Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 166929 |
|---|---|
| ensemblid | ENSG00000164023.15 |
| hgncid | 28395 |
| symbol | SGMS2 |
| name | sphingomyelin synthase 2 |
| refseq_nuc | NM_001375905.1 |
| refseq_prot | NP_001362834.1 |
| ensembl_nuc | ENST00000690982.1 |
| ensembl_prot | ENSP00000508566.1 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 107824932 |
| end | 107915047 |
| strand | + |
| ver | v1.2 |
| region | chr4:107824932-107915047 |
| region5000 | chr4:107819932-107920047 |
| regionname0 | SGMS2_chr4_107824932_107915047 |
| regionname5000 | SGMS2_chr4_107819932_107920047 |
| 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 | 365 | 267 | 85 | 69 | 66 | 14 | 31 | 48 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0002 | 0/0 | 365 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0003 | 0/0 | 365 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0004 | 0/0 | 365 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| 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 | 1098 | 261 | 79 | 69 | 66 | 14 | 31 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| c0002 | 0/0 | 1098 | 2 | 2 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| c0003 | 0/0 | 1098 | 2 | 2 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| c0004 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| c0005 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| c0006 | 0/0 | 1098 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| c0007 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| c0008 | 0/0 | 1098 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| 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 | 1/1 | 5143 | 168 | 31 | 48 | 58 | 6 | 23 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0002 | 0/0 | 5143 | 25 | 7 | 7 | 4 | 5 | 2 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0003 | 0/0 | 5143 | 14 | 12 | 2 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0004 | 0/0 | 5143 | 12 | 9 | 2 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0005 | 0/0 | 5143 | 9 | 7 | 2 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0006 | 0/0 | 5143 | 5 | 3 | 2 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0007 | 0/0 | 5143 | 4 | 2 | 1 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0008 | 0/0 | 5144 | 3 | 3 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0009 | 0/0 | 5143 | 3 | 0 | 1 | 0 | 0 | 2 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0010 | 0/0 | 5140 | 2 | 2 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0011 | 0/0 | 5451 | 2 | 0 | 0 | 0 | 0 | 2 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0012 | 0/0 | 5143 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0013 | 0/0 | 5143 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0014 | 0/0 | 5143 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0015 | 0/0 | 5143 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0016 | 0/0 | 5143 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0017 | 0/0 | 5143 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0018 | 0/0 | 5143 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0019 | 0/0 | 5143 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0020 | 0/0 | 5143 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0021 | 0/0 | 5143 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0022 | 0/0 | 5143 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0023 | 0/0 | 5143 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0024 | 0/0 | 5143 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0025 | 0/0 | 5143 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0026 | 0/0 | 5143 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0027 | 0/0 | 5143 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0028 | 0/0 | 5143 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0029 | 0/0 | 5140 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0030 | 0/0 | 5143 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0031 | 0/0 | 5143 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0032 | 0/0 | 5143 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0033 | 0/0 | 5143 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| t0034 | 0/0 | 5143 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| 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 | 4 | 0 | 2 | 0 | 1 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0002 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0010 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0045 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0131 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| 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 | 1098 | 261 | 79 | 69 | 66 | 14 | 31 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0002 | 0/0 | 1098 | 2 | 2 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0003 | 0/0 | 1098 | 2 | 2 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0005 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0007 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0002c0004 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0003c0008 | 0/0 | 1098 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0004c0006 | 0/0 | 1098 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 6240 | 164 | 29 | 47 | 58 | 6 | 22 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0002 | 0/0 | 6240 | 23 | 5 | 7 | 4 | 5 | 2 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0003 | 0/0 | 6240 | 14 | 12 | 2 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0004 | 0/0 | 6240 | 12 | 9 | 2 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0005 | 0/0 | 6240 | 9 | 7 | 2 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0006 | 0/0 | 6240 | 5 | 3 | 2 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0007 | 0/0 | 6240 | 4 | 2 | 1 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0008 | 0/0 | 6241 | 3 | 3 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0009 | 0/0 | 6240 | 3 | 0 | 1 | 0 | 0 | 2 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0010 | 0/0 | 6237 | 2 | 2 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0011 | 0/0 | 6548 | 2 | 0 | 0 | 0 | 0 | 2 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0012 | 0/0 | 6240 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0013 | 0/0 | 6240 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0014 | 0/0 | 6240 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0015 | 0/0 | 6240 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0016 | 0/0 | 6240 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0017 | 0/0 | 6240 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0018 | 0/0 | 6240 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0019 | 0/0 | 6240 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0020 | 0/0 | 6240 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0021 | 0/0 | 6240 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0022 | 0/0 | 6240 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0024 | 0/0 | 6240 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0026 | 0/0 | 6240 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0027 | 0/0 | 6240 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0028 | 0/0 | 6240 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0029 | 0/0 | 6237 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0030 | 0/0 | 6240 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0032 | 0/0 | 6240 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0033 | 0/0 | 6240 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0001t0034 | 0/0 | 6240 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0002t0001 | 0/0 | 6240 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0002t0023 | 0/0 | 6240 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0003t0002 | 0/0 | 6240 | 2 | 2 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0005t0031 | 0/0 | 6240 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0001c0007t0025 | 0/0 | 6240 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0002c0004t0001 | 0/0 | 6240 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0003c0008t0001 | 0/0 | 6240 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| a0004c0006t0001 | 0/0 | 6240 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | copy fasta | chr4 | 107819932 | 107920047 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0045 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0131 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0004g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0005g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0006g0002 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0006g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0007g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0007g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0007g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0007g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0008g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0008g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0009g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0009g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0009g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0010g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0010g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0011g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0011g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0012g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0013g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0014g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0015g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0016g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0017g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0018g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0019g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0020g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0021g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0022g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0024g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0026g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0027g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0028g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0029g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0030g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0032g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0033g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0001t0034g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0002t0023g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0003t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0003t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0005t0031g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0001c0007t0025g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0002c0004t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0003c0008t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| a0004c0006t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0102 | EUR | GBR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0106 | EUR | FIN | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG00323 | hp1 | a0001 | c0001 | t0024 | g0074 | EUR | FIN | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | FIN | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG00544 | hp1 | a0001 | c0001 | t0032 | g0155 | EAS | CHS | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG00733 | hp2 | a0001 | c0001 | t0009 | g0080 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG00735 | hp1 | a0001 | c0001 | t0034 | g0088 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0122 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01069 | hp2 | a0001 | c0001 | t0006 | g0002 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01071 | hp2 | a0001 | c0001 | t0006 | g0002 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01109 | hp2 | a0001 | c0001 | t0015 | g0208 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0248 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0255 | AMR | PUR | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0212 | AMR | CLM | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01255 | hp2 | a0001 | c0001 | t0033 | g0242 | AMR | CLM | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0066 | AMR | CLM | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01346 | hp1 | a0001 | c0001 | t0020 | g0159 | AMR | CLM | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | IBS | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | IBS | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01516 | hp1 | a0001 | c0001 | t0022 | g0035 | EUR | IBS | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01516 | hp2 | a0001 | c0001 | t0007 | g0091 | EUR | IBS | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0116 | AFR | ACB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01934 | hp2 | a0003 | c0008 | t0001 | g0009 | AMR | PEL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0218 | AMR | PEL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01981 | hp1 | a0001 | c0001 | t0026 | g0148 | AMR | PEL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01981 | hp2 | a0001 | c0001 | t0007 | g0090 | AMR | PEL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02015 | hp1 | a0001 | c0001 | t0017 | g0003 | EAS | KHV | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | ACB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02257 | hp1 | a0001 | c0001 | t0029 | g0230 | AFR | ACB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02280 | hp1 | a0001 | c0001 | t0028 | g0203 | AFR | ACB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0253 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0162 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0117 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0100 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0172 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0247 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0227 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0232 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0007 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0226 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0220 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0007 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0176 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02922 | hp1 | a0001 | c0003 | t0002 | g0133 | AFR | ESN | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02965 | hp1 | a0001 | c0001 | t0027 | g0118 | AFR | ESN | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0115 | AFR | ESN | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02976 | hp1 | a0001 | c0002 | t0023 | g0237 | AFR | ESN | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03017 | hp2 | a0004 | c0006 | t0001 | g0010 | SAS | PJL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03041 | hp1 | a0001 | c0001 | t0030 | g0044 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0224 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0104 | AFR | MSL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | MSL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0251 | AFR | ESN | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0239 | AFR | ESN | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | MSL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0250 | AFR | MSL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03225 | hp2 | a0001 | c0001 | t0018 | g0228 | AFR | MSL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03453 | hp1 | a0001 | c0001 | t0010 | g0210 | AFR | MSL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0240 | AFR | MSL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03486 | hp1 | a0001 | c0007 | t0025 | g0114 | AFR | MSL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0197 | AFR | MSL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03490 | hp1 | a0001 | c0001 | t0011 | g0040 | SAS | PJL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03490 | hp2 | a0001 | c0001 | t0009 | g0032 | SAS | PJL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03492 | hp2 | a0001 | c0001 | t0011 | g0170 | SAS | PJL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0181 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | MSL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03579 | hp2 | a0002 | c0004 | t0001 | g0233 | AFR | MSL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03688 | hp1 | a0001 | c0001 | t0014 | g0026 | SAS | STU | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | STU | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0110 | SAS | PJL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03710 | hp2 | a0001 | c0001 | t0009 | g0112 | SAS | PJL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03831 | hp2 | a0001 | c0001 | t0016 | g0204 | SAS | BEB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | STU | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | STU | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | STU | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | STU | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0234 | AFR | YRI | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0143 | AFR | YRI | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | CHB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | YRI | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18906 | hp2 | a0001 | c0001 | t0021 | g0043 | AFR | YRI | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18962 | hp1 | a0001 | c0001 | t0019 | g0038 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | LWK | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA19030 | hp2 | a0001 | c0001 | t0010 | g0238 | AFR | LWK | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA19085 | hp1 | a0001 | c0001 | t0013 | g0156 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | YRI | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | YRI | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0103 | AFR | ASW | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA20129 | hp2 | a0001 | c0005 | t0031 | g0012 | AFR | ASW | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0173 | EUR | TSI | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0128 | EUR | TSI | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0077 | EUR | TSI | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0107 | SAS | GIH | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | GIH | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0219 | AFR | ACB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02486 | hp2 | a0001 | c0003 | t0002 | g0246 | AFR | ACB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0249 | AFR | ACB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0123 | AFR | ACB | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0067 | AFR | MSL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | USA | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | USA | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | LWK | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| NA21309 | hp2 | a0001 | c0001 | t0012 | g0196 | AFR | LWK | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0131 | REF | REF | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0045 | REF | REF | SGMS2_chr4_107819932_107920047 | SGMS2 | chr4 | 107819932 | 107920047 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:107895824
|
G | A | 1 | a0002 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.271G>A | p.Val91Ile | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/7 | 919/6240 | 271/1098 | 91/365 | chr4 | 107895824 | ||
| chr4:107908648
|
G | A | 1 | a0004 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.811G>A | p.Glu271Lys | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/7 | 1459/6240 | 811/1098 | 271/365 | chr4 | 107908648 | ||
| chr4:107910545
|
T | A | 1 | a0003 | 1 | HG01934.hp2 | missense_variant | MODERATE | c.1090T>A | p.Ser364Thr | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 1738/6240 | 1090/1098 | 364/365 | chr4 | 107910545 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:107895724
|
G | A | 1 | a0001c0002 | 2 | HG02976.hp1 HG03471.hp1 |
synonymous_variant | LOW | c.171G>A | p.Pro57Pro | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/7 | 819/6240 | 171/1098 | 57/365 | chr4 | 107895724 | ||
| chr4:107895958
|
G | A | 1 | a0001c0005 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.405G>A | p.Gly135Gly | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/7 | 1053/6240 | 405/1098 | 135/365 | chr4 | 107895958 | ||
| chr4:107903355
|
G | A | 1 | a0001c0003 | 2 | HG02486.hp2 HG02922.hp1 |
synonymous_variant | LOW | c.696G>A | p.Thr232Thr | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/7 | 1344/6240 | 696/1098 | 232/365 | chr4 | 107903355 | ||
| chr4:107910463
|
G | A | 1 | a0001c0007 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.1008G>A | p.Pro336Pro | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 1656/6240 | 1008/1098 | 336/365 | chr4 | 107910463 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:107824969
|
A | G | 1 | a0001c0001t0034 | 1 | HG00735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-611A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/7 | 70585 | chr4 | 107824969 | |||||
| chr4:107895383
|
T | C | 1 | a0001c0001t0012 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-171T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/7 | 171 | chr4 | 107895383 | |||||
| chr4:107910573
|
A | C | 1 | a0001c0001t0033 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*20A>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 20 | chr4 | 107910573 | |||||
| chr4:107910684
|
A | G | 1 | a0001c0001t0032 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*131A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 131 | chr4 | 107910684 | |||||
| chr4:107910715
|
G | C | 1 | a0001c0001t0007 | 4 | HG01516.hp2 HG01981.hp2 HG02717.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*162G>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 162 | chr4 | 107910715 | |||||
| chr4:107910788
|
G | A | 1 | a0001c0001t0013 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*235G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 235 | chr4 | 107910788 | |||||
| chr4:107911071
|
C | T | 1 | a0001c0005t0031 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*518C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 518 | chr4 | 107911071 | |||||
| chr4:107911130
|
A | G | 18 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(15): Show | 73 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*577A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 577 | chr4 | 107911130 | |||||
| chr4:107911213
|
A | G | 1 | a0001c0001t0022 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*660A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 660 | chr4 | 107911213 | |||||
| chr4:107911318
|
G | A | 1 | a0001c0002t0023 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*765G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 765 | chr4 | 107911318 | |||||
| chr4:107911375
|
A | G | 1 | a0001c0001t0021 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*822A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 822 | chr4 | 107911375 | |||||
| chr4:107911571
|
T | C | 7 | a0001c0001t0002a0001c0001t0024a0001c0001t0026others(4): Show | 30 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1018T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 1018 | chr4 | 107911571 | |||||
| chr4:107911664
|
G | A | 1 | a0001c0001t0006 | 5 | HG01069.hp2 HG01071.hp2 HG02572.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1111G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 1111 | chr4 | 107911664 | |||||
| chr4:107911698
|
T | C | 1 | a0001c0001t0014 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1145T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 1145 | chr4 | 107911698 | |||||
| chr4:107911741
|
T | TA | 1 | a0001c0001t0008 | 3 | HG02895.hp2 HG02897.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1189dupA | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 1190 | INFO_REALIGN_3_PRIME | chr4 | 107911741 | ||||
| chr4:107911811
|
T | TAAAAAAT others(301): Show |
1 | a0001c0001t0011 | 2 | HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1273_*1274insGGCC others(304): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 1274 | INFO_REALIGN_3_PRIME | chr4 | 107911811 | ||||
| chr4:107911906
|
T | C | 1 | a0001c0001t0011 | 2 | HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1353T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 1353 | chr4 | 107911906 | |||||
| chr4:107912103
|
A | G | 1 | a0001c0001t0020 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1550A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 1550 | chr4 | 107912103 | |||||
| chr4:107912703
|
A | G | 1 | a0001c0001t0009 | 3 | HG00733.hp2 HG03490.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2150A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 2150 | chr4 | 107912703 | |||||
| chr4:107912770
|
T | C | 1 | a0001c0001t0027 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2217T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 2217 | chr4 | 107912770 | |||||
| chr4:107912789
|
C | A | 4 | a0001c0001t0004a0001c0001t0015a0001c0001t0028others(1): Show | 15 | HG00735.hp2 HG01109.hp2 HG01257.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2236C>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 2236 | chr4 | 107912789 | |||||
| chr4:107912842
|
C | T | 1 | a0001c0001t0019 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2289C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 2289 | chr4 | 107912842 | |||||
| chr4:107913007
|
A | G | 1 | a0001c0001t0018 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2454A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 2454 | chr4 | 107913007 | |||||
| chr4:107913248
|
T | C | 1 | a0001c0001t0016 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2695T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 2695 | chr4 | 107913248 | |||||
| chr4:107913353
|
A | G | 1 | a0001c0005t0031 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2800A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 2800 | chr4 | 107913353 | |||||
| chr4:107913373
|
G | T | 2 | a0001c0001t0004a0001c0002t0023 | 13 | HG00735.hp2 HG01257.hp1 HG02559.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2820G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 2820 | chr4 | 107913373 | |||||
| chr4:107913380
|
G | T | 1 | a0001c0001t0030 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2827G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 2827 | chr4 | 107913380 | |||||
| chr4:107913811
|
G | T | 1 | a0001c0001t0026 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3258G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 3258 | chr4 | 107913811 | |||||
| chr4:107913898
|
C | G | 1 | a0001c0001t0018 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3345C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 3345 | chr4 | 107913898 | |||||
| chr4:107914019
|
G | A | 1 | a0001c0001t0029 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3466G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 3466 | chr4 | 107914019 | |||||
| chr4:107914154
|
A | G | 1 | a0001c0001t0017 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3601A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 3601 | chr4 | 107914154 | |||||
| chr4:107914181
|
G | T | 1 | a0001c0007t0025 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3628G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 3628 | chr4 | 107914181 | |||||
| chr4:107914467
|
G | A | 1 | a0001c0001t0005 | 9 | HG01192.hp2 HG01884.hp1 HG01975.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3914G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 3914 | chr4 | 107914467 | |||||
| chr4:107914621
|
TATG | T | 2 | a0001c0001t0010a0001c0001t0029 | 3 | HG02257.hp1 HG03453.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4071_*4073delGAT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 4071 | INFO_REALIGN_3_PRIME | chr4 | 107914621 | ||||
| chr4:107914861
|
A | G | 1 | a0001c0001t0024 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4308A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 7/7 | 4308 | chr4 | 107914861 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:107825620
|
C | CT | 44 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(41): Show | 45 | HG01123.hp2 HG01167.hp1 HG01167.hp2 others(42): Show |
intron_variant | MODIFIER | c.-327+388dupT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107825620 | |||||
| chr4:107825620
|
C | CTT | 5 | a0001c0001t0001g0252a0001c0001t0001g0254a0001c0001t0003g0250others(2): Show | 5 | HG02572.hp1 HG02572.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-327+387_-327+388d others(4): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107825620 | |||||
| chr4:107825620
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0256a0001c0001t0003g0255 | 2 | HG01243.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-327+379_-327+388d others(12): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107825620 | |||||
| chr4:107825620
|
CT | C | 13 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0033others(10): Show | 13 | HG00323.hp2 HG01069.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.-327+388delT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107825620 | |||||
| chr4:107825620
|
CTTTTTT | C | 19 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(16): Show | 19 | HG01175.hp1 HG01361.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.-327+383_-327+388d others(8): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107825620 | |||||
| chr4:107825622
|
T | C | 1 | a0001c0005t0031g0012 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-327+369T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107825622 | ||||||
| chr4:107825834
|
C | T | 28 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(25): Show | 28 | HG01167.hp1 HG01175.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.-327+581C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107825834 | ||||||
| chr4:107825911
|
C | G | 2 | a0001c0001t0002g0207a0001c0001t0015g0208 | 2 | HG01109.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-327+658C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107825911 | ||||||
| chr4:107826054
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-327+801C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107826054 | ||||||
| chr4:107826076
|
A | G | 1 | a0001c0001t0001g0206 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-327+823A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107826076 | ||||||
| chr4:107826400
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-327+1147T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107826400 | ||||||
| chr4:107826548
|
C | CT | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0205others(3): Show | 7 | HG01255.hp2 HG01515.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-327+1305dupT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107826548 | |||||
| chr4:107826653
|
G | GT | 17 | a0001c0001t0001g0201a0001c0001t0001g0229a0001c0001t0001g0231others(14): Show | 17 | HG01109.hp1 HG01175.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-327+1411dupT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107826653 | |||||
| chr4:107826653
|
G | GTT | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0205others(3): Show | 7 | HG01255.hp2 HG01515.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-327+1410_-327+141 others(6): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107826653 | |||||
| chr4:107826653
|
G | T | 1 | a0001c0001t0016g0204 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-327+1400G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107826653 | ||||||
| chr4:107826842
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-327+1589G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107826842 | ||||||
| chr4:107826886
|
C | T | 2 | a0001c0001t0001g0256a0001c0001t0003g0255 | 2 | HG01243.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-327+1633C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107826886 | ||||||
| chr4:107827039
|
A | C | 2 | a0001c0001t0001g0199a0001c0001t0002g0200 | 2 | HG00642.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.-327+1786A>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107827039 | ||||||
| chr4:107827089
|
G | A | 2 | a0001c0001t0003g0250a0001c0001t0021g0043 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-327+1836G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107827089 | ||||||
| chr4:107827534
|
C | T | 4 | a0001c0001t0001g0198a0001c0001t0001g0256a0001c0001t0002g0008others(1): Show | 5 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.-327+2281C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107827534 | ||||||
| chr4:107827554
|
G | A | 21 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(18): Show | 21 | HG01175.hp1 HG01361.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.-327+2301G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107827554 | ||||||
| chr4:107827823
|
T | C | 1 | a0001c0001t0030g0044 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-327+2570T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107827823 | ||||||
| chr4:107827943
|
G | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0213a0001c0001t0001g0214others(3): Show | 6 | HG01123.hp2 HG01167.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.-327+2690G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107827943 | ||||||
| chr4:107827984
|
T | TCAAAA | 2 | a0001c0001t0005g0197a0001c0001t0006g0002 | 4 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-327+2752_-327+275 others(9): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107827984 | |||||
| chr4:107828023
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-327+2770C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107828023 | ||||||
| chr4:107828239
|
C | T | 3 | a0001c0001t0005g0197a0001c0001t0006g0002a0001c0001t0012g0196 | 5 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-327+2986C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107828239 | ||||||
| chr4:107828566
|
C | CT | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0014g0026 | 3 | HG02735.hp2 HG03688.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-327+3314dupT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107828566 | |||||
| chr4:107828833
|
C | G | 22 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0201others(19): Show | 23 | HG01109.hp1 HG01255.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.-327+3580C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107828833 | ||||||
| chr4:107828955
|
T | A | 1 | a0001c0001t0001g0030 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-327+3702T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107828955 | ||||||
| chr4:107829013
|
AAGG | A | 23 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0201others(20): Show | 24 | HG01109.hp1 HG01255.hp2 HG01515.hp1 others(21): Show |
intron_variant | MODIFIER | c.-327+3763_-327+376 others(7): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107829013 | |||||
| chr4:107829017
|
A | G | 23 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0201others(20): Show | 24 | HG01109.hp1 HG01255.hp2 HG01515.hp1 others(21): Show |
intron_variant | MODIFIER | c.-327+3764A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107829017 | ||||||
| chr4:107829116
|
T | C | 28 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(25): Show | 28 | HG01167.hp1 HG01175.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.-327+3863T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107829116 | ||||||
| chr4:107829199
|
T | A | 1 | a0001c0001t0012g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-327+3946T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107829199 | ||||||
| chr4:107829225
|
G | T | 1 | a0001c0001t0001g0198 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-327+3972G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107829225 | ||||||
| chr4:107829301
|
C | T | 4 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(1): Show | 4 | HG01106.hp1 HG01256.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.-327+4048C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107829301 | ||||||
| chr4:107829477
|
T | G | 2 | a0001c0001t0001g0256a0001c0001t0003g0255 | 2 | HG01243.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-327+4224T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107829477 | ||||||
| chr4:107829659
|
C | T | 1 | a0001c0001t0002g0202 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-327+4406C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107829659 | ||||||
| chr4:107829840
|
G | GC | 49 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(46): Show | 50 | HG01109.hp1 HG01167.hp1 HG01175.hp1 others(47): Show |
intron_variant | MODIFIER | c.-327+4587_-327+458 others(5): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107829840 | ||||||
| chr4:107829841
|
G | T | 49 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(46): Show | 50 | HG01109.hp1 HG01167.hp1 HG01175.hp1 others(47): Show |
intron_variant | MODIFIER | c.-327+4588G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107829841 | ||||||
| chr4:107829930
|
A | T | 1 | a0001c0001t0001g0244 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-327+4677A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107829930 | ||||||
| chr4:107830064
|
G | T | 27 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(24): Show | 27 | HG01167.hp1 HG01175.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.-327+4811G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107830064 | ||||||
| chr4:107830152
|
T | C | 2 | a0001c0001t0001g0245a0001c0003t0002g0246 | 2 | HG01167.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-327+4899T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107830152 | ||||||
| chr4:107830649
|
C | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(54): Show | 60 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.-327+5396C>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107830649 | ||||||
| chr4:107830727
|
G | GT | 3 | a0001c0001t0005g0197a0001c0001t0006g0002a0001c0001t0012g0196 | 5 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-327+5482dupT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107830727 | |||||
| chr4:107830811
|
G | A | 2 | a0001c0001t0003g0250a0001c0001t0021g0043 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-327+5558G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107830811 | ||||||
| chr4:107830973
|
G | A | 1 | a0001c0001t0002g0202 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-327+5720G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107830973 | ||||||
| chr4:107831140
|
G | T | 258 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(255): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-327+5887G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107831140 | ||||||
| chr4:107831230
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-327+5977G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107831230 | ||||||
| chr4:107831247
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-327+5994A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107831247 | ||||||
| chr4:107831294
|
G | C | 23 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0201others(20): Show | 26 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-327+6041G>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107831294 | ||||||
| chr4:107831383
|
C | T | 2 | a0001c0001t0005g0197a0001c0001t0006g0002 | 4 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-327+6130C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107831383 | ||||||
| chr4:107831434
|
T | C | 7 | a0001c0001t0001g0201a0001c0001t0002g0202a0001c0001t0003g0250others(4): Show | 9 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-327+6181T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107831434 | ||||||
| chr4:107831661
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-327+6408A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107831661 | ||||||
| chr4:107831811
|
A | T | 1 | a0001c0001t0001g0189 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-327+6558A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107831811 | ||||||
| chr4:107831907
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG02135.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-327+6654G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107831907 | ||||||
| chr4:107831966
|
A | G | 1 | a0001c0001t0002g0188 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-327+6713A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107831966 | ||||||
| chr4:107831996
|
C | T | 2 | a0001c0001t0001g0256a0001c0001t0003g0255 | 2 | HG01243.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-327+6743C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107831996 | ||||||
| chr4:107832246
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-327+6993C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107832246 | ||||||
| chr4:107832483
|
G | A | 24 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0033others(21): Show | 24 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.-327+7230G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107832483 | ||||||
| chr4:107832629
|
A | G | 6 | a0001c0001t0001g0186a0001c0001t0001g0241a0001c0001t0004g0239others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-327+7376A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107832629 | ||||||
| chr4:107832678
|
T | C | 1 | a0001c0001t0004g0066 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-327+7425T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107832678 | ||||||
| chr4:107832681
|
G | A | 63 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 68 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-327+7428G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107832681 | ||||||
| chr4:107832699
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-327+7446T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107832699 | ||||||
| chr4:107832803
|
G | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(66): Show | 74 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.-327+7550G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107832803 | ||||||
| chr4:107832960
|
T | C | 16 | a0001c0001t0001g0231a0001c0001t0002g0106a0001c0001t0002g0107others(13): Show | 16 | HG00280.hp1 HG01109.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-327+7707T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107832960 | ||||||
| chr4:107833234
|
G | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(73): Show | 81 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.-327+7981G>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107833234 | ||||||
| chr4:107833409
|
G | A | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-327+8156G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107833409 | ||||||
| chr4:107833537
|
A | C | 5 | a0001c0001t0001g0013a0001c0001t0001g0062a0001c0001t0001g0063others(2): Show | 5 | HG00733.hp1 HG01346.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-327+8284A>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107833537 | ||||||
| chr4:107833552
|
T | C | 2 | a0001c0001t0001g0241a0001c0001t0028g0203 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-327+8299T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107833552 | ||||||
| chr4:107833576
|
G | A | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-327+8323G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107833576 | ||||||
| chr4:107833663
|
A | T | 1 | a0001c0002t0023g0237 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-327+8410A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107833663 | ||||||
| chr4:107834037
|
A | G | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-327+8784A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107834037 | ||||||
| chr4:107834706
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-327+9453A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107834706 | ||||||
| chr4:107835115
|
G | A | 5 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0207others(2): Show | 5 | HG00280.hp1 HG01109.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-327+9862G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107835115 | ||||||
| chr4:107835132
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-327+9879A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107835132 | ||||||
| chr4:107835361
|
C | T | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-327+10108C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107835361 | ||||||
| chr4:107835387
|
G | A | 1 | a0001c0001t0005g0248 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-327+10134G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107835387 | ||||||
| chr4:107835586
|
C | T | 9 | a0001c0001t0001g0186a0001c0001t0001g0245a0001c0001t0001g0254others(6): Show | 9 | HG01167.hp1 HG02055.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.-327+10333C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107835586 | ||||||
| chr4:107835653
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-327+10400C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107835653 | ||||||
| chr4:107835782
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-327+10529C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107835782 | ||||||
| chr4:107835847
|
A | T | 1 | a0001c0001t0002g0060 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-327+10594A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107835847 | ||||||
| chr4:107835916
|
A | T | 2 | a0001c0001t0001g0241a0001c0001t0028g0203 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-327+10663A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107835916 | ||||||
| chr4:107835941
|
C | T | 2 | a0001c0001t0002g0101a0001c0001t0002g0102 | 2 | HG00099.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-327+10688C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107835941 | ||||||
| chr4:107836571
|
G | A | 16 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(13): Show | 16 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-327+11318G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107836571 | ||||||
| chr4:107836629
|
A | G | 1 | a0001c0001t0002g0042 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-327+11376A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107836629 | ||||||
| chr4:107836709
|
C | T | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-327+11456C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107836709 | ||||||
| chr4:107836798
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-327+11545G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107836798 | ||||||
| chr4:107836839
|
A | G | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0201others(2): Show | 5 | HG01109.hp1 HG01192.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-327+11586A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107836839 | ||||||
| chr4:107836870
|
G | A | 16 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(13): Show | 16 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-327+11617G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107836870 | ||||||
| chr4:107836964
|
G | A | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-327+11711G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107836964 | ||||||
| chr4:107837037
|
T | G | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-327+11784T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107837037 | ||||||
| chr4:107837114
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-327+11861T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107837114 | ||||||
| chr4:107837264
|
A | T | 2 | a0001c0001t0001g0183a0001c0001t0018g0228 | 2 | HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-327+12011A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107837264 | ||||||
| chr4:107837314
|
A | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(72): Show | 80 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.-327+12061A>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107837314 | ||||||
| chr4:107837423
|
A | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(108): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.-327+12170A>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107837423 | ||||||
| chr4:107837446
|
A | G | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-327+12193A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107837446 | ||||||
| chr4:107837790
|
C | T | 2 | a0001c0001t0001g0241a0001c0001t0028g0203 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-327+12537C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107837790 | ||||||
| chr4:107838101
|
G | T | 1 | a0001c0001t0002g0217 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-327+12848G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107838101 | ||||||
| chr4:107838320
|
T | A | 1 | a0001c0001t0001g0121 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-327+13067T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107838320 | ||||||
| chr4:107838422
|
A | ACTT | 22 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(19): Show | 22 | HG00735.hp2 HG01109.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.-327+13191_-327+13 others(9): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107838422 | |||||
| chr4:107838422
|
ACTT | A | 6 | a0001c0001t0001g0186a0001c0001t0003g0103a0001c0001t0004g0104others(3): Show | 6 | HG02055.hp2 HG03098.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-327+13191_-327+13 others(9): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107838422 | |||||
| chr4:107838468
|
A | AT | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-327+13216dupT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107838468 | |||||
| chr4:107838470
|
A | T | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-327+13217A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107838470 | ||||||
| chr4:107838488
|
A | T | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-327+13235A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107838488 | ||||||
| chr4:107838918
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-327+13665T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107838918 | ||||||
| chr4:107838927
|
T | C | 1 | a0001c0001t0024g0074 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-327+13674T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107838927 | ||||||
| chr4:107839082
|
A | G | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-327+13829A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107839082 | ||||||
| chr4:107839102
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-327+13849G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107839102 | ||||||
| chr4:107839149
|
T | G | 1 | a0001c0001t0004g0066 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-327+13896T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107839149 | ||||||
| chr4:107839242
|
T | G | 1 | a0001c0001t0001g0124 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-327+13989T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107839242 | ||||||
| chr4:107839347
|
G | A | 1 | a0001c0001t0003g0249 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-327+14094G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107839347 | ||||||
| chr4:107839377
|
G | GGTT | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-327+14125_-327+14 others(9): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107839377 | |||||
| chr4:107839378
|
G | A | 17 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(14): Show | 17 | HG01175.hp1 HG01361.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.-327+14125G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107839378 | ||||||
| chr4:107839510
|
A | G | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-327+14257A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107839510 | ||||||
| chr4:107839904
|
T | A | 1 | a0001c0001t0001g0126 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-327+14651T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107839904 | ||||||
| chr4:107840113
|
A | G | 2 | a0001c0001t0001g0241a0001c0001t0028g0203 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-327+14860A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107840113 | ||||||
| chr4:107840230
|
A | G | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-327+14977A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107840230 | ||||||
| chr4:107840307
|
A | G | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-327+15054A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107840307 | ||||||
| chr4:107840348
|
T | G | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-327+15095T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107840348 | ||||||
| chr4:107840568
|
C | A | 1 | a0001c0001t0001g0127 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-327+15315C>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107840568 | ||||||
| chr4:107840703
|
A | G | 2 | a0001c0001t0001g0241a0001c0001t0028g0203 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-327+15450A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107840703 | ||||||
| chr4:107840720
|
A | G | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-327+15467A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107840720 | ||||||
| chr4:107840881
|
C | A | 1 | a0001c0001t0001g0198 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-327+15628C>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107840881 | ||||||
| chr4:107840958
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-327+15705G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107840958 | ||||||
| chr4:107841047
|
G | A | 16 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(13): Show | 16 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-327+15794G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107841047 | ||||||
| chr4:107841130
|
A | G | 3 | a0001c0001t0001g0256a0001c0001t0003g0255a0001c0001t0012g0196 | 3 | HG01243.hp2 HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-327+15877A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107841130 | ||||||
| chr4:107841385
|
T | C | 8 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0207others(5): Show | 8 | HG00280.hp1 HG01109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-327+16132T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107841385 | ||||||
| chr4:107841416
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-327+16163C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107841416 | ||||||
| chr4:107841457
|
A | G | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0002g0173 | 3 | HG01106.hp2 HG01123.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-327+16204A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107841457 | ||||||
| chr4:107841618
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-327+16365T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107841618 | ||||||
| chr4:107841813
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-327+16560A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107841813 | ||||||
| chr4:107841823
|
A | AT | 5 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0207others(2): Show | 5 | HG00280.hp1 HG01109.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-327+16578dupT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107841823 | |||||
| chr4:107841832
|
G | C | 16 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(13): Show | 16 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-327+16579G>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107841832 | ||||||
| chr4:107841946
|
C | T | 2 | a0001c0001t0001g0241a0001c0001t0028g0203 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-326-16526C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107841946 | ||||||
| chr4:107841961
|
A | AT | 6 | a0001c0001t0001g0011a0001c0001t0001g0205a0001c0001t0001g0243others(3): Show | 7 | HG01255.hp2 HG01515.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-326-16502dupT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107841961 | |||||
| chr4:107841962
|
T | A | 19 | a0001c0001t0001g0062a0001c0001t0001g0119a0001c0001t0001g0120others(16): Show | 19 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-326-16510T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107841962 | ||||||
| chr4:107842169
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-326-16303A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107842169 | ||||||
| chr4:107842189
|
TAAAG | T | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0201others(2): Show | 5 | HG01109.hp1 HG01192.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-326-16279_-326-16 others(10): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107842189 | |||||
| chr4:107842284
|
T | A | 1 | a0001c0001t0004g0110 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-326-16188T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107842284 | ||||||
| chr4:107842465
|
A | G | 9 | a0001c0001t0001g0236a0001c0001t0001g0256a0001c0001t0002g0202others(6): Show | 11 | HG01069.hp2 HG01071.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.-326-16007A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107842465 | ||||||
| chr4:107842587
|
T | C | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-326-15885T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107842587 | ||||||
| chr4:107842614
|
A | G | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-326-15858A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107842614 | ||||||
| chr4:107842814
|
G | C | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-326-15658G>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107842814 | ||||||
| chr4:107842908
|
T | C | 16 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(13): Show | 16 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-326-15564T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107842908 | ||||||
| chr4:107842947
|
A | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(108): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.-326-15525A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107842947 | ||||||
| chr4:107842948
|
A | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(108): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.-326-15524A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107842948 | ||||||
| chr4:107842980
|
G | T | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-326-15492G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107842980 | ||||||
| chr4:107843173
|
T | C | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-326-15299T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107843173 | ||||||
| chr4:107843223
|
A | C | 2 | a0001c0001t0001g0241a0001c0001t0028g0203 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-326-15249A>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107843223 | ||||||
| chr4:107843296
|
T | C | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-326-15176T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107843296 | ||||||
| chr4:107843320
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-326-15152A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107843320 | ||||||
| chr4:107843347
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-326-15125G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107843347 | ||||||
| chr4:107843616
|
A | G | 1 | a0001c0001t0001g0206 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-326-14856A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107843616 | ||||||
| chr4:107843866
|
A | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0174a0001c0001t0001g0175others(1): Show | 4 | HG01106.hp2 HG01123.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.-326-14606A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107843866 | ||||||
| chr4:107844119
|
G | A | 1 | a0001c0001t0002g0128 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-326-14353G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107844119 | ||||||
| chr4:107844126
|
G | T | 1 | a0001c0001t0001g0121 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-326-14346G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107844126 | ||||||
| chr4:107844152
|
C | G | 1 | a0001c0001t0021g0043 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-326-14320C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107844152 | ||||||
| chr4:107844323
|
C | CA | 20 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(17): Show | 20 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.-326-14138dupA | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107844323 | |||||
| chr4:107844627
|
C | G | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-326-13845C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107844627 | ||||||
| chr4:107844638
|
C | T | 16 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(13): Show | 16 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-326-13834C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107844638 | ||||||
| chr4:107844696
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-326-13776A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107844696 | ||||||
| chr4:107844701
|
G | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0071others(12): Show | 18 | HG00099.hp2 HG00733.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.-326-13771G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107844701 | ||||||
| chr4:107844881
|
A | G | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-326-13591A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107844881 | ||||||
| chr4:107844949
|
A | G | 2 | a0001c0001t0011g0040a0001c0001t0011g0170 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-326-13523A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107844949 | ||||||
| chr4:107845156
|
C | A | 16 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(13): Show | 16 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-326-13316C>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107845156 | ||||||
| chr4:107845391
|
G | T | 1 | a0001c0001t0002g0169 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-326-13081G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107845391 | ||||||
| chr4:107845435
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-326-13037T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107845435 | ||||||
| chr4:107845676
|
G | A | 5 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0207others(2): Show | 5 | HG00280.hp1 HG01109.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-326-12796G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107845676 | ||||||
| chr4:107845818
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-326-12654G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107845818 | ||||||
| chr4:107845829
|
C | G | 16 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(13): Show | 16 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-326-12643C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107845829 | ||||||
| chr4:107845864
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-326-12608G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107845864 | ||||||
| chr4:107845882
|
C | T | 16 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(13): Show | 16 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-326-12590C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107845882 | ||||||
| chr4:107845909
|
A | T | 2 | a0001c0001t0001g0241a0001c0001t0028g0203 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-326-12563A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107845909 | ||||||
| chr4:107845921
|
T | C | 16 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(13): Show | 16 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-326-12551T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107845921 | ||||||
| chr4:107845977
|
G | A | 1 | a0001c0002t0023g0237 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-326-12495G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107845977 | ||||||
| chr4:107846000
|
T | G | 1 | a0001c0001t0006g0002 | 3 | HG01069.hp2 HG01071.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-326-12472T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107846000 | ||||||
| chr4:107846115
|
T | A | 1 | a0001c0001t0003g0249 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-326-12357T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107846115 | ||||||
| chr4:107846166
|
G | T | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-326-12306G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107846166 | ||||||
| chr4:107846179
|
G | T | 1 | a0001c0001t0027g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-326-12293G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107846179 | ||||||
| chr4:107846209
|
C | T | 2 | a0001c0002t0023g0237a0001c0003t0002g0246 | 2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-326-12263C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107846209 | ||||||
| chr4:107846252
|
AC | A | 16 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(13): Show | 16 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-326-12217delC | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107846252 | |||||
| chr4:107846257
|
C | T | 16 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(13): Show | 16 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-326-12215C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107846257 | ||||||
| chr4:107846374
|
G | C | 1 | a0001c0001t0003g0212 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-326-12098G>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107846374 | ||||||
| chr4:107846434
|
A | G | 2 | a0001c0001t0001g0241a0001c0001t0028g0203 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-326-12038A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107846434 | ||||||
| chr4:107846570
|
C | T | 2 | a0001c0001t0001g0241a0001c0001t0028g0203 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-326-11902C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107846570 | ||||||
| chr4:107846772
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-326-11700C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107846772 | ||||||
| chr4:107846798
|
T | C | 2 | a0001c0001t0001g0241a0001c0001t0028g0203 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-326-11674T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107846798 | ||||||
| chr4:107846879
|
T | C | 1 | a0001c0001t0001g0131 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-326-11593T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107846879 | ||||||
| chr4:107846883
|
A | G | 1 | a0001c0001t0001g0033 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-326-11589A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107846883 | ||||||
| chr4:107846957
|
C | G | 1 | a0001c0001t0002g0168 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-326-11515C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107846957 | ||||||
| chr4:107847038
|
G | A | 2 | a0001c0001t0001g0241a0001c0001t0028g0203 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-326-11434G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107847038 | ||||||
| chr4:107847110
|
T | G | 1 | a0001c0003t0002g0246 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-326-11362T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107847110 | ||||||
| chr4:107847144
|
T | G | 1 | a0001c0001t0001g0126 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-326-11328T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107847144 | ||||||
| chr4:107847217
|
G | T | 1 | a0001c0001t0001g0198 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-326-11255G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107847217 | ||||||
| chr4:107847247
|
G | A | 16 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(13): Show | 16 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-326-11225G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107847247 | ||||||
| chr4:107847397
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-326-11075C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107847397 | ||||||
| chr4:107847435
|
G | A | 4 | a0001c0001t0001g0083a0001c0001t0001g0199a0001c0001t0002g0008others(1): Show | 5 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-326-11037G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107847435 | ||||||
| chr4:107847544
|
G | A | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-326-10928G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107847544 | ||||||
| chr4:107847572
|
G | T | 7 | a0001c0001t0001g0039a0001c0001t0001g0165a0001c0001t0001g0166others(4): Show | 7 | NA18747.hp1 NA18941.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.-326-10900G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107847572 | ||||||
| chr4:107847594
|
C | T | 7 | a0001c0001t0001g0039a0001c0001t0001g0165a0001c0001t0001g0166others(4): Show | 7 | NA18747.hp1 NA18941.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.-326-10878C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107847594 | ||||||
| chr4:107847604
|
T | G | 1 | a0001c0001t0001g0132 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-326-10868T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107847604 | ||||||
| chr4:107847931
|
A | T | 1 | a0001c0001t0002g0129 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-326-10541A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107847931 | ||||||
| chr4:107848046
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-326-10426C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107848046 | ||||||
| chr4:107848500
|
C | T | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-326-9972C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107848500 | ||||||
| chr4:107848712
|
A | T | 2 | a0001c0001t0001g0241a0001c0001t0028g0203 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-326-9760A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107848712 | ||||||
| chr4:107849038
|
A | G | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-326-9434A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107849038 | ||||||
| chr4:107849048
|
G | A | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-326-9424G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107849048 | ||||||
| chr4:107849158
|
C | T | 2 | a0001c0001t0001g0241a0001c0001t0028g0203 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-326-9314C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107849158 | ||||||
| chr4:107849165
|
C | T | 2 | a0001c0001t0001g0241a0001c0001t0028g0203 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-326-9307C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107849165 | ||||||
| chr4:107849198
|
A | G | 2 | a0001c0001t0029g0230a0001c0005t0031g0012 | 2 | HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-326-9274A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107849198 | ||||||
| chr4:107849203
|
G | A | 4 | a0001c0001t0003g0235a0001c0001t0003g0250a0001c0001t0004g0234others(1): Show | 4 | HG02922.hp1 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-326-9269G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107849203 | ||||||
| chr4:107849319
|
G | A | 1 | a0001c0001t0006g0172 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-326-9153G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107849319 | ||||||
| chr4:107849433
|
C | A | 1 | a0001c0001t0003g0250 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-326-9039C>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107849433 | ||||||
| chr4:107849458
|
G | T | 16 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(13): Show | 16 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-326-9014G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107849458 | ||||||
| chr4:107849459
|
A | T | 16 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(13): Show | 16 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-326-9013A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107849459 | ||||||
| chr4:107849480
|
A | G | 2 | a0001c0001t0008g0007a0001c0001t0008g0224 | 3 | HG02895.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-326-8992A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107849480 | ||||||
| chr4:107849610
|
G | C | 6 | a0001c0001t0005g0115a0001c0001t0005g0116a0001c0001t0005g0117others(3): Show | 6 | HG01884.hp1 HG02647.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-326-8862G>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107849610 | ||||||
| chr4:107849635
|
GTGACTTT others(14): Show |
G | 18 | a0001c0001t0001g0119a0001c0001t0001g0183a0001c0001t0001g0201others(15): Show | 18 | HG00735.hp2 HG01109.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-326-8815_-326-879 others(25): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107849635 | |||||
| chr4:107849657
|
T | G | 1 | a0001c0001t0001g0171 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-326-8815T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107849657 | ||||||
| chr4:107849660
|
CTTTTTAA others(10): Show |
C | 1 | a0001c0001t0001g0229 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-326-8811_-326-879 others(21): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107849660 | ||||||
| chr4:107849754
|
C | G | 1 | a0001c0001t0001g0059 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-326-8718C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107849754 | ||||||
| chr4:107849867
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-326-8605A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107849867 | ||||||
| chr4:107850179
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-326-8293C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107850179 | ||||||
| chr4:107850186
|
C | A | 4 | a0001c0001t0001g0130a0001c0001t0001g0241a0001c0001t0003g0249others(1): Show | 4 | HG02258.hp1 HG02559.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-326-8286C>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107850186 | ||||||
| chr4:107850264
|
T | G | 23 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0130others(20): Show | 24 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.-326-8208T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107850264 | ||||||
| chr4:107850286
|
TA | T | 4 | a0001c0001t0001g0013a0001c0001t0001g0058a0001c0001t0001g0164others(1): Show | 4 | HG03490.hp2 NA18942.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.-326-8183delA | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107850286 | |||||
| chr4:107850339
|
C | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(47): Show | 55 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.-326-8133C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107850339 | ||||||
| chr4:107850348
|
T | C | 6 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0216others(3): Show | 6 | HG02809.hp1 HG02895.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-326-8124T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107850348 | ||||||
| chr4:107850490
|
G | A | 19 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(16): Show | 20 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.-326-7982G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107850490 | ||||||
| chr4:107850501
|
G | A | 2 | a0001c0001t0001g0254a0001c0007t0025g0114 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-326-7971G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107850501 | ||||||
| chr4:107850595
|
A | T | 23 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0130others(20): Show | 24 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.-326-7877A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107850595 | ||||||
| chr4:107850852
|
T | C | 19 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(16): Show | 19 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-326-7620T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107850852 | ||||||
| chr4:107850913
|
G | C | 4 | a0001c0001t0001g0119a0001c0001t0001g0201a0001c0001t0008g0007others(1): Show | 5 | HG01109.hp1 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-326-7559G>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107850913 | ||||||
| chr4:107851115
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-326-7357G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107851115 | ||||||
| chr4:107851123
|
T | C | 3 | a0001c0001t0001g0256a0001c0001t0003g0255a0001c0001t0012g0196 | 3 | HG01243.hp2 HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-326-7349T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107851123 | ||||||
| chr4:107851225
|
C | G | 1 | a0001c0001t0001g0023 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-326-7247C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107851225 | ||||||
| chr4:107851303
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-326-7169A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107851303 | ||||||
| chr4:107851411
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-326-7061T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107851411 | ||||||
| chr4:107851477
|
A | G | 19 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(16): Show | 20 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.-326-6995A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107851477 | ||||||
| chr4:107851488
|
C | G | 1 | a0001c0003t0002g0246 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-326-6984C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107851488 | ||||||
| chr4:107851577
|
A | G | 2 | a0001c0001t0011g0040a0001c0001t0011g0170 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-326-6895A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107851577 | ||||||
| chr4:107851603
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(118): Show | 127 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.-326-6869C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107851603 | ||||||
| chr4:107851763
|
G | T | 23 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0130others(20): Show | 24 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.-326-6709G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107851763 | ||||||
| chr4:107852033
|
G | A | 23 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0130others(20): Show | 24 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.-326-6439G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107852033 | ||||||
| chr4:107852040
|
A | G | 20 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(17): Show | 21 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-326-6432A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107852040 | ||||||
| chr4:107852071
|
A | AT | 27 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(24): Show | 27 | HG00280.hp1 HG00738.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.-326-6386dupT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107852071 | |||||
| chr4:107852071
|
AT | A | 5 | a0001c0001t0001g0034a0001c0001t0001g0059a0001c0001t0001g0135others(2): Show | 5 | HG01167.hp1 HG02976.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.-326-6386delT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107852071 | |||||
| chr4:107852090
|
A | G | 3 | a0001c0001t0001g0024a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG00544.hp2 HG02015.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.-326-6382A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107852090 | ||||||
| chr4:107852129
|
C | T | 3 | a0001c0001t0001g0130a0001c0001t0003g0249a0001c0001t0021g0043 | 3 | HG02258.hp1 HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-326-6343C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107852129 | ||||||
| chr4:107852402
|
T | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-326-6070T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107852402 | ||||||
| chr4:107852525
|
A | T | 2 | a0001c0001t0001g0130a0001c0001t0021g0043 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-326-5947A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107852525 | ||||||
| chr4:107852544
|
C | T | 7 | a0001c0001t0001g0186a0001c0001t0003g0103a0001c0001t0004g0104others(4): Show | 7 | HG02055.hp2 HG02615.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-326-5928C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107852544 | ||||||
| chr4:107852578
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0021g0043 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-326-5894G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107852578 | ||||||
| chr4:107852582
|
CAGG | C | 6 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0216others(3): Show | 6 | HG02809.hp1 HG02895.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-326-5887_-326-588 others(7): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107852582 | |||||
| chr4:107852746
|
A | AT | 51 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(48): Show | 57 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.-326-5714dupT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107852746 | |||||
| chr4:107852746
|
A | ATT | 17 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(14): Show | 17 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-326-5715_-326-571 others(6): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107852746 | |||||
| chr4:107852746
|
A | ATTTTTTT | 22 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(19): Show | 22 | HG00280.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.-326-5720_-326-571 others(11): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107852746 | |||||
| chr4:107852955
|
G | A | 26 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(23): Show | 26 | HG00280.hp1 HG01175.hp1 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.-326-5517G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107852955 | ||||||
| chr4:107853036
|
G | T | 3 | a0001c0001t0001g0130a0001c0001t0003g0249a0001c0001t0021g0043 | 3 | HG02258.hp1 HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-326-5436G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107853036 | ||||||
| chr4:107853077
|
C | T | 1 | a0001c0001t0001g0161 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-326-5395C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107853077 | ||||||
| chr4:107853089
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(75): Show | 83 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.-326-5383C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107853089 | ||||||
| chr4:107853092
|
T | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(66): Show | 74 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.-326-5380T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107853092 | ||||||
| chr4:107853432
|
A | G | 2 | a0001c0001t0001g0130a0001c0001t0021g0043 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-326-5040A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107853432 | ||||||
| chr4:107853780
|
C | G | 2 | a0001c0001t0001g0046a0001c0001t0001g0076 | 2 | HG02080.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.-326-4692C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107853780 | ||||||
| chr4:107853909
|
T | G | 1 | a0001c0001t0001g0186 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-326-4563T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107853909 | ||||||
| chr4:107853984
|
G | A | 1 | a0001c0001t0003g0249 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-326-4488G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107853984 | ||||||
| chr4:107854045
|
A | G | 1 | a0001c0001t0002g0128 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-326-4427A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107854045 | ||||||
| chr4:107854098
|
A | T | 23 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG00280.hp1 HG01175.hp1 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.-326-4374A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107854098 | ||||||
| chr4:107854186
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-326-4286A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107854186 | ||||||
| chr4:107854369
|
A | G | 3 | a0001c0001t0001g0130a0001c0001t0003g0249a0001c0001t0021g0043 | 3 | HG02258.hp1 HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-326-4103A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107854369 | ||||||
| chr4:107854380
|
TTC | T | 18 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(15): Show | 18 | HG01175.hp1 HG01361.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-326-4090_-326-408 others(6): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107854380 | |||||
| chr4:107854851
|
G | C | 4 | a0001c0001t0001g0135a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 4 | NA18612.hp2 NA18948.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.-326-3621G>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107854851 | ||||||
| chr4:107854909
|
A | G | 3 | a0001c0001t0001g0130a0001c0001t0003g0249a0001c0001t0021g0043 | 3 | HG02258.hp1 HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-326-3563A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107854909 | ||||||
| chr4:107855300
|
T | C | 2 | a0001c0001t0001g0130a0001c0001t0021g0043 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-326-3172T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107855300 | ||||||
| chr4:107855407
|
T | G | 3 | a0001c0001t0001g0130a0001c0001t0003g0249a0001c0001t0021g0043 | 3 | HG02258.hp1 HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-326-3065T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107855407 | ||||||
| chr4:107855520
|
G | A | 1 | a0001c0001t0002g0188 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-326-2952G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107855520 | ||||||
| chr4:107855582
|
G | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0140a0001c0001t0001g0191 | 3 | HG03688.hp2 HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-326-2890G>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107855582 | ||||||
| chr4:107855643
|
A | T | 2 | a0001c0001t0001g0126a0001c0001t0020g0159 | 2 | HG00738.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-326-2829A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107855643 | ||||||
| chr4:107855663
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-326-2809C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107855663 | ||||||
| chr4:107855681
|
G | A | 1 | a0001c0001t0030g0044 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-326-2791G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107855681 | ||||||
| chr4:107855980
|
A | G | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0201others(2): Show | 5 | HG01109.hp1 HG01192.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-326-2492A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107855980 | ||||||
| chr4:107856121
|
C | G | 1 | a0001c0001t0001g0241 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-326-2351C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107856121 | ||||||
| chr4:107856637
|
C | T | 3 | a0001c0001t0001g0130a0001c0001t0010g0238a0001c0001t0021g0043 | 3 | HG02258.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-326-1835C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107856637 | ||||||
| chr4:107856661
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-326-1811A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107856661 | ||||||
| chr4:107857104
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-326-1368T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107857104 | ||||||
| chr4:107857157
|
G | T | 6 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0216others(3): Show | 6 | HG02809.hp1 HG02895.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-326-1315G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107857157 | ||||||
| chr4:107857363
|
T | G | 44 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(41): Show | 45 | HG00280.hp1 HG01109.hp1 HG01175.hp1 others(42): Show |
intron_variant | MODIFIER | c.-326-1109T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107857363 | ||||||
| chr4:107857531
|
G | GAT | 52 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(49): Show | 57 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.-326-920_-326-919d others(4): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107857531 | |||||
| chr4:107857531
|
G | GATAT | 14 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0079others(11): Show | 14 | HG01192.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-326-922_-326-919d others(6): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107857531 | |||||
| chr4:107857531
|
G | GATATAT | 33 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(30): Show | 33 | HG01175.hp1 HG01361.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.-326-924_-326-919d others(8): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107857531 | |||||
| chr4:107857531
|
GAT | G | 5 | a0001c0001t0005g0115a0001c0001t0005g0116a0001c0001t0005g0117others(2): Show | 5 | HG01884.hp1 HG02647.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-326-920_-326-919d others(4): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107857531 | |||||
| chr4:107857531
|
GATAT | G | 10 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0190others(7): Show | 11 | HG01109.hp1 HG01192.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-326-922_-326-919d others(6): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107857531 | |||||
| chr4:107857630
|
A | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0214others(2): Show | 5 | HG01123.hp2 HG01167.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.-326-842A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107857630 | ||||||
| chr4:107857638
|
C | G | 1 | a0001c0001t0001g0158 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-326-834C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107857638 | ||||||
| chr4:107857751
|
A | G | 1 | a0001c0001t0003g0249 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-326-721A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107857751 | ||||||
| chr4:107857756
|
G | A | 1 | a0001c0001t0002g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-326-716G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107857756 | ||||||
| chr4:107857903
|
G | A | 4 | a0001c0001t0001g0135a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 4 | NA18612.hp2 NA18948.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.-326-569G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107857903 | ||||||
| chr4:107858010
|
A | AC | 43 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(40): Show | 44 | HG01109.hp1 HG01175.hp1 HG01261.hp2 others(41): Show |
intron_variant | MODIFIER | c.-326-454dupC | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 107858010 | |||||
| chr4:107858069
|
A | G | 1 | a0001c0001t0003g0249 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-326-403A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107858069 | ||||||
| chr4:107858151
|
T | C | 19 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(16): Show | 19 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-326-321T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107858151 | ||||||
| chr4:107858179
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(98): Show | 107 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.-326-293C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107858179 | ||||||
| chr4:107858259
|
G | A | 6 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0216others(3): Show | 6 | HG02809.hp1 HG02895.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-326-213G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107858259 | ||||||
| chr4:107858294
|
G | A | 42 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(39): Show | 43 | HG00280.hp1 HG01109.hp1 HG01175.hp1 others(40): Show |
intron_variant | MODIFIER | c.-326-178G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107858294 | ||||||
| chr4:107858459
|
T | C | 3 | a0001c0001t0001g0130a0001c0001t0003g0249a0001c0001t0021g0043 | 3 | HG02258.hp1 HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-326-13T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 1/6 | chr4 | 107858459 | ||||||
| chr4:107858669
|
TTGC | T | 45 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(42): Show | 46 | HG00280.hp1 HG01109.hp1 HG01175.hp1 others(43): Show |
intron_variant | MODIFIER | c.-245+124_-245+126d others(5): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107858669 | |||||
| chr4:107858850
|
T | C | 45 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(42): Show | 46 | HG00280.hp1 HG01109.hp1 HG01175.hp1 others(43): Show |
intron_variant | MODIFIER | c.-245+297T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107858850 | ||||||
| chr4:107858883
|
A | C | 1 | a0001c0001t0016g0204 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-245+330A>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107858883 | ||||||
| chr4:107858959
|
C | T | 45 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(42): Show | 46 | HG00280.hp1 HG01109.hp1 HG01175.hp1 others(43): Show |
intron_variant | MODIFIER | c.-245+406C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107858959 | ||||||
| chr4:107858984
|
A | G | 19 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(16): Show | 19 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-245+431A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107858984 | ||||||
| chr4:107859035
|
A | C | 1 | a0001c0001t0003g0232 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-245+482A>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107859035 | ||||||
| chr4:107859050
|
A | T | 2 | a0001c0001t0001g0130a0001c0001t0021g0043 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-245+497A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107859050 | ||||||
| chr4:107859522
|
C | A | 1 | a0001c0001t0004g0143 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-245+969C>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107859522 | ||||||
| chr4:107859628
|
C | T | 6 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0216others(3): Show | 6 | HG02809.hp1 HG02895.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-245+1075C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107859628 | ||||||
| chr4:107859743
|
G | C | 1 | a0001c0001t0001g0198 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-245+1190G>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107859743 | ||||||
| chr4:107859862
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-245+1309A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107859862 | ||||||
| chr4:107859959
|
GT | G | 45 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(42): Show | 46 | HG00280.hp1 HG01109.hp1 HG01175.hp1 others(43): Show |
intron_variant | MODIFIER | c.-245+1416delT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107859959 | |||||
| chr4:107860035
|
C | T | 10 | a0001c0001t0001g0252a0001c0001t0005g0115a0001c0001t0005g0116others(7): Show | 10 | HG01884.hp1 HG01975.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-245+1482C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107860035 | ||||||
| chr4:107860254
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-245+1701G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107860254 | ||||||
| chr4:107860258
|
C | G | 1 | a0001c0001t0004g0162 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-245+1705C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107860258 | ||||||
| chr4:107860429
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-245+1876A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107860429 | ||||||
| chr4:107860492
|
G | T | 3 | a0001c0001t0001g0130a0001c0001t0003g0249a0001c0001t0021g0043 | 3 | HG02258.hp1 HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-245+1939G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107860492 | ||||||
| chr4:107860508
|
A | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(132): Show | 142 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.-245+1955A>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107860508 | ||||||
| chr4:107860525
|
GT | G | 26 | a0001c0001t0001g0085a0001c0001t0001g0119a0001c0001t0001g0120others(23): Show | 26 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-245+1986delT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107860525 | |||||
| chr4:107860526
|
T | C | 1 | a0001c0001t0020g0159 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-245+1973T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107860526 | ||||||
| chr4:107860584
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-245+2031C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107860584 | ||||||
| chr4:107860590
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-245+2037C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107860590 | ||||||
| chr4:107860668
|
A | G | 45 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(42): Show | 46 | HG00280.hp1 HG01109.hp1 HG01175.hp1 others(43): Show |
intron_variant | MODIFIER | c.-245+2115A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107860668 | ||||||
| chr4:107860713
|
T | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(239): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.-245+2160T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107860713 | ||||||
| chr4:107860777
|
G | A | 18 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(15): Show | 18 | HG01175.hp1 HG01361.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-245+2224G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107860777 | ||||||
| chr4:107860843
|
A | G | 45 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(42): Show | 46 | HG00280.hp1 HG01109.hp1 HG01175.hp1 others(43): Show |
intron_variant | MODIFIER | c.-245+2290A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107860843 | ||||||
| chr4:107860930
|
C | T | 3 | a0001c0001t0001g0130a0001c0001t0003g0249a0001c0001t0021g0043 | 3 | HG02258.hp1 HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-245+2377C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107860930 | ||||||
| chr4:107860971
|
A | G | 2 | a0001c0001t0001g0164a0001c0001t0032g0155 | 2 | HG00544.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.-245+2418A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107860971 | ||||||
| chr4:107860984
|
T | G | 2 | a0001c0001t0001g0130a0001c0001t0021g0043 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-245+2431T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107860984 | ||||||
| chr4:107861039
|
G | A | 1 | a0001c0001t0003g0249 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-245+2486G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107861039 | ||||||
| chr4:107861534
|
TATTTCTT others(1): Show |
T | 2 | a0001c0001t0008g0007a0001c0001t0008g0224 | 3 | HG02895.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-245+2982_-245+298 others(12): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107861534 | ||||||
| chr4:107861600
|
T | C | 18 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(15): Show | 18 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-245+3047T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107861600 | ||||||
| chr4:107861817
|
A | G | 43 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(40): Show | 44 | HG00280.hp1 HG01109.hp1 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.-245+3264A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107861817 | ||||||
| chr4:107862131
|
G | A | 1 | a0001c0001t0001g0004 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-245+3578G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107862131 | ||||||
| chr4:107862247
|
C | T | 23 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0017others(20): Show | 23 | HG01167.hp2 HG01175.hp1 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.-245+3694C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107862247 | ||||||
| chr4:107862603
|
A | T | 128 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(125): Show | 134 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.-245+4050A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107862603 | ||||||
| chr4:107862697
|
C | T | 5 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0216others(2): Show | 5 | HG02809.hp1 HG02895.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-245+4144C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107862697 | ||||||
| chr4:107862975
|
G | A | 22 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0201others(19): Show | 22 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.-245+4422G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107862975 | ||||||
| chr4:107863036
|
C | G | 3 | a0001c0001t0002g0177a0001c0001t0003g0176a0001c0001t0003g0226 | 3 | HG02723.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-245+4483C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107863036 | ||||||
| chr4:107863358
|
A | G | 128 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(125): Show | 134 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.-245+4805A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107863358 | ||||||
| chr4:107863499
|
T | C | 4 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0207others(1): Show | 4 | HG00280.hp1 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-245+4946T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107863499 | ||||||
| chr4:107864176
|
G | T | 128 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(125): Show | 134 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.-245+5623G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107864176 | ||||||
| chr4:107864207
|
C | G | 2 | a0001c0001t0004g0006a0001c0001t0004g0143 | 3 | HG02622.hp2 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-245+5654C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107864207 | ||||||
| chr4:107864312
|
G | A | 128 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(125): Show | 134 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.-245+5759G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107864312 | ||||||
| chr4:107864420
|
G | T | 4 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0207others(1): Show | 4 | HG00280.hp1 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-245+5867G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107864420 | ||||||
| chr4:107864590
|
G | A | 138 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(135): Show | 144 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.-245+6037G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107864590 | ||||||
| chr4:107864635
|
G | T | 1 | a0001c0001t0001g0036 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-245+6082G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107864635 | ||||||
| chr4:107864647
|
G | A | 7 | a0001c0001t0001g0254a0001c0001t0001g0256a0001c0001t0003g0249others(4): Show | 7 | HG01243.hp2 HG02559.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.-245+6094G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107864647 | ||||||
| chr4:107864651
|
A | G | 128 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(125): Show | 134 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.-245+6098A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107864651 | ||||||
| chr4:107864746
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-245+6193G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107864746 | ||||||
| chr4:107864764
|
C | G | 1 | a0001c0001t0013g0156 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-245+6211C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107864764 | ||||||
| chr4:107864873
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-245+6320G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107864873 | ||||||
| chr4:107864973
|
A | G | 128 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(125): Show | 134 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.-245+6420A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107864973 | ||||||
| chr4:107865028
|
A | G | 6 | a0001c0001t0001g0086a0001c0001t0001g0097a0001c0001t0001g0121others(3): Show | 6 | HG00642.hp2 HG01099.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.-245+6475A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107865028 | ||||||
| chr4:107865116
|
G | A | 128 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(125): Show | 134 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.-245+6563G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107865116 | ||||||
| chr4:107865255
|
G | T | 1 | a0001c0001t0010g0238 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-245+6702G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107865255 | ||||||
| chr4:107865517
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-245+6964T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107865517 | ||||||
| chr4:107865573
|
G | T | 128 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(125): Show | 134 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.-245+7020G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107865573 | ||||||
| chr4:107865653
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-245+7100C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107865653 | ||||||
| chr4:107865760
|
T | A | 1 | a0001c0001t0029g0230 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-245+7207T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107865760 | ||||||
| chr4:107865827
|
C | T | 128 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(125): Show | 134 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.-245+7274C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107865827 | ||||||
| chr4:107865840
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-245+7287T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107865840 | ||||||
| chr4:107866331
|
C | T | 1 | a0001c0001t0029g0230 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-245+7778C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107866331 | ||||||
| chr4:107866568
|
A | T | 11 | a0001c0001t0001g0011a0001c0001t0001g0174a0001c0001t0001g0175others(8): Show | 14 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.-245+8015A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107866568 | ||||||
| chr4:107866582
|
A | C | 3 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0082 | 3 | HG01192.hp1 HG03654.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-245+8029A>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107866582 | ||||||
| chr4:107866828
|
A | G | 1 | a0001c0001t0002g0060 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-245+8275A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107866828 | ||||||
| chr4:107866969
|
T | C | 138 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(135): Show | 144 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.-245+8416T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107866969 | ||||||
| chr4:107867108
|
G | A | 138 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(135): Show | 144 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.-245+8555G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107867108 | ||||||
| chr4:107867333
|
A | G | 2 | a0001c0001t0001g0039a0001c0001t0001g0167 | 2 | NA18941.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.-245+8780A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107867333 | ||||||
| chr4:107867471
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-245+8918A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107867471 | ||||||
| chr4:107867524
|
A | G | 70 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0014others(67): Show | 72 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.-245+8971A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107867524 | ||||||
| chr4:107867525
|
C | T | 138 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(135): Show | 144 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.-245+8972C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107867525 | ||||||
| chr4:107867682
|
A | G | 128 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(125): Show | 134 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.-245+9129A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107867682 | ||||||
| chr4:107867705
|
TAATC | T | 1 | a0001c0001t0001g0001 | 4 | HG00099.hp2 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-245+9155_-245+915 others(8): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107867705 | |||||
| chr4:107867825
|
G | A | 23 | a0001c0001t0001g0087a0001c0001t0001g0119a0001c0001t0001g0120others(20): Show | 23 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.-245+9272G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107867825 | ||||||
| chr4:107867900
|
G | A | 1 | a0001c0001t0029g0230 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-245+9347G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107867900 | ||||||
| chr4:107867914
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-245+9361C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107867914 | ||||||
| chr4:107868042
|
A | G | 128 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(125): Show | 134 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.-245+9489A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107868042 | ||||||
| chr4:107868151
|
T | C | 1 | a0001c0001t0002g0188 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-245+9598T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107868151 | ||||||
| chr4:107868195
|
G | T | 4 | a0001c0001t0004g0162a0001c0001t0004g0239a0001c0001t0004g0240others(1): Show | 4 | HG02280.hp1 HG02615.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-245+9642G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107868195 | ||||||
| chr4:107868240
|
G | A | 128 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(125): Show | 134 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.-245+9687G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107868240 | ||||||
| chr4:107868528
|
C | A | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0201others(2): Show | 5 | HG01109.hp1 HG01192.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-245+9975C>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107868528 | ||||||
| chr4:107868582
|
G | T | 1 | a0001c0001t0001g0053 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-245+10029G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107868582 | ||||||
| chr4:107868590
|
C | T | 3 | a0001c0001t0001g0132a0001c0001t0001g0161a0001c0001t0001g0185 | 3 | HG01070.hp2 HG01993.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-245+10037C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107868590 | ||||||
| chr4:107868987
|
T | G | 1 | a0001c0001t0001g0048 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-245+10434T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107868987 | ||||||
| chr4:107869081
|
A | C | 8 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(5): Show | 8 | HG01884.hp2 HG02145.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-245+10528A>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107869081 | ||||||
| chr4:107869115
|
G | A | 3 | a0001c0001t0002g0177a0001c0001t0003g0176a0001c0001t0003g0226 | 3 | HG02723.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-245+10562G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107869115 | ||||||
| chr4:107869229
|
C | T | 5 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0216others(2): Show | 5 | HG02809.hp1 HG02895.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-245+10676C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107869229 | ||||||
| chr4:107869578
|
C | T | 134 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(131): Show | 140 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.-245+11025C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107869578 | ||||||
| chr4:107869789
|
G | A | 128 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(125): Show | 134 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.-245+11236G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107869789 | ||||||
| chr4:107869805
|
T | A | 129 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(126): Show | 135 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.-245+11252T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107869805 | ||||||
| chr4:107869874
|
A | G | 1 | a0001c0001t0029g0230 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-245+11321A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107869874 | ||||||
| chr4:107869944
|
G | A | 1 | a0001c0001t0020g0159 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-245+11391G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107869944 | ||||||
| chr4:107870205
|
A | T | 1 | a0001c0001t0001g0131 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-245+11652A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107870205 | ||||||
| chr4:107870291
|
A | G | 2 | a0001c0001t0004g0122a0001c0001t0004g0123 | 2 | HG00735.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-245+11738A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107870291 | ||||||
| chr4:107870517
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-245+11964A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107870517 | ||||||
| chr4:107870546
|
C | T | 129 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(126): Show | 135 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.-245+11993C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107870546 | ||||||
| chr4:107870611
|
T | G | 1 | a0001c0001t0001g0222 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-245+12058T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107870611 | ||||||
| chr4:107870630
|
A | G | 3 | a0001c0001t0001g0236a0001c0001t0006g0172a0001c0001t0006g0253 | 3 | HG02572.hp2 HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-245+12077A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107870630 | ||||||
| chr4:107870876
|
C | G | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096 | 3 | NA19065.hp2 NA19070.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.-245+12323C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107870876 | ||||||
| chr4:107871579
|
A | G | 117 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0014others(114): Show | 119 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.-245+13026A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107871579 | ||||||
| chr4:107871607
|
T | A | 1 | a0001c0001t0001g0061 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-245+13054T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107871607 | ||||||
| chr4:107871808
|
A | G | 46 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0031others(43): Show | 46 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.-245+13255A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107871808 | ||||||
| chr4:107871857
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-245+13304C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107871857 | ||||||
| chr4:107871914
|
A | G | 175 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(172): Show | 181 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.-245+13361A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107871914 | ||||||
| chr4:107871925
|
G | A | 81 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(78): Show | 86 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.-245+13372G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107871925 | ||||||
| chr4:107872349
|
G | A | 2 | a0001c0001t0001g0254a0001c0007t0025g0114 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-245+13796G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107872349 | ||||||
| chr4:107872376
|
G | C | 177 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(174): Show | 183 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.-245+13823G>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107872376 | ||||||
| chr4:107872377
|
T | C | 17 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0017others(14): Show | 17 | HG01167.hp2 HG01175.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.-245+13824T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107872377 | ||||||
| chr4:107872389
|
A | G | 1 | a0001c0005t0031g0012 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-245+13836A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107872389 | ||||||
| chr4:107872671
|
TA | T | 175 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(172): Show | 181 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.-245+14126delA | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107872671 | |||||
| chr4:107872748
|
A | G | 46 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0031others(43): Show | 46 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.-245+14195A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107872748 | ||||||
| chr4:107873301
|
AG | A | 52 | a0001c0001t0001g0010a0001c0001t0001g0025a0001c0001t0001g0034others(49): Show | 54 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-245+14750delG | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107873301 | |||||
| chr4:107873343
|
TCTA | T | 5 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0216others(2): Show | 5 | HG02809.hp1 HG02895.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-245+14793_-245+14 others(9): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107873343 | |||||
| chr4:107873388
|
G | A | 180 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(177): Show | 186 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.-245+14835G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107873388 | ||||||
| chr4:107873515
|
G | A | 1 | a0001c0001t0006g0172 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-245+14962G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107873515 | ||||||
| chr4:107873644
|
A | G | 1 | a0001c0001t0001g0165 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-245+15091A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107873644 | ||||||
| chr4:107873657
|
C | T | 11 | a0001c0001t0001g0011a0001c0001t0001g0174a0001c0001t0001g0175others(8): Show | 14 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.-245+15104C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107873657 | ||||||
| chr4:107873749
|
C | T | 258 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(255): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-245+15196C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107873749 | ||||||
| chr4:107873757
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-245+15204C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107873757 | ||||||
| chr4:107874155
|
T | C | 2 | a0001c0001t0002g0101a0001c0001t0002g0102 | 2 | HG00099.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-245+15602T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107874155 | ||||||
| chr4:107874412
|
C | T | 175 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(172): Show | 181 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.-245+15859C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107874412 | ||||||
| chr4:107874785
|
G | T | 175 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(172): Show | 181 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.-245+16232G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107874785 | ||||||
| chr4:107874932
|
G | A | 52 | a0001c0001t0001g0010a0001c0001t0001g0025a0001c0001t0001g0034others(49): Show | 54 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-245+16379G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107874932 | ||||||
| chr4:107875390
|
C | G | 1 | a0001c0001t0029g0230 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-245+16837C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107875390 | ||||||
| chr4:107875486
|
A | G | 5 | a0001c0001t0001g0236a0001c0001t0002g0202a0001c0001t0006g0002others(2): Show | 7 | HG01069.hp2 HG01071.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.-245+16933A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107875486 | ||||||
| chr4:107875553
|
G | A | 64 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0025others(61): Show | 69 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.-245+17000G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107875553 | ||||||
| chr4:107875667
|
T | C | 177 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(174): Show | 183 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.-245+17114T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107875667 | ||||||
| chr4:107875752
|
C | G | 1 | a0001c0001t0001g0054 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-245+17199C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107875752 | ||||||
| chr4:107875977
|
A | G | 1 | a0001c0007t0025g0114 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-245+17424A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107875977 | ||||||
| chr4:107876297
|
C | T | 8 | a0001c0001t0001g0186a0001c0001t0003g0103a0001c0001t0004g0104others(5): Show | 8 | HG02055.hp2 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-245+17744C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107876297 | ||||||
| chr4:107876585
|
G | A | 64 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0025others(61): Show | 69 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.-245+18032G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107876585 | ||||||
| chr4:107876761
|
C | G | 5 | a0001c0001t0005g0115a0001c0001t0005g0116a0001c0001t0005g0117others(2): Show | 5 | HG01884.hp1 HG02647.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-245+18208C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107876761 | ||||||
| chr4:107876803
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0023 | 2 | HG01934.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.-245+18250A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107876803 | ||||||
| chr4:107876812
|
T | A | 1 | a0001c0001t0029g0230 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-245+18259T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107876812 | ||||||
| chr4:107877102
|
C | A | 11 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(8): Show | 11 | HG00733.hp2 HG00741.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.-244-18208C>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107877102 | ||||||
| chr4:107877260
|
A | G | 2 | a0001c0001t0001g0039a0001c0001t0001g0167 | 2 | NA18941.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.-244-18050A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107877260 | ||||||
| chr4:107877545
|
C | G | 181 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(178): Show | 187 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.-244-17765C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107877545 | ||||||
| chr4:107877715
|
C | T | 182 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(179): Show | 188 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.-244-17595C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107877715 | ||||||
| chr4:107877740
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-244-17570G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107877740 | ||||||
| chr4:107877742
|
C | T | 1 | a0001c0001t0028g0203 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-244-17568C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107877742 | ||||||
| chr4:107877910
|
T | C | 1 | a0001c0001t0004g0239 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-244-17400T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107877910 | ||||||
| chr4:107877913
|
C | CT | 42 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0078others(39): Show | 45 | HG00280.hp1 HG00323.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.-244-17377dupT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107877913 | |||||
| chr4:107877913
|
C | CTT | 6 | a0001c0001t0001g0254a0001c0001t0001g0256a0001c0001t0006g0253others(3): Show | 7 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-244-17378_-244-17 others(8): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107877913 | |||||
| chr4:107877913
|
C | CTTT | 16 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0201others(13): Show | 16 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-244-17379_-244-17 others(9): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107877913 | |||||
| chr4:107877913
|
C | T | 2 | a0001c0001t0002g0207a0001c0001t0002g0217 | 2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-244-17397C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107877913 | ||||||
| chr4:107877913
|
CT | C | 46 | a0001c0001t0001g0010a0001c0001t0001g0025a0001c0001t0001g0034others(43): Show | 47 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.-244-17377delT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107877913 | |||||
| chr4:107877918
|
T | TC | 16 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0017others(13): Show | 16 | HG01167.hp2 HG01175.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.-244-17392_-244-17 others(7): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107877918 | ||||||
| chr4:107878001
|
C | T | 1 | a0001c0001t0005g0117 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-244-17309C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107878001 | ||||||
| chr4:107878058
|
G | T | 1 | a0001c0001t0010g0238 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-244-17252G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107878058 | ||||||
| chr4:107878088
|
G | A | 69 | a0001c0001t0001g0010a0001c0001t0001g0025a0001c0001t0001g0034others(66): Show | 72 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.-244-17222G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107878088 | ||||||
| chr4:107878152
|
G | A | 1 | a0001c0001t0016g0204 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-244-17158G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107878152 | ||||||
| chr4:107878446
|
A | G | 2 | a0001c0001t0008g0007a0001c0001t0008g0224 | 3 | HG02895.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-244-16864A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107878446 | ||||||
| chr4:107878628
|
A | G | 71 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0014others(68): Show | 74 | HG00280.hp1 HG01109.hp1 HG01167.hp2 others(71): Show |
intron_variant | MODIFIER | c.-244-16682A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107878628 | ||||||
| chr4:107878665
|
T | C | 17 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0017others(14): Show | 17 | HG01167.hp2 HG01175.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.-244-16645T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107878665 | ||||||
| chr4:107879108
|
A | AT | 53 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0031others(50): Show | 53 | HG00438.hp2 HG00544.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.-244-16186dupT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107879108 | |||||
| chr4:107879108
|
A | ATT | 80 | a0001c0001t0001g0010a0001c0001t0001g0025a0001c0001t0001g0034others(77): Show | 83 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.-244-16187_-244-16 others(8): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107879108 | |||||
| chr4:107879108
|
ATT | A | 26 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0082others(23): Show | 28 | HG01192.hp1 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-244-16187_-244-16 others(8): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107879108 | |||||
| chr4:107879139
|
C | T | 1 | a0001c0001t0001g0004 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-244-16171C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107879139 | ||||||
| chr4:107879438
|
C | A | 6 | a0001c0001t0001g0011a0001c0001t0001g0243a0001c0001t0002g0106others(3): Show | 7 | HG00280.hp1 HG02647.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-244-15872C>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107879438 | ||||||
| chr4:107879478
|
T | TTC | 112 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0025others(109): Show | 115 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.-244-15832_-244-15 others(8): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107879478 | ||||||
| chr4:107879517
|
G | A | 113 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0025others(110): Show | 116 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.-244-15793G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107879517 | ||||||
| chr4:107879682
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-244-15628G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107879682 | ||||||
| chr4:107879711
|
C | G | 43 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0031others(40): Show | 43 | HG00438.hp2 HG00544.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.-244-15599C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107879711 | ||||||
| chr4:107879751
|
C | T | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096 | 3 | NA19065.hp2 NA19070.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.-244-15559C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107879751 | ||||||
| chr4:107879759
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-244-15551G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107879759 | ||||||
| chr4:107879827
|
T | TA | 23 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0014others(20): Show | 24 | HG00280.hp1 HG01167.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.-244-15479dupA | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107879827 | |||||
| chr4:107880103
|
A | G | 1 | a0001c0001t0003g0232 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-244-15207A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107880103 | ||||||
| chr4:107880211
|
A | G | 1 | a0001c0001t0001g0153 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-244-15099A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107880211 | ||||||
| chr4:107880384
|
G | C | 140 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0025others(137): Show | 145 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.-244-14926G>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107880384 | ||||||
| chr4:107880508
|
T | C | 184 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(181): Show | 190 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.-244-14802T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107880508 | ||||||
| chr4:107880592
|
A | C | 1 | a0001c0001t0002g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-244-14718A>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107880592 | ||||||
| chr4:107880667
|
C | T | 9 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0236others(6): Show | 11 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.-244-14643C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107880667 | ||||||
| chr4:107880806
|
A | G | 17 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0017others(14): Show | 17 | HG01167.hp2 HG01175.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.-244-14504A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107880806 | ||||||
| chr4:107880851
|
C | CA | 18 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0086others(15): Show | 18 | HG00323.hp2 HG01109.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.-244-14443dupA | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107880851 | |||||
| chr4:107880864
|
A | AAG | 7 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0154others(4): Show | 7 | HG00733.hp2 HG01261.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.-244-14445_-244-14 others(8): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107880864 | |||||
| chr4:107880864
|
A | AG | 134 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0025others(131): Show | 139 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.-244-14446_-244-14 others(7): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107880864 | ||||||
| chr4:107880985
|
C | G | 17 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0017others(14): Show | 17 | HG01167.hp2 HG01175.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.-244-14325C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107880985 | ||||||
| chr4:107881225
|
C | A | 10 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0236others(7): Show | 12 | HG00735.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-244-14085C>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107881225 | ||||||
| chr4:107881241
|
A | G | 17 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0017others(14): Show | 17 | HG01167.hp2 HG01175.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.-244-14069A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107881241 | ||||||
| chr4:107881255
|
A | G | 89 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0014others(86): Show | 94 | HG00280.hp1 HG00558.hp2 HG00735.hp1 others(91): Show |
intron_variant | MODIFIER | c.-244-14055A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107881255 | ||||||
| chr4:107881352
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-244-13958G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107881352 | ||||||
| chr4:107881354
|
A | G | 2 | a0001c0001t0001g0126a0001c0001t0020g0159 | 2 | HG00738.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-244-13956A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107881354 | ||||||
| chr4:107881460
|
A | AT | 6 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0216others(3): Show | 6 | HG02809.hp1 HG02895.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-244-13840dupT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107881460 | |||||
| chr4:107881606
|
G | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(101): Show | 109 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.-244-13704G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107881606 | ||||||
| chr4:107881847
|
A | G | 9 | a0001c0001t0001g0141a0001c0001t0001g0211a0001c0001t0004g0104others(6): Show | 9 | HG02145.hp2 HG02615.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.-244-13463A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107881847 | ||||||
| chr4:107881939
|
A | G | 6 | a0001c0001t0001g0027a0001c0001t0001g0085a0001c0001t0001g0140others(3): Show | 6 | HG00639.hp1 HG03579.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.-244-13371A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107881939 | ||||||
| chr4:107882123
|
C | T | 6 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0002g0099others(3): Show | 6 | HG00735.hp1 HG01106.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-244-13187C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107882123 | ||||||
| chr4:107882142
|
G | A | 1 | a0001c0005t0031g0012 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-244-13168G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107882142 | ||||||
| chr4:107882226
|
A | G | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0216others(4): Show | 7 | HG01243.hp2 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-244-13084A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107882226 | ||||||
| chr4:107882320
|
A | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0139 | 2 | NA18948.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.-244-12990A>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107882320 | ||||||
| chr4:107882582
|
T | A | 9 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0216others(6): Show | 9 | HG01243.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-244-12728T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107882582 | ||||||
| chr4:107882724
|
T | C | 8 | a0001c0001t0001g0141a0001c0001t0001g0211a0001c0001t0004g0104others(5): Show | 8 | HG02145.hp2 HG02615.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.-244-12586T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107882724 | ||||||
| chr4:107883125
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-244-12185G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107883125 | ||||||
| chr4:107883231
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-244-12079C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107883231 | ||||||
| chr4:107883468
|
T | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.-244-11842T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107883468 | ||||||
| chr4:107883504
|
T | C | 2 | a0001c0001t0007g0100a0001c0001t0007g0227 | 2 | HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-244-11806T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107883504 | ||||||
| chr4:107883753
|
G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(100): Show | 108 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.-244-11557G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107883753 | ||||||
| chr4:107883858
|
T | C | 5 | a0001c0001t0005g0197a0001c0001t0005g0218a0001c0001t0005g0219others(2): Show | 5 | HG01192.hp2 HG01975.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-244-11452T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107883858 | ||||||
| chr4:107884032
|
C | T | 1 | a0001c0001t0034g0088 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-244-11278C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107884032 | ||||||
| chr4:107884089
|
A | AT | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.-244-11215dupT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107884089 | |||||
| chr4:107884500
|
AG | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.-244-10802delG | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107884500 | |||||
| chr4:107884503
|
G | C | 1 | a0001c0001t0001g0131 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-244-10807G>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107884503 | ||||||
| chr4:107884508
|
G | T | 1 | a0001c0001t0012g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-244-10802G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107884508 | ||||||
| chr4:107884644
|
C | T | 1 | a0001c0001t0005g0116 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-244-10666C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107884644 | ||||||
| chr4:107884774
|
A | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 173 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.-244-10536A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107884774 | ||||||
| chr4:107884849
|
C | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0113 | 2 | HG01261.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-244-10461C>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107884849 | ||||||
| chr4:107884998
|
A | G | 2 | a0001c0001t0009g0080a0001c0001t0009g0112 | 2 | HG00733.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-244-10312A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107884998 | ||||||
| chr4:107885227
|
A | AT | 32 | a0001c0001t0001g0065a0001c0001t0001g0071a0001c0001t0001g0073others(29): Show | 32 | HG00642.hp2 HG00733.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.-244-10072dupT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107885227 | |||||
| chr4:107885227
|
A | T | 20 | a0001c0001t0001g0034a0001c0001t0001g0059a0001c0001t0001g0119others(17): Show | 21 | HG00544.hp1 HG01109.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.-244-10083A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107885227 | ||||||
| chr4:107885227
|
AT | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(46): Show | 55 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.-244-10072delT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107885227 | |||||
| chr4:107885603
|
T | C | 7 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0216others(4): Show | 7 | HG01243.hp2 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-244-9707T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107885603 | ||||||
| chr4:107885639
|
T | C | 5 | a0001c0001t0001g0051a0001c0001t0001g0070a0001c0001t0001g0072others(2): Show | 5 | HG02523.hp2 HG03490.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.-244-9671T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107885639 | ||||||
| chr4:107885681
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-244-9629A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107885681 | ||||||
| chr4:107885876
|
A | G | 1 | a0001c0001t0001g0016 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-244-9434A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107885876 | ||||||
| chr4:107886204
|
T | G | 1 | a0001c0001t0001g0130 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-244-9106T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107886204 | ||||||
| chr4:107886207
|
T | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 117 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.-244-9103T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107886207 | ||||||
| chr4:107886364
|
A | AT | 14 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0046others(11): Show | 14 | HG01081.hp1 HG01243.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.-244-8916dupT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107886364 | |||||
| chr4:107886364
|
AT | A | 9 | a0001c0001t0001g0041a0001c0001t0001g0051a0001c0001t0001g0241others(6): Show | 11 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-244-8916delT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107886364 | |||||
| chr4:107886364
|
ATTTTTTT others(1): Show |
A | 20 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(17): Show | 20 | HG01123.hp1 HG01175.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.-244-8923_-244-891 others(12): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107886364 | |||||
| chr4:107886364
|
ATTTTTTT others(2): Show |
A | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(165): Show | 177 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.-244-8924_-244-891 others(13): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107886364 | |||||
| chr4:107886364
|
ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0001g0119a0001c0001t0019g0038 | 2 | HG02280.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.-244-8925_-244-891 others(14): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107886364 | |||||
| chr4:107886401
|
C | T | 6 | a0001c0001t0001g0071a0001c0001t0001g0111a0001c0001t0001g0113others(3): Show | 6 | HG00733.hp2 HG01261.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.-244-8909C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107886401 | ||||||
| chr4:107886430
|
G | A | 1 | a0001c0001t0003g0068 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-244-8880G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107886430 | ||||||
| chr4:107886853
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-244-8457T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107886853 | ||||||
| chr4:107886862
|
C | T | 44 | a0001c0001t0001g0011a0001c0001t0001g0055a0001c0001t0001g0081others(41): Show | 47 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-244-8448C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107886862 | ||||||
| chr4:107886890
|
G | C | 1 | a0001c0001t0001g0153 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-244-8420G>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107886890 | ||||||
| chr4:107886897
|
A | G | 2 | a0001c0001t0018g0228a0001c0001t0029g0230 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-244-8413A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107886897 | ||||||
| chr4:107886960
|
C | T | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG01106.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.-244-8350C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107886960 | ||||||
| chr4:107887030
|
C | T | 1 | a0001c0007t0025g0114 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-244-8280C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107887030 | ||||||
| chr4:107887093
|
G | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.-244-8217G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107887093 | ||||||
| chr4:107887141
|
A | T | 2 | a0001c0001t0004g0006a0001c0001t0004g0143 | 3 | HG02622.hp2 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-244-8169A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107887141 | ||||||
| chr4:107887205
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-244-8105T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107887205 | ||||||
| chr4:107888001
|
G | A | 20 | a0001c0001t0001g0034a0001c0001t0001g0059a0001c0001t0001g0119others(17): Show | 21 | HG00544.hp1 HG01109.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.-244-7309G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107888001 | ||||||
| chr4:107888099
|
C | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0139 | 2 | NA18948.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.-244-7211C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107888099 | ||||||
| chr4:107888159
|
A | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.-244-7151A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107888159 | ||||||
| chr4:107888271
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0075 | 3 | HG00280.hp2 HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-244-7039C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107888271 | ||||||
| chr4:107888332
|
T | C | 8 | a0001c0001t0001g0071a0001c0001t0001g0111a0001c0001t0001g0113others(5): Show | 8 | HG00733.hp2 HG01255.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.-244-6978T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107888332 | ||||||
| chr4:107888540
|
G | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.-244-6770G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107888540 | ||||||
| chr4:107888805
|
T | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(123): Show | 131 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.-244-6505T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107888805 | ||||||
| chr4:107888995
|
A | C | 4 | a0001c0001t0007g0090a0001c0001t0007g0091a0001c0001t0007g0100others(1): Show | 4 | HG01516.hp2 HG01981.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-244-6315A>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107888995 | ||||||
| chr4:107889298
|
C | G | 1 | a0001c0001t0001g0121 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-244-6012C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107889298 | ||||||
| chr4:107889358
|
A | G | 1 | a0001c0001t0029g0230 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-244-5952A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107889358 | ||||||
| chr4:107889615
|
C | T | 6 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0002g0099others(3): Show | 6 | HG00735.hp1 HG01106.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-244-5695C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107889615 | ||||||
| chr4:107889937
|
G | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(1): Show | 4 | HG02015.hp1 NA18990.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-244-5373G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107889937 | ||||||
| chr4:107890034
|
A | T | 1 | a0001c0001t0006g0172 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-244-5276A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107890034 | ||||||
| chr4:107890073
|
C | A | 4 | a0001c0001t0001g0119a0001c0001t0001g0201a0001c0003t0002g0133others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-244-5237C>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107890073 | ||||||
| chr4:107890111
|
G | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.-244-5199G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107890111 | ||||||
| chr4:107890136
|
G | C | 2 | a0001c0001t0008g0007a0001c0001t0008g0224 | 3 | HG02895.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-244-5174G>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107890136 | ||||||
| chr4:107890176
|
C | T | 1 | a0001c0001t0029g0230 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-244-5134C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107890176 | ||||||
| chr4:107890550
|
G | A | 1 | a0001c0005t0031g0012 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-244-4760G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107890550 | ||||||
| chr4:107890674
|
C | CA | 28 | a0001c0001t0001g0034a0001c0001t0001g0051a0001c0001t0001g0059others(25): Show | 29 | HG00438.hp2 HG00544.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.-244-4619dupA | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107890674 | |||||
| chr4:107890760
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-244-4550G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107890760 | ||||||
| chr4:107890802
|
C | T | 2 | a0001c0001t0018g0228a0001c0001t0029g0230 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-244-4508C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107890802 | ||||||
| chr4:107890940
|
G | T | 1 | a0001c0001t0002g0008 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-244-4370G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107890940 | ||||||
| chr4:107890953
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-244-4357G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107890953 | ||||||
| chr4:107890993
|
A | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 202 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.-244-4317A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107890993 | ||||||
| chr4:107891099
|
C | CT | 18 | a0001c0001t0001g0034a0001c0001t0001g0059a0001c0001t0001g0119others(15): Show | 18 | HG00544.hp1 HG01109.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.-244-4202dupT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107891099 | |||||
| chr4:107891129
|
TC | T | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 214 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.-244-4174delC | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107891129 | |||||
| chr4:107891308
|
A | T | 6 | a0001c0001t0001g0071a0001c0001t0001g0111a0001c0001t0001g0113others(3): Show | 6 | HG00733.hp2 HG01261.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.-244-4002A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107891308 | ||||||
| chr4:107891325
|
CA | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.-244-3975delA | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107891325 | |||||
| chr4:107891485
|
G | C | 1 | a0001c0001t0005g0218 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-244-3825G>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107891485 | ||||||
| chr4:107891495
|
CTTG | C | 44 | a0001c0001t0001g0011a0001c0001t0001g0055a0001c0001t0001g0081others(41): Show | 47 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-244-3810_-244-380 others(7): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107891495 | |||||
| chr4:107891619
|
C | T | 6 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0002g0099others(3): Show | 6 | HG00735.hp1 HG01106.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-244-3691C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107891619 | ||||||
| chr4:107891675
|
A | G | 1 | a0001c0007t0025g0114 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-244-3635A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107891675 | ||||||
| chr4:107891841
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-244-3469T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107891841 | ||||||
| chr4:107892057
|
T | G | 189 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(186): Show | 195 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.-244-3253T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107892057 | ||||||
| chr4:107892085
|
C | G | 3 | a0001c0001t0001g0055a0001c0001t0001g0189a0001c0001t0013g0156 | 3 | HG00558.hp2 NA19070.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-244-3225C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107892085 | ||||||
| chr4:107892110
|
GA | G | 109 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0055others(106): Show | 113 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.-244-3185delA | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107892110 | |||||
| chr4:107892156
|
G | A | 1 | a0001c0001t0003g0249 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-244-3154G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107892156 | ||||||
| chr4:107892234
|
C | CA | 10 | a0001c0001t0001g0052a0001c0001t0001g0134a0001c0001t0001g0174others(7): Show | 10 | HG00735.hp1 HG01106.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-244-3053dupA | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107892234 | |||||
| chr4:107892234
|
CA | C | 158 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(155): Show | 164 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.-244-3053delA | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107892234 | |||||
| chr4:107892234
|
CAA | C | 11 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0180others(8): Show | 11 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.-244-3054_-244-305 others(6): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107892234 | |||||
| chr4:107892234
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0182 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-244-3064_-244-305 others(16): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107892234 | |||||
| chr4:107892404
|
G | A | 1 | a0001c0001t0004g0110 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-244-2906G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107892404 | ||||||
| chr4:107892434
|
CAG | C | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(120): Show | 125 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.-244-2874_-244-287 others(6): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107892434 | |||||
| chr4:107892633
|
A | G | 9 | a0001c0001t0001g0073a0001c0001t0001g0078a0001c0001t0001g0079others(6): Show | 9 | HG00642.hp2 HG01192.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.-244-2677A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107892633 | ||||||
| chr4:107892655
|
C | T | 121 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(118): Show | 123 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.-244-2655C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107892655 | ||||||
| chr4:107892661
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-244-2649G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107892661 | ||||||
| chr4:107893041
|
T | C | 2 | a0001c0001t0003g0181a0001c0001t0003g0212 | 2 | HG01255.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-244-2269T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107893041 | ||||||
| chr4:107893354
|
G | A | 2 | a0001c0001t0004g0122a0001c0001t0004g0123 | 2 | HG00735.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-244-1956G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107893354 | ||||||
| chr4:107893569
|
G | C | 2 | a0001c0001t0004g0006a0001c0001t0004g0143 | 3 | HG02622.hp2 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-244-1741G>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107893569 | ||||||
| chr4:107893592
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-244-1718C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107893592 | ||||||
| chr4:107893732
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0152 | 2 | HG00438.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.-244-1578G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107893732 | ||||||
| chr4:107894192
|
C | CG | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(183): Show | 194 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.-244-1114dupG | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107894192 | |||||
| chr4:107894207
|
G | C | 2 | a0001c0001t0001g0241a0001c0001t0012g0196 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-244-1103G>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107894207 | ||||||
| chr4:107894207
|
G | T | 1 | a0001c0001t0001g0130 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-244-1103G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107894207 | ||||||
| chr4:107894213
|
A | C | 1 | a0001c0001t0014g0026 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-244-1097A>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107894213 | ||||||
| chr4:107894444
|
G | A | 13 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(10): Show | 13 | HG01943.hp1 HG01993.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.-244-866G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107894444 | ||||||
| chr4:107894511
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-244-799G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107894511 | ||||||
| chr4:107894659
|
C | G | 1 | a0001c0001t0001g0193 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-244-651C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107894659 | ||||||
| chr4:107894855
|
A | AAG | 239 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.-244-452_-244-451d others(4): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 107894855 | |||||
| chr4:107894988
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-244-322G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 2/6 | chr4 | 107894988 | ||||||
| chr4:107896022
|
A | C | 1 | a0001c0001t0030g0044 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.455+14A>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107896022 | ||||||
| chr4:107896040
|
A | T | 2 | a0001c0001t0001g0254a0001c0001t0027g0118 | 2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.455+32A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107896040 | ||||||
| chr4:107896109
|
A | G | 1 | a0001c0001t0022g0035 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.455+101A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107896109 | ||||||
| chr4:107896269
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.455+261G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107896269 | ||||||
| chr4:107896271
|
A | G | 1 | a0001c0001t0001g0020 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.455+263A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107896271 | ||||||
| chr4:107896431
|
T | C | 3 | a0001c0001t0001g0241a0001c0001t0001g0256a0001c0001t0012g0196 | 3 | HG03139.hp2 HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.455+423T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107896431 | ||||||
| chr4:107896474
|
T | G | 1 | a0001c0001t0001g0192 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.455+466T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107896474 | ||||||
| chr4:107896874
|
A | G | 4 | a0001c0001t0005g0115a0001c0001t0005g0116a0001c0001t0005g0117others(1): Show | 4 | HG01884.hp1 HG02647.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.455+866A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107896874 | ||||||
| chr4:107896991
|
C | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.455+983C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107896991 | ||||||
| chr4:107897048
|
T | G | 1 | a0001c0001t0009g0032 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.455+1040T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107897048 | ||||||
| chr4:107897249
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.455+1241A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107897249 | ||||||
| chr4:107897454
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.455+1446C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107897454 | ||||||
| chr4:107897497
|
T | C | 11 | a0001c0001t0001g0050a0001c0001t0001g0071a0001c0001t0001g0161others(8): Show | 11 | HG00438.hp1 HG00733.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.455+1489T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107897497 | ||||||
| chr4:107897601
|
C | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.455+1593C>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107897601 | ||||||
| chr4:107897624
|
GTTA | G | 4 | a0001c0001t0001g0241a0001c0001t0001g0256a0001c0001t0012g0196others(1): Show | 4 | HG01109.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.455+1623_455+1625d others(5): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr4 | 107897624 | |||||
| chr4:107897700
|
A | C | 1 | a0001c0001t0030g0044 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.455+1692A>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107897700 | ||||||
| chr4:107897718
|
T | A | 1 | a0001c0001t0002g0128 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.455+1710T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107897718 | ||||||
| chr4:107897766
|
A | G | 4 | a0001c0001t0002g0177a0001c0001t0003g0103a0001c0001t0003g0176others(1): Show | 4 | HG02723.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.455+1758A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107897766 | ||||||
| chr4:107897791
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.455+1783A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107897791 | ||||||
| chr4:107898145
|
T | A | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.456-1430T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107898145 | ||||||
| chr4:107898263
|
A | AT | 221 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.456-1302dupT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr4 | 107898263 | |||||
| chr4:107898297
|
C | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0244 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.456-1278C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107898297 | ||||||
| chr4:107898525
|
AAT | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.456-1047_456-1046d others(4): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr4 | 107898525 | |||||
| chr4:107898547
|
A | G | 1 | a0001c0005t0031g0012 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.456-1028A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107898547 | ||||||
| chr4:107898577
|
G | A | 1 | a0001c0001t0004g0143 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.456-998G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107898577 | ||||||
| chr4:107898735
|
C | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.456-840C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107898735 | ||||||
| chr4:107899065
|
A | G | 1 | a0001c0001t0005g0220 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.456-510A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107899065 | ||||||
| chr4:107899093
|
A | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0051a0001c0001t0001g0105others(3): Show | 6 | HG01123.hp2 HG01167.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.456-482A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107899093 | ||||||
| chr4:107899313
|
C | A | 1 | a0001c0001t0002g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.456-262C>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107899313 | ||||||
| chr4:107899494
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.456-81T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 3/6 | chr4 | 107899494 | ||||||
| chr4:107899825
|
A | G | 1 | a0001c0001t0033g0242 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.573+133A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | chr4 | 107899825 | ||||||
| chr4:107900075
|
C | G | 11 | a0001c0001t0001g0119a0001c0001t0001g0157a0001c0001t0001g0199others(8): Show | 11 | HG00733.hp2 HG01109.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.573+383C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | chr4 | 107900075 | ||||||
| chr4:107900196
|
C | G | 67 | a0001c0001t0001g0119a0001c0001t0001g0141a0001c0001t0001g0171others(64): Show | 70 | HG00280.hp1 HG00639.hp2 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.573+504C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | chr4 | 107900196 | ||||||
| chr4:107900280
|
A | G | 47 | a0001c0001t0001g0141a0001c0001t0001g0171a0001c0001t0001g0190others(44): Show | 50 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.573+588A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | chr4 | 107900280 | ||||||
| chr4:107900448
|
G | A | 1 | a0001c0001t0001g0048 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.573+756G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | chr4 | 107900448 | ||||||
| chr4:107900796
|
A | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0125 | 2 | NA18961.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.573+1104A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | chr4 | 107900796 | ||||||
| chr4:107900836
|
T | A | 1 | a0001c0001t0001g0160 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.573+1144T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | chr4 | 107900836 | ||||||
| chr4:107901099
|
G | C | 1 | a0001c0001t0001g0213 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.573+1407G>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | chr4 | 107901099 | ||||||
| chr4:107901137
|
G | A | 1 | a0001c0001t0016g0204 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.573+1445G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | chr4 | 107901137 | ||||||
| chr4:107901142
|
A | G | 11 | a0001c0001t0001g0119a0001c0001t0001g0199a0001c0001t0001g0201others(8): Show | 11 | HG00733.hp2 HG01109.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.573+1450A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | chr4 | 107901142 | ||||||
| chr4:107901463
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.574-1770G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | chr4 | 107901463 | ||||||
| chr4:107901859
|
T | C | 2 | a0001c0001t0001g0119a0001c0001t0001g0201 | 2 | HG01109.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.574-1374T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | chr4 | 107901859 | ||||||
| chr4:107901961
|
C | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0167a0001c0001t0001g0189 | 3 | NA18941.hp2 NA18983.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.574-1272C>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | chr4 | 107901961 | ||||||
| chr4:107901978
|
C | A | 3 | a0001c0001t0006g0002a0001c0001t0006g0172a0001c0001t0006g0253 | 5 | HG01069.hp2 HG01071.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.574-1255C>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | chr4 | 107901978 | ||||||
| chr4:107902086
|
C | CT | 5 | a0001c0001t0001g0119a0001c0001t0001g0201a0001c0001t0010g0238others(2): Show | 5 | HG01109.hp1 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.574-1135dupT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 107902086 | |||||
| chr4:107902115
|
C | G | 1 | a0001c0001t0014g0026 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.574-1118C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | chr4 | 107902115 | ||||||
| chr4:107902164
|
T | C | 11 | a0001c0001t0001g0119a0001c0001t0001g0199a0001c0001t0001g0201others(8): Show | 11 | HG00733.hp2 HG01109.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.574-1069T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | chr4 | 107902164 | ||||||
| chr4:107902207
|
G | C | 3 | a0001c0001t0006g0002a0001c0001t0006g0172a0001c0001t0006g0253 | 5 | HG01069.hp2 HG01071.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.574-1026G>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | chr4 | 107902207 | ||||||
| chr4:107902289
|
C | CA | 32 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0141others(29): Show | 34 | HG00280.hp1 HG00639.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.574-932dupA | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 107902289 | |||||
| chr4:107902289
|
C | CAAAAAAA others(3): Show |
4 | a0001c0001t0001g0199a0001c0001t0009g0032a0001c0001t0009g0080others(1): Show | 4 | HG00733.hp2 HG01515.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.574-941_574-932dup others(10): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 107902289 | |||||
| chr4:107902289
|
C | CAAAAAAA others(4): Show |
1 | a0001c0005t0031g0012 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.574-942_574-932dup others(11): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 107902289 | |||||
| chr4:107902289
|
C | CAAAAAAA others(5): Show |
6 | a0001c0001t0001g0201a0001c0001t0001g0254a0001c0001t0010g0210others(3): Show | 6 | HG01109.hp1 HG01109.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-943_574-932dup others(12): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 107902289 | |||||
| chr4:107902289
|
C | CAAAAAAA others(6): Show |
8 | a0001c0001t0001g0119a0001c0001t0001g0241a0001c0001t0001g0256others(5): Show | 8 | HG01175.hp2 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.574-932_574-931ins others(13): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 107902289 | |||||
| chr4:107902289
|
C | CAAAAAAA others(7): Show |
9 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0181others(6): Show | 9 | HG01243.hp2 HG01255.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.574-932_574-931ins others(14): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 107902289 | |||||
| chr4:107902289
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0003g0216 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.574-932_574-931ins others(16): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 107902289 | |||||
| chr4:107902289
|
C | CAAAAAAA others(19): Show |
1 | a0001c0001t0004g0066 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.574-932_574-931ins others(26): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 107902289 | |||||
| chr4:107902289
|
C | CAAAAAAA others(20): Show |
2 | a0001c0001t0004g0122a0001c0001t0004g0123 | 2 | HG00735.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.574-932_574-931ins others(27): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 107902289 | |||||
| chr4:107902289
|
C | CAAAAAAA others(21): Show |
3 | a0001c0001t0004g0110a0001c0001t0004g0234a0001c0001t0004g0239 | 3 | HG03195.hp1 HG03704.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.574-932_574-931ins others(28): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 107902289 | |||||
| chr4:107902289
|
C | CAAAAAAA others(22): Show |
6 | a0001c0001t0004g0006a0001c0001t0004g0104a0001c0001t0004g0143others(3): Show | 7 | HG02280.hp1 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.574-932_574-931ins others(29): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 107902289 | |||||
| chr4:107902289
|
C | CAAAAAAA others(25): Show |
1 | a0001c0002t0023g0237 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.574-932_574-931ins others(32): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 107902289 | |||||
| chr4:107902289
|
C | CAAAAAAA others(26): Show |
1 | a0001c0002t0001g0067 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.574-932_574-931ins others(33): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 107902289 | |||||
| chr4:107902302
|
G | A | 1 | a0001c0001t0033g0242 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.574-931G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | chr4 | 107902302 | ||||||
| chr4:107902313
|
A | G | 5 | a0001c0001t0001g0241a0001c0001t0001g0256a0001c0001t0012g0196others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.574-920A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | chr4 | 107902313 | ||||||
| chr4:107902388
|
A | G | 2 | a0001c0001t0001g0205a0001c0001t0002g0128 | 2 | HG01515.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.574-845A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | chr4 | 107902388 | ||||||
| chr4:107902422
|
C | T | 1 | a0001c0001t0002g0128 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.574-811C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | chr4 | 107902422 | ||||||
| chr4:107902588
|
G | A | 1 | a0001c0001t0014g0026 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.574-645G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | chr4 | 107902588 | ||||||
| chr4:107903046
|
A | G | 3 | a0001c0001t0001g0241a0001c0001t0001g0256a0001c0001t0012g0196 | 3 | HG03139.hp2 HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.574-187A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | chr4 | 107903046 | ||||||
| chr4:107903083
|
G | A | 24 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0181others(21): Show | 25 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.574-150G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | chr4 | 107903083 | ||||||
| chr4:107903173
|
G | C | 19 | a0001c0001t0001g0141a0001c0001t0001g0171a0001c0001t0001g0190others(16): Show | 19 | HG00280.hp1 HG00639.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.574-60G>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 4/6 | chr4 | 107903173 | ||||||
| chr4:107903499
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0075others(5): Show | 12 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(9): Show |
intron_variant | MODIFIER | c.727+113G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107903499 | ||||||
| chr4:107903511
|
A | G | 16 | a0001c0001t0001g0171a0001c0001t0002g0060a0001c0001t0002g0106others(13): Show | 16 | HG00280.hp1 HG00639.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.727+125A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107903511 | ||||||
| chr4:107903544
|
C | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0195 | 2 | HG01106.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.727+158C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107903544 | ||||||
| chr4:107903737
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.727+351A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107903737 | ||||||
| chr4:107903829
|
T | C | 2 | a0001c0001t0001g0254a0001c0001t0027g0118 | 2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.727+443T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107903829 | ||||||
| chr4:107903897
|
T | G | 1 | a0001c0001t0004g0066 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.727+511T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107903897 | ||||||
| chr4:107904403
|
A | G | 17 | a0001c0001t0001g0171a0001c0001t0002g0060a0001c0001t0002g0106others(14): Show | 17 | HG00280.hp1 HG00639.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.727+1017A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107904403 | ||||||
| chr4:107904552
|
T | G | 16 | a0001c0001t0001g0171a0001c0001t0002g0060a0001c0001t0002g0106others(13): Show | 16 | HG00280.hp1 HG00639.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.727+1166T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107904552 | ||||||
| chr4:107904565
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.727+1179G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107904565 | ||||||
| chr4:107904631
|
T | G | 19 | a0001c0001t0001g0141a0001c0001t0001g0171a0001c0001t0001g0190others(16): Show | 19 | HG00280.hp1 HG00639.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.727+1245T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107904631 | ||||||
| chr4:107904690
|
T | G | 19 | a0001c0001t0001g0141a0001c0001t0001g0171a0001c0001t0001g0190others(16): Show | 19 | HG00280.hp1 HG00639.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.727+1304T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107904690 | ||||||
| chr4:107904843
|
C | G | 2 | a0001c0001t0001g0119a0001c0001t0001g0201 | 2 | HG01109.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.727+1457C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107904843 | ||||||
| chr4:107904891
|
T | C | 16 | a0001c0001t0001g0171a0001c0001t0002g0060a0001c0001t0002g0106others(13): Show | 16 | HG00280.hp1 HG00639.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.727+1505T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107904891 | ||||||
| chr4:107904915
|
A | T | 4 | a0001c0001t0001g0254a0001c0001t0010g0238a0001c0001t0027g0118others(1): Show | 4 | HG02257.hp1 HG02965.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.727+1529A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107904915 | ||||||
| chr4:107905126
|
A | T | 225 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(222): Show | 235 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.727+1740A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107905126 | ||||||
| chr4:107905227
|
T | C | 70 | a0001c0001t0001g0011a0001c0001t0001g0061a0001c0001t0001g0081others(67): Show | 73 | HG00438.hp2 HG00735.hp2 HG01099.hp2 others(70): Show |
intron_variant | MODIFIER | c.727+1841T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107905227 | ||||||
| chr4:107905411
|
T | A | 1 | a0001c0001t0001g0152 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.727+2025T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107905411 | ||||||
| chr4:107905550
|
A | G | 236 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(233): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.727+2164A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107905550 | ||||||
| chr4:107905556
|
G | T | 1 | a0001c0001t0004g0066 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.727+2170G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107905556 | ||||||
| chr4:107905621
|
G | C | 70 | a0001c0001t0001g0241a0001c0001t0002g0008a0001c0001t0002g0042others(67): Show | 74 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.727+2235G>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107905621 | ||||||
| chr4:107905658
|
G | C | 71 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0211others(68): Show | 75 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.727+2272G>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107905658 | ||||||
| chr4:107905737
|
G | A | 1 | a0001c0001t0018g0228 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.727+2351G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107905737 | ||||||
| chr4:107905914
|
A | G | 1 | a0001c0001t0002g0173 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.727+2528A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107905914 | ||||||
| chr4:107905967
|
A | T | 33 | a0001c0001t0002g0008a0001c0001t0002g0042a0001c0001t0002g0060others(30): Show | 36 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.727+2581A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107905967 | ||||||
| chr4:107906012
|
C | T | 9 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0181others(6): Show | 9 | HG01243.hp2 HG01255.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.728-2553C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107906012 | ||||||
| chr4:107906181
|
G | A | 4 | a0001c0001t0006g0002a0001c0001t0006g0172a0001c0001t0006g0253others(1): Show | 6 | HG01069.hp2 HG01071.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.728-2384G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107906181 | ||||||
| chr4:107906198
|
A | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(1): Show | 4 | HG02015.hp1 NA18990.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.728-2367A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107906198 | ||||||
| chr4:107906222
|
A | C | 29 | a0001c0001t0002g0008a0001c0001t0002g0042a0001c0001t0002g0060others(26): Show | 30 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.728-2343A>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107906222 | ||||||
| chr4:107906311
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.728-2254C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107906311 | ||||||
| chr4:107906313
|
A | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0191 | 2 | HG03704.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.728-2252A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107906313 | ||||||
| chr4:107906348
|
G | A | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | HG01167.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.728-2217G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107906348 | ||||||
| chr4:107906422
|
A | G | 3 | a0001c0001t0006g0002a0001c0001t0006g0172a0001c0001t0006g0253 | 5 | HG01069.hp2 HG01071.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.728-2143A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107906422 | ||||||
| chr4:107906749
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0002g0008 | 3 | HG01070.hp1 HG01071.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.728-1816G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107906749 | ||||||
| chr4:107907061
|
G | A | 4 | a0001c0001t0006g0002a0001c0001t0006g0172a0001c0001t0006g0253others(1): Show | 6 | HG01069.hp2 HG01071.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.728-1504G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107907061 | ||||||
| chr4:107907097
|
C | G | 6 | a0001c0001t0004g0104a0001c0001t0004g0162a0001c0001t0004g0234others(3): Show | 6 | HG02280.hp1 HG02615.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.728-1468C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107907097 | ||||||
| chr4:107907198
|
A | G | 1 | a0001c0001t0003g0249 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.728-1367A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107907198 | ||||||
| chr4:107907262
|
C | G | 5 | a0001c0001t0004g0006a0001c0001t0004g0066a0001c0001t0004g0110others(2): Show | 6 | HG01257.hp1 HG02622.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.728-1303C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107907262 | ||||||
| chr4:107907618
|
T | A | 1 | a0001c0001t0001g0063 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.728-947T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107907618 | ||||||
| chr4:107908029
|
T | C | 42 | a0001c0001t0002g0008a0001c0001t0002g0042a0001c0001t0002g0060others(39): Show | 43 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.728-536T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107908029 | ||||||
| chr4:107908169
|
C | A | 5 | a0001c0001t0003g0249a0001c0001t0006g0002a0001c0001t0006g0172others(2): Show | 7 | HG01069.hp2 HG01071.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.728-396C>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107908169 | ||||||
| chr4:107908187
|
T | C | 70 | a0001c0001t0001g0186a0001c0001t0002g0008a0001c0001t0002g0042others(67): Show | 74 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.728-378T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107908187 | ||||||
| chr4:107908222
|
C | T | 57 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0018others(54): Show | 58 | HG00438.hp1 HG00544.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.728-343C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107908222 | ||||||
| chr4:107908360
|
C | T | 25 | a0001c0001t0002g0008a0001c0001t0002g0042a0001c0001t0002g0060others(22): Show | 26 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.728-205C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107908360 | ||||||
| chr4:107908361
|
G | A | 1 | a0001c0001t0001g0039 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.728-204G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 5/6 | chr4 | 107908361 | ||||||
| chr4:107908859
|
A | G | 1 | a0001c0001t0002g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.894+128A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107908859 | ||||||
| chr4:107909026
|
G | C | 2 | a0001c0001t0001g0034a0001c0001t0032g0155 | 2 | HG00544.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.894+295G>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909026 | ||||||
| chr4:107909109
|
A | AT | 27 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0002g0008others(24): Show | 28 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.894+392dupT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr4 | 107909109 | |||||
| chr4:107909109
|
A | ATT | 12 | a0001c0001t0002g0060a0001c0001t0002g0129a0001c0001t0003g0068others(9): Show | 12 | HG01243.hp2 HG01255.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.894+391_894+392dup others(2): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr4 | 107909109 | |||||
| chr4:107909109
|
AT | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0061a0001c0001t0001g0180others(4): Show | 7 | HG00323.hp2 HG01884.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.894+392delT | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr4 | 107909109 | |||||
| chr4:107909184
|
C | T | 3 | a0001c0001t0009g0032a0001c0001t0009g0080a0001c0001t0009g0112 | 3 | HG00733.hp2 HG03490.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.894+453C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909184 | ||||||
| chr4:107909264
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0125 | 2 | NA18961.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.894+533C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909264 | ||||||
| chr4:107909271
|
A | G | 62 | a0001c0001t0002g0008a0001c0001t0002g0042a0001c0001t0002g0060others(59): Show | 64 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.894+540A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909271 | ||||||
| chr4:107909320
|
A | G | 72 | a0001c0001t0001g0241a0001c0001t0001g0256a0001c0001t0002g0008others(69): Show | 76 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.894+589A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909320 | ||||||
| chr4:107909386
|
T | C | 72 | a0001c0001t0001g0241a0001c0001t0001g0256a0001c0001t0002g0008others(69): Show | 76 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.894+655T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909386 | ||||||
| chr4:107909500
|
G | T | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.894+769G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909500 | ||||||
| chr4:107909504
|
C | A | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.894+773C>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909504 | ||||||
| chr4:107909507
|
T | A | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.894+776T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909507 | ||||||
| chr4:107909509
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.894+778C>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909509 | ||||||
| chr4:107909510
|
T | A | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.894+779T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909510 | ||||||
| chr4:107909511
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.894+780G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909511 | ||||||
| chr4:107909513
|
T | A | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.894+782T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909513 | ||||||
| chr4:107909516
|
T | A | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.894+785T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909516 | ||||||
| chr4:107909517
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.894+786T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909517 | ||||||
| chr4:107909518
|
C | A | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.894+787C>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909518 | ||||||
| chr4:107909520
|
T | A | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.894+789T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909520 | ||||||
| chr4:107909521
|
C | A | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.894+790C>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909521 | ||||||
| chr4:107909523
|
T | A | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.894+792T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909523 | ||||||
| chr4:107909525
|
T | A | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.894+794T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909525 | ||||||
| chr4:107909526
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.894+795G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909526 | ||||||
| chr4:107909527
|
C | A | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.894+796C>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909527 | ||||||
| chr4:107909528
|
T | A | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.894+797T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909528 | ||||||
| chr4:107909534
|
T | A | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.894+803T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909534 | ||||||
| chr4:107909536
|
C | G | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.894+805C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909536 | ||||||
| chr4:107909539
|
C | G | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.894+808C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909539 | ||||||
| chr4:107909540
|
C | G | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.894+809C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909540 | ||||||
| chr4:107909542
|
T | A | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-808T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909542 | ||||||
| chr4:107909544
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-806T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909544 | ||||||
| chr4:107909545
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-805T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909545 | ||||||
| chr4:107909548
|
C | G | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-802C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909548 | ||||||
| chr4:107909550
|
G | T | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-800G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909550 | ||||||
| chr4:107909552
|
T | A | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-798T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909552 | ||||||
| chr4:107909553
|
G | T | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-797G>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909553 | ||||||
| chr4:107909556
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-794T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909556 | ||||||
| chr4:107909557
|
T | G | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-793T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909557 | ||||||
| chr4:107909558
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-792T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909558 | ||||||
| chr4:107909562
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-788T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909562 | ||||||
| chr4:107909564
|
C | G | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-786C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909564 | ||||||
| chr4:107909565
|
T | G | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-785T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909565 | ||||||
| chr4:107909566
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-784T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909566 | ||||||
| chr4:107909567
|
C | G | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-783C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909567 | ||||||
| chr4:107909568
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-782T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909568 | ||||||
| chr4:107909571
|
C | G | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-779C>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909571 | ||||||
| chr4:107909572
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-778A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909572 | ||||||
| chr4:107909573
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-777T>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909573 | ||||||
| chr4:107909577
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-773A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909577 | ||||||
| chr4:107909578
|
A | T | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-772A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909578 | ||||||
| chr4:107909581
|
T | A | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-769T>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909581 | ||||||
| chr4:107909582
|
A | C | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-768A>C | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909582 | ||||||
| chr4:107909595
|
AAATGCCA others(4): Show |
A | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-754_895-744del others(11): Show |
SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909595 | ||||||
| chr4:107909608
|
T | G | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-742T>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909608 | ||||||
| chr4:107909609
|
C | A | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-741C>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909609 | ||||||
| chr4:107909611
|
A | T | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895-739A>T | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909611 | ||||||
| chr4:107909785
|
G | A | 3 | a0001c0001t0006g0002a0001c0001t0006g0172a0001c0001t0006g0253 | 5 | HG01069.hp2 HG01071.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.895-565G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909785 | ||||||
| chr4:107909800
|
A | G | 1 | a0001c0001t0002g0202 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.895-550A>G | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107909800 | ||||||
| chr4:107910174
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.895-176G>A | SGMS2 | ENSG00000164023.15 | transcript | ENST00000690982.1 | protein_coding | 6/6 | chr4 | 107910174 |