003t0005g0215a0001c0003t0005g0216others(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 | a0001c0001t0001g0154a0001c0001t0001g0157a0001c0001t0001g0162 | 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 | a0001c0001t0005g0205a0001c0003t0005g0215a0001c0003t0005g0216others(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 | 227 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(224): Show | 227 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.634+15741T>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38705635 | ||||||
| chr2:38705898
|
C | T | 78 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0123others(75): 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 | a0002c0002t0001g0297a0002c0002t0006g0275a0002c0002t0006g0296others(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 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172others(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 | 37 | a0001c0001t0001g0010a0001c0001t0002g0015a0001c0001t0002g0016others(34): Show | 37 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.634+16579G>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38706473 | ||||||
| chr2:38706511
|
C | CA | 20 | a0001c0001t0001g0069a0001c0001t0001g0101a0001c0001t0001g0189others(17): 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 | 82 | a0001c0001t0001g0011a0001c0001t0001g0078a0001c0001t0001g0123others(79): 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 | a0001c0001t0001g0154a0001c0001t0001g0157a0001c0001t0001g0162 | 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 | a0002c0002t0012g0326a0002c0002t0014g0152a0002c0002t0014g0153others(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 | a0001c0001t0001g0241a0001c0001t0001g0254 | 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 | 69 | a0001c0001t0001g0011a0001c0001t0001g0123a0001c0001t0001g0148others(66): 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 | ||||||
| chr2:38706838
|
C | G | 327 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(324): Show | 327 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.634+16944C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38706838 | ||||||
| chr2:38706875
|
A | AG | 35 | a0001c0001t0001g0009a0001c0001t0001g0158a0001c0001t0001g0159others(32): 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 | a0001c0001t0025g0161 | 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 | a0001c0001t0001g0193a0001c0001t0002g0170a0001c0001t0002g0229others(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 | a0001c0001t0031g0256 | 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 | a0002c0002t0006g0060a0002c0002t0013g0209 | 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 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165 | 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 | a0001c0001t0003g0308a0001c0001t0003g0310a0001c0001t0019g0309others(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 | a0002c0002t0006g0275a0002c0002t0006g0296a0002c0002t0006g0299 | 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0004g0003others(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 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(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 | a0001c0001t0002g0229a0001c0001t0002g0230 | 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 | a0001c0001t0001g0150 | 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0123 | 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 | a0002c0002t0001g0273 | 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 | a0002c0002t0012g0326 | 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 | a0001c0001t0001g0119 | 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 | 70 | a0001c0001t0001g0011a0001c0001t0001g0123a0001c0001t0001g0148others(67): 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 | a0001c0001t0001g0026 | 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 | 70 | a0001c0001t0001g0011a0001c0001t0001g0123a0001c0001t0001g0148others(67): 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 | 40 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0002g0015others(37): Show | 40 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(37): 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 |
23 | a0001c0001t0001g0179a0001c0001t0002g0317a0001c0001t0004g0003others(20): 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 |
53 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0123others(50): 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 | a0001c0001t0001g0167a0002c0002t0001g0201a0002c0002t0001g0258others(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 | a0001c0001t0001g0151 | 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 | a0001c0001t0005g0205a0001c0001t0007g0097a0001c0001t0019g0202others(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 | a0001c0001t0001g0154a0001c0001t0001g0157a0001c0001t0001g0162others(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 | a0002c0002t0014g0152a0002c0002t0014g0153a0002c0002t0018g0008 | 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 | 142 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(139): Show | 142 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(139): Show |
intron_variant | MODIFIER | c.634+18217T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38708111 | ||||||
| chr2:38708111
|
TTAAAA | T | 120 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(117): 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 | 70 | a0001c0001t0001g0011a0001c0001t0001g0123a0001c0001t0001g0148others(67): 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 | a0002c0002t0001g0289 | 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 | a0003c0004t0004g0211a0003c0004t0004g0212 | 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 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0004g0003others(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 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0004g0003others(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 | a0001c0001t0011g0020 | 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 | 36 | a0001c0001t0001g0010a0001c0001t0002g0015a0001c0001t0002g0016others(33): Show | 36 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(33): 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 | a0001c0001t0003g0308a0001c0001t0003g0310a0001c0001t0006g0206others(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 | a0001c0001t0001g0154a0001c0001t0001g0157a0001c0001t0001g0162others(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 | 116 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0026others(113): 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 | a0002c0002t0001g0306 | 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 | 10 | a0002c0002t0006g0232a0002c0002t0009g0001a0002c0002t0009g0231others(7): 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 | a0001c0001t0006g0206a0001c0001t0031g0256 | 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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0162 | 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 | a0001c0001t0002g0015a0001c0001t0002g0016 | 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 | a0001c0001t0001g0129a0001c0001t0001g0130 | 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 | a0002c0002t0001g0290 | 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 | 25 | a0001c0001t0005g0205a0001c0003t0005g0215a0001c0003t0005g0216others(22): 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 | 71 | a0001c0001t0001g0011a0001c0001t0001g0123a0001c0001t0001g0148others(68): 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 | ||||||
| chr2:38709484
|
C | G | 327 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(324): Show | 327 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.634+19590C>G | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38709484 | ||||||
| chr2:38709486
|
A | G | 4 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0141others(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 | a0001c0001t0033g0214a0003c0004t0004g0211a0003c0004t0004g0212 | 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 | a0001c0001t0001g0026a0001c0001t0004g0003a0001c0001t0004g0004others(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 | a0001c0001t0001g0121 | 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 | a0001c0001t0001g0007a0001c0001t0001g0069a0001c0001t0001g0082others(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 | a0001c0001t0002g0312a0001c0001t0002g0313a0001c0001t0002g0314others(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 | a0001c0001t0002g0312a0001c0001t0002g0313a0001c0001t0002g0314others(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 | a0001c0001t0001g0121a0001c0001t0001g0301 | 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 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0004g0003others(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 | a0002c0002t0012g0326 | 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 | a0001c0001t0002g0044 | 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 | a0001c0001t0002g0312a0001c0001t0002g0313a0001c0001t0002g0314others(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 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0004g0003others(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 | a0001c0001t0031g0256 | 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 | a0001c0001t0001g0182a0001c0001t0001g0254a0001c0001t0002g0045others(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 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0074others(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 | a0002c0002t0006g0060 | 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 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0004g0003others(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 | 71 | a0001c0001t0001g0011a0001c0001t0001g0123a0001c0001t0001g0148others(68): 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 | 11 | a0002c0002t0006g0232a0002c0002t0009g0001a0002c0002t0009g0231others(8): 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 | a0001c0001t0002g0312a0001c0001t0002g0313a0001c0001t0002g0314others(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 | 39 | a0001c0001t0001g0010a0001c0001t0002g0015a0001c0001t0002g0016others(36): Show | 39 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(36): 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 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0004g0003others(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 | 115 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(112): 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 | 43 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0002g0015others(40): Show | 43 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(40): 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 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0004g0003others(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 | a0001c0001t0005g0205a0001c0003t0005g0215a0001c0003t0005g0216others(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 | a0002c0002t0014g0152a0002c0002t0014g0153a0002c0002t0018g0008 | 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 | 11 | a0002c0002t0006g0232a0002c0002t0009g0001a0002c0002t0009g0231others(8): 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 | a0002c0002t0014g0152a0002c0002t0014g0153a0002c0002t0018g0008 | 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 | a0002c0002t0014g0152a0002c0002t0014g0153a0002c0002t0018g0008 | 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 | a0001c0001t0017g0031 | 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 | a0001c0001t0002g0047 | 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 |
35 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0002g0015others(32): Show | 35 | HG00639.hp2 HG00673.hp2 HG00735.hp1 others(32): 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 | a0001c0001t0027g0035 | 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 | a0001c0001t0002g0048 | 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 | a0002c0002t0014g0152a0002c0002t0014g0153a0002c0002t0018g0008 | 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 | 43 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0002g0015others(40): Show | 43 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(40): 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 | a0001c0001t0001g0246 | 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 | a0001c0001t0033g0214 | 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 | a0003c0004t0004g0211a0003c0004t0004g0212 | 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 | a0001c0001t0001g0251 | 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 | a0001c0001t0002g0312a0001c0001t0002g0313a0001c0001t0002g0314others(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 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172others(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 | a0001c0001t0032g0324 | 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 | a0001c0001t0001g0154a0001c0001t0001g0157a0002c0002t0001g0186 | 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 | a0001c0001t0003g0308a0001c0001t0003g0310a0001c0001t0019g0309others(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 | a0001c0001t0003g0053a0001c0001t0003g0055a0001c0001t0003g0056others(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 | a0001c0001t0001g0162a0001c0001t0003g0145a0001c0001t0003g0166others(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 | a0001c0001t0001g0121 | 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 | a0001c0001t0003g0059 | 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 | a0002c0002t0006g0060 | 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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0076 | 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 | a0001c0001t0016g0169 | 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 | a0001c0001t0001g0129 | 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 | a0001c0001t0001g0128 | 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 | a0001c0001t0001g0099 | 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 |
112 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0062others(109): 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 | a0002c0002t0004g0320a0002c0002t0004g0321a0002c0002t0004g0322 | 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 | a0001c0001t0001g0026 | 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 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0012others(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 | a0001c0001t0001g0002a0001c0001t0004g0039 | 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 | a0001c0001t0001g0146a0001c0001t0001g0191 | 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 | a0001c0001t0031g0256 | 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 |
11 | a0002c0002t0006g0232a0002c0002t0009g0001a0002c0002t0009g0231others(8): 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 | a0001c0001t0005g0205a0001c0003t0005g0215a0001c0003t0005g0216others(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 | a0001c0001t0001g0131 | 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 | 76 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0123others(73): 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 | 76 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0123others(73): 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 | a0002c0002t0030g0140 | 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 | 76 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0123others(73): 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 | a0002c0002t0001g0274 | 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 | a0002c0002t0001g0273 | 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 | a0002c0002t0001g0262 | 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 | a0001c0001t0001g0180 | 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 | a0002c0002t0001g0286 | 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 |
2 | a0002c0002t0001g0280a0002c0002t0001g0281 | 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0011a0001c0001t0001g0123a0001c0001t0001g0148others(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 | a0002c0002t0001g0283a0002c0002t0001g0297a0002c0002t0006g0275others(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 | a0002c0002t0001g0258 | 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 | a0002c0002t0001g0295 | 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 | a0002c0002t0001g0290 | 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 | a0001c0001t0001g0009a0001c0001t0011g0156a0001c0001t0011g0160others(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 | a0001c0001t0001g0158a0001c0001t0001g0159 | 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 | a0001c0001t0001g0167 | 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0002g0312a0001c0001t0002g0313a0001c0001t0002g0314others(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 | a0001c0001t0033g0214a0001c0001t0034g0213 | 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 | a0001c0001t0001g0240 | 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 | 79 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0011others(76): 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 | a0001c0001t0001g0109 | 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 | a0001c0003t0005g0222 | 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 | a0001c0001t0001g0183a0001c0001t0003g0145a0001c0001t0031g0256others(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 | a0002c0002t0018g0008 | 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 | 258 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(255): Show | 258 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(255): 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 | a0001c0001t0032g0324 | 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 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0115 | 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 | a0002c0002t0001g0260 | 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 | 287 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(284): Show | 287 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(284): 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 | a0001c0001t0003g0308a0001c0001t0028g0307 | 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 | 306 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(303): Show | 306 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(303): 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 | a0001c0001t0032g0324a0002c0002t0006g0060 | 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 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0141others(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 | a0001c0001t0032g0324 | 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 | a0001c0001t0003g0308a0001c0001t0003g0310a0001c0001t0019g0309others(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 | a0001c0001t0031g0256a0002c0002t0004g0320a0002c0002t0004g0321others(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 | 221 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(218): Show | 221 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(218): 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 | 69 | a0001c0001t0001g0011a0001c0001t0001g0064a0001c0001t0001g0086others(66): 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 | a0001c0001t0003g0308a0001c0001t0003g0310a0001c0001t0019g0309others(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 | a0001c0001t0002g0312a0001c0001t0002g0313a0001c0001t0002g0314others(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 | a0001c0001t0032g0324a0002c0002t0006g0060 | 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 | a0001c0001t0020g0095 | 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 | a0001c0001t0007g0087 | 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 | a0001c0001t0003g0308a0001c0001t0003g0310a0001c0001t0028g0307 | 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 | a0001c0003t0005g0225 | 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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(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 | a0002c0002t0001g0278a0002c0002t0001g0285 | 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 | a0001c0003t0005g0225 | 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 | 51 | a0001c0001t0001g0034a0001c0001t0002g0015a0001c0001t0002g0016others(48): Show | 51 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.635-13769T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38715787 | ||||||
| chr2:38715882
|
G | C | 208 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(205): 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 | a0002c0002t0001g0306 | 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 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0004g0003others(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 | a0002c0002t0014g0152a0002c0002t0014g0153a0002c0002t0018g0008 | 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 | a0002c0002t0001g0286 | 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 | a0001c0001t0008g0006a0001c0001t0008g0137a0001c0001t0008g0228 | 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 | a0001c0001t0001g0138 | 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 | 316 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(313): Show | 316 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(313): 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 | a0002c0002t0012g0326 | 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 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0004g0003others(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 | a0001c0001t0001g0005a0001c0001t0001g0098 | 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 | a0001c0001t0001g0070 | 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 | a0001c0001t0005g0116a0001c0001t0005g0205a0001c0001t0033g0214others(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 | a0001c0001t0001g0074 | 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 | 16 | a0001c0001t0003g0308a0001c0001t0003g0310a0001c0001t0028g0307others(13): 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 | a0001c0001t0001g0078a0001c0001t0001g0093a0001c0001t0001g0096others(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 | a0001c0001t0001g0072a0001c0001t0001g0154a0001c0001t0001g0157others(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 | 61 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0063others(58): 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 | a0001c0001t0001g0134a0001c0001t0001g0142a0001c0001t0001g0143others(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 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0131others(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 | 50 | a0001c0001t0001g0138a0001c0001t0002g0015a0001c0001t0002g0016others(47): Show | 50 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(47): 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 | a0001c0001t0001g0254 | 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 | a0001c0001t0002g0029a0001c0001t0002g0045a0001c0001t0002g0046 | 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 | a0004c0005t0002g0126 | 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 | a0001c0001t0019g0309a0002c0002t0013g0209 | 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 | 196 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(193): 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 | 197 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(194): 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 | 196 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(193): 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 | a0001c0001t0002g0229a0001c0001t0002g0230a0004c0005t0002g0126 | 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 | a0002c0002t0012g0326 | 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 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0004g0003others(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 | a0002c0002t0001g0261 | 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 | a0002c0002t0001g0286 | 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 | a0001c0001t0001g0083 | 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 | a0001c0001t0001g0072 | 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 | a0002c0002t0001g0288 | 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 | a0001c0001t0002g0229a0001c0001t0002g0230a0004c0005t0002g0126 | 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 | a0001c0001t0001g0123a0001c0001t0003g0077a0001c0001t0003g0080others(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 | 186 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(183): 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 | a0001c0001t0005g0116a0001c0001t0005g0205a0001c0003t0005g0215others(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 | a0002c0002t0006g0060 | 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 | 198 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(195): 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 | a0001c0001t0001g0251 | 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 | 195 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(192): 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 | a0001c0001t0013g0227a0002c0002t0004g0320a0002c0002t0004g0321others(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 | a0001c0001t0001g0154a0001c0001t0001g0157 | 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 | 316 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(313): Show | 316 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(313): 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 | a0001c0001t0013g0117 | 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 | 8 | a0002c0002t0006g0232a0002c0002t0009g0001a0002c0002t0009g0231others(5): 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0092a0001c0001t0001g0100 | 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 | a0001c0001t0005g0205a0001c0003t0005g0215a0001c0003t0005g0219others(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 | 11 | a0002c0002t0006g0232a0002c0002t0009g0001a0002c0002t0009g0231others(8): 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 | a0001c0001t0007g0097a0001c0001t0013g0117 | 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 | 272 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(269): Show | 272 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(269): 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 | a0001c0001t0003g0145 | 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 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0065others(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 | 185 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(182): 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 | a0001c0001t0001g0134a0001c0001t0001g0167a0001c0001t0001g0179others(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 | a0002c0002t0001g0297 | 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 | a0001c0001t0032g0324 | 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 | a0001c0001t0001g0241 | 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 | a0001c0001t0031g0256 | 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 | a0001c0001t0001g0005a0001c0001t0001g0092a0001c0001t0001g0098others(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 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0026others(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 | 163 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(160): 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 | 101 | a0001c0001t0001g0063a0001c0001t0001g0075a0001c0001t0001g0076others(98): Show | 101 | HG00639.hp2 HG00673.hp2 HG00735.hp1 others(98): 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 | a0001c0001t0002g0046a0001c0001t0004g0003a0001c0001t0004g0004others(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 | 30 | a0001c0001t0001g0011a0001c0001t0001g0065a0001c0001t0001g0081others(27): 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 | 152 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(149): 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 | a0001c0001t0001g0063a0001c0001t0001g0075a0001c0001t0001g0076others(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 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0004g0003others(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 | 47 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(44): Show | 47 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(44): 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 | a0001c0003t0005g0216a0001c0003t0005g0217a0001c0003t0005g0218others(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 | a0001c0001t0006g0173 | 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 | a0001c0001t0002g0023 | 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 | a0002c0002t0006g0060a0002c0002t0013g0209 | 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 | 55 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(52): Show | 55 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.635-8005T>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38721551 | ||||||
| chr2:38721588
|
C | T | 290 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(287): Show | 290 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(287): 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 | a0001c0001t0003g0308a0001c0001t0028g0307 | 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 | 99 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(96): 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 | 195 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(192): 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 | a0001c0001t0003g0308a0001c0001t0003g0310a0001c0001t0019g0309others(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 | a0001c0001t0001g0064a0001c0001t0001g0083a0001c0001t0001g0104others(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 | a0001c0001t0001g0107 | 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 | a0001c0001t0001g0007a0001c0001t0001g0062a0001c0001t0001g0073others(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 | a0001c0001t0001g0070a0001c0001t0001g0088a0001c0001t0001g0101others(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 | 41 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(38): Show | 41 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(38): 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 | 80 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(77): 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 | a0001c0001t0001g0065a0001c0001t0001g0069a0001c0001t0001g0079others(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 | a0001c0001t0001g0002a0001c0001t0002g0022a0001c0001t0002g0041others(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 | a0001c0001t0002g0171a0001c0001t0002g0172a0001c0001t0003g0053others(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 | 177 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(174): 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 | a0001c0001t0001g0154a0001c0001t0001g0157a0001c0001t0004g0003others(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 | 21 | a0001c0001t0001g0026a0001c0001t0004g0012a0001c0001t0004g0013others(18): 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 | a0001c0001t0006g0176a0001c0001t0008g0068a0001c0001t0008g0228 | 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 | a0001c0001t0001g0002a0001c0001t0002g0022a0001c0001t0002g0045others(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 | 48 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(45): Show | 48 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(45): 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 | a0001c0001t0001g0154a0001c0001t0001g0157 | 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 | a0001c0001t0001g0147 | 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 | a0001c0001t0001g0148a0001c0001t0001g0149 | 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 | a0002c0002t0001g0267 | 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 | 208 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(205): 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 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0004g0003others(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 | a0002c0002t0012g0326 | 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 | a0002c0002t0001g0269 | 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 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0004g0003others(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 | 11 | a0002c0002t0006g0232a0002c0002t0009g0001a0002c0002t0009g0231others(8): 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 | a0002c0002t0006g0060 | 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 | a0002c0002t0006g0060a0002c0002t0013g0209 | 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 | a0001c0001t0001g0063a0001c0001t0001g0076a0001c0001t0001g0107 | 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 | a0002c0002t0006g0060a0002c0002t0013g0209 | 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 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0004g0003others(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 | a0001c0001t0001g0154a0001c0001t0001g0157 | 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 | a0001c0001t0031g0256 | 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 | a0001c0001t0004g0004a0001c0001t0004g0040a0001c0001t0004g0050 | 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 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0154others(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 | a0002c0002t0001g0262a0002c0002t0010g0187 | 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 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0006g0052others(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 | 305 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(302): Show | 305 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(302): 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 | a0001c0001t0001g0154a0001c0001t0001g0157 | 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 | 197 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(194): 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 | a0002c0002t0004g0320a0002c0002t0004g0321a0002c0002t0004g0322 | 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 | a0001c0001t0005g0116a0001c0001t0005g0205a0001c0003t0005g0215others(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 | 210 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(207): 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 | a0001c0001t0001g0063a0001c0001t0001g0076a0001c0001t0001g0107 | 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 | a0001c0001t0013g0227a0002c0002t0004g0320a0002c0002t0004g0321others(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 | a0001c0001t0001g0010a0001c0001t0001g0065 | 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 | a0001c0001t0001g0026a0001c0001t0004g0003a0001c0001t0004g0004others(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 | a0001c0003t0005g0215a0001c0003t0005g0222a0001c0003t0005g0223others(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 | a0002c0002t0003g0304a0002c0002t0003g0305 | 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 | a0001c0001t0002g0198a0001c0001t0002g0199a0001c0001t0002g0200 | 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 | 55 | a0001c0001t0001g0034a0001c0001t0002g0015a0001c0001t0002g0016others(52): Show | 55 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(52): 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 | a0001c0001t0003g0053a0001c0001t0003g0055a0001c0001t0003g0056others(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 | a0002c0002t0001g0268 | 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 | a0002c0002t0012g0326 | 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 | a0004c0005t0002g0126 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.635-3768C>T | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38725788 | ||||||
| chr2:38725858
|
T | C | 327 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(324): Show | 327 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.635-3698T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38725858 | ||||||
| chr2:38726154
|
T | C | 1 | a0001c0001t0001g0099 | 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 | 96 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(93): Show | 96 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(93): 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 | a0001c0001t0002g0188a0001c0003t0005g0215a0002c0002t0012g0326 | 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 | 212 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(209): 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 | a0001c0001t0001g0074a0001c0001t0001g0084a0002c0002t0001g0306others(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 | 212 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(209): 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 | 211 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(208): 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0005g0116a0001c0001t0005g0205a0001c0003t0005g0215others(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 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0012others(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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0005a0001c0001t0001g0098 | 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 | a0001c0001t0011g0252 | 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 | a0001c0001t0001g0124 | 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 | a0001c0001t0003g0166 | 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 | a0002c0002t0001g0283 | 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 | a0001c0001t0001g0011a0001c0001t0001g0163 | 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 | 54 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(51): Show | 54 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.635-2679C>A | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | chr2 | 38726877 | ||||||
| chr2:38726896
|
T | TA | 327 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(324): Show | 327 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.635-2651dupA | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 38726896 | |||||
| chr2:38726983
|
A | AGGT | 4 | a0001c0001t0032g0324a0002c0002t0006g0060a0002c0002t0012g0326others(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 | a0001c0001t0031g0256 | 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 | a0001c0001t0031g0256 | 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 | a0001c0001t0005g0116a0001c0001t0005g0205a0001c0003t0005g0215others(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 | a0001c0001t0001g0246 | 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 | 69 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(66): Show | 69 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(66): 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 | a0001c0001t0031g0256 | 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 | 98 | a0001c0001t0001g0026a0001c0001t0002g0015a0001c0001t0002g0016others(95): Show | 98 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(95): 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 | 216 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(213): 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 | a0001c0001t0013g0227a0002c0002t0004g0320a0002c0002t0004g0321others(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 | a0001c0001t0005g0116a0001c0001t0005g0205a0001c0003t0005g0215others(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 | a0001c0001t0001g0105 | 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 | 54 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(51): Show | 54 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(51): 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 | a0001c0001t0001g0100a0001c0001t0003g0053a0001c0001t0004g0003others(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 | a0001c0001t0001g0142a0001c0001t0001g0154a0001c0001t0001g0301others(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 | a0001c0001t0032g0324a0002c0002t0012g0326 | 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 | a0002c0002t0014g0152a0002c0002t0014g0153a0002c0002t0018g0008others(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 | a0002c0002t0001g0263a0002c0002t0001g0264a0002c0002t0001g0265others(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 | 199 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(196): 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 | a0001c0001t0005g0116a0001c0001t0005g0205a0001c0003t0005g0215others(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 | a0001c0001t0001g0081a0001c0001t0001g0144a0001c0001t0008g0068 | 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 | 199 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(196): 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 | 298 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(295): Show | 298 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(295): 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 | a0001c0001t0001g0165 | 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 | 198 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(195): 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 | 199 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(196): 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 | a0001c0001t0001g0093a0001c0001t0001g0133a0001c0001t0001g0135others(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 | 196 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(193): 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 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0006g0052others(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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0246 | 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 | a0001c0001t0001g0155 | 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 | 75 | a0001c0001t0001g0034a0001c0001t0002g0015a0001c0001t0002g0016others(72): Show | 75 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(72): 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 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0012others(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 | a0001c0001t0031g0256 | 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 | a0001c0001t0001g0005a0001c0001t0001g0098 | 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 |
191 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(188): 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 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0247others(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 | a0001c0001t0017g0032 | 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 | 199 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(196): 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 | 199 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(196): 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 | 199 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(196): 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 | 198 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(195): 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 | 198 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(195): 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 | a0001c0001t0006g0052 | 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 | 199 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(196): 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 | 54 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(51): Show | 54 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(51): 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 | a0002c0002t0001g0263a0002c0002t0001g0264a0002c0002t0001g0265others(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 | 199 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(196): 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 | 198 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(195): 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 | a0002c0002t0014g0152a0002c0002t0014g0153a0002c0002t0018g0008others(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 | a0001c0001t0032g0324a0002c0002t0006g0060a0002c0002t0012g0326others(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 | a0002c0002t0014g0152a0002c0002t0014g0153a0002c0002t0018g0008others(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 | ||||||
| chr2:38729913
|
T | C | 327 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(324): Show | 327 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.776+216T>C | GALM | ENSG00000143891.17 | transcript | ENST00000272252.10 | protein_coding | 5/6 | chr2 | 38729913 | ||||||
| chr2:38729921
|
G | A | 1 | a0001c0001t0001g0250 | 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 | a0002c0002t0001g0291 | 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 | 198 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(195): 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 | a0001c0001t0024g0120 | 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 | a0002c0002t0004g0320a0002c0002t0004g0321a0002c0002t0004g0322others(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 | 198 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(195): 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 | a0001c0001t0003g0059a0004c0005t0002g0126 | 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 | a0001c0001t0001g0162 | 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 | a0001c0001t0003g0308a0001c0001t0013g0227a0001c0001t0028g0307others(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 | 65 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(62): Show | 65 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(62): 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 | a0001c0001t0005g0116a0001c0001t0005g0205a0001c0001t0033g0214others(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 | 301 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(298): Show | 301 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(298): 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 | a0001c0001t0001g0114a0001c0001t0001g0254a0001c0001t0004g0003others(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 | 187 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(184): 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 | a0001c0001t0001g0154a0001c0001t0001g0196a0001c0001t0001g0247others(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 | 68 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(65): Show | 68 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(65): 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 | a0002c0002t0018g0008 | 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 | a0001c0001t0001g0010a0001c0001t0001g0065 | 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 | a0002c0002t0012g0233a0002c0002t0012g0239 | 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 | a0001c0001t0011g0252 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0006g0052 | 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 | a0001c0001t0002g0317 | 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 | 200 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(197): 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 | a0001c0001t0001g0129 | 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 | a0001c0001t0001g0247a0002c0002t0001g0277 | 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 | a0001c0001t0001g0083 | 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 | a0001c0001t0031g0256 | 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 | a0004c0005t0002g0126 | 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 | a0001c0001t0001g0123a0001c0001t0001g0167a0001c0001t0001g0168others(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 | a0001c0001t0003g0310a0001c0001t0005g0116a0001c0001t0005g0205others(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 | 187 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(184): 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 | a0001c0001t0005g0205a0001c0003t0005g0215a0001c0003t0005g0216others(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 | a0001c0001t0003g0308a0001c0001t0019g0309a0001c0001t0028g0307others(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 | 201 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(198): 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 | 70 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(67): Show | 70 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(67): 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 | a0001c0001t0003g0166 | 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 | 15 | a0001c0001t0003g0308a0001c0001t0003g0310a0001c0001t0019g0309others(12): 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 | 55 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(52): Show | 55 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(52): 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 | a0001c0001t0003g0053 | 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 | a0001c0001t0032g0324a0002c0002t0012g0234a0002c0002t0012g0326 | 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 | a0001c0001t0003g0310a0001c0001t0019g0202a0001c0001t0019g0309others(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 |