| geneid | 57620 |
|---|---|
| ensemblid | ENSG00000109689.20 |
| hgncid | 19205 |
| symbol | STIM2 |
| name | stromal interaction molecule 2 |
| refseq_nuc | NM_020860.4 |
| refseq_prot | NP_065911.3 |
| ensembl_nuc | ENST00000467087.7 |
| ensembl_prot | ENSP00000419073.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 26860841 |
| end | 27025381 |
| strand | + |
| ver | v1.2 |
| region | chr4:26860841-27025381 |
| region5000 | chr4:26855841-27030381 |
| regionname0 | STIM2_chr4_26860841_27025381 |
| regionname5000 | STIM2_chr4_26855841_27030381 |
| 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 | 30 | 336 | 80 | 58 | 154 | 8 | 34 | 112 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| 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 | 0/1 | 2241 | 323 | 75 | 55 | 151 | 8 | 33 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| c0002 | 1/0 | 2241 | 9 | 5 | 3 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| c0003 | 0/0 | 2241 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| c0004 | 0/0 | 2241 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| c0005 | 0/0 | 2241 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| c0006 | 0/0 | 2241 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2763 | 64 | 12 | 15 | 27 | 0 | 9 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0002 | 0/0 | 2764 | 52 | 6 | 3 | 39 | 1 | 3 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0003 | 0/0 | 2764 | 46 | 6 | 11 | 23 | 2 | 4 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0004 | 0/0 | 2763 | 40 | 1 | 5 | 25 | 1 | 8 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0005 | 0/0 | 2764 | 18 | 8 | 1 | 8 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0006 | 0/0 | 2762 | 12 | 0 | 6 | 4 | 2 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0007 | 0/0 | 2765 | 11 | 7 | 1 | 3 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0008 | 0/0 | 2763 | 10 | 0 | 0 | 10 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0009 | 0/0 | 2762 | 9 | 4 | 3 | 0 | 0 | 2 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0010 | 0/0 | 2761 | 8 | 5 | 3 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0011 | 1/0 | 2764 | 7 | 2 | 0 | 4 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0012 | 0/0 | 2761 | 5 | 5 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0013 | 0/0 | 2760 | 4 | 4 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0014 | 0/0 | 2764 | 4 | 0 | 1 | 1 | 0 | 2 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0015 | 0/0 | 2764 | 4 | 4 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0016 | 0/0 | 2763 | 3 | 2 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0017 | 0/0 | 2764 | 3 | 0 | 3 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0018 | 0/0 | 2762 | 3 | 1 | 1 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0019 | 0/0 | 2762 | 2 | 2 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0020 | 0/0 | 2763 | 2 | 0 | 1 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0021 | 0/0 | 2764 | 2 | 2 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0022 | 0/0 | 2764 | 2 | 0 | 0 | 2 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0023 | 0/0 | 2763 | 2 | 0 | 1 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0024 | 0/0 | 2765 | 2 | 0 | 0 | 0 | 1 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0025 | 0/0 | 2762 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0026 | 0/0 | 2762 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0027 | 0/0 | 2763 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0028 | 0/0 | 2762 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0029 | 0/0 | 2761 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0030 | 0/0 | 2761 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0031 | 0/0 | 2764 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0032 | 0/0 | 2763 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0033 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0034 | 0/0 | 2764 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0035 | 0/0 | 2764 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0036 | 0/0 | 2764 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0037 | 0/0 | 2762 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0038 | 0/0 | 2762 | 1 | 0 | 0 | 0 | 1 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0039 | 0/0 | 2764 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0040 | 0/0 | 2764 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0041 | 0/0 | 2763 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0042 | 0/0 | 2765 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0043 | 0/0 | 2765 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0044 | 0/0 | 2765 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| t0045 | 0/0 | 2763 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0042 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0269 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| 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 | 0/1 | 2241 | 323 | 75 | 55 | 151 | 8 | 33 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0002 | 1/0 | 2241 | 9 | 5 | 3 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0003 | 0/0 | 2241 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0004 | 0/0 | 2241 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0005 | 0/0 | 2241 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0006 | 0/0 | 2241 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5003 | 63 | 12 | 15 | 26 | 0 | 9 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0002 | 0/0 | 5004 | 51 | 6 | 3 | 38 | 1 | 3 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0003 | 0/0 | 5004 | 45 | 6 | 11 | 22 | 2 | 4 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0004 | 0/0 | 5003 | 40 | 1 | 5 | 25 | 1 | 8 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0005 | 0/0 | 5004 | 18 | 8 | 1 | 8 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0006 | 0/0 | 5002 | 12 | 0 | 6 | 4 | 2 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0007 | 0/0 | 5005 | 11 | 7 | 1 | 3 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0008 | 0/0 | 5003 | 10 | 0 | 0 | 10 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0009 | 0/0 | 5002 | 5 | 2 | 1 | 0 | 0 | 2 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0010 | 0/0 | 5001 | 8 | 5 | 3 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0011 | 0/0 | 5004 | 6 | 2 | 0 | 4 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0012 | 0/0 | 5001 | 5 | 5 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0013 | 0/0 | 5000 | 3 | 3 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0014 | 0/0 | 5004 | 4 | 0 | 1 | 1 | 0 | 2 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0015 | 0/0 | 5004 | 4 | 4 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0016 | 0/0 | 5003 | 3 | 2 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0017 | 0/0 | 5004 | 3 | 0 | 3 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0018 | 0/0 | 5002 | 3 | 1 | 1 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0019 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0020 | 0/0 | 5003 | 2 | 0 | 1 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0021 | 0/0 | 5004 | 2 | 2 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0022 | 0/0 | 5004 | 2 | 0 | 0 | 2 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0023 | 0/0 | 5003 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0024 | 0/0 | 5005 | 2 | 0 | 0 | 0 | 1 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0025 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0027 | 0/0 | 5003 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0028 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0029 | 0/0 | 5001 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0030 | 0/0 | 5001 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0031 | 0/0 | 5004 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0032 | 0/0 | 5003 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0033 | 0/0 | 5005 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0034 | 0/0 | 5004 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0035 | 0/0 | 5004 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0036 | 0/0 | 5004 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0037 | 0/0 | 5002 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0038 | 0/0 | 5002 | 1 | 0 | 0 | 0 | 1 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0040 | 0/0 | 5004 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0041 | 0/0 | 5003 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0042 | 0/0 | 5005 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0043 | 0/0 | 5005 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0044 | 0/0 | 5005 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0001t0045 | 0/0 | 5003 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0002t0009 | 0/0 | 5002 | 4 | 2 | 2 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0002t0011 | 1/0 | 5004 | 1 | 0 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0002t0013 | 0/0 | 5000 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0002t0019 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0002t0023 | 0/0 | 5003 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0002t0026 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0003t0001 | 0/0 | 5003 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0004t0039 | 0/0 | 5004 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0005t0002 | 0/0 | 5004 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| a0001c0006t0003 | 0/0 | 5004 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | copy fasta | chr4 | 26855841 | 27030381 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0042 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0006g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0006g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0006g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0006g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0006g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0006g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0006g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0006g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0006g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0006g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0006g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0007g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0007g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0007g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0007g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0007g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0007g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0007g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0007g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0008g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0008g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0008g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0008g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0008g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0008g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0008g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0008g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0008g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0008g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0009g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0009g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0009g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0009g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0009g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0010g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0010g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0010g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0010g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0010g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0010g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0010g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0010g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0011g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0011g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0011g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0011g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0011g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0011g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0012g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0012g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0012g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0012g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0012g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0013g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0013g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0013g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0014g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0014g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0014g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0014g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0015g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0015g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0015g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0015g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0016g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0016g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0016g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0017g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0017g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0017g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0018g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0018g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0018g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0019g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0020g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0020g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0021g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0021g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0022g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0022g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0023g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0024g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0024g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0025g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0027g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0028g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0029g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0030g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0031g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0032g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0033g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0034g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0035g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0036g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0037g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0038g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0040g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0041g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0042g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0043g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0044g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0045g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0002t0009g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0002t0009g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0002t0009g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0002t0009g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0002t0011g0269 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0002t0013g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0002t0019g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0002t0023g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0002t0026g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0004t0039g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0005t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0006t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0200 | EUR | GBR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0244 | EUR | GBR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00408 | hp1 | a0001 | c0001 | t0044 | g0270 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0274 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00544 | hp1 | a0001 | c0001 | t0005 | g0067 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00544 | hp2 | a0001 | c0005 | t0002 | g0088 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0233 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0262 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00597 | hp2 | a0001 | c0001 | t0007 | g0248 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00621 | hp2 | a0001 | c0001 | t0023 | g0160 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00642 | hp2 | a0001 | c0001 | t0014 | g0121 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00733 | hp1 | a0001 | c0002 | t0023 | g0155 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00735 | hp1 | a0001 | c0001 | t0010 | g0132 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00738 | hp2 | a0001 | c0001 | t0017 | g0186 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00741 | hp1 | a0001 | c0001 | t0016 | g0017 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0178 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01071 | hp1 | a0001 | c0001 | t0042 | g0250 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01071 | hp2 | a0001 | c0001 | t0010 | g0135 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01074 | hp1 | a0001 | c0001 | t0006 | g0129 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01074 | hp2 | a0001 | c0001 | t0006 | g0253 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0137 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0226 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01106 | hp1 | a0001 | c0001 | t0029 | g0136 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01106 | hp2 | a0001 | c0002 | t0009 | g0114 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0247 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01167 | hp2 | a0001 | c0001 | t0017 | g0187 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01169 | hp2 | a0001 | c0001 | t0017 | g0185 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0196 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01243 | hp1 | a0001 | c0001 | t0007 | g0091 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01255 | hp2 | a0001 | c0002 | t0009 | g0115 | AMR | CLM | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01256 | hp1 | a0001 | c0001 | t0006 | g0133 | AMR | CLM | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0162 | AMR | CLM | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01261 | hp1 | a0001 | c0001 | t0009 | g0328 | AMR | CLM | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0251 | AMR | CLM | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01358 | hp1 | a0001 | c0001 | t0018 | g0275 | AMR | CLM | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0265 | AMR | CLM | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0266 | AMR | CLM | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0276 | AMR | CLM | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01433 | hp1 | a0001 | c0001 | t0010 | g0131 | AMR | CLM | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | CLM | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01515 | hp1 | a0001 | c0001 | t0006 | g0001 | EUR | IBS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0188 | EUR | IBS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01517 | hp1 | a0001 | c0001 | t0038 | g0130 | EUR | IBS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01517 | hp2 | a0001 | c0001 | t0006 | g0001 | EUR | IBS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0180 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0203 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0206 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0166 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0179 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0117 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0157 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01975 | hp2 | a0001 | c0001 | t0020 | g0294 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01981 | hp2 | a0001 | c0001 | t0005 | g0097 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0169 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01993 | hp2 | a0001 | c0001 | t0006 | g0116 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0175 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0234 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02056 | hp2 | a0001 | c0006 | t0003 | g0174 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0231 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02135 | hp2 | a0001 | c0001 | t0006 | g0239 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02145 | hp1 | a0001 | c0001 | t0012 | g0215 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0236 | EAS | CDX | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | CDX | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0151 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02280 | hp1 | a0001 | c0001 | t0012 | g0221 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02280 | hp2 | a0001 | c0001 | t0036 | g0016 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02451 | hp1 | a0001 | c0001 | t0015 | g0333 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0182 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02572 | hp1 | a0001 | c0001 | t0010 | g0101 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02572 | hp2 | a0001 | c0001 | t0028 | g0284 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0243 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0212 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0110 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02622 | hp2 | a0001 | c0001 | t0010 | g0106 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02630 | hp2 | a0001 | c0001 | t0016 | g0019 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02647 | hp2 | a0001 | c0001 | t0012 | g0280 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0268 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0158 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0208 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0168 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0314 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0286 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02809 | hp1 | a0001 | c0001 | t0027 | g0104 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02809 | hp2 | a0001 | c0001 | t0018 | g0112 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02896 | hp1 | a0001 | c0002 | t0009 | g0149 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0146 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0118 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0145 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02922 | hp1 | a0001 | c0002 | t0013 | g0099 | AFR | ESN | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02922 | hp2 | a0001 | c0001 | t0030 | g0195 | AFR | ESN | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | ESN | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02965 | hp2 | a0001 | c0001 | t0015 | g0330 | AFR | ESN | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03041 | hp1 | a0001 | c0002 | t0019 | g0107 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03041 | hp2 | a0001 | c0001 | t0012 | g0223 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0279 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03130 | hp1 | a0001 | c0001 | t0019 | g0150 | AFR | ESN | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0211 | AFR | ESN | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0209 | AFR | ESN | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03139 | hp2 | a0001 | c0001 | t0012 | g0222 | AFR | ESN | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ESN | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0210 | AFR | ESN | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03209 | hp2 | a0001 | c0001 | t0016 | g0018 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03225 | hp2 | a0001 | c0001 | t0011 | g0213 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0192 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03239 | hp2 | a0001 | c0001 | t0009 | g0126 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03453 | hp1 | a0001 | c0002 | t0026 | g0102 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03453 | hp2 | a0001 | c0001 | t0013 | g0218 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03486 | hp1 | a0001 | c0001 | t0011 | g0214 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03486 | hp2 | a0001 | c0001 | t0010 | g0327 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0246 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0245 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0307 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03669 | hp1 | a0001 | c0001 | t0014 | g0122 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0334 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | STU | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03688 | hp2 | a0001 | c0001 | t0009 | g0216 | SAS | STU | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03704 | hp1 | a0001 | c0001 | t0043 | g0312 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0261 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03710 | hp1 | a0001 | c0001 | t0018 | g0171 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0201 | SAS | BEB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0003 | SAS | BEB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03834 | hp2 | a0001 | c0004 | t0039 | g0161 | SAS | BEB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0242 | SAS | BEB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03927 | hp2 | a0001 | c0001 | t0014 | g0119 | SAS | BEB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG04115 | hp1 | a0001 | c0001 | t0037 | g0134 | SAS | STU | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0252 | SAS | STU | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0108 | AFR | YRI | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18522 | hp2 | a0001 | c0001 | t0021 | g0205 | AFR | YRI | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | CHB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0227 | EAS | CHB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | CHB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18906 | hp1 | a0001 | c0001 | t0013 | g0217 | AFR | YRI | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18906 | hp2 | a0001 | c0002 | t0009 | g0103 | AFR | YRI | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18944 | hp2 | a0001 | c0001 | t0011 | g0229 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18948 | hp1 | a0001 | c0001 | t0008 | g0076 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18948 | hp2 | a0001 | c0001 | t0007 | g0255 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18949 | hp2 | a0001 | c0001 | t0031 | g0009 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18950 | hp2 | a0001 | c0001 | t0008 | g0063 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18951 | hp1 | a0001 | c0001 | t0005 | g0034 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18953 | hp1 | a0001 | c0001 | t0005 | g0301 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18954 | hp2 | a0001 | c0001 | t0008 | g0029 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18968 | hp2 | a0001 | c0001 | t0014 | g0123 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0230 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18970 | hp2 | a0001 | c0001 | t0005 | g0300 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18973 | hp1 | a0001 | c0001 | t0011 | g0241 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18973 | hp2 | a0001 | c0001 | t0006 | g0062 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18980 | hp1 | a0001 | c0001 | t0032 | g0298 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0264 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18985 | hp1 | a0001 | c0001 | t0005 | g0291 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18985 | hp2 | a0001 | c0003 | t0001 | g0285 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18989 | hp1 | a0001 | c0001 | t0005 | g0140 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18991 | hp1 | a0001 | c0001 | t0008 | g0094 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18993 | hp2 | a0001 | c0001 | t0041 | g0235 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18994 | hp1 | a0001 | c0001 | t0008 | g0068 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18995 | hp2 | a0001 | c0001 | t0008 | g0028 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18997 | hp1 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18998 | hp1 | a0001 | c0001 | t0011 | g0087 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0259 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0096 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19011 | hp1 | a0001 | c0001 | t0040 | g0079 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19030 | hp1 | a0001 | c0001 | t0021 | g0204 | AFR | LWK | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19030 | hp2 | a0001 | c0001 | t0033 | g0144 | AFR | LWK | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19058 | hp2 | a0001 | c0001 | t0022 | g0318 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19060 | hp2 | a0001 | c0001 | t0005 | g0080 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19063 | hp1 | a0001 | c0001 | t0008 | g0147 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19063 | hp2 | a0001 | c0001 | t0020 | g0004 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19068 | hp1 | a0001 | c0001 | t0022 | g0302 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19070 | hp1 | a0001 | c0001 | t0008 | g0069 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19074 | hp1 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19077 | hp2 | a0001 | c0001 | t0007 | g0254 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19078 | hp1 | a0001 | c0001 | t0006 | g0023 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19078 | hp2 | a0001 | c0001 | t0011 | g0287 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19080 | hp2 | a0001 | c0001 | t0008 | g0027 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0249 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19086 | hp1 | a0001 | c0001 | t0008 | g0074 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19090 | hp1 | a0001 | c0001 | t0006 | g0072 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19091 | hp2 | a0001 | c0001 | t0035 | g0289 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0278 | AFR | YRI | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19240 | hp2 | a0001 | c0001 | t0010 | g0105 | AFR | YRI | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA20805 | hp1 | a0001 | c0001 | t0024 | g0308 | EUR | TSI | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0290 | EUR | TSI | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | GIH | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA20905 | hp2 | a0001 | c0001 | t0024 | g0309 | SAS | GIH | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02109 | hp1 | a0001 | c0001 | t0015 | g0331 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0202 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02486 | hp1 | a0001 | c0001 | t0010 | g0100 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0109 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02559 | hp1 | a0001 | c0001 | t0013 | g0219 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02559 | hp2 | a0001 | c0001 | t0009 | g0283 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG06807 | hp1 | a0001 | c0001 | t0045 | g0183 | AFR | USA | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG06807 | hp2 | a0001 | c0001 | t0034 | g0120 | AFR | USA | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA20300 | hp1 | a0001 | c0001 | t0015 | g0332 | AFR | USA | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA20300 | hp2 | a0001 | c0001 | t0025 | g0220 | AFR | USA | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0042 | REF | REF | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0011 | g0269 | REF | REF | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:27007598
|
T | G | 1 | a0001 | 1 | NA18985.hp2 | missense_variant | MODERATE | c.1047T>G | p.Asp349Glu | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 8/12 | 1425/5004 | 1047/2241 | 349/746 | chr4 | 27007598 | ||
| chr4:27008800
|
A | T | 1 | a0001 | 1 | NA18985.hp2 | missense_variant | MODERATE | c.1287A>T | p.Glu429Asp | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/12 | 1665/5004 | 1287/2241 | 429/746 | chr4 | 27008800 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:27002389
|
G | A | 5 | a0001c0001a0001c0003a0001c0004others(2): Show | 327 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(324): Show |
synonymous_variant | LOW | c.798G>A | p.Gln266Gln | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 6/12 | 1176/5004 | 798/2241 | 266/746 | chr4 | 27002389 | ||
| chr4:27017737
|
T | C | 1 | a0001c0004 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.1516T>C | p.Leu506Leu | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/12 | 1894/5004 | 1516/2241 | 506/746 | chr4 | 27017737 | ||
| chr4:27022600
|
G | A | 1 | a0001c0005 | 1 | HG00544.hp2 | synonymous_variant | LOW | c.1845G>A | p.Glu615Glu | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 12/12 | 2223/5004 | 1845/2241 | 615/746 | chr4 | 27022600 | ||
| chr4:27022954
|
G | A | 1 | a0001c0006 | 1 | HG02056.hp2 | synonymous_variant | LOW | c.2199G>A | p.Lys733Lys | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 12/12 | 2577/5004 | 2199/2241 | 733/746 | chr4 | 27022954 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:26860921
|
C | A | 2 | a0001c0001t0019a0001c0002t0019 | 2 | HG03041.hp1 HG03130.hp1 |
5_prime_UTR_variant | MODIFIER | c.-298C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/12 | 298 | chr4 | 26860921 | |||||
| chr4:26860924
|
CT | C | 28 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(25): Show | 235 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(232): Show |
5_prime_UTR_variant | MODIFIER | c.-277delT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/12 | 277 | INFO_REALIGN_3_PRIME | chr4 | 26860924 | ||||
| chr4:26860924
|
CTT | C | 11 | a0001c0001t0009a0001c0001t0010a0001c0001t0019others(8): Show | 26 | HG00735.hp1 HG01071.hp2 HG01106.hp1 others(23): Show |
5_prime_UTR_variant | MODIFIER | c.-278_-277delTT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/12 | 277 | INFO_REALIGN_3_PRIME | chr4 | 26860924 | ||||
| chr4:26860924
|
CTTT | C | 4 | a0001c0001t0012a0001c0001t0013a0001c0001t0025others(1): Show | 10 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-279_-277delTTT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/12 | 277 | INFO_REALIGN_3_PRIME | chr4 | 26860924 | ||||
| chr4:26860951
|
G | C | 1 | a0001c0001t0021 | 2 | NA18522.hp2 NA19030.hp1 |
5_prime_UTR_variant | MODIFIER | c.-268G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/12 | 268 | chr4 | 26860951 | |||||
| chr4:26861086
|
T | A | 1 | a0001c0001t0041 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-133T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/12 | 133 | chr4 | 26861086 | |||||
| chr4:26861112
|
C | T | 1 | a0001c0001t0040 | 1 | NA19011.hp1 | 5_prime_UTR_variant | MODIFIER | c.-107C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/12 | 107 | chr4 | 26861112 | |||||
| chr4:26861114
|
G | C | 1 | a0001c0001t0031 | 1 | NA18949.hp2 | 5_prime_UTR_variant | MODIFIER | c.-105G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/12 | 105 | chr4 | 26861114 | |||||
| chr4:26861132
|
C | T | 9 | a0001c0001t0003a0001c0001t0017a0001c0001t0018others(6): Show | 57 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(54): Show |
5_prime_UTR_variant | MODIFIER | c.-87C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/12 | 87 | chr4 | 26861132 | |||||
| chr4:26861160
|
C | G | 9 | a0001c0001t0003a0001c0001t0017a0001c0001t0018others(6): Show | 57 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(54): Show |
5_prime_UTR_variant | MODIFIER | c.-59C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/12 | 59 | chr4 | 26861160 | |||||
| chr4:27023019
|
T | C | 1 | a0001c0002t0026 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*23T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 12/12 | 23 | chr4 | 27023019 | |||||
| chr4:27023183
|
T | C | 1 | a0001c0001t0032 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*187T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 12/12 | 187 | chr4 | 27023183 | |||||
| chr4:27023336
|
C | G | 1 | a0001c0001t0022 | 2 | NA19058.hp2 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*340C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 12/12 | 340 | chr4 | 27023336 | |||||
| chr4:27023452
|
C | G | 1 | a0001c0001t0022 | 2 | NA19058.hp2 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*456C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 12/12 | 456 | chr4 | 27023452 | |||||
| chr4:27023470
|
G | GA | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(20): Show | 153 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*486dupA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 12/12 | 487 | INFO_REALIGN_3_PRIME | chr4 | 27023470 | ||||
| chr4:27023470
|
GA | G | 12 | a0001c0001t0004a0001c0001t0006a0001c0001t0010others(9): Show | 73 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*486delA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 12/12 | 486 | INFO_REALIGN_3_PRIME | chr4 | 27023470 | ||||
| chr4:27023506
|
A | G | 1 | a0001c0001t0022 | 2 | NA19058.hp2 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*510A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 12/12 | 510 | chr4 | 27023506 | |||||
| chr4:27023550
|
A | T | 1 | a0001c0004t0039 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*554A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 12/12 | 554 | chr4 | 27023550 | |||||
| chr4:27023616
|
G | A | 2 | a0001c0001t0014a0001c0001t0042 | 5 | HG00642.hp2 HG01071.hp1 HG03669.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*620G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 12/12 | 620 | chr4 | 27023616 | |||||
| chr4:27023624
|
A | G | 1 | a0001c0001t0036 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*628A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 12/12 | 628 | chr4 | 27023624 | |||||
| chr4:27023875
|
A | G | 13 | a0001c0001t0002a0001c0001t0008a0001c0001t0017others(10): Show | 77 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*879A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 12/12 | 879 | chr4 | 27023875 | |||||
| chr4:27024212
|
A | G | 1 | a0001c0001t0038 | 1 | HG01517.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1216A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 12/12 | 1216 | chr4 | 27024212 | |||||
| chr4:27024259
|
T | TA | 3 | a0001c0001t0015a0001c0001t0025a0001c0001t0033 | 6 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1270dupA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 12/12 | 1271 | INFO_REALIGN_3_PRIME | chr4 | 27024259 | ||||
| chr4:27024403
|
T | A | 1 | a0001c0001t0029 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1407T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 12/12 | 1407 | chr4 | 27024403 | |||||
| chr4:27024545
|
C | A | 1 | a0001c0001t0035 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1549C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 12/12 | 1549 | chr4 | 27024545 | |||||
| chr4:27024564
|
A | G | 1 | a0001c0001t0034 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1568A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 12/12 | 1568 | chr4 | 27024564 | |||||
| chr4:27025059
|
G | C | 2 | a0001c0001t0016a0001c0001t0028 | 4 | HG00741.hp1 HG02572.hp2 HG02630.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2063G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 12/12 | 2063 | chr4 | 27025059 | |||||
| chr4:27025061
|
G | C | 1 | a0001c0001t0043 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2065G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 12/12 | 2065 | chr4 | 27025061 | |||||
| chr4:27025230
|
A | G | 1 | a0001c0001t0044 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2234A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 12/12 | 2234 | chr4 | 27025230 | |||||
| chr4:27025294
|
G | T | 1 | a0001c0001t0037 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2298G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 12/12 | 2298 | chr4 | 27025294 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:26861414
|
G | GACCTCT | 7 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(4): Show | 7 | HG03579.hp1 HG03834.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.151+45_151+46insAC others(4): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26861414 | ||||||
| chr4:26861416
|
G | C | 7 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(4): Show | 7 | HG03579.hp1 HG03834.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.151+47G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26861416 | ||||||
| chr4:26861452
|
G | C | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012 | 3 | HG01192.hp2 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.151+83G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26861452 | ||||||
| chr4:26861458
|
C | G | 1 | a0001c0001t0003g0334 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.151+89C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26861458 | ||||||
| chr4:26861469
|
G | C | 1 | a0001c0001t0001g0013 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.151+100G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26861469 | ||||||
| chr4:26861695
|
A | AT | 13 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0002g0277others(10): Show | 13 | HG01358.hp1 HG01361.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.151+348dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26861695 | |||||
| chr4:26861695
|
A | ATT | 56 | a0001c0001t0001g0306a0001c0001t0001g0319a0001c0001t0002g0005others(53): Show | 56 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.151+347_151+348dup others(2): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26861695 | |||||
| chr4:26861695
|
AT | A | 106 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(103): Show | 107 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.151+348delT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26861695 | |||||
| chr4:26861709
|
T | G | 6 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0016g0017others(3): Show | 6 | HG00741.hp1 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.151+340T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26861709 | ||||||
| chr4:26861755
|
T | C | 1 | a0001c0001t0004g0118 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.151+386T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26861755 | ||||||
| chr4:26861819
|
T | C | 280 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(277): Show | 282 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(279): Show |
intron_variant | MODIFIER | c.151+450T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26861819 | ||||||
| chr4:26861900
|
C | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.151+531C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26861900 | ||||||
| chr4:26861921
|
C | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+552C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26861921 | ||||||
| chr4:26861960
|
C | T | 10 | a0001c0001t0009g0216a0001c0001t0012g0215a0001c0001t0012g0221others(7): Show | 10 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+591C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26861960 | ||||||
| chr4:26861997
|
G | A | 1 | a0001c0001t0014g0119 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.151+628G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26861997 | ||||||
| chr4:26862219
|
G | A | 19 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0002g0127others(16): Show | 19 | HG00642.hp2 HG00735.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.151+850G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26862219 | ||||||
| chr4:26862274
|
C | T | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+905C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26862274 | ||||||
| chr4:26862315
|
A | G | 1 | a0001c0001t0012g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.151+946A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26862315 | ||||||
| chr4:26862318
|
G | GT | 19 | a0001c0001t0001g0225a0001c0001t0002g0329a0001c0001t0004g0271others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.151+966dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26862318 | |||||
| chr4:26862318
|
GT | G | 113 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0006others(110): Show | 114 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.151+966delT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26862318 | |||||
| chr4:26862318
|
GTT | G | 28 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0124others(25): Show | 28 | HG00735.hp1 HG00741.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.151+965_151+966del others(2): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26862318 | |||||
| chr4:26862318
|
GTTT | G | 90 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(87): Show | 91 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.151+964_151+966del others(3): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26862318 | |||||
| chr4:26862539
|
A | ATAGGATA others(38): Show |
1 | a0001c0001t0002g0012 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.151+1173_151+1217d others(47): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26862539 | |||||
| chr4:26862557
|
TAG | T | 13 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(10): Show | 13 | HG01106.hp2 HG01255.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+1194_151+1195d others(4): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26862557 | |||||
| chr4:26862694
|
A | T | 11 | a0001c0001t0009g0216a0001c0001t0009g0328a0001c0001t0012g0215others(8): Show | 11 | HG01261.hp1 HG02145.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+1325A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26862694 | ||||||
| chr4:26862813
|
A | T | 3 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019 | 3 | HG00741.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.151+1444A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26862813 | ||||||
| chr4:26862846
|
A | G | 6 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(3): Show | 6 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+1477A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26862846 | ||||||
| chr4:26862939
|
G | A | 1 | a0001c0001t0018g0275 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.151+1570G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26862939 | ||||||
| chr4:26863267
|
G | A | 1 | a0001c0001t0009g0328 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.151+1898G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26863267 | ||||||
| chr4:26863464
|
A | G | 4 | a0001c0001t0005g0206a0001c0001t0007g0203a0001c0001t0021g0204others(1): Show | 4 | HG01884.hp2 HG01891.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+2095A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26863464 | ||||||
| chr4:26864058
|
G | T | 1 | a0001c0001t0043g0312 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.151+2689G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26864058 | ||||||
| chr4:26864127
|
A | G | 11 | a0001c0001t0009g0216a0001c0001t0009g0328a0001c0001t0012g0215others(8): Show | 11 | HG01261.hp1 HG02145.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+2758A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26864127 | ||||||
| chr4:26864179
|
G | A | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+2810G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26864179 | ||||||
| chr4:26864252
|
C | T | 11 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0006g0129others(8): Show | 11 | HG00735.hp1 HG01071.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+2883C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26864252 | ||||||
| chr4:26864663
|
A | G | 1 | a0001c0001t0002g0093 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.151+3294A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26864663 | ||||||
| chr4:26864698
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+3329A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26864698 | ||||||
| chr4:26864800
|
C | G | 1 | a0001c0001t0001g0092 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.151+3431C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26864800 | ||||||
| chr4:26864832
|
G | T | 6 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(3): Show | 6 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+3463G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26864832 | ||||||
| chr4:26864862
|
C | T | 10 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(7): Show | 10 | HG02109.hp1 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.151+3493C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26864862 | ||||||
| chr4:26865080
|
A | G | 12 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(9): Show | 12 | HG02109.hp1 HG02451.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.151+3711A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26865080 | ||||||
| chr4:26865088
|
G | C | 3 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0110 | 3 | HG02486.hp2 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.151+3719G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26865088 | ||||||
| chr4:26865089
|
T | C | 273 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(270): Show | 275 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(272): Show |
intron_variant | MODIFIER | c.151+3720T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26865089 | ||||||
| chr4:26865125
|
TTC | T | 3 | a0001c0001t0007g0091a0001c0001t0007g0145a0001c0001t0007g0146 | 3 | HG01243.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.151+3760_151+3761d others(4): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26865125 | |||||
| chr4:26865141
|
C | T | 110 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(107): Show | 111 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.151+3772C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26865141 | ||||||
| chr4:26865178
|
T | G | 3 | a0001c0001t0007g0091a0001c0001t0007g0145a0001c0001t0007g0146 | 3 | HG01243.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.151+3809T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26865178 | ||||||
| chr4:26865344
|
C | T | 1 | a0001c0001t0002g0311 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.151+3975C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26865344 | ||||||
| chr4:26865349
|
G | A | 1 | a0001c0001t0003g0151 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.151+3980G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26865349 | ||||||
| chr4:26865350
|
T | C | 125 | a0001c0001t0001g0020a0001c0001t0001g0224a0001c0001t0001g0225others(122): Show | 126 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.151+3981T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26865350 | ||||||
| chr4:26865407
|
G | T | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.151+4038G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26865407 | ||||||
| chr4:26865580
|
A | G | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.151+4211A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26865580 | ||||||
| chr4:26865601
|
C | T | 3 | a0001c0001t0007g0091a0001c0001t0007g0145a0001c0001t0007g0146 | 3 | HG01243.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.151+4232C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26865601 | ||||||
| chr4:26865639
|
T | C | 55 | a0001c0001t0001g0306a0001c0001t0001g0319a0001c0001t0002g0005others(52): Show | 55 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.151+4270T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26865639 | ||||||
| chr4:26865827
|
T | TA | 12 | a0001c0001t0004g0228a0001c0001t0004g0230a0001c0001t0004g0231others(9): Show | 12 | HG00558.hp2 HG02040.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.151+4466dupA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26865827 | |||||
| chr4:26865945
|
A | G | 7 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0206others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.151+4576A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26865945 | ||||||
| chr4:26865989
|
GT | G | 330 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(327): Show | 332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.151+4631delT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26865989 | |||||
| chr4:26866037
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.151+4668A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26866037 | ||||||
| chr4:26866389
|
C | T | 1 | a0001c0001t0007g0278 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.151+5020C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26866389 | ||||||
| chr4:26866461
|
C | T | 3 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0110 | 3 | HG02486.hp2 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.151+5092C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26866461 | ||||||
| chr4:26866618
|
A | G | 6 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(3): Show | 6 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+5249A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26866618 | ||||||
| chr4:26866814
|
CTA | C | 4 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019others(1): Show | 4 | HG00741.hp1 HG02630.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+5447_151+5448d others(4): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26866814 | |||||
| chr4:26866978
|
A | T | 8 | a0001c0001t0004g0232a0001c0001t0004g0233a0001c0001t0004g0234others(5): Show | 8 | HG00558.hp2 HG02040.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.151+5609A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26866978 | ||||||
| chr4:26866983
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.151+5614G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26866983 | ||||||
| chr4:26867056
|
A | G | 10 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0206others(7): Show | 10 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.151+5687A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26867056 | ||||||
| chr4:26867145
|
C | G | 1 | a0001c0001t0004g0268 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.151+5776C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26867145 | ||||||
| chr4:26867146
|
G | A | 1 | a0001c0002t0023g0155 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.151+5777G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26867146 | ||||||
| chr4:26867251
|
A | G | 3 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0110 | 3 | HG02486.hp2 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.151+5882A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26867251 | ||||||
| chr4:26867469
|
T | C | 1 | a0001c0002t0013g0099 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.151+6100T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26867469 | ||||||
| chr4:26867524
|
A | G | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0009g0126 | 3 | HG03239.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.151+6155A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26867524 | ||||||
| chr4:26867544
|
C | T | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.151+6175C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26867544 | ||||||
| chr4:26867657
|
G | T | 1 | a0001c0001t0006g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.151+6288G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26867657 | ||||||
| chr4:26867716
|
G | C | 112 | a0001c0001t0001g0020a0001c0001t0001g0306a0001c0001t0001g0319others(109): Show | 113 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.151+6347G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26867716 | ||||||
| chr4:26867781
|
C | T | 4 | a0001c0001t0005g0206a0001c0001t0007g0203a0001c0001t0021g0204others(1): Show | 4 | HG01884.hp2 HG01891.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+6412C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26867781 | ||||||
| chr4:26867911
|
A | G | 2 | a0001c0001t0002g0089a0001c0005t0002g0088 | 2 | HG00544.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.151+6542A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26867911 | ||||||
| chr4:26868459
|
A | T | 55 | a0001c0001t0001g0306a0001c0001t0001g0319a0001c0001t0002g0005others(52): Show | 55 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.151+7090A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26868459 | ||||||
| chr4:26868670
|
A | G | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0011g0087 | 3 | NA18968.hp1 NA18998.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.151+7301A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26868670 | ||||||
| chr4:26868696
|
A | G | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.151+7327A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26868696 | ||||||
| chr4:26868818
|
C | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+7449C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26868818 | ||||||
| chr4:26868862
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+7493A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26868862 | ||||||
| chr4:26868889
|
C | T | 1 | a0001c0001t0004g0267 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.151+7520C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26868889 | ||||||
| chr4:26868912
|
A | G | 2 | a0001c0001t0003g0201a0001c0001t0003g0202 | 2 | HG02109.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.151+7543A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26868912 | ||||||
| chr4:26869022
|
C | G | 1 | a0001c0001t0009g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.151+7653C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26869022 | ||||||
| chr4:26869093
|
G | A | 1 | a0001c0001t0010g0327 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.151+7724G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26869093 | ||||||
| chr4:26869104
|
G | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0138 | 2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.151+7735G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26869104 | ||||||
| chr4:26869273
|
T | C | 3 | a0001c0001t0007g0091a0001c0001t0007g0145a0001c0001t0007g0146 | 3 | HG01243.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.151+7904T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26869273 | ||||||
| chr4:26869299
|
C | CA | 12 | a0001c0001t0005g0206a0001c0001t0007g0203a0001c0001t0009g0328others(9): Show | 12 | HG01261.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.151+7951dupA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26869299 | |||||
| chr4:26869299
|
CA | C | 189 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(186): Show | 191 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(188): Show |
intron_variant | MODIFIER | c.151+7951delA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26869299 | |||||
| chr4:26869317
|
A | G | 1 | a0001c0001t0003g0200 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.151+7948A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26869317 | ||||||
| chr4:26869633
|
A | G | 3 | a0001c0001t0007g0091a0001c0001t0007g0145a0001c0001t0007g0146 | 3 | HG01243.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.151+8264A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26869633 | ||||||
| chr4:26869650
|
T | C | 1 | a0001c0001t0018g0275 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.151+8281T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26869650 | ||||||
| chr4:26869719
|
C | T | 1 | a0001c0001t0005g0206 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.151+8350C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26869719 | ||||||
| chr4:26869890
|
A | G | 3 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0036g0016 | 3 | HG02280.hp2 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.151+8521A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26869890 | ||||||
| chr4:26869893
|
T | C | 5 | a0001c0001t0008g0027a0001c0001t0008g0028a0001c0001t0008g0029others(2): Show | 5 | NA18954.hp2 NA18991.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.151+8524T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26869893 | ||||||
| chr4:26870051
|
C | A | 7 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0206others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.151+8682C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26870051 | ||||||
| chr4:26870109
|
A | G | 8 | a0001c0001t0012g0215a0001c0001t0012g0221a0001c0001t0012g0222others(5): Show | 8 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.151+8740A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26870109 | ||||||
| chr4:26870169
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+8800A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26870169 | ||||||
| chr4:26870297
|
C | CA | 42 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(39): Show | 42 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.151+8942dupA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26870297 | |||||
| chr4:26870297
|
CA | C | 23 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0003g0159others(20): Show | 23 | HG01106.hp2 HG01255.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.151+8942delA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26870297 | |||||
| chr4:26870409
|
A | G | 23 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(20): Show | 23 | HG01106.hp2 HG01255.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.151+9040A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26870409 | ||||||
| chr4:26870630
|
T | C | 3 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0036g0016 | 3 | HG02280.hp2 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.151+9261T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26870630 | ||||||
| chr4:26870737
|
C | G | 4 | a0001c0001t0005g0206a0001c0001t0007g0203a0001c0001t0021g0204others(1): Show | 4 | HG01884.hp2 HG01891.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+9368C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26870737 | ||||||
| chr4:26870740
|
G | C | 23 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0206others(20): Show | 23 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.151+9371G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26870740 | ||||||
| chr4:26870776
|
G | A | 1 | a0001c0001t0028g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.151+9407G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26870776 | ||||||
| chr4:26870797
|
G | A | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+9428G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26870797 | ||||||
| chr4:26870838
|
G | A | 117 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(114): Show | 118 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.151+9469G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26870838 | ||||||
| chr4:26870844
|
A | G | 6 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(3): Show | 6 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+9475A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26870844 | ||||||
| chr4:26870845
|
T | C | 1 | a0001c0001t0008g0094 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.151+9476T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26870845 | ||||||
| chr4:26870883
|
G | A | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+9514G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26870883 | ||||||
| chr4:26870901
|
CT | C | 14 | a0001c0001t0001g0030a0001c0001t0001g0085a0001c0001t0002g0288others(11): Show | 14 | HG01106.hp2 HG01255.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.151+9547delT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26870901 | |||||
| chr4:26871095
|
A | C | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0012g0280 | 3 | HG02647.hp2 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.151+9726A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26871095 | ||||||
| chr4:26871100
|
A | G | 2 | a0001c0001t0001g0281a0001c0001t0001g0282 | 2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.151+9731A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26871100 | ||||||
| chr4:26871298
|
A | G | 2 | a0001c0001t0002g0083a0001c0001t0002g0084 | 2 | HG01934.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.151+9929A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26871298 | ||||||
| chr4:26871385
|
T | A | 1 | a0001c0001t0034g0120 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.151+10016T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26871385 | ||||||
| chr4:26871390
|
T | C | 1 | a0001c0001t0009g0328 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.151+10021T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26871390 | ||||||
| chr4:26871562
|
A | G | 1 | a0001c0001t0004g0231 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.151+10193A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26871562 | ||||||
| chr4:26871622
|
C | A | 1 | a0001c0001t0009g0328 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.151+10253C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26871622 | ||||||
| chr4:26871625
|
G | T | 2 | a0001c0001t0004g0265a0001c0001t0004g0266 | 2 | HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.151+10256G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26871625 | ||||||
| chr4:26871704
|
C | CT | 161 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(158): Show | 163 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.151+10353dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26871704 | |||||
| chr4:26871704
|
CT | C | 13 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(10): Show | 13 | HG01106.hp2 HG01255.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+10353delT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26871704 | |||||
| chr4:26871792
|
C | G | 1 | a0001c0001t0001g0013 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.151+10423C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26871792 | ||||||
| chr4:26872078
|
A | G | 181 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(178): Show | 183 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.151+10709A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26872078 | ||||||
| chr4:26872184
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.151+10815G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26872184 | ||||||
| chr4:26872226
|
T | C | 2 | a0001c0001t0002g0010a0001c0001t0002g0011 | 2 | HG01192.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.151+10857T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26872226 | ||||||
| chr4:26872424
|
T | G | 3 | a0001c0001t0014g0119a0001c0001t0014g0121a0001c0001t0014g0122 | 3 | HG00642.hp2 HG03669.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.151+11055T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26872424 | ||||||
| chr4:26872573
|
TTAA | T | 10 | a0001c0001t0004g0230a0001c0001t0004g0232a0001c0001t0004g0233others(7): Show | 10 | HG00558.hp2 HG02040.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.151+11210_151+1121 others(7): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26872573 | |||||
| chr4:26872652
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.151+11283C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26872652 | ||||||
| chr4:26872760
|
G | C | 2 | a0001c0001t0002g0127a0001c0001t0002g0128 | 2 | HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.151+11391G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26872760 | ||||||
| chr4:26872784
|
G | A | 121 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(118): Show | 122 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.151+11415G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26872784 | ||||||
| chr4:26872814
|
T | C | 121 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(118): Show | 122 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.151+11445T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26872814 | ||||||
| chr4:26872990
|
A | AT | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+11625dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26872990 | |||||
| chr4:26873081
|
C | T | 1 | a0001c0001t0002g0154 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.151+11712C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26873081 | ||||||
| chr4:26873170
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.151+11801C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26873170 | ||||||
| chr4:26873248
|
G | A | 8 | a0001c0001t0012g0215a0001c0001t0012g0221a0001c0001t0012g0222others(5): Show | 8 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.151+11879G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26873248 | ||||||
| chr4:26873253
|
G | A | 2 | a0001c0001t0004g0265a0001c0001t0004g0266 | 2 | HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.151+11884G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26873253 | ||||||
| chr4:26873303
|
A | C | 3 | a0001c0001t0004g0237a0001c0001t0004g0238a0001c0001t0006g0239 | 3 | HG02135.hp2 NA18989.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.151+11934A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26873303 | ||||||
| chr4:26873311
|
C | CT | 5 | a0001c0001t0014g0119a0001c0001t0014g0121a0001c0001t0014g0122others(2): Show | 5 | HG00642.hp2 HG03669.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.151+11944dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26873311 | |||||
| chr4:26873354
|
C | T | 1 | a0001c0001t0009g0328 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.151+11985C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26873354 | ||||||
| chr4:26873465
|
T | C | 1 | a0001c0001t0003g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.151+12096T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26873465 | ||||||
| chr4:26873635
|
C | T | 2 | a0001c0001t0002g0089a0001c0005t0002g0088 | 2 | HG00544.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.151+12266C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26873635 | ||||||
| chr4:26873644
|
A | G | 231 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(228): Show | 233 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(230): Show |
intron_variant | MODIFIER | c.151+12275A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26873644 | ||||||
| chr4:26873833
|
C | T | 87 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(84): Show | 88 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.151+12464C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26873833 | ||||||
| chr4:26873971
|
C | T | 1 | a0001c0001t0012g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.151+12602C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26873971 | ||||||
| chr4:26874028
|
C | T | 2 | a0001c0001t0003g0198a0001c0001t0003g0199 | 2 | HG02071.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.151+12659C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26874028 | ||||||
| chr4:26874394
|
C | G | 2 | a0001c0001t0019g0150a0001c0002t0019g0107 | 2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.151+13025C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26874394 | ||||||
| chr4:26874397
|
A | T | 2 | a0001c0001t0004g0227a0001c0001t0004g0262 | 2 | HG00597.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.151+13028A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26874397 | ||||||
| chr4:26874403
|
G | C | 1 | a0001c0001t0001g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.151+13034G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26874403 | ||||||
| chr4:26874659
|
T | C | 1 | a0001c0001t0004g0268 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.151+13290T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26874659 | ||||||
| chr4:26874754
|
G | A | 53 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0281others(50): Show | 53 | HG01192.hp2 HG01243.hp1 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.151+13385G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26874754 | ||||||
| chr4:26874818
|
T | C | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.151+13449T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26874818 | ||||||
| chr4:26875050
|
A | G | 1 | a0001c0001t0005g0080 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.151+13681A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26875050 | ||||||
| chr4:26875146
|
TCTTAA | T | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+13782_151+1378 others(9): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26875146 | |||||
| chr4:26875289
|
C | T | 1 | a0001c0001t0018g0275 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.151+13920C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26875289 | ||||||
| chr4:26875610
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.151+14241A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26875610 | ||||||
| chr4:26875649
|
C | T | 279 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(276): Show | 281 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(278): Show |
intron_variant | MODIFIER | c.151+14280C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26875649 | ||||||
| chr4:26875685
|
A | G | 1 | a0001c0001t0012g0222 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.151+14316A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26875685 | ||||||
| chr4:26875836
|
T | C | 4 | a0001c0001t0005g0034a0001c0001t0005g0080a0001c0001t0005g0096others(1): Show | 4 | HG01981.hp2 NA18951.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+14467T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26875836 | ||||||
| chr4:26875851
|
C | T | 4 | a0001c0001t0005g0206a0001c0001t0007g0203a0001c0001t0021g0204others(1): Show | 4 | HG01884.hp2 HG01891.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+14482C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26875851 | ||||||
| chr4:26875877
|
T | G | 1 | a0001c0001t0009g0328 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.151+14508T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26875877 | ||||||
| chr4:26876290
|
T | G | 6 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(3): Show | 6 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+14921T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26876290 | ||||||
| chr4:26876352
|
C | T | 1 | a0001c0001t0040g0079 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.151+14983C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26876352 | ||||||
| chr4:26876521
|
A | C | 3 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0110 | 3 | HG02486.hp2 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.151+15152A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26876521 | ||||||
| chr4:26876711
|
T | C | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0038others(1): Show | 4 | HG02523.hp1 NA18612.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+15342T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26876711 | ||||||
| chr4:26876792
|
TCTTA | T | 9 | a0001c0001t0005g0206a0001c0001t0007g0203a0001c0001t0014g0119others(6): Show | 9 | HG00642.hp2 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.151+15426_151+1542 others(8): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26876792 | |||||
| chr4:26876837
|
A | T | 1 | a0001c0001t0003g0197 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.151+15468A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26876837 | ||||||
| chr4:26877044
|
G | A | 2 | a0001c0001t0019g0150a0001c0002t0019g0107 | 2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.151+15675G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26877044 | ||||||
| chr4:26877310
|
C | A | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+15941C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26877310 | ||||||
| chr4:26877333
|
G | A | 2 | a0001c0001t0009g0328a0001c0001t0044g0270 | 2 | HG00408.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.151+15964G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26877333 | ||||||
| chr4:26877508
|
G | A | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+16139G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26877508 | ||||||
| chr4:26877516
|
G | GT | 6 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0003g0196others(3): Show | 6 | HG00733.hp1 HG01175.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.151+16160dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26877516 | |||||
| chr4:26877516
|
GT | G | 30 | a0001c0001t0001g0306a0001c0001t0001g0319a0001c0001t0002g0005others(27): Show | 30 | HG01192.hp2 HG01433.hp2 HG02129.hp2 others(27): Show |
intron_variant | MODIFIER | c.151+16160delT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26877516 | |||||
| chr4:26877519
|
T | G | 1 | a0001c0001t0004g0227 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.151+16150T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26877519 | ||||||
| chr4:26877587
|
G | A | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.151+16218G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26877587 | ||||||
| chr4:26877598
|
C | T | 2 | a0001c0001t0003g0113a0001c0001t0003g0194 | 2 | HG02015.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.151+16229C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26877598 | ||||||
| chr4:26877749
|
G | A | 2 | a0001c0001t0006g0129a0001c0001t0038g0130 | 2 | HG01074.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.151+16380G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26877749 | ||||||
| chr4:26878038
|
A | G | 1 | a0001c0001t0028g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.151+16669A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26878038 | ||||||
| chr4:26878268
|
C | T | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+16899C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26878268 | ||||||
| chr4:26878280
|
T | A | 2 | a0001c0001t0005g0206a0001c0001t0007g0203 | 2 | HG01884.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.151+16911T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26878280 | ||||||
| chr4:26878421
|
A | G | 3 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0110 | 3 | HG02486.hp2 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.151+17052A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26878421 | ||||||
| chr4:26878534
|
C | T | 1 | a0001c0001t0003g0193 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.151+17165C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26878534 | ||||||
| chr4:26878541
|
G | A | 1 | a0001c0001t0003g0162 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.151+17172G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26878541 | ||||||
| chr4:26878592
|
T | G | 1 | a0001c0001t0034g0120 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.151+17223T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26878592 | ||||||
| chr4:26879017
|
T | C | 57 | a0001c0001t0001g0020a0001c0001t0003g0002a0001c0001t0003g0111others(54): Show | 58 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.151+17648T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26879017 | ||||||
| chr4:26879133
|
A | G | 26 | a0001c0001t0001g0319a0001c0001t0002g0005a0001c0001t0002g0006others(23): Show | 26 | HG01192.hp2 HG01433.hp2 HG02129.hp2 others(23): Show |
intron_variant | MODIFIER | c.151+17764A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26879133 | ||||||
| chr4:26879154
|
C | T | 3 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0036g0016 | 3 | HG02280.hp2 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.151+17785C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26879154 | ||||||
| chr4:26879332
|
C | CT | 6 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(3): Show | 6 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+17975dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26879332 | |||||
| chr4:26879364
|
T | C | 1 | a0001c0001t0010g0327 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.151+17995T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26879364 | ||||||
| chr4:26879456
|
C | A | 1 | a0001c0001t0002g0154 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.151+18087C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26879456 | ||||||
| chr4:26879457
|
A | C | 1 | a0001c0001t0002g0154 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.151+18088A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26879457 | ||||||
| chr4:26879458
|
T | A | 1 | a0001c0001t0002g0154 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.151+18089T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26879458 | ||||||
| chr4:26879504
|
T | A | 8 | a0001c0001t0012g0215a0001c0001t0012g0221a0001c0001t0012g0222others(5): Show | 8 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.151+18135T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26879504 | ||||||
| chr4:26879546
|
A | G | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012 | 3 | HG01192.hp2 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.151+18177A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26879546 | ||||||
| chr4:26879719
|
A | G | 3 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0036g0016 | 3 | HG02280.hp2 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.151+18350A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26879719 | ||||||
| chr4:26879829
|
A | G | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.151+18460A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26879829 | ||||||
| chr4:26879997
|
CTT | C | 3 | a0001c0001t0007g0091a0001c0001t0007g0145a0001c0001t0007g0146 | 3 | HG01243.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.151+18630_151+1863 others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26879997 | |||||
| chr4:26880232
|
G | A | 122 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(119): Show | 123 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.151+18863G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26880232 | ||||||
| chr4:26880600
|
C | CATATATA others(17): Show |
96 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0039others(93): Show | 97 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.151+19286_151+1930 others(28): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26880600 | |||||
| chr4:26880600
|
C | CATATATA others(41): Show |
9 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0003g0163others(6): Show | 9 | HG01192.hp2 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+19262_151+1930 others(52): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26880600 | |||||
| chr4:26880600
|
C | CATATATA others(65): Show |
2 | a0001c0001t0002g0012a0001c0002t0026g0102 | 2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.151+19238_151+1930 others(76): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26880600 | |||||
| chr4:26880600
|
CATATATA others(17): Show |
C | 1 | a0001c0001t0038g0130 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.151+19286_151+1930 others(28): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26880600 | |||||
| chr4:26880639
|
A | G | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.151+19270A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26880639 | ||||||
| chr4:26880646
|
A | AATATATA others(43): Show |
2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.151+19309_151+1931 others(54): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26880646 | |||||
| chr4:26880647
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0003g0192 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.151+19285_151+1928 others(26): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26880647 | |||||
| chr4:26880655
|
A | ATAAATAT others(5): Show |
1 | a0001c0001t0005g0212 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.151+19310_151+1932 others(16): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26880655 | |||||
| chr4:26880655
|
A | ATAAATAT others(41): Show |
1 | a0001c0001t0003g0189 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.151+19309_151+1931 others(52): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26880655 | |||||
| chr4:26880655
|
A | ATAAATAT others(17): Show |
1 | a0001c0001t0003g0334 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.151+19298_151+1932 others(28): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26880655 | |||||
| chr4:26880682
|
A | AATAT | 3 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019 | 3 | HG00741.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.151+19322_151+1932 others(8): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26880682 | |||||
| chr4:26880682
|
AAT | A | 3 | a0001c0001t0007g0091a0001c0001t0007g0145a0001c0001t0007g0146 | 3 | HG01243.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.151+19324_151+1932 others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26880682 | |||||
| chr4:26880717
|
T | C | 1 | a0001c0001t0002g0154 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.151+19348T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26880717 | ||||||
| chr4:26880721
|
C | T | 1 | a0001c0001t0002g0154 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.151+19352C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26880721 | ||||||
| chr4:26880788
|
G | A | 1 | a0001c0001t0009g0328 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.151+19419G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26880788 | ||||||
| chr4:26880797
|
A | C | 1 | a0001c0001t0010g0105 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.151+19428A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26880797 | ||||||
| chr4:26880909
|
G | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0041 | 2 | NA18962.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.151+19540G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26880909 | ||||||
| chr4:26880922
|
A | G | 9 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(6): Show | 9 | HG01106.hp2 HG01255.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+19553A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26880922 | ||||||
| chr4:26881323
|
C | T | 1 | a0001c0001t0002g0154 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.151+19954C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26881323 | ||||||
| chr4:26881371
|
C | A | 1 | a0001c0001t0009g0328 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.151+20002C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26881371 | ||||||
| chr4:26881465
|
C | CA | 69 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0148others(66): Show | 70 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.151+20111dupA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26881465 | |||||
| chr4:26881465
|
C | CAA | 85 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(82): Show | 86 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.151+20110_151+2011 others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26881465 | |||||
| chr4:26881557
|
C | T | 1 | a0001c0004t0039g0161 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.151+20188C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26881557 | ||||||
| chr4:26881709
|
G | A | 9 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(6): Show | 9 | HG01106.hp2 HG01255.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+20340G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26881709 | ||||||
| chr4:26881877
|
C | T | 2 | a0001c0001t0005g0206a0001c0001t0007g0203 | 2 | HG01884.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.151+20508C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26881877 | ||||||
| chr4:26882017
|
A | G | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.151+20648A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26882017 | ||||||
| chr4:26882054
|
A | G | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.151+20685A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26882054 | ||||||
| chr4:26882142
|
C | T | 259 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(256): Show | 261 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(258): Show |
intron_variant | MODIFIER | c.151+20773C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26882142 | ||||||
| chr4:26882287
|
T | C | 60 | a0001c0001t0001g0020a0001c0001t0001g0095a0001c0001t0001g0098others(57): Show | 61 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.151+20918T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26882287 | ||||||
| chr4:26882397
|
C | A | 1 | a0001c0001t0009g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.151+21028C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26882397 | ||||||
| chr4:26882437
|
A | ATTTC | 179 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(176): Show | 181 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.151+21084_151+2108 others(8): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26882437 | |||||
| chr4:26882454
|
T | TTTC | 70 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0281others(67): Show | 70 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.151+21087_151+2108 others(7): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26882454 | |||||
| chr4:26882454
|
T | TTTCTTTC | 8 | a0001c0001t0012g0215a0001c0001t0012g0221a0001c0001t0012g0222others(5): Show | 8 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.151+21087_151+2108 others(11): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26882454 | |||||
| chr4:26882463
|
G | T | 80 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0281others(77): Show | 80 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.151+21094G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26882463 | ||||||
| chr4:26882469
|
G | T | 1 | a0001c0001t0002g0154 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.151+21100G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26882469 | ||||||
| chr4:26882470
|
T | G | 1 | a0001c0001t0002g0154 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.151+21101T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26882470 | ||||||
| chr4:26882596
|
T | A | 1 | a0001c0001t0038g0130 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.151+21227T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26882596 | ||||||
| chr4:26882695
|
C | G | 1 | a0001c0001t0001g0306 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.151+21326C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26882695 | ||||||
| chr4:26882700
|
A | C | 3 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0036g0016 | 3 | HG02280.hp2 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.151+21331A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26882700 | ||||||
| chr4:26882774
|
T | C | 3 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0110 | 3 | HG02486.hp2 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.151+21405T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26882774 | ||||||
| chr4:26882786
|
C | T | 259 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(256): Show | 261 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(258): Show |
intron_variant | MODIFIER | c.151+21417C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26882786 | ||||||
| chr4:26882839
|
C | CT | 13 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(10): Show | 13 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.151+21483dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26882839 | |||||
| chr4:26882843
|
T | C | 1 | a0001c0001t0036g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.151+21474T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26882843 | ||||||
| chr4:26882923
|
C | T | 1 | a0001c0001t0004g0261 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.151+21554C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26882923 | ||||||
| chr4:26882963
|
G | A | 1 | a0001c0001t0004g0263 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.151+21594G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26882963 | ||||||
| chr4:26883004
|
A | AT | 114 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(111): Show | 116 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.151+21651dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26883004 | |||||
| chr4:26883004
|
A | ATT | 45 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0031others(42): Show | 45 | HG00438.hp2 HG00544.hp1 HG01934.hp2 others(42): Show |
intron_variant | MODIFIER | c.151+21650_151+2165 others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26883004 | |||||
| chr4:26883287
|
TGGTATAT others(21): Show |
T | 1 | a0001c0001t0002g0154 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.151+21919_151+2194 others(32): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26883287 | ||||||
| chr4:26883313
|
C | G | 1 | a0001c0001t0009g0126 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.151+21944C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26883313 | ||||||
| chr4:26883325
|
A | G | 4 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0110others(1): Show | 4 | HG02486.hp2 HG02622.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+21956A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26883325 | ||||||
| chr4:26883752
|
A | T | 3 | a0001c0001t0017g0185a0001c0001t0017g0186a0001c0001t0017g0187 | 3 | HG00738.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.151+22383A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26883752 | ||||||
| chr4:26883843
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+22474A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26883843 | ||||||
| chr4:26883857
|
G | A | 1 | a0001c0001t0001g0306 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.151+22488G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26883857 | ||||||
| chr4:26884092
|
T | A | 1 | a0001c0001t0014g0121 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.151+22723T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26884092 | ||||||
| chr4:26884126
|
G | A | 3 | a0001c0001t0007g0091a0001c0001t0007g0145a0001c0001t0007g0146 | 3 | HG01243.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.151+22757G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26884126 | ||||||
| chr4:26884151
|
G | T | 123 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(120): Show | 124 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.151+22782G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26884151 | ||||||
| chr4:26884173
|
A | C | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.151+22804A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26884173 | ||||||
| chr4:26884192
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.151+22823G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26884192 | ||||||
| chr4:26884279
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.151+22910A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26884279 | ||||||
| chr4:26884584
|
C | A | 9 | a0001c0001t0006g0129a0001c0001t0006g0133a0001c0001t0006g0137others(6): Show | 9 | HG00735.hp1 HG01071.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+23215C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26884584 | ||||||
| chr4:26884584
|
C | T | 1 | a0001c0001t0004g0274 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.151+23215C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26884584 | ||||||
| chr4:26884674
|
C | T | 101 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(98): Show | 102 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.151+23305C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26884674 | ||||||
| chr4:26885043
|
T | C | 3 | a0001c0001t0007g0091a0001c0001t0007g0145a0001c0001t0007g0146 | 3 | HG01243.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.151+23674T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26885043 | ||||||
| chr4:26885134
|
TTGTGTTC others(28): Show |
T | 8 | a0001c0001t0001g0025a0001c0001t0001g0058a0001c0001t0001g0059others(5): Show | 8 | HG00438.hp2 NA18973.hp2 NA18989.hp1 others(5): Show |
intron_variant | MODIFIER | c.151+23768_151+2380 others(39): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885134 | |||||
| chr4:26885353
|
C | A | 1 | a0001c0001t0007g0203 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.151+23984C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26885353 | ||||||
| chr4:26885483
|
C | A | 2 | a0001c0002t0009g0114a0001c0002t0009g0115 | 2 | HG01106.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.151+24114C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26885483 | ||||||
| chr4:26885601
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+24232A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26885601 | ||||||
| chr4:26885821
|
T | TTA | 10 | a0001c0001t0001g0282a0001c0001t0004g0236a0001c0001t0004g0251others(7): Show | 10 | HG01256.hp1 HG01261.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+24504_151+2450 others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885821 | |||||
| chr4:26885821
|
T | TTATA | 11 | a0001c0001t0001g0281a0001c0001t0004g0226a0001c0001t0004g0227others(8): Show | 11 | HG00558.hp2 HG00597.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+24502_151+2450 others(8): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885821 | |||||
| chr4:26885821
|
T | TTATATA | 4 | a0001c0001t0004g0231a0001c0001t0004g0232a0001c0001t0006g0247others(1): Show | 4 | HG01167.hp1 HG02080.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+24500_151+2450 others(10): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885821 | |||||
| chr4:26885821
|
T | TTATATAT others(1): Show |
6 | a0001c0001t0004g0243a0001c0001t0004g0244a0001c0001t0004g0245others(3): Show | 6 | HG00099.hp2 HG00423.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.151+24498_151+2450 others(12): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885821 | |||||
| chr4:26885821
|
T | TTATATAT others(3): Show |
4 | a0001c0001t0004g0242a0001c0001t0004g0271a0001c0001t0007g0203others(1): Show | 4 | HG01884.hp2 HG03927.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+24496_151+2450 others(14): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885821 | |||||
| chr4:26885821
|
T | TTATATAT others(5): Show |
4 | a0001c0001t0004g0118a0001c0001t0004g0263a0001c0001t0006g0116others(1): Show | 4 | HG01993.hp2 HG02559.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+24494_151+2450 others(16): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885821 | |||||
| chr4:26885821
|
T | TTATATAT others(9): Show |
1 | a0001c0001t0004g0264 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.151+24490_151+2450 others(20): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885821 | |||||
| chr4:26885821
|
T | TTATATAT others(19): Show |
1 | a0001c0001t0004g0240 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.151+24480_151+2450 others(30): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885821 | |||||
| chr4:26885821
|
TTA | T | 11 | a0001c0001t0002g0154a0001c0001t0004g0228a0001c0001t0004g0257others(8): Show | 11 | HG00597.hp1 HG00741.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.151+24504_151+2450 others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885821 | |||||
| chr4:26885821
|
TTATATA | T | 5 | a0001c0001t0005g0206a0001c0001t0006g0129a0001c0001t0010g0327others(2): Show | 5 | HG01074.hp1 HG01517.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.151+24500_151+2450 others(10): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885821 | |||||
| chr4:26885821
|
TTATATAT others(1): Show |
T | 4 | a0001c0001t0004g0237a0001c0001t0004g0238a0001c0001t0004g0259others(1): Show | 4 | HG02451.hp1 NA18989.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+24498_151+2450 others(12): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885821 | |||||
| chr4:26885821
|
TTATATAT others(3): Show |
T | 3 | a0001c0001t0004g0117a0001c0001t0004g0260a0001c0002t0026g0102 | 3 | HG01943.hp2 HG03453.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.151+24496_151+2450 others(14): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885821 | |||||
| chr4:26885821
|
TTATATAT others(5): Show |
T | 1 | a0001c0001t0029g0136 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.151+24494_151+2450 others(16): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885821 | |||||
| chr4:26885821
|
TTATATAT others(7): Show |
T | 3 | a0001c0001t0006g0239a0001c0001t0015g0332a0001c0001t0021g0205 | 3 | HG02135.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.151+24492_151+2450 others(18): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885821 | |||||
| chr4:26885821
|
TTATATAT others(9): Show |
T | 4 | a0001c0001t0019g0150a0001c0001t0044g0270a0001c0002t0013g0099others(1): Show | 4 | HG00408.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+24490_151+2450 others(20): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885821 | |||||
| chr4:26885821
|
TTATATAT others(11): Show |
T | 1 | a0001c0001t0004g0261 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.151+24488_151+2450 others(22): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885821 | |||||
| chr4:26885821
|
TTATATAT others(13): Show |
T | 2 | a0001c0001t0001g0057a0001c0001t0006g0137 | 2 | HG00621.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.151+24486_151+2450 others(24): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885821 | |||||
| chr4:26885821
|
TTATATAT others(17): Show |
T | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.151+24482_151+2450 others(28): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885821 | |||||
| chr4:26885821
|
TTATATAT others(19): Show |
T | 2 | a0001c0001t0003g0113a0001c0001t0011g0229 | 2 | HG02015.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.151+24480_151+2450 others(30): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885821 | |||||
| chr4:26885821
|
TTATATAT others(21): Show |
T | 14 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0003g0156others(11): Show | 14 | HG01243.hp1 HG01243.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.151+24478_151+2450 others(32): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885821 | |||||
| chr4:26885821
|
TTATATAT others(23): Show |
T | 117 | a0001c0001t0001g0020a0001c0001t0001g0306a0001c0001t0001g0319others(114): Show | 118 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.151+24476_151+2450 others(34): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885821 | |||||
| chr4:26885821
|
TTATATAT others(27): Show |
T | 1 | a0001c0001t0014g0121 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.151+24472_151+2450 others(38): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885821 | |||||
| chr4:26885821
|
TTATATAT others(29): Show |
T | 1 | a0001c0001t0004g0267 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.151+24470_151+2450 others(40): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885821 | |||||
| chr4:26885821
|
TTATATAT others(31): Show |
T | 10 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(7): Show | 10 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.151+24468_151+2450 others(42): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885821 | |||||
| chr4:26885831
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0002g0073 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.151+24487_151+2448 others(30): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885831 | |||||
| chr4:26885833
|
A | ATATACAT others(25): Show |
7 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(4): Show | 7 | NA18973.hp2 NA18989.hp1 NA18999.hp1 others(4): Show |
intron_variant | MODIFIER | c.151+24468_151+2446 others(36): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885833 | |||||
| chr4:26885833
|
A | ATATATAC others(23): Show |
2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | NA18944.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.151+24470_151+2447 others(34): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885833 | |||||
| chr4:26885842
|
T | C | 1 | a0001c0001t0011g0213 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.151+24473T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26885842 | ||||||
| chr4:26885853
|
ATATATAT others(15): Show |
A | 1 | a0001c0001t0005g0212 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.151+24490_151+2451 others(26): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885853 | |||||
| chr4:26885857
|
ATATATAT others(11): Show |
A | 1 | a0001c0001t0005g0211 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.151+24494_151+2451 others(22): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885857 | |||||
| chr4:26885859
|
A | ATATATAT others(31): Show |
2 | a0001c0001t0002g0037a0001c0001t0008g0063 | 2 | HG02523.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.151+24511_151+2451 others(42): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0031 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.151+24503_151+2450 others(44): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATAT others(57): Show |
1 | a0001c0001t0001g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.151+24503_151+2450 others(68): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATAT others(27): Show |
5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0090others(2): Show | 5 | HG01981.hp2 HG02004.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.151+24503_151+2450 others(38): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATAT others(33): Show |
1 | a0001c0001t0002g0064 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.151+24501_151+2450 others(44): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATAT others(31): Show |
1 | a0001c0001t0001g0038 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.151+24501_151+2450 others(42): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATAT others(25): Show |
3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0009g0126 | 3 | HG01192.hp1 HG02273.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.151+24501_151+2450 others(36): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATAT others(23): Show |
1 | a0001c0005t0002g0088 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.151+24501_151+2450 others(34): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATAT others(99): Show |
1 | a0001c0001t0001g0041 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.151+24501_151+2450 others(110): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATAT others(97): Show |
1 | a0001c0001t0001g0033 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.151+24501_151+2450 others(108): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATAT others(31): Show |
3 | a0001c0001t0001g0081a0001c0001t0001g0143a0001c0001t0002g0065 | 3 | HG02040.hp1 HG03490.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.151+24499_151+2450 others(42): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATAT others(29): Show |
2 | a0001c0001t0001g0013a0001c0001t0002g0066 | 2 | HG03491.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.151+24499_151+2450 others(40): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATAT others(27): Show |
2 | a0001c0001t0008g0027a0001c0001t0008g0094 | 2 | NA18991.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.151+24499_151+2450 others(38): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATAT others(25): Show |
1 | a0001c0001t0005g0096 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.151+24499_151+2450 others(36): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATAT others(23): Show |
6 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0048others(3): Show | 6 | HG00738.hp1 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.151+24499_151+2450 others(34): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATAT others(99): Show |
2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | NA18957.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.151+24499_151+2450 others(110): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATAT others(21): Show |
2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG00733.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.151+24499_151+2450 others(32): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATAT others(59): Show |
1 | a0001c0001t0001g0022 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.151+24499_151+2450 others(70): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATAT others(31): Show |
1 | a0001c0001t0002g0093 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.151+24497_151+2449 others(42): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATAT others(29): Show |
1 | a0001c0001t0005g0067 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.151+24497_151+2449 others(40): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATAT others(27): Show |
4 | a0001c0001t0001g0086a0001c0001t0002g0026a0001c0001t0008g0068others(1): Show | 4 | HG02135.hp1 NA18948.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+24497_151+2449 others(38): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATAT others(25): Show |
5 | a0001c0001t0001g0039a0001c0001t0001g0141a0001c0001t0008g0028others(2): Show | 5 | NA18995.hp2 NA19000.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.151+24497_151+2449 others(36): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0008g0029 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.151+24497_151+2449 others(34): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATAT others(21): Show |
4 | a0001c0001t0001g0021a0001c0001t0001g0032a0001c0001t0001g0051others(1): Show | 4 | HG00735.hp2 HG01928.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+24497_151+2449 others(32): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATAT others(19): Show |
2 | a0001c0001t0001g0052a0001c0001t0006g0001 | 3 | HG01515.hp1 HG01517.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.151+24497_151+2449 others(30): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATGT others(24): Show |
1 | a0001c0001t0006g0023 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.151+24495_151+2449 others(35): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATGT others(27): Show |
1 | a0001c0001t0001g0070 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.151+24495_151+2449 others(38): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATGT others(25): Show |
2 | a0001c0001t0001g0025a0001c0001t0001g0071 | 2 | HG00438.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.151+24495_151+2449 others(36): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATGT others(23): Show |
4 | a0001c0001t0001g0085a0001c0001t0002g0083a0001c0001t0008g0074others(1): Show | 4 | HG01934.hp2 NA18968.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+24495_151+2449 others(34): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATGT others(19): Show |
1 | a0001c0001t0001g0125 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.151+24495_151+2449 others(30): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATGT others(17): Show |
4 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(1): Show | 4 | HG02071.hp1 HG02083.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+24495_151+2449 others(28): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATATGT others(25): Show |
2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.151+24495_151+2449 others(36): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATGTAT others(23): Show |
2 | a0001c0001t0001g0040a0001c0001t0001g0092 | 2 | HG03540.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.151+24493_151+2449 others(34): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATGTAT others(21): Show |
1 | a0001c0001t0006g0072 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.151+24493_151+2449 others(32): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATATGTAT others(15): Show |
2 | a0001c0001t0001g0056a0001c0001t0002g0089 | 2 | HG02015.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.151+24493_151+2449 others(26): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATGTATAT others(21): Show |
1 | a0001c0001t0012g0221 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.151+24491_151+2449 others(32): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATGTATAT others(19): Show |
1 | a0001c0001t0002g0084 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.151+24491_151+2449 others(30): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | ATGTATAT others(31): Show |
1 | a0001c0001t0005g0080 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.151+24491_151+2449 others(42): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885859
|
A | G | 11 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0057others(8): Show | 11 | HG00621.hp1 HG02129.hp1 NA18944.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+24490A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26885859 | ||||||
| chr4:26885859
|
ATATATAT others(9): Show |
A | 1 | a0001c0001t0005g0208 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.151+24496_151+2451 others(20): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885859 | |||||
| chr4:26885865
|
ATATATAT others(3): Show |
A | 2 | a0001c0001t0005g0209a0001c0001t0005g0210 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.151+24502_151+2451 others(14): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26885865 | |||||
| chr4:26885867
|
A | G | 2 | a0001c0001t0014g0119a0001c0001t0014g0121 | 2 | HG00642.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.151+24498A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26885867 | ||||||
| chr4:26885869
|
A | G | 13 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(10): Show | 13 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.151+24500A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26885869 | ||||||
| chr4:26885871
|
A | G | 5 | a0001c0001t0014g0119a0001c0001t0014g0121a0001c0001t0016g0017others(2): Show | 5 | HG00642.hp2 HG00741.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.151+24502A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26885871 | ||||||
| chr4:26885877
|
A | C | 13 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(10): Show | 13 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.151+24508A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26885877 | ||||||
| chr4:26885889
|
A | G | 1 | a0001c0001t0003g0196 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.151+24520A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26885889 | ||||||
| chr4:26885934
|
A | G | 1 | a0001c0001t0004g0234 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.151+24565A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26885934 | ||||||
| chr4:26886021
|
C | T | 4 | a0001c0001t0010g0131a0001c0001t0010g0132a0001c0001t0010g0135others(1): Show | 4 | HG00735.hp1 HG01071.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+24652C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26886021 | ||||||
| chr4:26886079
|
T | G | 1 | a0001c0001t0001g0057 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.151+24710T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26886079 | ||||||
| chr4:26886085
|
G | A | 2 | a0001c0001t0009g0216a0001c0001t0028g0284 | 2 | HG02572.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.151+24716G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26886085 | ||||||
| chr4:26886183
|
G | T | 2 | a0001c0001t0004g0245a0001c0001t0004g0246 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.151+24814G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26886183 | ||||||
| chr4:26886227
|
A | G | 236 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(233): Show | 238 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(235): Show |
intron_variant | MODIFIER | c.151+24858A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26886227 | ||||||
| chr4:26886339
|
CGAT | C | 3 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0036g0016 | 3 | HG02280.hp2 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.151+24973_151+2497 others(7): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26886339 | |||||
| chr4:26886412
|
A | G | 1 | a0001c0001t0031g0009 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.151+25043A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26886412 | ||||||
| chr4:26886644
|
G | T | 1 | a0001c0001t0002g0305 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.151+25275G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26886644 | ||||||
| chr4:26886968
|
G | A | 1 | a0001c0001t0002g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.151+25599G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26886968 | ||||||
| chr4:26887030
|
G | A | 95 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(92): Show | 96 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.151+25661G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26887030 | ||||||
| chr4:26887125
|
G | A | 4 | a0001c0001t0005g0206a0001c0001t0007g0203a0001c0001t0021g0204others(1): Show | 4 | HG01884.hp2 HG01891.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+25756G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26887125 | ||||||
| chr4:26887183
|
C | CT | 39 | a0001c0001t0001g0086a0001c0001t0001g0125a0001c0001t0002g0153others(36): Show | 39 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.151+25838dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26887183 | |||||
| chr4:26887183
|
CT | C | 186 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(183): Show | 188 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(185): Show |
intron_variant | MODIFIER | c.151+25838delT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26887183 | |||||
| chr4:26887230
|
C | T | 3 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0006g0001 | 4 | HG00733.hp2 HG01255.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+25861C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26887230 | ||||||
| chr4:26887432
|
C | T | 233 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(230): Show | 235 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(232): Show |
intron_variant | MODIFIER | c.151+26063C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26887432 | ||||||
| chr4:26887450
|
C | G | 3 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0148 | 3 | HG02258.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.151+26081C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26887450 | ||||||
| chr4:26887600
|
A | G | 2 | a0001c0001t0009g0216a0001c0001t0028g0284 | 2 | HG02572.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.151+26231A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26887600 | ||||||
| chr4:26887660
|
G | A | 4 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(1): Show | 4 | HG02486.hp1 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+26291G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26887660 | ||||||
| chr4:26887701
|
G | T | 125 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(122): Show | 126 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.151+26332G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26887701 | ||||||
| chr4:26887702
|
T | C | 8 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0007g0091others(5): Show | 8 | HG01243.hp1 HG02559.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.151+26333T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26887702 | ||||||
| chr4:26887962
|
G | C | 1 | a0001c0001t0018g0275 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.151+26593G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26887962 | ||||||
| chr4:26888027
|
A | C | 1 | a0001c0001t0001g0090 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.151+26658A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26888027 | ||||||
| chr4:26888081
|
T | G | 1 | a0001c0001t0004g0252 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.151+26712T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26888081 | ||||||
| chr4:26888117
|
G | T | 1 | a0001c0001t0003g0189 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.151+26748G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26888117 | ||||||
| chr4:26888374
|
C | T | 1 | a0001c0001t0009g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.151+27005C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26888374 | ||||||
| chr4:26888488
|
G | C | 14 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(11): Show | 14 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.151+27119G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26888488 | ||||||
| chr4:26888575
|
C | T | 1 | a0001c0001t0004g0268 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.151+27206C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26888575 | ||||||
| chr4:26888699
|
G | A | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.151+27330G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26888699 | ||||||
| chr4:26888781
|
C | T | 1 | a0001c0003t0001g0285 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.151+27412C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26888781 | ||||||
| chr4:26888810
|
A | G | 192 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(189): Show | 194 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.151+27441A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26888810 | ||||||
| chr4:26888829
|
T | C | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+27460T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26888829 | ||||||
| chr4:26888863
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.151+27494G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26888863 | ||||||
| chr4:26888901
|
C | T | 1 | a0001c0001t0002g0304 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.151+27532C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26888901 | ||||||
| chr4:26888963
|
A | C | 1 | a0001c0001t0008g0076 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.151+27594A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26888963 | ||||||
| chr4:26889017
|
A | C | 2 | a0001c0001t0019g0150a0001c0002t0019g0107 | 2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.151+27648A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26889017 | ||||||
| chr4:26889190
|
G | C | 1 | a0001c0001t0010g0101 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.151+27821G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26889190 | ||||||
| chr4:26889291
|
T | C | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.151+27922T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26889291 | ||||||
| chr4:26889396
|
A | C | 1 | a0001c0001t0005g0067 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.151+28027A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26889396 | ||||||
| chr4:26889526
|
G | A | 2 | a0001c0001t0002g0127a0001c0001t0002g0128 | 2 | HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.151+28157G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26889526 | ||||||
| chr4:26889613
|
T | C | 1 | a0001c0001t0001g0092 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.151+28244T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26889613 | ||||||
| chr4:26889904
|
A | G | 14 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(11): Show | 14 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.151+28535A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26889904 | ||||||
| chr4:26890293
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.151+28924G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26890293 | ||||||
| chr4:26890324
|
T | C | 3 | a0001c0001t0006g0116a0001c0001t0006g0247a0001c0001t0006g0253 | 3 | HG01074.hp2 HG01167.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.151+28955T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26890324 | ||||||
| chr4:26890552
|
C | T | 57 | a0001c0001t0001g0306a0001c0001t0001g0319a0001c0001t0002g0005others(54): Show | 57 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.152-28952C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26890552 | ||||||
| chr4:26890562
|
C | T | 3 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019 | 3 | HG00741.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.152-28942C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26890562 | ||||||
| chr4:26890578
|
A | C | 1 | a0001c0001t0004g0226 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.152-28926A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26890578 | ||||||
| chr4:26890590
|
C | T | 81 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0281others(78): Show | 81 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.152-28914C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26890590 | ||||||
| chr4:26890607
|
G | A | 1 | a0001c0001t0006g0129 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.152-28897G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26890607 | ||||||
| chr4:26890642
|
T | G | 248 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(245): Show | 250 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(247): Show |
intron_variant | MODIFIER | c.152-28862T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26890642 | ||||||
| chr4:26890651
|
C | T | 14 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(11): Show | 14 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.152-28853C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26890651 | ||||||
| chr4:26890680
|
C | T | 1 | a0001c0001t0004g0227 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.152-28824C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26890680 | ||||||
| chr4:26890713
|
A | G | 2 | a0001c0001t0008g0028a0001c0001t0008g0147 | 2 | NA18995.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.152-28791A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26890713 | ||||||
| chr4:26890802
|
C | T | 1 | a0001c0001t0004g0252 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.152-28702C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26890802 | ||||||
| chr4:26890818
|
C | T | 4 | a0001c0001t0012g0215a0001c0001t0012g0222a0001c0001t0012g0223others(1): Show | 4 | HG02145.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-28686C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26890818 | ||||||
| chr4:26890823
|
C | CA | 23 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0095others(20): Show | 23 | HG00408.hp1 HG01256.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.152-28661dupA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26890823 | |||||
| chr4:26890823
|
CA | C | 7 | a0001c0001t0001g0043a0001c0001t0001g0081a0001c0001t0002g0303others(4): Show | 7 | HG02004.hp1 HG03225.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.152-28661delA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26890823 | |||||
| chr4:26891139
|
G | C | 1 | a0001c0001t0009g0328 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.152-28365G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26891139 | ||||||
| chr4:26891177
|
G | C | 138 | a0001c0001t0001g0020a0001c0001t0001g0224a0001c0001t0001g0225others(135): Show | 139 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.152-28327G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26891177 | ||||||
| chr4:26891190
|
A | G | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.152-28314A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26891190 | ||||||
| chr4:26891234
|
G | A | 14 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(11): Show | 14 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.152-28270G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26891234 | ||||||
| chr4:26891244
|
T | C | 1 | a0001c0001t0001g0042 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.152-28260T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26891244 | ||||||
| chr4:26891350
|
T | C | 57 | a0001c0001t0001g0306a0001c0001t0001g0319a0001c0001t0002g0005others(54): Show | 57 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.152-28154T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26891350 | ||||||
| chr4:26891555
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-27949A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26891555 | ||||||
| chr4:26891558
|
T | C | 1 | a0001c0001t0004g0262 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.152-27946T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26891558 | ||||||
| chr4:26891558
|
T | TAC | 14 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0242others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.152-27907_152-2790 others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26891558 | |||||
| chr4:26891558
|
T | TACAC | 5 | a0001c0001t0004g0261a0001c0001t0010g0101a0001c0001t0011g0241others(2): Show | 5 | HG02572.hp1 HG03453.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-27909_152-2790 others(8): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26891558 | |||||
| chr4:26891558
|
TAC | T | 17 | a0001c0001t0002g0292a0001c0001t0005g0014a0001c0001t0005g0208others(14): Show | 17 | HG00408.hp1 HG01993.hp2 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.152-27907_152-2790 others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26891558 | |||||
| chr4:26891558
|
TACAC | T | 60 | a0001c0001t0001g0020a0001c0001t0001g0306a0001c0001t0002g0005others(57): Show | 60 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.152-27909_152-2790 others(8): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26891558 | |||||
| chr4:26891558
|
TACACAC | T | 61 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0095others(58): Show | 62 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.152-27911_152-2790 others(10): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26891558 | |||||
| chr4:26891558
|
TACACACA others(1): Show |
T | 93 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0024others(90): Show | 94 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.152-27913_152-2790 others(12): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26891558 | |||||
| chr4:26891558
|
TACACACA others(3): Show |
T | 5 | a0001c0001t0001g0045a0001c0001t0015g0330a0001c0001t0015g0331others(2): Show | 5 | HG02109.hp1 HG02273.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-27915_152-2790 others(14): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26891558 | |||||
| chr4:26891558
|
TACACACA others(5): Show |
T | 8 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(5): Show | 8 | HG02071.hp1 HG02083.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-27917_152-2790 others(16): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26891558 | |||||
| chr4:26891558
|
TACACACA others(7): Show |
T | 1 | a0001c0003t0001g0285 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.152-27919_152-2790 others(18): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26891558 | |||||
| chr4:26891558
|
TACACACA others(9): Show |
T | 3 | a0001c0001t0007g0091a0001c0001t0007g0145a0001c0001t0007g0146 | 3 | HG01243.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.152-27921_152-2790 others(20): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26891558 | |||||
| chr4:26891591
|
ACACACAC others(1): Show |
A | 4 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019others(1): Show | 4 | HG00741.hp1 HG02630.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-27911_152-2790 others(12): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26891591 | |||||
| chr4:26891599
|
C | A | 1 | a0001c0001t0004g0233 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.152-27905C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26891599 | ||||||
| chr4:26891928
|
C | T | 2 | a0001c0001t0002g0005a0001c0001t0002g0008 | 2 | NA18991.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.152-27576C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26891928 | ||||||
| chr4:26891937
|
C | A | 3 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0148 | 3 | HG02258.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.152-27567C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26891937 | ||||||
| chr4:26891961
|
G | A | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-27543G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26891961 | ||||||
| chr4:26891980
|
T | A | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.152-27524T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26891980 | ||||||
| chr4:26892058
|
C | T | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-27446C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26892058 | ||||||
| chr4:26892085
|
C | T | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.152-27419C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26892085 | ||||||
| chr4:26892182
|
A | G | 1 | a0001c0001t0009g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.152-27322A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26892182 | ||||||
| chr4:26892192
|
C | T | 1 | a0001c0002t0019g0107 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.152-27312C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26892192 | ||||||
| chr4:26892198
|
C | T | 2 | a0001c0001t0004g0245a0001c0001t0004g0246 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.152-27306C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26892198 | ||||||
| chr4:26892397
|
G | A | 9 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0012g0215others(6): Show | 9 | HG01243.hp2 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-27107G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26892397 | ||||||
| chr4:26892529
|
G | T | 1 | a0001c0001t0004g0252 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.152-26975G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26892529 | ||||||
| chr4:26892617
|
T | C | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-26887T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26892617 | ||||||
| chr4:26892787
|
G | C | 1 | a0001c0001t0002g0307 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.152-26717G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26892787 | ||||||
| chr4:26892852
|
G | A | 46 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0306others(43): Show | 46 | HG01106.hp2 HG01192.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.152-26652G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26892852 | ||||||
| chr4:26893034
|
A | G | 110 | a0001c0001t0001g0020a0001c0001t0001g0224a0001c0001t0001g0225others(107): Show | 111 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(108): Show |
intron_variant | MODIFIER | c.152-26470A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26893034 | ||||||
| chr4:26893049
|
G | A | 2 | a0001c0001t0021g0204a0001c0001t0021g0205 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.152-26455G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26893049 | ||||||
| chr4:26893091
|
T | C | 14 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(11): Show | 14 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.152-26413T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26893091 | ||||||
| chr4:26893101
|
G | A | 1 | a0001c0001t0006g0253 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.152-26403G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26893101 | ||||||
| chr4:26893268
|
C | T | 1 | a0001c0001t0005g0211 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.152-26236C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26893268 | ||||||
| chr4:26893273
|
C | G | 1 | a0001c0001t0037g0134 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.152-26231C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26893273 | ||||||
| chr4:26893643
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-25861A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26893643 | ||||||
| chr4:26893683
|
C | T | 2 | a0001c0001t0009g0216a0001c0001t0028g0284 | 2 | HG02572.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.152-25821C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26893683 | ||||||
| chr4:26893730
|
G | A | 3 | a0001c0001t0007g0091a0001c0001t0007g0145a0001c0001t0007g0146 | 3 | HG01243.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.152-25774G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26893730 | ||||||
| chr4:26893771
|
AT | A | 233 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(230): Show | 235 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(232): Show |
intron_variant | MODIFIER | c.152-25723delT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26893771 | |||||
| chr4:26893928
|
G | A | 10 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0009g0216others(7): Show | 10 | HG01243.hp2 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.152-25576G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26893928 | ||||||
| chr4:26893980
|
C | T | 1 | a0001c0001t0002g0007 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.152-25524C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26893980 | ||||||
| chr4:26894152
|
G | C | 1 | a0001c0001t0001g0049 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.152-25352G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26894152 | ||||||
| chr4:26894181
|
C | G | 13 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0006g0129others(10): Show | 13 | HG00735.hp1 HG01071.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.152-25323C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26894181 | ||||||
| chr4:26894210
|
T | C | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-25294T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26894210 | ||||||
| chr4:26894270
|
G | GTA | 8 | a0001c0001t0001g0025a0001c0001t0001g0058a0001c0001t0001g0059others(5): Show | 8 | HG00438.hp2 NA18973.hp2 NA18989.hp1 others(5): Show |
intron_variant | MODIFIER | c.152-25233_152-2523 others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26894270 | |||||
| chr4:26894272
|
G | A | 120 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(117): Show | 121 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.152-25232G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26894272 | ||||||
| chr4:26894272
|
G | GTA | 9 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0012g0215others(6): Show | 9 | HG01243.hp2 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-25220_152-2521 others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26894272 | |||||
| chr4:26894272
|
GTA | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-25220_152-2521 others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26894272 | |||||
| chr4:26894517
|
T | C | 1 | a0001c0001t0003g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.152-24987T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26894517 | ||||||
| chr4:26894538
|
AT | A | 11 | a0001c0001t0002g0005a0001c0001t0002g0154a0001c0001t0002g0295others(8): Show | 11 | HG01167.hp1 HG01975.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.152-24953delT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26894538 | |||||
| chr4:26894632
|
T | C | 3 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0110 | 3 | HG02486.hp2 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.152-24872T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26894632 | ||||||
| chr4:26894635
|
G | C | 3 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019 | 3 | HG00741.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.152-24869G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26894635 | ||||||
| chr4:26894796
|
C | T | 1 | a0001c0001t0013g0219 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.152-24708C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26894796 | ||||||
| chr4:26894879
|
A | G | 2 | a0001c0001t0004g0243a0001c0001t0042g0250 | 2 | HG01071.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.152-24625A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26894879 | ||||||
| chr4:26894930
|
G | C | 1 | a0001c0001t0015g0331 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.152-24574G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26894930 | ||||||
| chr4:26895041
|
G | A | 4 | a0001c0001t0003g0167a0001c0001t0005g0014a0001c0001t0005g0015others(1): Show | 4 | HG02280.hp2 HG03209.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-24463G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26895041 | ||||||
| chr4:26895085
|
G | A | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-24419G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26895085 | ||||||
| chr4:26895284
|
A | G | 1 | a0001c0001t0021g0205 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.152-24220A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26895284 | ||||||
| chr4:26895423
|
A | C | 331 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(328): Show | 333 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(330): Show |
intron_variant | MODIFIER | c.152-24081A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26895423 | ||||||
| chr4:26895424
|
A | G | 331 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(328): Show | 333 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(330): Show |
intron_variant | MODIFIER | c.152-24080A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26895424 | ||||||
| chr4:26895436
|
C | T | 123 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(120): Show | 124 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.152-24068C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26895436 | ||||||
| chr4:26895451
|
C | A | 1 | a0001c0002t0009g0149 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.152-24053C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26895451 | ||||||
| chr4:26895484
|
A | G | 1 | a0001c0001t0013g0218 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.152-24020A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26895484 | ||||||
| chr4:26895745
|
A | C | 4 | a0001c0001t0002g0311a0001c0001t0005g0291a0001c0001t0005g0300others(1): Show | 4 | NA18953.hp1 NA18953.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-23759A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26895745 | ||||||
| chr4:26895876
|
A | G | 2 | a0001c0001t0003g0111a0001c0001t0003g0156 | 2 | HG02027.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.152-23628A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26895876 | ||||||
| chr4:26896041
|
T | C | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.152-23463T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26896041 | ||||||
| chr4:26896069
|
T | C | 1 | a0001c0001t0003g0168 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.152-23435T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26896069 | ||||||
| chr4:26896082
|
G | C | 123 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(120): Show | 124 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.152-23422G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26896082 | ||||||
| chr4:26896152
|
G | C | 1 | a0001c0001t0009g0328 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.152-23352G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26896152 | ||||||
| chr4:26896506
|
A | G | 2 | a0001c0001t0005g0206a0001c0001t0007g0203 | 2 | HG01884.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.152-22998A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26896506 | ||||||
| chr4:26896544
|
T | A | 3 | a0001c0001t0007g0091a0001c0001t0007g0145a0001c0001t0007g0146 | 3 | HG01243.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.152-22960T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26896544 | ||||||
| chr4:26896551
|
C | T | 1 | a0001c0001t0009g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.152-22953C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26896551 | ||||||
| chr4:26896686
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0038others(1): Show | 4 | HG02523.hp1 NA18612.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-22818G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26896686 | ||||||
| chr4:26896970
|
C | T | 1 | a0001c0001t0021g0205 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.152-22534C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26896970 | ||||||
| chr4:26897156
|
T | C | 1 | a0001c0001t0002g0152 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.152-22348T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26897156 | ||||||
| chr4:26897170
|
C | T | 14 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(11): Show | 14 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.152-22334C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26897170 | ||||||
| chr4:26897251
|
G | T | 1 | a0001c0001t0005g0014 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.152-22253G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26897251 | ||||||
| chr4:26897265
|
G | T | 1 | a0001c0001t0003g0188 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.152-22239G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26897265 | ||||||
| chr4:26897424
|
C | T | 12 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0206others(9): Show | 12 | HG00642.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.152-22080C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26897424 | ||||||
| chr4:26897430
|
T | C | 1 | a0001c0001t0001g0092 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.152-22074T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26897430 | ||||||
| chr4:26897494
|
A | G | 1 | a0001c0001t0003g0158 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.152-22010A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26897494 | ||||||
| chr4:26897637
|
A | T | 1 | a0001c0001t0004g0252 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.152-21867A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26897637 | ||||||
| chr4:26897918
|
C | T | 1 | a0001c0001t0012g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.152-21586C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26897918 | ||||||
| chr4:26897955
|
C | T | 88 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(85): Show | 89 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.152-21549C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26897955 | ||||||
| chr4:26898077
|
A | G | 1 | a0001c0001t0002g0008 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.152-21427A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26898077 | ||||||
| chr4:26898151
|
A | G | 1 | a0001c0001t0006g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.152-21353A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26898151 | ||||||
| chr4:26898504
|
A | G | 1 | a0001c0001t0037g0134 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.152-21000A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26898504 | ||||||
| chr4:26898650
|
C | T | 1 | a0001c0001t0024g0309 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.152-20854C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26898650 | ||||||
| chr4:26898864
|
A | T | 2 | a0001c0001t0009g0216a0001c0001t0028g0284 | 2 | HG02572.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.152-20640A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26898864 | ||||||
| chr4:26898887
|
T | G | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.152-20617T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26898887 | ||||||
| chr4:26899048
|
A | G | 57 | a0001c0001t0001g0020a0001c0001t0003g0002a0001c0001t0003g0111others(54): Show | 58 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.152-20456A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26899048 | ||||||
| chr4:26899150
|
T | C | 57 | a0001c0001t0001g0020a0001c0001t0003g0002a0001c0001t0003g0111others(54): Show | 58 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.152-20354T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26899150 | ||||||
| chr4:26899251
|
T | G | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0009g0126 | 3 | HG03239.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.152-20253T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26899251 | ||||||
| chr4:26899350
|
A | G | 1 | a0001c0001t0027g0104 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.152-20154A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26899350 | ||||||
| chr4:26899425
|
T | C | 1 | a0001c0001t0011g0229 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.152-20079T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26899425 | ||||||
| chr4:26899881
|
T | A | 1 | a0001c0001t0009g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.152-19623T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26899881 | ||||||
| chr4:26900607
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-18897A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26900607 | ||||||
| chr4:26900739
|
G | T | 180 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(177): Show | 182 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.152-18765G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26900739 | ||||||
| chr4:26900792
|
A | T | 2 | a0001c0001t0002g0152a0001c0001t0002g0153 | 2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.152-18712A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26900792 | ||||||
| chr4:26900894
|
G | A | 2 | a0001c0001t0002g0064a0001c0001t0002g0066 | 2 | NA18961.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.152-18610G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26900894 | ||||||
| chr4:26901070
|
G | T | 8 | a0001c0001t0004g0232a0001c0001t0004g0233a0001c0001t0004g0234others(5): Show | 8 | HG00558.hp2 HG02040.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-18434G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26901070 | ||||||
| chr4:26901158
|
G | T | 1 | a0001c0001t0028g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.152-18346G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26901158 | ||||||
| chr4:26901168
|
G | A | 30 | a0001c0001t0001g0306a0001c0001t0001g0319a0001c0001t0002g0005others(27): Show | 30 | HG01192.hp2 HG01261.hp1 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.152-18336G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26901168 | ||||||
| chr4:26901487
|
T | C | 1 | a0001c0001t0006g0072 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.152-18017T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26901487 | ||||||
| chr4:26901531
|
C | T | 3 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0110 | 3 | HG02486.hp2 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.152-17973C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26901531 | ||||||
| chr4:26901666
|
G | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.152-17838G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26901666 | ||||||
| chr4:26901679
|
G | A | 1 | a0001c0001t0002g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.152-17825G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26901679 | ||||||
| chr4:26901827
|
C | G | 38 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0030others(35): Show | 39 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.152-17677C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26901827 | ||||||
| chr4:26901990
|
C | T | 1 | a0001c0001t0036g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.152-17514C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26901990 | ||||||
| chr4:26902271
|
T | C | 1 | a0001c0001t0007g0108 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.152-17233T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26902271 | ||||||
| chr4:26902405
|
G | A | 95 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(92): Show | 96 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.152-17099G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26902405 | ||||||
| chr4:26902563
|
G | A | 1 | a0001c0001t0008g0028 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.152-16941G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26902563 | ||||||
| chr4:26902582
|
T | C | 4 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(1): Show | 4 | NA18999.hp1 NA19062.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-16922T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26902582 | ||||||
| chr4:26902591
|
G | A | 123 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(120): Show | 124 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.152-16913G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26902591 | ||||||
| chr4:26902990
|
G | A | 5 | a0001c0001t0014g0119a0001c0001t0014g0121a0001c0001t0014g0122others(2): Show | 5 | HG00642.hp2 HG03669.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-16514G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26902990 | ||||||
| chr4:26903023
|
A | G | 1 | a0001c0001t0004g0268 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.152-16481A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26903023 | ||||||
| chr4:26903213
|
C | G | 1 | a0001c0001t0004g0273 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.152-16291C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26903213 | ||||||
| chr4:26903216
|
G | C | 1 | a0001c0001t0008g0063 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.152-16288G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26903216 | ||||||
| chr4:26903250
|
A | G | 2 | a0001c0001t0005g0014a0001c0001t0005g0015 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.152-16254A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26903250 | ||||||
| chr4:26903419
|
G | A | 1 | a0001c0001t0009g0328 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.152-16085G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26903419 | ||||||
| chr4:26903421
|
A | G | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.152-16083A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26903421 | ||||||
| chr4:26903447
|
A | G | 2 | a0001c0001t0001g0038a0001c0001t0002g0037 | 2 | HG02523.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.152-16057A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26903447 | ||||||
| chr4:26903664
|
T | C | 1 | a0001c0001t0041g0235 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.152-15840T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26903664 | ||||||
| chr4:26903738
|
G | C | 1 | a0001c0001t0005g0097 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.152-15766G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26903738 | ||||||
| chr4:26903877
|
T | G | 1 | a0001c0001t0001g0039 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.152-15627T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26903877 | ||||||
| chr4:26903949
|
C | CT | 7 | a0001c0001t0005g0206a0001c0001t0007g0108a0001c0001t0007g0109others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.152-15546dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26903949 | |||||
| chr4:26904042
|
C | T | 5 | a0001c0001t0005g0208a0001c0001t0005g0209a0001c0001t0005g0210others(2): Show | 5 | HG02615.hp1 HG02717.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-15462C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26904042 | ||||||
| chr4:26904096
|
T | TC | 54 | a0001c0001t0001g0031a0001c0001t0001g0043a0001c0001t0001g0051others(51): Show | 54 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.152-15402dupC | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26904096 | |||||
| chr4:26904102
|
C | A | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-15402C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26904102 | ||||||
| chr4:26904577
|
A | G | 28 | a0001c0001t0001g0319a0001c0001t0002g0005a0001c0001t0002g0006others(25): Show | 28 | HG01192.hp2 HG01433.hp2 HG02129.hp2 others(25): Show |
intron_variant | MODIFIER | c.152-14927A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26904577 | ||||||
| chr4:26904596
|
C | A | 1 | a0001c0001t0009g0328 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.152-14908C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26904596 | ||||||
| chr4:26904682
|
C | T | 1 | a0001c0001t0009g0328 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.152-14822C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26904682 | ||||||
| chr4:26904801
|
A | G | 1 | a0001c0001t0001g0036 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.152-14703A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26904801 | ||||||
| chr4:26904810
|
T | A | 1 | a0001c0001t0009g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.152-14694T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26904810 | ||||||
| chr4:26904814
|
C | A | 233 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(230): Show | 235 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(232): Show |
intron_variant | MODIFIER | c.152-14690C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26904814 | ||||||
| chr4:26905267
|
C | T | 1 | a0001c0001t0037g0134 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.152-14237C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26905267 | ||||||
| chr4:26905268
|
G | A | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-14236G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26905268 | ||||||
| chr4:26905436
|
G | C | 2 | a0001c0001t0005g0206a0001c0001t0007g0203 | 2 | HG01884.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.152-14068G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26905436 | ||||||
| chr4:26905524
|
G | A | 1 | a0001c0001t0015g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.152-13980G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26905524 | ||||||
| chr4:26905618
|
G | A | 3 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0036g0016 | 3 | HG02280.hp2 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.152-13886G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26905618 | ||||||
| chr4:26905742
|
T | C | 279 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(276): Show | 281 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(278): Show |
intron_variant | MODIFIER | c.152-13762T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26905742 | ||||||
| chr4:26905946
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.152-13558G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26905946 | ||||||
| chr4:26905972
|
A | T | 1 | a0001c0001t0003g0200 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.152-13532A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26905972 | ||||||
| chr4:26905978
|
T | C | 3 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019 | 3 | HG00741.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.152-13526T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26905978 | ||||||
| chr4:26906077
|
T | C | 2 | a0001c0001t0009g0216a0001c0001t0028g0284 | 2 | HG02572.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.152-13427T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26906077 | ||||||
| chr4:26906230
|
G | A | 127 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(124): Show | 128 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(125): Show |
intron_variant | MODIFIER | c.152-13274G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26906230 | ||||||
| chr4:26906235
|
T | C | 3 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019 | 3 | HG00741.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.152-13269T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26906235 | ||||||
| chr4:26906241
|
C | G | 157 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(154): Show | 159 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.152-13263C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26906241 | ||||||
| chr4:26906440
|
G | GT | 6 | a0001c0001t0001g0031a0001c0001t0001g0061a0001c0001t0001g0141others(3): Show | 6 | HG02074.hp1 NA18956.hp1 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-13046dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26906440 | |||||
| chr4:26906440
|
GT | G | 8 | a0001c0001t0001g0013a0001c0001t0001g0033a0001c0001t0001g0281others(5): Show | 8 | HG01891.hp2 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.152-13046delT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26906440 | |||||
| chr4:26906444
|
T | G | 1 | a0001c0001t0004g0226 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.152-13060T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26906444 | ||||||
| chr4:26906966
|
CA | C | 225 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(222): Show | 227 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(224): Show |
intron_variant | MODIFIER | c.152-12521delA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26906966 | |||||
| chr4:26906966
|
CAA | C | 11 | a0001c0001t0002g0310a0001c0001t0003g0176a0001c0001t0003g0197others(8): Show | 11 | HG00438.hp1 HG02145.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-12522_152-1252 others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26906966 | |||||
| chr4:26906981
|
A | C | 1 | a0001c0001t0003g0181 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.152-12523A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26906981 | ||||||
| chr4:26906989
|
T | C | 1 | a0001c0002t0013g0099 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.152-12515T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26906989 | ||||||
| chr4:26907243
|
G | A | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-12261G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26907243 | ||||||
| chr4:26907325
|
A | G | 3 | a0001c0001t0017g0185a0001c0001t0017g0186a0001c0001t0017g0187 | 3 | HG00738.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.152-12179A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26907325 | ||||||
| chr4:26907430
|
C | T | 2 | a0001c0001t0002g0152a0001c0001t0002g0153 | 2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.152-12074C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26907430 | ||||||
| chr4:26907450
|
T | C | 1 | a0001c0001t0014g0122 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.152-12054T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26907450 | ||||||
| chr4:26907458
|
A | G | 168 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(165): Show | 170 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.152-12046A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26907458 | ||||||
| chr4:26907913
|
C | T | 1 | a0001c0001t0002g0315 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.152-11591C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26907913 | ||||||
| chr4:26907997
|
C | T | 1 | a0001c0002t0023g0155 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.152-11507C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26907997 | ||||||
| chr4:26908015
|
G | A | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-11489G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26908015 | ||||||
| chr4:26908053
|
C | A | 3 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0036g0016 | 3 | HG02280.hp2 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.152-11451C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26908053 | ||||||
| chr4:26908082
|
A | G | 9 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0012g0215others(6): Show | 9 | HG01243.hp2 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-11422A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26908082 | ||||||
| chr4:26908114
|
C | G | 1 | a0001c0001t0004g0261 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.152-11390C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26908114 | ||||||
| chr4:26908475
|
T | TTTTG | 26 | a0001c0001t0002g0154a0001c0001t0002g0288a0001c0001t0002g0290others(23): Show | 26 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.152-11012_152-1100 others(8): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26908475 | |||||
| chr4:26908530
|
C | A | 3 | a0001c0001t0017g0185a0001c0001t0017g0186a0001c0001t0017g0187 | 3 | HG00738.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.152-10974C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26908530 | ||||||
| chr4:26908586
|
C | T | 3 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019 | 3 | HG00741.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.152-10918C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26908586 | ||||||
| chr4:26908635
|
T | C | 1 | a0001c0001t0005g0209 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.152-10869T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26908635 | ||||||
| chr4:26908696
|
C | G | 3 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0036g0016 | 3 | HG02280.hp2 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.152-10808C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26908696 | ||||||
| chr4:26908730
|
C | T | 2 | a0001c0001t0021g0204a0001c0001t0021g0205 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.152-10774C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26908730 | ||||||
| chr4:26908735
|
C | T | 1 | a0001c0001t0003g0189 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.152-10769C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26908735 | ||||||
| chr4:26908779
|
C | A | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.152-10725C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26908779 | ||||||
| chr4:26908815
|
C | G | 10 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(7): Show | 10 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.152-10689C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26908815 | ||||||
| chr4:26908920
|
C | A | 50 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0281others(47): Show | 50 | HG01192.hp2 HG01243.hp2 HG01261.hp1 others(47): Show |
intron_variant | MODIFIER | c.152-10584C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26908920 | ||||||
| chr4:26909049
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-10455A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26909049 | ||||||
| chr4:26909078
|
C | T | 9 | a0001c0001t0006g0129a0001c0001t0006g0133a0001c0001t0006g0137others(6): Show | 9 | HG00735.hp1 HG01071.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-10426C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26909078 | ||||||
| chr4:26909118
|
A | T | 40 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0024others(37): Show | 41 | HG00544.hp2 HG00621.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.152-10386A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26909118 | ||||||
| chr4:26909231
|
A | G | 1 | a0001c0001t0005g0080 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.152-10273A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26909231 | ||||||
| chr4:26909378
|
T | C | 151 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(148): Show | 153 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.152-10126T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26909378 | ||||||
| chr4:26909547
|
T | C | 59 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0306others(56): Show | 59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.152-9957T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26909547 | ||||||
| chr4:26909601
|
G | A | 5 | a0001c0001t0005g0208a0001c0001t0005g0209a0001c0001t0005g0210others(2): Show | 5 | HG02615.hp1 HG02717.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-9903G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26909601 | ||||||
| chr4:26909740
|
G | A | 3 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0148 | 3 | HG02258.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.152-9764G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26909740 | ||||||
| chr4:26909777
|
A | G | 5 | a0001c0001t0014g0119a0001c0001t0014g0121a0001c0001t0014g0122others(2): Show | 5 | HG00642.hp2 HG03669.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-9727A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26909777 | ||||||
| chr4:26910013
|
A | T | 2 | a0001c0001t0009g0216a0001c0001t0028g0284 | 2 | HG02572.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.152-9491A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26910013 | ||||||
| chr4:26910086
|
G | T | 1 | a0001c0001t0005g0067 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.152-9418G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26910086 | ||||||
| chr4:26910088
|
G | A | 1 | a0001c0001t0002g0292 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.152-9416G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26910088 | ||||||
| chr4:26910169
|
A | G | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-9335A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26910169 | ||||||
| chr4:26910212
|
A | G | 1 | a0001c0002t0026g0102 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.152-9292A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26910212 | ||||||
| chr4:26910299
|
A | T | 171 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(168): Show | 173 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.152-9205A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26910299 | ||||||
| chr4:26910391
|
G | T | 2 | a0001c0001t0009g0279a0001c0001t0009g0283 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.152-9113G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26910391 | ||||||
| chr4:26910504
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.152-9000A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26910504 | ||||||
| chr4:26910582
|
C | T | 2 | a0001c0001t0024g0309a0001c0001t0043g0312 | 2 | HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.152-8922C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26910582 | ||||||
| chr4:26910639
|
G | A | 1 | a0001c0001t0002g0299 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.152-8865G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26910639 | ||||||
| chr4:26910732
|
A | G | 1 | a0001c0001t0010g0327 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.152-8772A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26910732 | ||||||
| chr4:26911146
|
A | G | 1 | a0001c0001t0003g0175 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.152-8358A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26911146 | ||||||
| chr4:26911231
|
AAAAT | A | 50 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0281others(47): Show | 50 | HG01192.hp2 HG01243.hp2 HG01261.hp1 others(47): Show |
intron_variant | MODIFIER | c.152-8249_152-8246d others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26911231 | |||||
| chr4:26911231
|
AAAATAAA others(1): Show |
A | 13 | a0001c0001t0006g0129a0001c0001t0006g0133a0001c0001t0006g0137others(10): Show | 13 | HG00642.hp2 HG00735.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.152-8253_152-8246d others(10): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26911231 | |||||
| chr4:26911231
|
AAAATAAA others(5): Show |
A | 1 | a0001c0001t0034g0120 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.152-8257_152-8246d others(14): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26911231 | |||||
| chr4:26911305
|
T | C | 1 | a0001c0001t0044g0270 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.152-8199T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26911305 | ||||||
| chr4:26911472
|
C | G | 185 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(182): Show | 187 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(184): Show |
intron_variant | MODIFIER | c.152-8032C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26911472 | ||||||
| chr4:26911569
|
C | A | 28 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(25): Show | 28 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.152-7935C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26911569 | ||||||
| chr4:26911599
|
A | G | 1 | a0001c0004t0039g0161 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.152-7905A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26911599 | ||||||
| chr4:26911756
|
G | A | 1 | a0001c0001t0009g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.152-7748G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26911756 | ||||||
| chr4:26911850
|
T | G | 7 | a0001c0001t0012g0215a0001c0001t0012g0222a0001c0001t0012g0223others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.152-7654T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26911850 | ||||||
| chr4:26912016
|
C | A | 3 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019 | 3 | HG00741.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.152-7488C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26912016 | ||||||
| chr4:26912053
|
C | T | 1 | a0001c0001t0036g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.152-7451C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26912053 | ||||||
| chr4:26912161
|
T | C | 1 | a0001c0001t0004g0118 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.152-7343T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26912161 | ||||||
| chr4:26912231
|
G | T | 1 | a0001c0001t0009g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.152-7273G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26912231 | ||||||
| chr4:26912755
|
G | A | 1 | a0001c0001t0024g0308 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.152-6749G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26912755 | ||||||
| chr4:26912917
|
G | C | 189 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(186): Show | 191 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(188): Show |
intron_variant | MODIFIER | c.152-6587G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26912917 | ||||||
| chr4:26912990
|
A | G | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.152-6514A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26912990 | ||||||
| chr4:26913022
|
C | A | 237 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(234): Show | 239 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(236): Show |
intron_variant | MODIFIER | c.152-6482C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26913022 | ||||||
| chr4:26913215
|
A | G | 60 | a0001c0001t0001g0020a0001c0001t0003g0002a0001c0001t0003g0111others(57): Show | 61 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.152-6289A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26913215 | ||||||
| chr4:26913458
|
G | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0070a0001c0001t0001g0071 | 3 | HG02735.hp2 HG03491.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.152-6046G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26913458 | ||||||
| chr4:26913475
|
A | G | 2 | a0001c0001t0004g0230a0001c0001t0011g0229 | 2 | NA18944.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.152-6029A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26913475 | ||||||
| chr4:26913586
|
C | G | 1 | a0001c0001t0001g0056 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.152-5918C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26913586 | ||||||
| chr4:26913762
|
T | C | 1 | a0001c0001t0008g0027 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.152-5742T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26913762 | ||||||
| chr4:26913896
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-5608A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26913896 | ||||||
| chr4:26913911
|
G | A | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-5593G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26913911 | ||||||
| chr4:26913987
|
A | G | 9 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0012g0215others(6): Show | 9 | HG01243.hp2 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-5517A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26913987 | ||||||
| chr4:26914189
|
C | G | 58 | a0001c0001t0001g0306a0001c0001t0001g0319a0001c0001t0002g0005others(55): Show | 58 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.152-5315C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26914189 | ||||||
| chr4:26914196
|
T | C | 1 | a0001c0001t0001g0046 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.152-5308T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26914196 | ||||||
| chr4:26914212
|
A | G | 1 | a0001c0001t0002g0307 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.152-5292A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26914212 | ||||||
| chr4:26914310
|
T | A | 2 | a0001c0001t0005g0206a0001c0001t0007g0203 | 2 | HG01884.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.152-5194T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26914310 | ||||||
| chr4:26914348
|
C | A | 2 | a0001c0001t0009g0216a0001c0001t0028g0284 | 2 | HG02572.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.152-5156C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26914348 | ||||||
| chr4:26914440
|
C | T | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.152-5064C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26914440 | ||||||
| chr4:26914472
|
C | T | 46 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0281others(43): Show | 46 | HG01192.hp2 HG01243.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.152-5032C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26914472 | ||||||
| chr4:26914517
|
C | T | 1 | a0001c0001t0002g0320 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.152-4987C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26914517 | ||||||
| chr4:26914785
|
G | A | 4 | a0001c0001t0014g0119a0001c0001t0014g0121a0001c0001t0014g0122others(1): Show | 4 | HG00642.hp2 HG03669.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-4719G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26914785 | ||||||
| chr4:26915150
|
C | T | 3 | a0001c0001t0002g0311a0001c0001t0005g0291a0001c0001t0005g0300 | 3 | NA18953.hp2 NA18970.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.152-4354C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26915150 | ||||||
| chr4:26915162
|
G | A | 89 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(86): Show | 90 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.152-4342G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26915162 | ||||||
| chr4:26915199
|
A | G | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0012g0280 | 3 | HG02647.hp2 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.152-4305A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26915199 | ||||||
| chr4:26915260
|
A | G | 3 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019 | 3 | HG00741.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.152-4244A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26915260 | ||||||
| chr4:26915395
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.152-4109C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26915395 | ||||||
| chr4:26915411
|
T | C | 1 | a0001c0001t0003g0177 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.152-4093T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26915411 | ||||||
| chr4:26915415
|
C | T | 1 | a0001c0006t0003g0174 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.152-4089C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26915415 | ||||||
| chr4:26915416
|
G | A | 1 | a0001c0001t0003g0196 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.152-4088G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26915416 | ||||||
| chr4:26915512
|
G | C | 1 | a0001c0001t0002g0322 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.152-3992G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26915512 | ||||||
| chr4:26915639
|
G | A | 34 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0030others(31): Show | 35 | HG00544.hp2 HG00621.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.152-3865G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26915639 | ||||||
| chr4:26915777
|
C | T | 3 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0110 | 3 | HG02486.hp2 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.152-3727C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26915777 | ||||||
| chr4:26915859
|
G | C | 4 | a0001c0001t0003g0157a0001c0001t0003g0169a0001c0001t0003g0175others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-3645G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26915859 | ||||||
| chr4:26915908
|
G | A | 10 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(7): Show | 10 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.152-3596G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26915908 | ||||||
| chr4:26916012
|
G | A | 10 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(7): Show | 10 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.152-3492G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26916012 | ||||||
| chr4:26916227
|
A | G | 5 | a0001c0001t0005g0208a0001c0001t0005g0209a0001c0001t0005g0210others(2): Show | 5 | HG02615.hp1 HG02717.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-3277A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26916227 | ||||||
| chr4:26916297
|
A | G | 2 | a0001c0001t0009g0283a0001c0001t0012g0280 | 2 | HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.152-3207A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26916297 | ||||||
| chr4:26916660
|
C | T | 10 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(7): Show | 10 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.152-2844C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26916660 | ||||||
| chr4:26916729
|
T | G | 282 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(279): Show | 284 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(281): Show |
intron_variant | MODIFIER | c.152-2775T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26916729 | ||||||
| chr4:26916763
|
C | G | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.152-2741C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26916763 | ||||||
| chr4:26916958
|
G | A | 1 | a0001c0001t0002g0083 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.152-2546G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26916958 | ||||||
| chr4:26917014
|
A | G | 3 | a0001c0001t0007g0091a0001c0001t0007g0145a0001c0001t0007g0146 | 3 | HG01243.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.152-2490A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26917014 | ||||||
| chr4:26917564
|
C | A | 89 | a0001c0001t0001g0020a0001c0001t0001g0306a0001c0001t0001g0319others(86): Show | 90 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.152-1940C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26917564 | ||||||
| chr4:26917571
|
TTAAA | T | 94 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(91): Show | 95 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.152-1925_152-1922d others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26917571 | |||||
| chr4:26917746
|
A | G | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.152-1758A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26917746 | ||||||
| chr4:26917770
|
G | A | 94 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(91): Show | 95 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.152-1734G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26917770 | ||||||
| chr4:26917985
|
G | C | 2 | a0001c0001t0002g0326a0001c0001t0002g0329 | 2 | NA19004.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.152-1519G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26917985 | ||||||
| chr4:26918228
|
C | CT | 16 | a0001c0001t0001g0013a0001c0001t0001g0070a0001c0001t0001g0071others(13): Show | 16 | HG00642.hp2 HG01081.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.152-1258dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26918228 | |||||
| chr4:26918228
|
CT | C | 12 | a0001c0001t0001g0020a0001c0001t0002g0066a0001c0001t0003g0111others(9): Show | 12 | HG01169.hp1 HG01943.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.152-1258delT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26918228 | |||||
| chr4:26918302
|
T | A | 2 | a0001c0001t0004g0227a0001c0001t0004g0262 | 2 | HG00597.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.152-1202T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26918302 | ||||||
| chr4:26918341
|
T | C | 1 | a0001c0001t0003g0196 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.152-1163T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26918341 | ||||||
| chr4:26918363
|
G | T | 1 | a0001c0001t0002g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.152-1141G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26918363 | ||||||
| chr4:26918433
|
A | G | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-1071A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26918433 | ||||||
| chr4:26918599
|
A | T | 1 | a0001c0001t0009g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.152-905A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26918599 | ||||||
| chr4:26918645
|
G | A | 92 | a0001c0001t0001g0020a0001c0001t0001g0306a0001c0001t0001g0319others(89): Show | 93 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.152-859G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26918645 | ||||||
| chr4:26918674
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.152-830C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26918674 | ||||||
| chr4:26918907
|
T | A | 1 | a0001c0001t0003g0170 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.152-597T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26918907 | ||||||
| chr4:26918934
|
T | G | 4 | a0001c0001t0003g0159a0001c0001t0003g0182a0001c0001t0018g0112others(1): Show | 4 | HG02451.hp2 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-570T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26918934 | ||||||
| chr4:26918944
|
C | T | 4 | a0001c0001t0003g0157a0001c0001t0003g0169a0001c0001t0003g0175others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-560C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26918944 | ||||||
| chr4:26919017
|
G | A | 1 | a0001c0001t0009g0328 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.152-487G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26919017 | ||||||
| chr4:26919034
|
C | T | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.152-470C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26919034 | ||||||
| chr4:26919126
|
G | GT | 6 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0283others(3): Show | 6 | HG00733.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-366dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 26919126 | |||||
| chr4:26919128
|
T | G | 1 | a0001c0001t0003g0196 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.152-376T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26919128 | ||||||
| chr4:26919233
|
A | G | 1 | a0001c0001t0036g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.152-271A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26919233 | ||||||
| chr4:26919472
|
C | G | 7 | a0001c0001t0012g0215a0001c0001t0012g0222a0001c0001t0012g0223others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.152-32C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26919472 | ||||||
| chr4:26919845
|
G | T | 111 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0281others(108): Show | 112 | HG00099.hp1 HG00438.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.282+211G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26919845 | ||||||
| chr4:26920224
|
A | G | 112 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(109): Show | 113 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.282+590A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26920224 | ||||||
| chr4:26920391
|
T | A | 1 | a0001c0001t0004g0286 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.282+757T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26920391 | ||||||
| chr4:26920414
|
G | A | 1 | a0001c0001t0003g0196 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.282+780G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26920414 | ||||||
| chr4:26920440
|
CT | C | 3 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0036g0016 | 3 | HG02280.hp2 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.282+807delT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26920440 | ||||||
| chr4:26920446
|
G | A | 1 | a0001c0001t0004g0262 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.282+812G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26920446 | ||||||
| chr4:26920519
|
T | G | 5 | a0001c0001t0003g0188a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG00099.hp1 HG01515.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+885T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26920519 | ||||||
| chr4:26920596
|
C | A | 2 | a0001c0001t0005g0034a0001c0001t0005g0096 | 2 | NA18951.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.282+962C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26920596 | ||||||
| chr4:26920849
|
T | G | 3 | a0001c0001t0007g0091a0001c0001t0007g0145a0001c0001t0007g0146 | 3 | HG01243.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.282+1215T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26920849 | ||||||
| chr4:26921071
|
C | T | 1 | a0001c0002t0019g0107 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.282+1437C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26921071 | ||||||
| chr4:26921088
|
C | G | 109 | a0001c0001t0001g0020a0001c0001t0001g0224a0001c0001t0001g0225others(106): Show | 110 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.282+1454C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26921088 | ||||||
| chr4:26921099
|
C | T | 7 | a0001c0001t0003g0151a0001c0001t0003g0162a0001c0001t0003g0166others(4): Show | 7 | HG00642.hp1 HG00741.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.282+1465C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26921099 | ||||||
| chr4:26921198
|
A | G | 1 | a0001c0001t0003g0165 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.282+1564A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26921198 | ||||||
| chr4:26921238
|
G | A | 1 | a0001c0001t0010g0327 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.282+1604G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26921238 | ||||||
| chr4:26921290
|
C | A | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.282+1656C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26921290 | ||||||
| chr4:26921355
|
G | T | 3 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0148 | 3 | HG02258.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.282+1721G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26921355 | ||||||
| chr4:26921698
|
G | A | 1 | a0001c0001t0002g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.282+2064G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26921698 | ||||||
| chr4:26921746
|
G | A | 1 | a0001c0001t0004g0231 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.282+2112G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26921746 | ||||||
| chr4:26921949
|
C | T | 1 | a0001c0004t0039g0161 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.282+2315C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26921949 | ||||||
| chr4:26922027
|
A | C | 2 | a0001c0001t0005g0209a0001c0001t0005g0210 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.282+2393A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26922027 | ||||||
| chr4:26922148
|
C | T | 1 | a0001c0001t0009g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.282+2514C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26922148 | ||||||
| chr4:26922178
|
C | A | 109 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(106): Show | 110 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.282+2544C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26922178 | ||||||
| chr4:26922217
|
A | G | 1 | a0001c0001t0009g0328 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.282+2583A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26922217 | ||||||
| chr4:26922220
|
A | G | 4 | a0001c0001t0005g0206a0001c0001t0007g0203a0001c0001t0021g0204others(1): Show | 4 | HG01884.hp2 HG01891.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+2586A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26922220 | ||||||
| chr4:26922414
|
AG | A | 108 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(105): Show | 109 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.282+2781delG | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26922414 | ||||||
| chr4:26922710
|
G | C | 1 | a0001c0001t0001g0098 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.282+3076G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26922710 | ||||||
| chr4:26922822
|
G | T | 108 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(105): Show | 109 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.282+3188G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26922822 | ||||||
| chr4:26923211
|
C | T | 14 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(11): Show | 14 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.282+3577C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26923211 | ||||||
| chr4:26923433
|
G | A | 1 | a0001c0001t0003g0196 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.282+3799G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26923433 | ||||||
| chr4:26923465
|
C | A | 5 | a0001c0001t0014g0119a0001c0001t0014g0121a0001c0001t0014g0122others(2): Show | 5 | HG00642.hp2 HG03669.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+3831C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26923465 | ||||||
| chr4:26923550
|
C | T | 1 | a0001c0001t0009g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.282+3916C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26923550 | ||||||
| chr4:26923646
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+4012A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26923646 | ||||||
| chr4:26923652
|
A | G | 2 | a0001c0001t0002g0296a0001c0001t0005g0301 | 2 | NA18953.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.282+4018A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26923652 | ||||||
| chr4:26923706
|
T | G | 2 | a0001c0001t0005g0209a0001c0001t0005g0210 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.282+4072T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26923706 | ||||||
| chr4:26923709
|
G | C | 2 | a0001c0001t0005g0209a0001c0001t0005g0210 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.282+4075G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26923709 | ||||||
| chr4:26923761
|
T | C | 52 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0031others(49): Show | 52 | HG00438.hp2 HG01934.hp2 HG01943.hp1 others(49): Show |
intron_variant | MODIFIER | c.282+4127T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26923761 | ||||||
| chr4:26923884
|
C | G | 3 | a0001c0001t0004g0259a0001c0001t0004g0260a0001c0001t0011g0241 | 3 | NA18973.hp1 NA18980.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.282+4250C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26923884 | ||||||
| chr4:26923935
|
A | T | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+4301A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26923935 | ||||||
| chr4:26923967
|
G | A | 3 | a0001c0001t0007g0091a0001c0001t0007g0145a0001c0001t0007g0146 | 3 | HG01243.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.282+4333G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26923967 | ||||||
| chr4:26923969
|
G | A | 1 | a0001c0001t0002g0026 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.282+4335G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26923969 | ||||||
| chr4:26924057
|
G | T | 3 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0148 | 3 | HG02258.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.282+4423G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26924057 | ||||||
| chr4:26924062
|
C | T | 1 | a0001c0001t0018g0171 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.282+4428C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26924062 | ||||||
| chr4:26924093
|
T | C | 266 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(263): Show | 268 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(265): Show |
intron_variant | MODIFIER | c.282+4459T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26924093 | ||||||
| chr4:26924106
|
T | C | 1 | a0001c0001t0002g0293 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.282+4472T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26924106 | ||||||
| chr4:26924118
|
C | T | 4 | a0001c0001t0005g0206a0001c0001t0007g0203a0001c0001t0021g0204others(1): Show | 4 | HG01884.hp2 HG01891.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+4484C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26924118 | ||||||
| chr4:26924221
|
T | C | 14 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0014others(11): Show | 14 | HG00642.hp2 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.282+4587T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26924221 | ||||||
| chr4:26924237
|
C | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+4603C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26924237 | ||||||
| chr4:26924294
|
A | G | 116 | a0001c0001t0001g0020a0001c0001t0001g0306a0001c0001t0001g0319others(113): Show | 117 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.282+4660A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26924294 | ||||||
| chr4:26924295
|
A | C | 14 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(11): Show | 14 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.282+4661A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26924295 | ||||||
| chr4:26924385
|
A | G | 266 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(263): Show | 268 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(265): Show |
intron_variant | MODIFIER | c.282+4751A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26924385 | ||||||
| chr4:26924437
|
T | C | 2 | a0001c0001t0005g0014a0001c0001t0005g0015 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.282+4803T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26924437 | ||||||
| chr4:26924505
|
A | G | 1 | a0001c0001t0005g0206 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.282+4871A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26924505 | ||||||
| chr4:26924626
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.282+4992G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26924626 | ||||||
| chr4:26924716
|
T | TG | 7 | a0001c0001t0012g0215a0001c0001t0012g0222a0001c0001t0012g0223others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.282+5082_282+5083i others(3): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26924716 | ||||||
| chr4:26924717
|
C | A | 7 | a0001c0001t0012g0215a0001c0001t0012g0222a0001c0001t0012g0223others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.282+5083C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26924717 | ||||||
| chr4:26924717
|
C | G | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.282+5083C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26924717 | ||||||
| chr4:26924725
|
C | T | 1 | a0001c0001t0009g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.282+5091C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26924725 | ||||||
| chr4:26924776
|
G | A | 1 | a0001c0001t0002g0307 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.282+5142G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26924776 | ||||||
| chr4:26924825
|
A | G | 1 | a0001c0001t0004g0259 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.282+5191A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26924825 | ||||||
| chr4:26924855
|
G | A | 1 | a0001c0001t0009g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.282+5221G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26924855 | ||||||
| chr4:26924905
|
C | T | 6 | a0001c0001t0003g0157a0001c0001t0003g0169a0001c0001t0003g0175others(3): Show | 6 | HG01361.hp2 HG01975.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.282+5271C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26924905 | ||||||
| chr4:26924924
|
C | G | 2 | a0001c0001t0005g0209a0001c0001t0005g0210 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.282+5290C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26924924 | ||||||
| chr4:26925063
|
G | A | 2 | a0001c0001t0002g0083a0001c0001t0002g0084 | 2 | HG01934.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.282+5429G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26925063 | ||||||
| chr4:26925086
|
C | T | 123 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(120): Show | 124 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(121): Show |
intron_variant | MODIFIER | c.282+5452C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26925086 | ||||||
| chr4:26925099
|
A | T | 2 | a0001c0001t0003g0173a0001c0006t0003g0174 | 2 | HG02056.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.282+5465A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26925099 | ||||||
| chr4:26925208
|
G | A | 123 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(120): Show | 124 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(121): Show |
intron_variant | MODIFIER | c.282+5574G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26925208 | ||||||
| chr4:26925296
|
C | T | 95 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(92): Show | 96 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.282+5662C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26925296 | ||||||
| chr4:26925328
|
C | G | 1 | a0001c0001t0007g0203 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.282+5694C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26925328 | ||||||
| chr4:26925422
|
A | C | 7 | a0001c0001t0012g0215a0001c0001t0012g0222a0001c0001t0012g0223others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.282+5788A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26925422 | ||||||
| chr4:26925499
|
C | G | 1 | a0001c0001t0006g0133 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.282+5865C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26925499 | ||||||
| chr4:26925553
|
A | C | 330 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(327): Show | 332 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(329): Show |
intron_variant | MODIFIER | c.282+5919A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26925553 | ||||||
| chr4:26925596
|
C | G | 1 | a0001c0001t0003g0169 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.282+5962C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26925596 | ||||||
| chr4:26925642
|
G | A | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.282+6008G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26925642 | ||||||
| chr4:26925701
|
A | T | 244 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(241): Show | 246 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(243): Show |
intron_variant | MODIFIER | c.282+6067A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26925701 | ||||||
| chr4:26925783
|
C | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.282+6149C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26925783 | ||||||
| chr4:26925786
|
C | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.282+6152C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26925786 | ||||||
| chr4:26925848
|
A | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | NA18944.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.282+6214A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26925848 | ||||||
| chr4:26925863
|
A | C | 1 | a0001c0001t0002g0288 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.282+6229A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26925863 | ||||||
| chr4:26926006
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.282+6372C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26926006 | ||||||
| chr4:26926130
|
T | C | 2 | a0001c0001t0002g0152a0001c0001t0002g0153 | 2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.282+6496T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26926130 | ||||||
| chr4:26926198
|
C | T | 5 | a0001c0001t0005g0208a0001c0001t0005g0209a0001c0001t0005g0210others(2): Show | 5 | HG02615.hp1 HG02717.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+6564C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26926198 | ||||||
| chr4:26926232
|
G | A | 11 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0009g0216others(8): Show | 11 | HG01243.hp2 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.282+6598G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26926232 | ||||||
| chr4:26926259
|
T | C | 266 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(263): Show | 268 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(265): Show |
intron_variant | MODIFIER | c.282+6625T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26926259 | ||||||
| chr4:26926289
|
C | G | 1 | a0001c0001t0019g0150 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.282+6655C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26926289 | ||||||
| chr4:26926376
|
A | G | 114 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(111): Show | 115 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(112): Show |
intron_variant | MODIFIER | c.282+6742A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26926376 | ||||||
| chr4:26926382
|
A | C | 1 | a0001c0001t0004g0268 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.282+6748A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26926382 | ||||||
| chr4:26926406
|
C | T | 9 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0012g0215others(6): Show | 9 | HG01243.hp2 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.282+6772C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26926406 | ||||||
| chr4:26926454
|
G | A | 1 | a0001c0001t0021g0205 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.282+6820G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26926454 | ||||||
| chr4:26926478
|
G | A | 2 | a0001c0001t0003g0189a0001c0001t0005g0067 | 2 | HG00544.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.282+6844G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26926478 | ||||||
| chr4:26926686
|
A | C | 238 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(235): Show | 240 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(237): Show |
intron_variant | MODIFIER | c.282+7052A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26926686 | ||||||
| chr4:26926737
|
C | T | 1 | a0001c0001t0003g0200 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.282+7103C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26926737 | ||||||
| chr4:26926789
|
G | C | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+7155G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26926789 | ||||||
| chr4:26926857
|
A | C | 1 | a0001c0001t0003g0202 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.282+7223A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26926857 | ||||||
| chr4:26926947
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.282+7313C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26926947 | ||||||
| chr4:26927006
|
C | T | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+7372C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927006 | ||||||
| chr4:26927009
|
T | C | 1 | a0001c0001t0009g0328 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.282+7375T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927009 | ||||||
| chr4:26927027
|
A | G | 3 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019 | 3 | HG00741.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.282+7393A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927027 | ||||||
| chr4:26927063
|
T | C | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+7429T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927063 | ||||||
| chr4:26927079
|
G | A | 89 | a0001c0001t0001g0306a0001c0001t0001g0319a0001c0001t0002g0005others(86): Show | 90 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.282+7445G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927079 | ||||||
| chr4:26927158
|
G | T | 5 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(2): Show | 5 | HG02486.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+7524G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927158 | ||||||
| chr4:26927180
|
G | A | 1 | a0001c0001t0002g0313 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.282+7546G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927180 | ||||||
| chr4:26927180
|
G | C | 7 | a0001c0001t0012g0215a0001c0001t0012g0222a0001c0001t0012g0223others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.282+7546G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927180 | ||||||
| chr4:26927244
|
G | A | 1 | a0001c0001t0005g0014 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.282+7610G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927244 | ||||||
| chr4:26927256
|
A | G | 1 | a0001c0001t0009g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.282+7622A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927256 | ||||||
| chr4:26927327
|
A | G | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+7693A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927327 | ||||||
| chr4:26927328
|
C | T | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+7694C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927328 | ||||||
| chr4:26927370
|
A | G | 1 | a0001c0001t0003g0181 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.282+7736A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927370 | ||||||
| chr4:26927402
|
C | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+7768C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927402 | ||||||
| chr4:26927432
|
A | C | 1 | a0001c0001t0002g0314 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.282+7798A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927432 | ||||||
| chr4:26927456
|
C | T | 3 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0110 | 3 | HG02486.hp2 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.282+7822C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927456 | ||||||
| chr4:26927458
|
C | T | 2 | a0001c0001t0021g0204a0001c0001t0021g0205 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.282+7824C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927458 | ||||||
| chr4:26927495
|
A | G | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.282+7861A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927495 | ||||||
| chr4:26927498
|
G | A | 3 | a0001c0001t0007g0091a0001c0001t0007g0145a0001c0001t0007g0146 | 3 | HG01243.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.282+7864G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927498 | ||||||
| chr4:26927528
|
G | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.282+7894G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927528 | ||||||
| chr4:26927536
|
C | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.282+7902C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927536 | ||||||
| chr4:26927537
|
G | A | 1 | a0001c0001t0004g0237 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.282+7903G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927537 | ||||||
| chr4:26927540
|
G | A | 5 | a0001c0001t0002g0311a0001c0001t0005g0291a0001c0001t0005g0300others(2): Show | 5 | NA18953.hp2 NA18970.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+7906G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927540 | ||||||
| chr4:26927544
|
G | A | 1 | a0001c0001t0003g0158 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.282+7910G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927544 | ||||||
| chr4:26927566
|
A | T | 5 | a0001c0001t0014g0119a0001c0001t0014g0121a0001c0001t0014g0122others(2): Show | 5 | HG00642.hp2 HG03669.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+7932A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927566 | ||||||
| chr4:26927587
|
A | G | 1 | a0001c0001t0019g0150 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.282+7953A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927587 | ||||||
| chr4:26927588
|
C | A | 1 | a0001c0001t0019g0150 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.282+7954C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927588 | ||||||
| chr4:26927589
|
A | G | 1 | a0001c0001t0019g0150 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.282+7955A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927589 | ||||||
| chr4:26927604
|
G | A | 3 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0148 | 3 | HG02258.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.282+7970G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927604 | ||||||
| chr4:26927680
|
T | TA | 66 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0092others(63): Show | 66 | HG00423.hp2 HG00558.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.282+8073dupA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26927680 | |||||
| chr4:26927680
|
T | TAA | 6 | a0001c0001t0001g0141a0001c0001t0002g0026a0001c0001t0002g0297others(3): Show | 6 | HG00408.hp2 HG02135.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+8072_282+8073d others(4): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26927680 | |||||
| chr4:26927680
|
TA | T | 47 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0024others(44): Show | 48 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.282+8073delA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26927680 | |||||
| chr4:26927680
|
TAA | T | 75 | a0001c0001t0001g0020a0001c0001t0001g0306a0001c0001t0001g0319others(72): Show | 76 | HG00099.hp1 HG00438.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.282+8072_282+8073d others(4): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26927680 | |||||
| chr4:26927680
|
TAAA | T | 17 | a0001c0001t0002g0128a0001c0001t0003g0159a0001c0001t0003g0180others(14): Show | 17 | HG01515.hp2 HG01884.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.282+8071_282+8073d others(5): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26927680 | |||||
| chr4:26927680
|
TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0002g0320 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.282+8061_282+8073d others(15): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26927680 | |||||
| chr4:26927690
|
AAAAAAAA others(17): Show |
A | 14 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(11): Show | 14 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.282+8068_282+8091d others(26): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26927690 | |||||
| chr4:26927715
|
A | C | 14 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(11): Show | 14 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.282+8081A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927715 | ||||||
| chr4:26927726
|
C | A | 5 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(2): Show | 5 | NA18973.hp2 NA18999.hp1 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+8092C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927726 | ||||||
| chr4:26927747
|
C | G | 1 | a0001c0001t0015g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.282+8113C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927747 | ||||||
| chr4:26927756
|
TA | T | 104 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(101): Show | 105 | HG00438.hp2 HG00733.hp2 HG00735.hp2 others(102): Show |
intron_variant | MODIFIER | c.282+8133delA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26927756 | |||||
| chr4:26927756
|
TAA | T | 43 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(40): Show | 43 | HG00544.hp2 HG00621.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.282+8132_282+8133d others(4): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26927756 | |||||
| chr4:26927767
|
AT | A | 3 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0320 | 3 | HG02129.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.282+8134delT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927767 | ||||||
| chr4:26927829
|
A | AATTATAT others(23): Show |
1 | a0001c0001t0001g0013 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.282+8225_282+8254d others(32): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26927829 | |||||
| chr4:26927829
|
AATTATAT others(23): Show |
A | 14 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(11): Show | 14 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.282+8225_282+8254d others(32): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26927829 | |||||
| chr4:26927843
|
T | C | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+8209T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927843 | ||||||
| chr4:26927849
|
A | T | 3 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0110 | 3 | HG02486.hp2 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.282+8215A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927849 | ||||||
| chr4:26927875
|
T | G | 1 | a0001c0001t0001g0092 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.282+8241T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927875 | ||||||
| chr4:26927888
|
T | C | 1 | a0001c0001t0002g0311 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.282+8254T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927888 | ||||||
| chr4:26927916
|
T | G | 1 | a0001c0001t0012g0221 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.282+8282T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26927916 | ||||||
| chr4:26928115
|
C | T | 2 | a0001c0001t0005g0014a0001c0001t0005g0015 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.282+8481C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26928115 | ||||||
| chr4:26928279
|
A | G | 1 | a0001c0001t0003g0166 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.282+8645A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26928279 | ||||||
| chr4:26928352
|
G | A | 1 | a0001c0001t0005g0067 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.282+8718G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26928352 | ||||||
| chr4:26928382
|
G | A | 1 | a0001c0001t0003g0163 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.282+8748G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26928382 | ||||||
| chr4:26928526
|
T | G | 90 | a0001c0001t0001g0020a0001c0001t0001g0306a0001c0001t0001g0319others(87): Show | 91 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.282+8892T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26928526 | ||||||
| chr4:26928554
|
A | G | 14 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(11): Show | 14 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.282+8920A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26928554 | ||||||
| chr4:26928588
|
G | A | 2 | a0001c0001t0019g0150a0001c0002t0019g0107 | 2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.282+8954G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26928588 | ||||||
| chr4:26928663
|
C | T | 1 | a0001c0001t0002g0304 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.282+9029C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26928663 | ||||||
| chr4:26928731
|
A | T | 5 | a0001c0001t0014g0119a0001c0001t0014g0121a0001c0001t0014g0122others(2): Show | 5 | HG00642.hp2 HG03669.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+9097A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26928731 | ||||||
| chr4:26928824
|
A | G | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.282+9190A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26928824 | ||||||
| chr4:26928885
|
A | G | 2 | a0001c0001t0004g0245a0001c0001t0004g0246 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.282+9251A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26928885 | ||||||
| chr4:26928936
|
C | T | 59 | a0001c0001t0003g0002a0001c0001t0003g0111a0001c0001t0003g0113others(56): Show | 60 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.282+9302C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26928936 | ||||||
| chr4:26929235
|
G | A | 1 | a0001c0001t0002g0297 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.282+9601G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26929235 | ||||||
| chr4:26929264
|
C | T | 1 | a0001c0001t0005g0003 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.282+9630C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26929264 | ||||||
| chr4:26929270
|
T | C | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+9636T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26929270 | ||||||
| chr4:26929577
|
T | TA | 7 | a0001c0001t0012g0215a0001c0001t0012g0222a0001c0001t0012g0223others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.282+9951dupA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26929577 | |||||
| chr4:26929877
|
TAG | T | 4 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019others(1): Show | 4 | HG00741.hp1 HG02630.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+10247_282+1024 others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26929877 | |||||
| chr4:26929884
|
G | A | 4 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019others(1): Show | 4 | HG00741.hp1 HG02630.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+10250G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26929884 | ||||||
| chr4:26929952
|
A | G | 1 | a0001c0001t0009g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.282+10318A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26929952 | ||||||
| chr4:26930475
|
GT | G | 172 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(169): Show | 174 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.282+10850delT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26930475 | |||||
| chr4:26930629
|
T | A | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+10995T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26930629 | ||||||
| chr4:26930790
|
T | A | 7 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0110others(4): Show | 7 | HG00741.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.282+11156T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26930790 | ||||||
| chr4:26930831
|
G | A | 221 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(218): Show | 223 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.282+11197G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26930831 | ||||||
| chr4:26930890
|
T | C | 1 | a0001c0001t0004g0226 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.282+11256T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26930890 | ||||||
| chr4:26931047
|
A | G | 6 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(3): Show | 6 | HG02486.hp1 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+11413A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26931047 | ||||||
| chr4:26931108
|
G | C | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.282+11474G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26931108 | ||||||
| chr4:26931119
|
G | A | 1 | a0001c0001t0029g0136 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.282+11485G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26931119 | ||||||
| chr4:26931147
|
C | T | 2 | a0001c0001t0002g0322a0001c0001t0002g0325 | 2 | NA19062.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.282+11513C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26931147 | ||||||
| chr4:26931370
|
G | A | 1 | a0001c0001t0001g0319 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.282+11736G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26931370 | ||||||
| chr4:26931370
|
G | C | 1 | a0001c0001t0004g0267 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.282+11736G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26931370 | ||||||
| chr4:26931643
|
T | A | 4 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019others(1): Show | 4 | HG00741.hp1 HG02630.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+12009T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26931643 | ||||||
| chr4:26932222
|
A | G | 1 | a0001c0001t0009g0328 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.282+12588A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26932222 | ||||||
| chr4:26932223
|
C | T | 235 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(232): Show | 237 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(234): Show |
intron_variant | MODIFIER | c.282+12589C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26932223 | ||||||
| chr4:26932676
|
G | A | 1 | a0001c0001t0002g0320 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.282+13042G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26932676 | ||||||
| chr4:26933042
|
A | C | 1 | a0001c0001t0024g0308 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.282+13408A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26933042 | ||||||
| chr4:26933054
|
G | A | 3 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0148 | 3 | HG02258.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.282+13420G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26933054 | ||||||
| chr4:26933190
|
C | CA | 7 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0002g0007others(4): Show | 7 | HG01243.hp2 HG02071.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.282+13572dupA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26933190 | |||||
| chr4:26933243
|
T | A | 3 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0036g0016 | 3 | HG02280.hp2 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.282+13609T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26933243 | ||||||
| chr4:26933262
|
C | T | 99 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0306others(96): Show | 100 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.282+13628C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26933262 | ||||||
| chr4:26933297
|
A | G | 1 | a0001c0001t0002g0307 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.282+13663A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26933297 | ||||||
| chr4:26933498
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+13864A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26933498 | ||||||
| chr4:26933574
|
C | G | 1 | a0001c0002t0013g0099 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.282+13940C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26933574 | ||||||
| chr4:26933613
|
G | T | 7 | a0001c0001t0012g0215a0001c0001t0012g0222a0001c0001t0012g0223others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.282+13979G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26933613 | ||||||
| chr4:26933733
|
C | CA | 33 | a0001c0001t0001g0045a0001c0001t0001g0070a0001c0001t0001g0281others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.282+14121dupA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26933733 | |||||
| chr4:26933733
|
C | CAA | 6 | a0001c0001t0002g0093a0001c0001t0005g0206a0001c0001t0007g0203others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+14120_282+1412 others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26933733 | |||||
| chr4:26933733
|
C | CAAA | 7 | a0001c0001t0002g0207a0001c0001t0005g0003a0001c0001t0014g0119others(4): Show | 7 | HG00642.hp2 HG03669.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.282+14119_282+1412 others(7): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26933733 | |||||
| chr4:26933733
|
CA | C | 28 | a0001c0001t0001g0024a0001c0001t0001g0044a0001c0001t0002g0083others(25): Show | 28 | HG00099.hp2 HG00733.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.282+14121delA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26933733 | |||||
| chr4:26933754
|
A | G | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.282+14120A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26933754 | ||||||
| chr4:26933781
|
G | A | 1 | a0001c0001t0009g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.282+14147G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26933781 | ||||||
| chr4:26933833
|
G | A | 237 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(234): Show | 239 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(236): Show |
intron_variant | MODIFIER | c.282+14199G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26933833 | ||||||
| chr4:26933852
|
A | G | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.282+14218A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26933852 | ||||||
| chr4:26933901
|
C | T | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+14267C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26933901 | ||||||
| chr4:26934064
|
C | T | 4 | a0001c0001t0012g0215a0001c0001t0012g0222a0001c0001t0012g0223others(1): Show | 4 | HG02145.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+14430C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26934064 | ||||||
| chr4:26934125
|
C | T | 1 | a0001c0001t0004g0271 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.282+14491C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26934125 | ||||||
| chr4:26934405
|
T | G | 4 | a0001c0001t0005g0206a0001c0001t0007g0203a0001c0001t0021g0204others(1): Show | 4 | HG01884.hp2 HG01891.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+14771T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26934405 | ||||||
| chr4:26934504
|
G | A | 1 | a0001c0006t0003g0174 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.282+14870G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26934504 | ||||||
| chr4:26934690
|
A | G | 234 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(231): Show | 236 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(233): Show |
intron_variant | MODIFIER | c.282+15056A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26934690 | ||||||
| chr4:26934867
|
C | T | 1 | a0001c0001t0002g0207 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.282+15233C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26934867 | ||||||
| chr4:26934877
|
A | C | 137 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(134): Show | 138 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.282+15243A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26934877 | ||||||
| chr4:26934913
|
C | CA | 22 | a0001c0001t0001g0224a0001c0001t0001g0281a0001c0001t0001g0282others(19): Show | 22 | HG01169.hp2 HG01261.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.282+15302dupA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26934913 | |||||
| chr4:26934913
|
CA | C | 110 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0022others(107): Show | 111 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.282+15302delA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26934913 | |||||
| chr4:26935035
|
A | G | 1 | a0001c0001t0001g0086 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.282+15401A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26935035 | ||||||
| chr4:26935067
|
G | A | 2 | a0001c0001t0005g0014a0001c0001t0005g0015 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.282+15433G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26935067 | ||||||
| chr4:26935210
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+15576A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26935210 | ||||||
| chr4:26935419
|
G | A | 18 | a0001c0001t0002g0026a0001c0001t0002g0064a0001c0001t0002g0065others(15): Show | 18 | HG01934.hp2 HG01943.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.282+15785G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26935419 | ||||||
| chr4:26935563
|
G | A | 3 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0148 | 3 | HG02258.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.282+15929G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26935563 | ||||||
| chr4:26936088
|
A | G | 14 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(11): Show | 14 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.282+16454A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26936088 | ||||||
| chr4:26936386
|
A | G | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012 | 3 | HG01192.hp2 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.282+16752A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26936386 | ||||||
| chr4:26936401
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.282+16767C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26936401 | ||||||
| chr4:26936496
|
A | G | 1 | a0001c0001t0005g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.282+16862A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26936496 | ||||||
| chr4:26936514
|
C | T | 238 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(235): Show | 240 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(237): Show |
intron_variant | MODIFIER | c.282+16880C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26936514 | ||||||
| chr4:26936556
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0138 | 2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.282+16922G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26936556 | ||||||
| chr4:26936599
|
G | A | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+16965G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26936599 | ||||||
| chr4:26936612
|
A | T | 1 | a0001c0001t0002g0154 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.282+16978A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26936612 | ||||||
| chr4:26937017
|
G | T | 1 | a0001c0001t0001g0022 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.282+17383G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26937017 | ||||||
| chr4:26937030
|
T | C | 263 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(260): Show | 265 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(262): Show |
intron_variant | MODIFIER | c.282+17396T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26937030 | ||||||
| chr4:26937139
|
G | C | 129 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(126): Show | 130 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.282+17505G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26937139 | ||||||
| chr4:26937297
|
G | A | 14 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(11): Show | 14 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.282+17663G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26937297 | ||||||
| chr4:26937316
|
G | T | 2 | a0001c0002t0009g0114a0001c0002t0009g0115 | 2 | HG01106.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.282+17682G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26937316 | ||||||
| chr4:26937391
|
C | G | 4 | a0001c0001t0012g0215a0001c0001t0012g0222a0001c0001t0012g0223others(1): Show | 4 | HG02145.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+17757C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26937391 | ||||||
| chr4:26937634
|
C | T | 14 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(11): Show | 14 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.282+18000C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26937634 | ||||||
| chr4:26937812
|
T | C | 1 | a0001c0001t0009g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.282+18178T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26937812 | ||||||
| chr4:26937950
|
T | G | 1 | a0001c0001t0004g0267 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.282+18316T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26937950 | ||||||
| chr4:26937974
|
A | G | 4 | a0001c0001t0005g0206a0001c0001t0007g0203a0001c0001t0021g0204others(1): Show | 4 | HG01884.hp2 HG01891.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+18340A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26937974 | ||||||
| chr4:26937981
|
A | AT | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+18353dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26937981 | |||||
| chr4:26938009
|
AAATTTAA others(10): Show |
A | 15 | a0001c0001t0004g0260a0001c0001t0010g0100a0001c0001t0010g0101others(12): Show | 15 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.282+18392_282+1840 others(21): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26938009 | |||||
| chr4:26938050
|
T | C | 14 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(11): Show | 14 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.282+18416T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26938050 | ||||||
| chr4:26938062
|
T | A | 1 | a0001c0001t0030g0195 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.282+18428T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26938062 | ||||||
| chr4:26938087
|
A | G | 3 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0036g0016 | 3 | HG02280.hp2 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.282+18453A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26938087 | ||||||
| chr4:26938180
|
C | CT | 9 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0032others(6): Show | 9 | HG00738.hp1 HG01175.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.282+18557dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26938180 | |||||
| chr4:26938191
|
T | A | 1 | a0001c0001t0011g0213 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.282+18557T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26938191 | ||||||
| chr4:26938338
|
G | A | 3 | a0001c0001t0004g0259a0001c0001t0004g0260a0001c0001t0011g0241 | 3 | NA18973.hp1 NA18980.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.282+18704G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26938338 | ||||||
| chr4:26938435
|
A | G | 1 | a0001c0002t0013g0099 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.282+18801A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26938435 | ||||||
| chr4:26938615
|
T | C | 101 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(98): Show | 102 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.282+18981T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26938615 | ||||||
| chr4:26938727
|
G | A | 1 | a0001c0001t0003g0194 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.283-18885G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26938727 | ||||||
| chr4:26938727
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.283-18885G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26938727 | ||||||
| chr4:26938887
|
A | C | 2 | a0001c0001t0002g0296a0001c0001t0005g0301 | 2 | NA18953.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.283-18725A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26938887 | ||||||
| chr4:26938887
|
A | G | 1 | a0001c0002t0009g0115 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.283-18725A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26938887 | ||||||
| chr4:26938923
|
A | T | 1 | a0001c0001t0002g0303 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.283-18689A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26938923 | ||||||
| chr4:26938972
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-18640A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26938972 | ||||||
| chr4:26939065
|
A | G | 90 | a0001c0001t0001g0020a0001c0001t0001g0306a0001c0001t0001g0319others(87): Show | 91 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.283-18547A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26939065 | ||||||
| chr4:26939095
|
C | A | 14 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(11): Show | 14 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.283-18517C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26939095 | ||||||
| chr4:26939098
|
G | A | 1 | a0001c0002t0009g0149 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.283-18514G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26939098 | ||||||
| chr4:26939227
|
C | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | NA18944.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.283-18385C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26939227 | ||||||
| chr4:26939299
|
A | T | 1 | a0001c0001t0003g0169 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.283-18313A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26939299 | ||||||
| chr4:26939362
|
G | C | 3 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019 | 3 | HG00741.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.283-18250G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26939362 | ||||||
| chr4:26939382
|
C | T | 1 | a0001c0001t0001g0042 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.283-18230C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26939382 | ||||||
| chr4:26939547
|
A | T | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-18065A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26939547 | ||||||
| chr4:26939571
|
T | G | 1 | a0001c0001t0002g0307 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.283-18041T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26939571 | ||||||
| chr4:26939676
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.283-17936G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26939676 | ||||||
| chr4:26939763
|
G | T | 1 | a0001c0001t0003g0181 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.283-17849G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26939763 | ||||||
| chr4:26939944
|
C | T | 1 | a0001c0001t0004g0272 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.283-17668C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26939944 | ||||||
| chr4:26940032
|
C | T | 1 | a0001c0001t0009g0328 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.283-17580C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26940032 | ||||||
| chr4:26940144
|
A | G | 1 | a0001c0001t0003g0191 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.283-17468A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26940144 | ||||||
| chr4:26940218
|
T | C | 4 | a0001c0001t0012g0215a0001c0001t0012g0222a0001c0001t0012g0223others(1): Show | 4 | HG02145.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-17394T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26940218 | ||||||
| chr4:26940360
|
C | G | 3 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0036g0016 | 3 | HG02280.hp2 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.283-17252C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26940360 | ||||||
| chr4:26940392
|
A | G | 3 | a0001c0001t0007g0091a0001c0001t0007g0145a0001c0001t0007g0146 | 3 | HG01243.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.283-17220A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26940392 | ||||||
| chr4:26940496
|
C | A | 1 | a0001c0001t0001g0020 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.283-17116C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26940496 | ||||||
| chr4:26940783
|
A | G | 3 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019 | 3 | HG00741.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.283-16829A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26940783 | ||||||
| chr4:26940942
|
G | T | 3 | a0001c0001t0013g0217a0001c0001t0013g0218a0001c0001t0013g0219 | 3 | HG02559.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.283-16670G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26940942 | ||||||
| chr4:26941126
|
C | A | 234 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(231): Show | 236 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(233): Show |
intron_variant | MODIFIER | c.283-16486C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26941126 | ||||||
| chr4:26941127
|
C | G | 236 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(233): Show | 238 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(235): Show |
intron_variant | MODIFIER | c.283-16485C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26941127 | ||||||
| chr4:26941252
|
G | T | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.283-16360G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26941252 | ||||||
| chr4:26941540
|
G | T | 2 | a0001c0001t0002g0152a0001c0001t0002g0153 | 2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.283-16072G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26941540 | ||||||
| chr4:26941667
|
A | C | 1 | a0001c0001t0001g0040 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.283-15945A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26941667 | ||||||
| chr4:26941684
|
T | TAATTATT others(303): Show |
4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-15912_283-1591 others(314): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26941684 | |||||
| chr4:26941692
|
G | C | 4 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(1): Show | 4 | NA18999.hp1 NA19062.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-15920G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26941692 | ||||||
| chr4:26941951
|
A | G | 2 | a0001c0001t0021g0204a0001c0001t0021g0205 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.283-15661A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26941951 | ||||||
| chr4:26942053
|
G | GATAT | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-15558_283-1555 others(8): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26942053 | |||||
| chr4:26942165
|
C | G | 1 | a0001c0001t0009g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.283-15447C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26942165 | ||||||
| chr4:26942380
|
C | T | 1 | a0001c0001t0003g0163 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.283-15232C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26942380 | ||||||
| chr4:26942429
|
G | A | 1 | a0001c0001t0004g0259 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.283-15183G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26942429 | ||||||
| chr4:26942433
|
A | G | 1 | a0001c0001t0004g0251 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.283-15179A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26942433 | ||||||
| chr4:26942548
|
C | A | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-15064C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26942548 | ||||||
| chr4:26942631
|
T | G | 3 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0006g0001 | 4 | HG00733.hp2 HG01255.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-14981T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26942631 | ||||||
| chr4:26942692
|
C | T | 88 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(85): Show | 89 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.283-14920C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26942692 | ||||||
| chr4:26942718
|
T | G | 1 | a0001c0001t0011g0241 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.283-14894T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26942718 | ||||||
| chr4:26942753
|
T | C | 282 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(279): Show | 284 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(281): Show |
intron_variant | MODIFIER | c.283-14859T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26942753 | ||||||
| chr4:26942900
|
A | G | 1 | a0001c0001t0009g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.283-14712A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26942900 | ||||||
| chr4:26942993
|
C | A | 3 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0110 | 3 | HG02486.hp2 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.283-14619C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26942993 | ||||||
| chr4:26943183
|
C | CT | 91 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(88): Show | 92 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.283-14421dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26943183 | |||||
| chr4:26943347
|
G | A | 2 | a0001c0001t0004g0265a0001c0001t0004g0266 | 2 | HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.283-14265G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26943347 | ||||||
| chr4:26943376
|
T | C | 2 | a0001c0001t0009g0216a0001c0001t0028g0284 | 2 | HG02572.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.283-14236T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26943376 | ||||||
| chr4:26943440
|
C | A | 1 | a0001c0001t0007g0255 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.283-14172C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26943440 | ||||||
| chr4:26943501
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.283-14111C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26943501 | ||||||
| chr4:26943527
|
G | A | 218 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(215): Show | 220 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(217): Show |
intron_variant | MODIFIER | c.283-14085G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26943527 | ||||||
| chr4:26943687
|
A | G | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.283-13925A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26943687 | ||||||
| chr4:26943905
|
T | C | 234 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(231): Show | 236 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(233): Show |
intron_variant | MODIFIER | c.283-13707T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26943905 | ||||||
| chr4:26943943
|
T | G | 1 | a0001c0001t0002g0292 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.283-13669T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26943943 | ||||||
| chr4:26943981
|
C | T | 1 | a0001c0001t0004g0231 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.283-13631C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26943981 | ||||||
| chr4:26944139
|
A | G | 1 | a0001c0002t0013g0099 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.283-13473A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26944139 | ||||||
| chr4:26944384
|
T | G | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.283-13228T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26944384 | ||||||
| chr4:26944466
|
C | T | 3 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0148 | 3 | HG02258.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.283-13146C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26944466 | ||||||
| chr4:26944611
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-13001A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26944611 | ||||||
| chr4:26944827
|
A | G | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-12785A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26944827 | ||||||
| chr4:26944832
|
T | C | 1 | a0001c0001t0044g0270 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.283-12780T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26944832 | ||||||
| chr4:26945145
|
G | A | 1 | a0001c0001t0009g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.283-12467G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26945145 | ||||||
| chr4:26945354
|
G | A | 14 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(11): Show | 14 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.283-12258G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26945354 | ||||||
| chr4:26945393
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.283-12219C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26945393 | ||||||
| chr4:26945436
|
A | G | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.283-12176A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26945436 | ||||||
| chr4:26945451
|
T | A | 1 | a0001c0001t0028g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283-12161T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26945451 | ||||||
| chr4:26945539
|
A | G | 5 | a0001c0001t0014g0119a0001c0001t0014g0121a0001c0001t0014g0122others(2): Show | 5 | HG00642.hp2 HG03669.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.283-12073A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26945539 | ||||||
| chr4:26945656
|
G | A | 330 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(327): Show | 332 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(329): Show |
intron_variant | MODIFIER | c.283-11956G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26945656 | ||||||
| chr4:26945747
|
A | G | 8 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0009g0216others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.283-11865A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26945747 | ||||||
| chr4:26945771
|
C | A | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.283-11841C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26945771 | ||||||
| chr4:26945793
|
G | T | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-11819G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26945793 | ||||||
| chr4:26945906
|
C | T | 1 | a0001c0001t0028g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283-11706C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26945906 | ||||||
| chr4:26946269
|
A | T | 53 | a0001c0001t0003g0002a0001c0001t0003g0111a0001c0001t0003g0113others(50): Show | 54 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.283-11343A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26946269 | ||||||
| chr4:26946387
|
G | A | 3 | a0001c0001t0013g0217a0001c0001t0013g0218a0001c0001t0013g0219 | 3 | HG02559.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.283-11225G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26946387 | ||||||
| chr4:26946405
|
G | A | 59 | a0001c0001t0003g0002a0001c0001t0003g0111a0001c0001t0003g0113others(56): Show | 60 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.283-11207G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26946405 | ||||||
| chr4:26946444
|
A | G | 1 | a0001c0001t0007g0255 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.283-11168A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26946444 | ||||||
| chr4:26946449
|
A | G | 1 | a0001c0001t0012g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.283-11163A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26946449 | ||||||
| chr4:26946464
|
C | CA | 3 | a0001c0001t0003g0159a0001c0001t0003g0182a0001c0001t0018g0112 | 3 | HG02451.hp2 HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.283-11146dupA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26946464 | |||||
| chr4:26946497
|
C | G | 3 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0110 | 3 | HG02486.hp2 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.283-11115C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26946497 | ||||||
| chr4:26946565
|
T | C | 1 | a0001c0001t0044g0270 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.283-11047T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26946565 | ||||||
| chr4:26946568
|
G | A | 2 | a0001c0001t0003g0190a0001c0001t0003g0191 | 2 | NA19085.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.283-11044G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26946568 | ||||||
| chr4:26946577
|
C | T | 1 | a0001c0001t0025g0220 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.283-11035C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26946577 | ||||||
| chr4:26946647
|
G | A | 4 | a0001c0001t0005g0206a0001c0001t0007g0203a0001c0001t0021g0204others(1): Show | 4 | HG01884.hp2 HG01891.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-10965G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26946647 | ||||||
| chr4:26946657
|
C | T | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-10955C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26946657 | ||||||
| chr4:26946662
|
T | C | 1 | a0001c0001t0004g0252 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.283-10950T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26946662 | ||||||
| chr4:26946706
|
A | G | 2 | a0001c0001t0004g0263a0001c0001t0004g0264 | 2 | NA18965.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.283-10906A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26946706 | ||||||
| chr4:26946817
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.283-10795G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26946817 | ||||||
| chr4:26946834
|
C | T | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-10778C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26946834 | ||||||
| chr4:26946864
|
C | G | 98 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(95): Show | 99 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.283-10748C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26946864 | ||||||
| chr4:26946914
|
A | T | 5 | a0001c0001t0014g0119a0001c0001t0014g0121a0001c0001t0014g0122others(2): Show | 5 | HG00642.hp2 HG03669.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.283-10698A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26946914 | ||||||
| chr4:26947150
|
C | T | 98 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(95): Show | 99 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.283-10462C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26947150 | ||||||
| chr4:26947242
|
A | G | 4 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019others(1): Show | 4 | HG00741.hp1 HG02630.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-10370A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26947242 | ||||||
| chr4:26947283
|
T | C | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-10329T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26947283 | ||||||
| chr4:26947373
|
G | A | 232 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(229): Show | 234 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(231): Show |
intron_variant | MODIFIER | c.283-10239G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26947373 | ||||||
| chr4:26947511
|
A | C | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-10101A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26947511 | ||||||
| chr4:26947751
|
C | T | 1 | a0001c0001t0004g0251 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.283-9861C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26947751 | ||||||
| chr4:26947889
|
C | T | 2 | a0001c0001t0003g0189a0001c0001t0005g0067 | 2 | HG00544.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.283-9723C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26947889 | ||||||
| chr4:26948084
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.283-9528C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26948084 | ||||||
| chr4:26948164
|
C | T | 1 | a0001c0002t0013g0099 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.283-9448C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26948164 | ||||||
| chr4:26948431
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.283-9181G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26948431 | ||||||
| chr4:26948643
|
C | T | 88 | a0001c0001t0001g0306a0001c0001t0001g0319a0001c0001t0002g0005others(85): Show | 89 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.283-8969C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26948643 | ||||||
| chr4:26948766
|
A | C | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-8846A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26948766 | ||||||
| chr4:26948781
|
G | GT | 6 | a0001c0001t0001g0020a0001c0001t0001g0281a0001c0001t0001g0282others(3): Show | 6 | HG01169.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-8820dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26948781 | |||||
| chr4:26948894
|
G | A | 1 | a0001c0001t0012g0221 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.283-8718G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26948894 | ||||||
| chr4:26948903
|
T | G | 1 | a0001c0001t0004g0267 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.283-8709T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26948903 | ||||||
| chr4:26948970
|
G | A | 1 | a0001c0001t0012g0221 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.283-8642G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26948970 | ||||||
| chr4:26949048
|
T | G | 1 | a0001c0002t0023g0155 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.283-8564T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26949048 | ||||||
| chr4:26949049
|
C | A | 2 | a0001c0001t0001g0139a0001c0001t0005g0140 | 2 | NA18989.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.283-8563C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26949049 | ||||||
| chr4:26949365
|
C | T | 98 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(95): Show | 99 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.283-8247C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26949365 | ||||||
| chr4:26949524
|
A | G | 2 | a0001c0001t0001g0038a0001c0001t0002g0037 | 2 | HG02523.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.283-8088A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26949524 | ||||||
| chr4:26949826
|
G | T | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.283-7786G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26949826 | ||||||
| chr4:26949898
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.283-7714G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26949898 | ||||||
| chr4:26949973
|
T | C | 1 | a0001c0001t0006g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.283-7639T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26949973 | ||||||
| chr4:26950077
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.283-7535A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26950077 | ||||||
| chr4:26950316
|
C | T | 1 | a0001c0001t0020g0004 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.283-7296C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26950316 | ||||||
| chr4:26950395
|
C | G | 5 | a0001c0001t0005g0208a0001c0001t0005g0209a0001c0001t0005g0210others(2): Show | 5 | HG02615.hp1 HG02717.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.283-7217C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26950395 | ||||||
| chr4:26950431
|
C | T | 10 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(7): Show | 10 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.283-7181C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26950431 | ||||||
| chr4:26950438
|
T | G | 1 | a0001c0001t0003g0159 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.283-7174T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26950438 | ||||||
| chr4:26950576
|
T | G | 1 | a0001c0001t0003g0159 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.283-7036T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26950576 | ||||||
| chr4:26950648
|
T | C | 4 | a0001c0001t0003g0157a0001c0001t0003g0169a0001c0001t0003g0175others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-6964T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26950648 | ||||||
| chr4:26950708
|
T | C | 117 | a0001c0001t0001g0306a0001c0001t0001g0319a0001c0001t0002g0005others(114): Show | 118 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.283-6904T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26950708 | ||||||
| chr4:26950937
|
G | A | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.283-6675G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26950937 | ||||||
| chr4:26951119
|
T | G | 1 | a0001c0001t0007g0248 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.283-6493T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26951119 | ||||||
| chr4:26951565
|
G | A | 1 | a0001c0001t0001g0306 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.283-6047G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26951565 | ||||||
| chr4:26951657
|
T | TA | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-5954dupA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26951657 | |||||
| chr4:26951819
|
A | T | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-5793A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26951819 | ||||||
| chr4:26951916
|
C | G | 1 | a0001c0001t0005g0003 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.283-5696C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26951916 | ||||||
| chr4:26951944
|
A | G | 1 | a0001c0001t0002g0315 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.283-5668A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26951944 | ||||||
| chr4:26952057
|
C | A | 1 | a0001c0001t0006g0133 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.283-5555C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26952057 | ||||||
| chr4:26952077
|
G | A | 10 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(7): Show | 10 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.283-5535G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26952077 | ||||||
| chr4:26952112
|
C | T | 97 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(94): Show | 98 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.283-5500C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26952112 | ||||||
| chr4:26952482
|
A | G | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.283-5130A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26952482 | ||||||
| chr4:26952832
|
T | C | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0012g0280 | 3 | HG02647.hp2 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.283-4780T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26952832 | ||||||
| chr4:26952844
|
C | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | NA18944.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.283-4768C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26952844 | ||||||
| chr4:26952906
|
G | A | 6 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0012g0215others(3): Show | 6 | HG01243.hp2 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-4706G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26952906 | ||||||
| chr4:26953165
|
T | C | 3 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0148 | 3 | HG02258.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.283-4447T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26953165 | ||||||
| chr4:26953242
|
A | T | 1 | a0001c0001t0020g0294 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.283-4370A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26953242 | ||||||
| chr4:26953366
|
G | A | 1 | a0001c0001t0009g0328 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.283-4246G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26953366 | ||||||
| chr4:26953399
|
G | A | 2 | a0001c0001t0002g0089a0001c0005t0002g0088 | 2 | HG00544.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.283-4213G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26953399 | ||||||
| chr4:26953409
|
A | G | 1 | a0001c0001t0003g0163 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.283-4203A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26953409 | ||||||
| chr4:26953420
|
C | T | 1 | a0001c0001t0009g0328 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.283-4192C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26953420 | ||||||
| chr4:26953421
|
T | G | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.283-4191T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26953421 | ||||||
| chr4:26953474
|
G | A | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-4138G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26953474 | ||||||
| chr4:26953478
|
T | C | 1 | a0001c0001t0016g0017 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.283-4134T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26953478 | ||||||
| chr4:26953654
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.283-3958A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26953654 | ||||||
| chr4:26953781
|
C | T | 1 | a0001c0001t0036g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.283-3831C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26953781 | ||||||
| chr4:26954002
|
A | G | 2 | a0001c0001t0001g0281a0001c0001t0001g0282 | 2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.283-3610A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26954002 | ||||||
| chr4:26954036
|
T | G | 4 | a0001c0001t0001g0033a0001c0001t0001g0092a0001c0001t0001g0141others(1): Show | 4 | NA18962.hp1 NA18962.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-3576T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26954036 | ||||||
| chr4:26954263
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-3349A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26954263 | ||||||
| chr4:26954329
|
TTGCTGAG others(1493): Show |
T | 21 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0005g0014others(18): Show | 21 | HG00642.hp2 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.283-3276_283-1777d others(2): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26954329 | |||||
| chr4:26954731
|
A | G | 1 | a0001c0001t0002g0207 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.283-2881A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26954731 | ||||||
| chr4:26954864
|
C | T | 13 | a0001c0001t0010g0100a0001c0001t0010g0105a0001c0001t0010g0106others(10): Show | 13 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.283-2748C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26954864 | ||||||
| chr4:26955142
|
T | C | 240 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(237): Show | 242 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(239): Show |
intron_variant | MODIFIER | c.283-2470T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26955142 | ||||||
| chr4:26955309
|
C | T | 101 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(98): Show | 102 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.283-2303C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26955309 | ||||||
| chr4:26955376
|
G | A | 113 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(110): Show | 114 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.283-2236G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26955376 | ||||||
| chr4:26955526
|
C | G | 1 | a0001c0001t0007g0278 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.283-2086C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26955526 | ||||||
| chr4:26955536
|
C | G | 9 | a0001c0001t0010g0100a0001c0001t0010g0105a0001c0001t0010g0106others(6): Show | 9 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.283-2076C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26955536 | ||||||
| chr4:26955885
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.283-1727A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26955885 | ||||||
| chr4:26956236
|
T | C | 3 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019 | 3 | HG00741.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.283-1376T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26956236 | ||||||
| chr4:26956380
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.283-1232A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26956380 | ||||||
| chr4:26956443
|
C | CTT | 8 | a0001c0001t0012g0215a0001c0001t0012g0222a0001c0001t0012g0223others(5): Show | 8 | HG02109.hp1 HG02145.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.283-1154_283-1153d others(4): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26956443 | |||||
| chr4:26956443
|
CT | C | 12 | a0001c0001t0004g0236a0001c0001t0004g0259a0001c0001t0011g0213others(9): Show | 12 | HG00642.hp2 HG01167.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.283-1153delT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26956443 | |||||
| chr4:26956687
|
CAGA | C | 10 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0105others(7): Show | 10 | HG00733.hp1 HG01106.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.283-920_283-918del others(3): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 26956687 | |||||
| chr4:26956801
|
A | G | 1 | a0001c0001t0002g0307 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.283-811A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26956801 | ||||||
| chr4:26957175
|
G | A | 1 | a0001c0001t0004g0260 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.283-437G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26957175 | ||||||
| chr4:26957252
|
C | A | 3 | a0001c0001t0007g0091a0001c0001t0007g0145a0001c0001t0007g0146 | 3 | HG01243.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.283-360C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26957252 | ||||||
| chr4:26957254
|
G | A | 92 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(89): Show | 93 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.283-358G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26957254 | ||||||
| chr4:26957385
|
T | A | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-227T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26957385 | ||||||
| chr4:26957585
|
T | C | 99 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(96): Show | 100 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.283-27T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26957585 | ||||||
| chr4:26957818
|
A | G | 3 | a0001c0001t0013g0217a0001c0001t0013g0218a0001c0001t0013g0219 | 3 | HG02559.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.397+92A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26957818 | ||||||
| chr4:26957877
|
T | C | 1 | a0001c0001t0043g0312 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.397+151T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26957877 | ||||||
| chr4:26958035
|
CA | C | 3 | a0001c0001t0004g0245a0001c0001t0004g0246a0001c0001t0004g0261 | 3 | HG03491.hp2 HG03492.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.397+312delA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26958035 | |||||
| chr4:26958037
|
A | C | 1 | a0001c0001t0008g0094 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.397+311A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26958037 | ||||||
| chr4:26958175
|
A | G | 4 | a0001c0001t0005g0206a0001c0001t0007g0203a0001c0001t0021g0204others(1): Show | 4 | HG01884.hp2 HG01891.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+449A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26958175 | ||||||
| chr4:26958284
|
A | G | 1 | a0001c0001t0002g0320 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.397+558A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26958284 | ||||||
| chr4:26958397
|
A | T | 1 | a0001c0001t0035g0289 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.397+671A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26958397 | ||||||
| chr4:26958422
|
T | C | 95 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0002g0152others(92): Show | 95 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.397+696T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26958422 | ||||||
| chr4:26958464
|
T | G | 1 | a0001c0001t0003g0163 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.397+738T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26958464 | ||||||
| chr4:26958478
|
T | G | 1 | a0001c0001t0030g0195 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.397+752T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26958478 | ||||||
| chr4:26958682
|
CT | C | 15 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0005g0014others(12): Show | 15 | HG01243.hp2 HG01261.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.397+960delT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26958682 | |||||
| chr4:26958686
|
T | A | 303 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(300): Show | 305 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.397+960T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26958686 | ||||||
| chr4:26958827
|
C | A | 1 | a0001c0001t0004g0271 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.397+1101C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26958827 | ||||||
| chr4:26959013
|
A | G | 1 | a0001c0002t0026g0102 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.397+1287A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26959013 | ||||||
| chr4:26959057
|
T | C | 2 | a0001c0001t0021g0204a0001c0001t0021g0205 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.397+1331T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26959057 | ||||||
| chr4:26959155
|
T | A | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+1429T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26959155 | ||||||
| chr4:26959617
|
A | T | 99 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(96): Show | 99 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.397+1891A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26959617 | ||||||
| chr4:26959712
|
A | AT | 8 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0009g0216others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.397+2000dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26959712 | |||||
| chr4:26960212
|
G | A | 1 | a0001c0002t0023g0155 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.397+2486G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26960212 | ||||||
| chr4:26960367
|
GTA | G | 5 | a0001c0001t0005g0208a0001c0001t0005g0209a0001c0001t0005g0210others(2): Show | 5 | HG02615.hp1 HG02717.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+2643_397+2644d others(4): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26960367 | |||||
| chr4:26960373
|
G | A | 1 | a0001c0005t0002g0088 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.397+2647G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26960373 | ||||||
| chr4:26960399
|
A | AAC | 3 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0006g0001 | 4 | HG00733.hp2 HG01255.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.397+2685_397+2686d others(4): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26960399 | |||||
| chr4:26960463
|
T | A | 3 | a0001c0001t0004g0227a0001c0001t0004g0262a0001c0001t0004g0271 | 3 | HG00597.hp1 NA18747.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.397+2737T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26960463 | ||||||
| chr4:26960506
|
A | G | 318 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(315): Show | 320 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(317): Show |
intron_variant | MODIFIER | c.397+2780A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26960506 | ||||||
| chr4:26960547
|
T | TGAAA | 3 | a0001c0001t0004g0251a0001c0001t0004g0265a0001c0001t0004g0266 | 3 | HG01261.hp2 HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.397+2824_397+2827d others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26960547 | |||||
| chr4:26960564
|
A | G | 1 | a0001c0001t0002g0295 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.397+2838A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26960564 | ||||||
| chr4:26960625
|
A | G | 1 | a0001c0001t0013g0218 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.397+2899A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26960625 | ||||||
| chr4:26960790
|
C | T | 5 | a0001c0001t0005g0208a0001c0001t0005g0209a0001c0001t0005g0210others(2): Show | 5 | HG02615.hp1 HG02717.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+3064C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26960790 | ||||||
| chr4:26960834
|
C | T | 4 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0148others(1): Show | 4 | HG02258.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.397+3108C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26960834 | ||||||
| chr4:26961001
|
C | G | 92 | a0001c0001t0001g0057a0001c0001t0001g0306a0001c0001t0002g0005others(89): Show | 93 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.397+3275C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26961001 | ||||||
| chr4:26961014
|
C | CA | 88 | a0001c0001t0001g0031a0001c0001t0002g0073a0001c0001t0002g0152others(85): Show | 88 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.397+3302dupA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26961014 | |||||
| chr4:26961038
|
C | T | 1 | a0001c0001t0005g0206 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.397+3312C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26961038 | ||||||
| chr4:26961116
|
A | G | 1 | a0001c0001t0002g0010 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.397+3390A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26961116 | ||||||
| chr4:26961185
|
A | G | 5 | a0001c0001t0005g0206a0001c0001t0009g0328a0001c0001t0016g0017others(2): Show | 5 | HG00741.hp1 HG01261.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+3459A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26961185 | ||||||
| chr4:26961251
|
A | G | 80 | a0001c0001t0001g0032a0001c0001t0001g0058a0001c0001t0001g0060others(77): Show | 81 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.397+3525A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26961251 | ||||||
| chr4:26961316
|
C | T | 1 | a0001c0001t0006g0239 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.397+3590C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26961316 | ||||||
| chr4:26961356
|
T | C | 4 | a0001c0001t0012g0215a0001c0001t0012g0222a0001c0001t0012g0223others(1): Show | 4 | HG02145.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+3630T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26961356 | ||||||
| chr4:26961480
|
A | G | 5 | a0001c0001t0001g0319a0001c0001t0012g0215a0001c0001t0012g0222others(2): Show | 5 | HG01433.hp2 HG02145.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+3754A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26961480 | ||||||
| chr4:26961480
|
A | T | 1 | a0001c0001t0009g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.397+3754A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26961480 | ||||||
| chr4:26961878
|
A | C | 1 | a0001c0001t0028g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.397+4152A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26961878 | ||||||
| chr4:26961940
|
G | A | 5 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0005g0291others(2): Show | 5 | NA18953.hp1 NA18970.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+4214G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26961940 | ||||||
| chr4:26962224
|
A | G | 1 | a0001c0001t0006g0133 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.397+4498A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26962224 | ||||||
| chr4:26962318
|
C | A | 1 | a0001c0001t0001g0306 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.397+4592C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26962318 | ||||||
| chr4:26962333
|
A | T | 1 | a0001c0001t0004g0271 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.397+4607A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26962333 | ||||||
| chr4:26962559
|
A | AGT | 19 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0281others(16): Show | 19 | HG00738.hp2 HG01071.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.397+4874_397+4875d others(4): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26962559 | |||||
| chr4:26962559
|
A | AGTGT | 4 | a0001c0001t0002g0006a0001c0001t0003g0193a0001c0001t0004g0257others(1): Show | 4 | HG02451.hp1 HG03579.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.397+4872_397+4875d others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26962559 | |||||
| chr4:26962559
|
AGT | A | 82 | a0001c0001t0002g0065a0001c0001t0002g0083a0001c0001t0002g0084others(79): Show | 82 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.397+4874_397+4875d others(4): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26962559 | |||||
| chr4:26962559
|
AGTGT | A | 30 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0058others(27): Show | 30 | HG00558.hp2 HG01081.hp2 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.397+4872_397+4875d others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26962559 | |||||
| chr4:26962559
|
AGTGTGT | A | 113 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0024others(110): Show | 114 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.397+4870_397+4875d others(8): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26962559 | |||||
| chr4:26962559
|
AGTGTGTG others(1): Show |
A | 7 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0051others(4): Show | 7 | HG00735.hp1 HG00735.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+4868_397+4875d others(10): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26962559 | |||||
| chr4:26962559
|
AGTGTGTG others(3): Show |
A | 4 | a0001c0001t0001g0041a0001c0001t0001g0077a0001c0001t0004g0251others(1): Show | 4 | HG01261.hp2 HG02572.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+4866_397+4875d others(12): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26962559 | |||||
| chr4:26962590
|
G | A | 1 | a0001c0001t0007g0278 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.397+4864G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26962590 | ||||||
| chr4:26962592
|
GTGTGTGT others(11): Show |
G | 1 | a0001c0001t0007g0278 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.397+4872_397+4889d others(20): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26962592 | |||||
| chr4:26962594
|
G | A | 2 | a0001c0001t0003g0188a0001c0006t0003g0174 | 2 | HG01515.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.397+4868G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26962594 | ||||||
| chr4:26962596
|
G | A | 3 | a0001c0001t0003g0165a0001c0001t0003g0173a0001c0001t0014g0122 | 3 | HG02155.hp2 HG03669.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.397+4870G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26962596 | ||||||
| chr4:26962596
|
GTGTGTAT others(7): Show |
G | 2 | a0001c0001t0003g0188a0001c0006t0003g0174 | 2 | HG01515.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.397+4876_397+4889d others(16): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26962596 | |||||
| chr4:26962598
|
GTGTA | G | 6 | a0001c0001t0005g0206a0001c0001t0005g0209a0001c0001t0005g0210others(3): Show | 6 | HG01891.hp2 HG03130.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.397+4876_397+4879d others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26962598 | |||||
| chr4:26962598
|
GTGTATGT others(5): Show |
G | 3 | a0001c0001t0003g0165a0001c0001t0003g0173a0001c0001t0014g0122 | 3 | HG02155.hp2 HG03669.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.397+4876_397+4887d others(14): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26962598 | |||||
| chr4:26962604
|
GTGTGTC | G | 106 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0006others(103): Show | 107 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.397+4890_397+4895d others(8): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26962604 | |||||
| chr4:26962608
|
G | A | 6 | a0001c0001t0005g0206a0001c0001t0005g0209a0001c0001t0005g0210others(3): Show | 6 | HG01891.hp2 HG03130.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.397+4882G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26962608 | ||||||
| chr4:26962610
|
C | G | 6 | a0001c0001t0005g0206a0001c0001t0005g0209a0001c0001t0005g0210others(3): Show | 6 | HG01891.hp2 HG03130.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.397+4884C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26962610 | ||||||
| chr4:26962728
|
A | G | 325 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.397+5002A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26962728 | ||||||
| chr4:26962767
|
T | C | 24 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0031others(21): Show | 24 | HG00438.hp2 HG00621.hp1 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.397+5041T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26962767 | ||||||
| chr4:26962783
|
T | C | 1 | a0001c0001t0009g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.397+5057T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26962783 | ||||||
| chr4:26962937
|
C | G | 1 | a0001c0001t0009g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.397+5211C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26962937 | ||||||
| chr4:26963010
|
A | G | 1 | a0001c0001t0007g0278 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.397+5284A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26963010 | ||||||
| chr4:26963154
|
G | A | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+5428G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26963154 | ||||||
| chr4:26963275
|
C | A | 3 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019 | 3 | HG00741.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.397+5549C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26963275 | ||||||
| chr4:26963452
|
G | A | 12 | a0001c0001t0004g0252a0001c0001t0006g0001a0001c0001t0006g0129others(9): Show | 13 | HG00735.hp1 HG01071.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+5726G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26963452 | ||||||
| chr4:26963465
|
ATC | A | 325 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.397+5741_397+5742d others(4): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26963465 | |||||
| chr4:26963475
|
G | A | 1 | a0001c0001t0009g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.397+5749G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26963475 | ||||||
| chr4:26963556
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.397+5830A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26963556 | ||||||
| chr4:26963601
|
G | GT | 3 | a0001c0001t0003g0159a0001c0001t0003g0182a0001c0001t0007g0278 | 3 | HG02451.hp2 HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.397+5879dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26963601 | |||||
| chr4:26963678
|
G | A | 2 | a0001c0001t0003g0190a0001c0001t0003g0191 | 2 | NA19085.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.397+5952G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26963678 | ||||||
| chr4:26963684
|
A | G | 196 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(193): Show | 197 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.397+5958A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26963684 | ||||||
| chr4:26963707
|
T | A | 2 | a0001c0001t0003g0198a0001c0001t0003g0199 | 2 | HG02071.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.397+5981T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26963707 | ||||||
| chr4:26963743
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+6017A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26963743 | ||||||
| chr4:26963893
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+6167A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26963893 | ||||||
| chr4:26964143
|
C | A | 1 | a0001c0001t0001g0319 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.397+6417C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26964143 | ||||||
| chr4:26964320
|
A | G | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+6594A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26964320 | ||||||
| chr4:26964537
|
T | C | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.397+6811T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26964537 | ||||||
| chr4:26964631
|
G | T | 1 | a0001c0001t0001g0042 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.397+6905G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26964631 | ||||||
| chr4:26964655
|
A | G | 55 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(52): Show | 55 | HG00438.hp2 HG00621.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.397+6929A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26964655 | ||||||
| chr4:26964705
|
G | A | 1 | a0001c0001t0009g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.397+6979G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26964705 | ||||||
| chr4:26964950
|
C | T | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(1): Show | 4 | HG02647.hp2 HG02723.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+7224C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26964950 | ||||||
| chr4:26965081
|
C | T | 6 | a0001c0001t0014g0119a0001c0001t0014g0121a0001c0001t0014g0122others(3): Show | 6 | HG00642.hp2 HG01071.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.397+7355C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26965081 | ||||||
| chr4:26965258
|
G | A | 1 | a0001c0001t0003g0173 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.397+7532G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26965258 | ||||||
| chr4:26965284
|
A | G | 124 | a0001c0001t0001g0039a0001c0001t0001g0085a0001c0001t0001g0086others(121): Show | 125 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.397+7558A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26965284 | ||||||
| chr4:26965337
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+7611A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26965337 | ||||||
| chr4:26965361
|
C | G | 62 | a0001c0001t0002g0037a0001c0001t0003g0002a0001c0001t0003g0111others(59): Show | 63 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.397+7635C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26965361 | ||||||
| chr4:26965420
|
T | C | 27 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0024others(24): Show | 27 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.397+7694T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26965420 | ||||||
| chr4:26965422
|
G | C | 1 | a0001c0001t0002g0305 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.397+7696G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26965422 | ||||||
| chr4:26965490
|
T | G | 1 | a0001c0001t0009g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.397+7764T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26965490 | ||||||
| chr4:26965500
|
G | C | 1 | a0001c0001t0004g0271 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.397+7774G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26965500 | ||||||
| chr4:26965547
|
CT | C | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+7823delT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26965547 | |||||
| chr4:26965702
|
A | AT | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+7980dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26965702 | |||||
| chr4:26965862
|
A | G | 166 | a0001c0001t0001g0039a0001c0001t0001g0085a0001c0001t0001g0086others(163): Show | 167 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.397+8136A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26965862 | ||||||
| chr4:26965954
|
C | T | 2 | a0001c0001t0003g0166a0001c0001t0003g0179 | 2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.397+8228C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26965954 | ||||||
| chr4:26966059
|
C | T | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.397+8333C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26966059 | ||||||
| chr4:26966191
|
G | A | 1 | a0001c0001t0009g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.397+8465G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26966191 | ||||||
| chr4:26966217
|
A | G | 7 | a0001c0001t0002g0288a0001c0001t0002g0292a0001c0001t0002g0293others(4): Show | 7 | HG00408.hp2 HG00423.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.397+8491A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26966217 | ||||||
| chr4:26966220
|
T | C | 59 | a0001c0001t0001g0039a0001c0001t0001g0085a0001c0001t0001g0086others(56): Show | 59 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.397+8494T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26966220 | ||||||
| chr4:26966381
|
A | G | 2 | a0001c0001t0002g0152a0001c0001t0002g0153 | 2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.397+8655A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26966381 | ||||||
| chr4:26966813
|
G | C | 155 | a0001c0001t0001g0039a0001c0001t0001g0085a0001c0001t0001g0086others(152): Show | 156 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.397+9087G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26966813 | ||||||
| chr4:26966932
|
C | T | 2 | a0001c0001t0002g0152a0001c0001t0002g0153 | 2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.397+9206C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26966932 | ||||||
| chr4:26966997
|
A | C | 1 | a0001c0001t0001g0090 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.397+9271A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26966997 | ||||||
| chr4:26967203
|
C | T | 1 | a0001c0001t0005g0301 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.397+9477C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26967203 | ||||||
| chr4:26967213
|
T | C | 1 | a0001c0001t0002g0307 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.397+9487T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26967213 | ||||||
| chr4:26967243
|
A | G | 1 | a0001c0002t0013g0099 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.397+9517A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26967243 | ||||||
| chr4:26967509
|
G | A | 1 | a0001c0001t0009g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.397+9783G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26967509 | ||||||
| chr4:26967578
|
T | C | 1 | a0001c0001t0004g0259 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.397+9852T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26967578 | ||||||
| chr4:26967633
|
G | A | 2 | a0001c0001t0009g0328a0001c0001t0019g0150 | 2 | HG01261.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.397+9907G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26967633 | ||||||
| chr4:26967683
|
G | A | 1 | a0001c0001t0003g0179 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.397+9957G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26967683 | ||||||
| chr4:26967785
|
G | C | 166 | a0001c0001t0001g0039a0001c0001t0001g0085a0001c0001t0001g0086others(163): Show | 167 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.397+10059G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26967785 | ||||||
| chr4:26967789
|
G | C | 1 | a0001c0001t0003g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.397+10063G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26967789 | ||||||
| chr4:26967858
|
A | G | 3 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019 | 3 | HG00741.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.397+10132A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26967858 | ||||||
| chr4:26967887
|
A | G | 2 | a0001c0001t0009g0328a0001c0001t0019g0150 | 2 | HG01261.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.397+10161A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26967887 | ||||||
| chr4:26968006
|
C | T | 55 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0226others(52): Show | 55 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.397+10280C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26968006 | ||||||
| chr4:26968129
|
C | T | 1 | a0001c0001t0009g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.397+10403C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26968129 | ||||||
| chr4:26968236
|
A | G | 13 | a0001c0001t0005g0206a0001c0001t0007g0108a0001c0001t0007g0109others(10): Show | 13 | HG00642.hp2 HG01071.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.397+10510A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26968236 | ||||||
| chr4:26968428
|
A | G | 1 | a0001c0001t0003g0189 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.397+10702A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26968428 | ||||||
| chr4:26968450
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.397+10724G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26968450 | ||||||
| chr4:26968581
|
A | G | 6 | a0001c0001t0014g0119a0001c0001t0014g0121a0001c0001t0014g0122others(3): Show | 6 | HG00642.hp2 HG01071.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.397+10855A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26968581 | ||||||
| chr4:26968754
|
T | C | 168 | a0001c0001t0001g0039a0001c0001t0001g0085a0001c0001t0001g0086others(165): Show | 169 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.397+11028T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26968754 | ||||||
| chr4:26968975
|
ATTTTG | A | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+11254_397+1125 others(9): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26968975 | |||||
| chr4:26969521
|
C | T | 100 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0006others(97): Show | 101 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.397+11795C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26969521 | ||||||
| chr4:26969533
|
G | A | 1 | a0001c0001t0004g0236 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.397+11807G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26969533 | ||||||
| chr4:26969671
|
C | T | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0012g0280 | 3 | HG02647.hp2 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.397+11945C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26969671 | ||||||
| chr4:26969905
|
T | A | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.397+12179T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26969905 | ||||||
| chr4:26969974
|
C | A | 1 | a0001c0002t0026g0102 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.397+12248C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26969974 | ||||||
| chr4:26969999
|
TAA | T | 112 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0006others(109): Show | 113 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.397+12274_397+1227 others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26969999 | ||||||
| chr4:26970042
|
G | T | 7 | a0001c0001t0005g0206a0001c0001t0007g0108a0001c0001t0007g0109others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+12316G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26970042 | ||||||
| chr4:26970065
|
A | G | 1 | a0001c0001t0001g0306 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.397+12339A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26970065 | ||||||
| chr4:26970197
|
GTGTATAT others(17): Show |
G | 25 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0292others(22): Show | 25 | HG00423.hp2 HG01934.hp2 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.397+12501_397+1252 others(28): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26970197 | |||||
| chr4:26970199
|
G | T | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0009g0216 | 3 | HG01243.hp2 HG02145.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.397+12473G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26970199 | ||||||
| chr4:26970199
|
GTATATAT others(13): Show |
G | 2 | a0001c0001t0001g0081a0001c0001t0034g0120 | 2 | HG03490.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.397+12477_397+1249 others(24): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26970199 | |||||
| chr4:26970199
|
GTATATAT others(15): Show |
G | 108 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0048others(105): Show | 109 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.397+12475_397+1249 others(26): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26970199 | |||||
| chr4:26970201
|
A | G | 76 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(73): Show | 76 | HG00438.hp2 HG00621.hp1 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.397+12475A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26970201 | ||||||
| chr4:26970201
|
ATATATAT others(15): Show |
A | 69 | a0001c0001t0001g0225a0001c0001t0002g0026a0001c0001t0002g0064others(66): Show | 70 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.397+12497_397+1251 others(26): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26970201 | |||||
| chr4:26970203
|
A | G | 4 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0021g0204others(1): Show | 4 | HG03209.hp1 HG03579.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+12477A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26970203 | ||||||
| chr4:26970203
|
ATATATAT others(13): Show |
A | 62 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0025others(59): Show | 62 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.397+12497_397+1251 others(24): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26970203 | |||||
| chr4:26970205
|
ATATATAT others(11): Show |
A | 22 | a0001c0001t0001g0021a0001c0001t0001g0039a0001c0001t0001g0041others(19): Show | 22 | HG01192.hp1 HG01255.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.397+12497_397+1251 others(22): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26970205 | |||||
| chr4:26970207
|
ATATATAT others(9): Show |
A | 13 | a0001c0001t0001g0022a0001c0001t0001g0050a0001c0001t0001g0053others(10): Show | 13 | HG00733.hp2 HG00741.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.397+12497_397+1251 others(20): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26970207 | |||||
| chr4:26970209
|
ATATATAT others(7): Show |
A | 4 | a0001c0001t0009g0328a0001c0001t0011g0214a0001c0001t0013g0218others(1): Show | 4 | HG01261.hp1 HG02922.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+12497_397+1251 others(18): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26970209 | |||||
| chr4:26970211
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0319 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.397+12497_397+1250 others(16): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26970211 | |||||
| chr4:26970213
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0045g0183 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.397+12497_397+1250 others(14): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26970213 | |||||
| chr4:26970217
|
ATATATG | A | 3 | a0001c0001t0012g0215a0001c0001t0012g0223a0001c0001t0025g0220 | 3 | HG02145.hp1 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.397+12497_397+1250 others(10): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26970217 | |||||
| chr4:26970217
|
ATATATGT others(23): Show |
A | 5 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0005g0291others(2): Show | 5 | NA18953.hp1 NA18970.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+12495_397+1252 others(34): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26970217 | |||||
| chr4:26970219
|
ATATG | A | 3 | a0001c0001t0007g0091a0001c0001t0007g0145a0001c0002t0026g0102 | 3 | HG01243.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.397+12497_397+1250 others(8): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26970219 | |||||
| chr4:26970219
|
ATATGTAT others(21): Show |
A | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0216others(2): Show | 5 | HG02647.hp2 HG02723.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+12501_397+1252 others(32): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26970219 | |||||
| chr4:26970221
|
A | G | 3 | a0001c0001t0001g0081a0001c0001t0034g0120a0001c0002t0013g0099 | 3 | HG02922.hp1 HG03490.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.397+12495A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26970221 | ||||||
| chr4:26970223
|
G | A | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.397+12497G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26970223 | ||||||
| chr4:26970225
|
A | G | 15 | a0001c0001t0002g0277a0001c0001t0002g0310a0001c0001t0002g0321others(12): Show | 15 | HG00642.hp2 HG01071.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.397+12499A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26970225 | ||||||
| chr4:26970227
|
A | G | 1 | a0001c0001t0034g0120 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.397+12501A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26970227 | ||||||
| chr4:26970232
|
TATATATA others(12): Show |
T | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.397+12507_397+1252 others(23): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26970232 | ||||||
| chr4:26970245
|
ATG | A | 78 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(75): Show | 79 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.397+12521_397+1252 others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26970245 | |||||
| chr4:26970247
|
G | A | 233 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(230): Show | 234 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.397+12521G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26970247 | ||||||
| chr4:26970250
|
TGTA | T | 3 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0148 | 3 | HG02258.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.397+12525_397+1252 others(7): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26970250 | ||||||
| chr4:26970295
|
C | T | 1 | a0001c0001t0012g0215 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.397+12569C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26970295 | ||||||
| chr4:26970409
|
C | G | 325 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.397+12683C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26970409 | ||||||
| chr4:26970932
|
G | A | 314 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(313): Show |
intron_variant | MODIFIER | c.397+13206G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26970932 | ||||||
| chr4:26970944
|
A | G | 2 | a0001c0001t0009g0328a0001c0001t0019g0150 | 2 | HG01261.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.397+13218A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26970944 | ||||||
| chr4:26971038
|
C | G | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.397+13312C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26971038 | ||||||
| chr4:26971047
|
A | C | 2 | a0001c0001t0003g0167a0001c0001t0003g0176 | 2 | NA18986.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.397+13321A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26971047 | ||||||
| chr4:26971095
|
C | T | 2 | a0001c0001t0003g0167a0001c0001t0003g0176 | 2 | NA18986.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.397+13369C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26971095 | ||||||
| chr4:26971301
|
G | T | 7 | a0001c0001t0005g0206a0001c0001t0007g0108a0001c0001t0007g0109others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+13575G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26971301 | ||||||
| chr4:26971318
|
C | T | 5 | a0001c0001t0001g0319a0001c0001t0012g0215a0001c0001t0012g0222others(2): Show | 5 | HG01433.hp2 HG02145.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+13592C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26971318 | ||||||
| chr4:26971319
|
G | A | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.397+13593G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26971319 | ||||||
| chr4:26971320
|
T | G | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.397+13594T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26971320 | ||||||
| chr4:26971425
|
G | A | 2 | a0001c0001t0005g0014a0001c0001t0005g0015 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.397+13699G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26971425 | ||||||
| chr4:26971503
|
C | G | 2 | a0001c0001t0009g0328a0001c0001t0019g0150 | 2 | HG01261.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.397+13777C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26971503 | ||||||
| chr4:26971527
|
C | T | 7 | a0001c0001t0005g0206a0001c0001t0007g0108a0001c0001t0007g0109others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+13801C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26971527 | ||||||
| chr4:26971617
|
A | T | 2 | a0001c0001t0002g0152a0001c0001t0002g0153 | 2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.397+13891A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26971617 | ||||||
| chr4:26971721
|
A | G | 9 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0148others(6): Show | 9 | HG00642.hp2 HG01071.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.397+13995A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26971721 | ||||||
| chr4:26971829
|
G | T | 3 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0148 | 3 | HG02258.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.397+14103G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26971829 | ||||||
| chr4:26971961
|
T | G | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(1): Show | 4 | HG02647.hp2 HG02723.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+14235T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26971961 | ||||||
| chr4:26972220
|
A | G | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0009g0216 | 3 | HG01243.hp2 HG02145.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.397+14494A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26972220 | ||||||
| chr4:26972303
|
G | A | 9 | a0001c0001t0004g0245a0001c0001t0004g0246a0001c0001t0004g0261others(6): Show | 9 | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.397+14577G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26972303 | ||||||
| chr4:26972431
|
T | C | 1 | a0001c0001t0025g0220 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.397+14705T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26972431 | ||||||
| chr4:26972443
|
G | A | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0009g0216 | 3 | HG01243.hp2 HG02145.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.397+14717G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26972443 | ||||||
| chr4:26972540
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.397+14814G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26972540 | ||||||
| chr4:26972599
|
T | C | 1 | a0001c0001t0003g0334 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.397+14873T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26972599 | ||||||
| chr4:26972600
|
G | A | 1 | a0001c0001t0003g0334 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.397+14874G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26972600 | ||||||
| chr4:26973006
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+15280A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26973006 | ||||||
| chr4:26973073
|
G | C | 1 | a0001c0002t0019g0107 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.397+15347G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26973073 | ||||||
| chr4:26973334
|
G | T | 6 | a0001c0001t0014g0119a0001c0001t0014g0121a0001c0001t0014g0122others(3): Show | 6 | HG00642.hp2 HG01071.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.397+15608G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26973334 | ||||||
| chr4:26973366
|
G | A | 1 | a0001c0001t0004g0118 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.397+15640G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26973366 | ||||||
| chr4:26973368
|
G | A | 3 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019 | 3 | HG00741.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.397+15642G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26973368 | ||||||
| chr4:26973379
|
G | A | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+15653G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26973379 | ||||||
| chr4:26973383
|
T | C | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+15657T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26973383 | ||||||
| chr4:26973518
|
A | G | 2 | a0001c0001t0002g0005a0001c0001t0002g0008 | 2 | NA18991.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.397+15792A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26973518 | ||||||
| chr4:26973544
|
C | T | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+15818C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26973544 | ||||||
| chr4:26973586
|
G | A | 1 | a0001c0001t0001g0306 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.397+15860G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26973586 | ||||||
| chr4:26973785
|
G | A | 5 | a0001c0001t0001g0319a0001c0001t0012g0215a0001c0001t0012g0222others(2): Show | 5 | HG01433.hp2 HG02145.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+16059G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26973785 | ||||||
| chr4:26973791
|
C | CT | 3 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0148 | 3 | HG02258.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.397+16067dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26973791 | |||||
| chr4:26973923
|
T | C | 81 | a0001c0001t0001g0039a0001c0001t0001g0085a0001c0001t0001g0086others(78): Show | 81 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.397+16197T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26973923 | ||||||
| chr4:26973983
|
C | T | 2 | a0001c0001t0003g0201a0001c0001t0003g0202 | 2 | HG02109.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.397+16257C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26973983 | ||||||
| chr4:26973997
|
C | T | 1 | a0001c0001t0002g0315 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.397+16271C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26973997 | ||||||
| chr4:26974189
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+16463A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26974189 | ||||||
| chr4:26974257
|
G | A | 1 | a0001c0001t0014g0122 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.397+16531G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26974257 | ||||||
| chr4:26974300
|
C | T | 1 | a0001c0001t0007g0278 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.397+16574C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26974300 | ||||||
| chr4:26974362
|
T | G | 5 | a0001c0001t0001g0319a0001c0001t0012g0215a0001c0001t0012g0222others(2): Show | 5 | HG01433.hp2 HG02145.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+16636T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26974362 | ||||||
| chr4:26974367
|
A | G | 178 | a0001c0001t0001g0039a0001c0001t0001g0085a0001c0001t0001g0086others(175): Show | 179 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.397+16641A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26974367 | ||||||
| chr4:26974551
|
T | A | 1 | a0001c0001t0028g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.397+16825T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26974551 | ||||||
| chr4:26974562
|
G | A | 3 | a0001c0001t0005g0034a0001c0001t0005g0080a0001c0001t0005g0096 | 3 | NA18951.hp1 NA19007.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.397+16836G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26974562 | ||||||
| chr4:26974575
|
T | C | 5 | a0001c0001t0005g0208a0001c0001t0005g0209a0001c0001t0005g0210others(2): Show | 5 | HG02615.hp1 HG02717.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+16849T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26974575 | ||||||
| chr4:26974577
|
G | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.397+16851G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26974577 | ||||||
| chr4:26974650
|
T | A | 5 | a0001c0001t0005g0208a0001c0001t0005g0209a0001c0001t0005g0210others(2): Show | 5 | HG02615.hp1 HG02717.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+16924T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26974650 | ||||||
| chr4:26974711
|
C | T | 1 | a0001c0002t0019g0107 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.397+16985C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26974711 | ||||||
| chr4:26974810
|
T | C | 6 | a0001c0001t0014g0119a0001c0001t0014g0121a0001c0001t0014g0122others(3): Show | 6 | HG00642.hp2 HG01071.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.397+17084T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26974810 | ||||||
| chr4:26974932
|
G | A | 1 | a0001c0001t0009g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.397+17206G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26974932 | ||||||
| chr4:26974981
|
T | C | 1 | a0001c0002t0026g0102 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.397+17255T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26974981 | ||||||
| chr4:26975244
|
A | G | 1 | a0001c0002t0026g0102 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.397+17518A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26975244 | ||||||
| chr4:26975299
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+17573A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26975299 | ||||||
| chr4:26975328
|
T | G | 1 | a0001c0001t0003g0172 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.397+17602T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26975328 | ||||||
| chr4:26975403
|
C | G | 325 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.397+17677C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26975403 | ||||||
| chr4:26975528
|
T | C | 1 | a0001c0001t0004g0226 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.397+17802T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26975528 | ||||||
| chr4:26975596
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+17870A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26975596 | ||||||
| chr4:26975650
|
A | G | 1 | a0001c0001t0009g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.397+17924A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26975650 | ||||||
| chr4:26975798
|
G | A | 1 | a0001c0001t0002g0290 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.397+18072G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26975798 | ||||||
| chr4:26975903
|
G | A | 1 | a0001c0001t0010g0327 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.397+18177G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26975903 | ||||||
| chr4:26976033
|
C | T | 2 | a0001c0001t0009g0328a0001c0001t0019g0150 | 2 | HG01261.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.397+18307C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26976033 | ||||||
| chr4:26976107
|
G | A | 16 | a0001c0001t0004g0252a0001c0001t0006g0001a0001c0001t0006g0129others(13): Show | 17 | HG00735.hp1 HG01071.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.397+18381G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26976107 | ||||||
| chr4:26976132
|
C | T | 150 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0006others(147): Show | 151 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.397+18406C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26976132 | ||||||
| chr4:26976203
|
C | T | 6 | a0001c0001t0014g0119a0001c0001t0014g0121a0001c0001t0014g0122others(3): Show | 6 | HG00642.hp2 HG01071.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.397+18477C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26976203 | ||||||
| chr4:26976211
|
G | A | 1 | a0001c0001t0002g0153 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.397+18485G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26976211 | ||||||
| chr4:26976382
|
C | CT | 127 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(124): Show | 128 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.397+18676dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26976382 | |||||
| chr4:26976382
|
CT | C | 6 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0004g0267others(3): Show | 6 | HG01169.hp2 HG02258.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.397+18676delT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26976382 | |||||
| chr4:26976570
|
G | T | 5 | a0001c0001t0001g0319a0001c0001t0012g0215a0001c0001t0012g0222others(2): Show | 5 | HG01433.hp2 HG02145.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-18809G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26976570 | ||||||
| chr4:26976674
|
C | T | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.398-18705C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26976674 | ||||||
| chr4:26976752
|
C | T | 1 | a0001c0002t0019g0107 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.398-18627C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26976752 | ||||||
| chr4:26976792
|
G | A | 325 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.398-18587G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26976792 | ||||||
| chr4:26976857
|
G | A | 1 | a0001c0001t0004g0252 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.398-18522G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26976857 | ||||||
| chr4:26976910
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.398-18469C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26976910 | ||||||
| chr4:26977084
|
C | A | 1 | a0001c0001t0012g0222 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.398-18295C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26977084 | ||||||
| chr4:26977174
|
G | A | 6 | a0001c0001t0017g0185a0001c0001t0017g0186a0001c0001t0017g0187others(3): Show | 6 | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.398-18205G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26977174 | ||||||
| chr4:26977201
|
A | G | 3 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0045 | 3 | HG01928.hp1 HG02004.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.398-18178A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26977201 | ||||||
| chr4:26977329
|
T | G | 1 | a0001c0001t0009g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.398-18050T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26977329 | ||||||
| chr4:26977341
|
G | A | 3 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0148 | 3 | HG02258.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.398-18038G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26977341 | ||||||
| chr4:26977522
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.398-17857G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26977522 | ||||||
| chr4:26977588
|
A | G | 3 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019 | 3 | HG00741.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.398-17791A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26977588 | ||||||
| chr4:26977733
|
C | G | 5 | a0001c0001t0001g0319a0001c0001t0012g0215a0001c0001t0012g0222others(2): Show | 5 | HG01433.hp2 HG02145.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-17646C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26977733 | ||||||
| chr4:26977807
|
G | A | 1 | a0001c0001t0009g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.398-17572G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26977807 | ||||||
| chr4:26977818
|
G | T | 325 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.398-17561G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26977818 | ||||||
| chr4:26977888
|
G | A | 2 | a0001c0001t0009g0328a0001c0001t0019g0150 | 2 | HG01261.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.398-17491G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26977888 | ||||||
| chr4:26978072
|
A | G | 325 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.398-17307A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26978072 | ||||||
| chr4:26978091
|
G | A | 325 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.398-17288G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26978091 | ||||||
| chr4:26978399
|
A | G | 60 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(57): Show | 60 | HG00438.hp2 HG00621.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.398-16980A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26978399 | ||||||
| chr4:26978426
|
G | A | 1 | a0001c0001t0012g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.398-16953G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26978426 | ||||||
| chr4:26978482
|
C | G | 1 | a0001c0001t0009g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.398-16897C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26978482 | ||||||
| chr4:26978483
|
T | C | 1 | a0001c0001t0005g0067 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.398-16896T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26978483 | ||||||
| chr4:26978665
|
T | G | 2 | a0001c0001t0033g0144a0001c0001t0036g0016 | 2 | HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.398-16714T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26978665 | ||||||
| chr4:26978688
|
G | A | 1 | a0001c0001t0003g0193 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.398-16691G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26978688 | ||||||
| chr4:26978717
|
C | T | 2 | a0001c0001t0005g0014a0001c0001t0005g0015 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.398-16662C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26978717 | ||||||
| chr4:26978799
|
A | C | 1 | a0001c0001t0004g0232 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.398-16580A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26978799 | ||||||
| chr4:26978876
|
G | A | 1 | a0001c0001t0036g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.398-16503G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26978876 | ||||||
| chr4:26979052
|
C | T | 1 | a0001c0001t0003g0159 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.398-16327C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26979052 | ||||||
| chr4:26979097
|
G | A | 328 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(325): Show | 330 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(327): Show |
intron_variant | MODIFIER | c.398-16282G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26979097 | ||||||
| chr4:26979171
|
C | T | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-16208C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26979171 | ||||||
| chr4:26979341
|
T | G | 1 | a0001c0001t0008g0028 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.398-16038T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26979341 | ||||||
| chr4:26979443
|
C | A | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-15936C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26979443 | ||||||
| chr4:26979684
|
T | C | 1 | a0001c0001t0003g0182 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.398-15695T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26979684 | ||||||
| chr4:26979818
|
G | T | 1 | a0001c0001t0007g0278 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.398-15561G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26979818 | ||||||
| chr4:26980031
|
C | T | 1 | a0001c0001t0006g0116 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.398-15348C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26980031 | ||||||
| chr4:26980039
|
C | T | 1 | a0001c0001t0004g0267 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.398-15340C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26980039 | ||||||
| chr4:26980184
|
A | G | 1 | a0001c0001t0004g0259 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.398-15195A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26980184 | ||||||
| chr4:26980497
|
C | A | 1 | a0001c0001t0003g0201 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.398-14882C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26980497 | ||||||
| chr4:26980606
|
A | G | 2 | a0001c0001t0033g0144a0001c0001t0036g0016 | 2 | HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.398-14773A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26980606 | ||||||
| chr4:26980607
|
C | G | 3 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0048 | 3 | HG00738.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.398-14772C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26980607 | ||||||
| chr4:26980644
|
A | G | 1 | a0001c0001t0002g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.398-14735A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26980644 | ||||||
| chr4:26980932
|
A | G | 3 | a0001c0001t0013g0218a0001c0001t0030g0195a0001c0001t0045g0183 | 3 | HG02922.hp2 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.398-14447A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26980932 | ||||||
| chr4:26980939
|
C | A | 3 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0110 | 3 | HG02486.hp2 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.398-14440C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26980939 | ||||||
| chr4:26980958
|
C | T | 1 | a0001c0001t0010g0327 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.398-14421C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26980958 | ||||||
| chr4:26981007
|
T | G | 325 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.398-14372T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26981007 | ||||||
| chr4:26981231
|
C | A | 1 | a0001c0001t0024g0308 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.398-14148C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26981231 | ||||||
| chr4:26981280
|
A | G | 1 | a0001c0001t0012g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.398-14099A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26981280 | ||||||
| chr4:26981402
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.398-13977C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26981402 | ||||||
| chr4:26981556
|
C | T | 4 | a0001c0001t0012g0215a0001c0001t0012g0222a0001c0001t0012g0223others(1): Show | 4 | HG02145.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-13823C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26981556 | ||||||
| chr4:26981633
|
C | T | 1 | a0001c0001t0009g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.398-13746C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26981633 | ||||||
| chr4:26981634
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.398-13745G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26981634 | ||||||
| chr4:26981843
|
T | C | 1 | a0001c0001t0002g0317 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.398-13536T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26981843 | ||||||
| chr4:26981934
|
A | G | 1 | a0001c0001t0003g0157 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.398-13445A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26981934 | ||||||
| chr4:26981969
|
C | CT | 184 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(181): Show | 185 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.398-13398dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26981969 | |||||
| chr4:26982131
|
C | T | 120 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0281others(117): Show | 121 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.398-13248C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26982131 | ||||||
| chr4:26982223
|
T | TTGAA | 5 | a0001c0001t0001g0319a0001c0001t0012g0215a0001c0001t0012g0222others(2): Show | 5 | HG01433.hp2 HG02145.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-13155_398-1315 others(8): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26982223 | |||||
| chr4:26982308
|
C | T | 4 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019others(1): Show | 4 | HG00741.hp1 HG02572.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-13071C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26982308 | ||||||
| chr4:26982407
|
A | G | 1 | a0001c0001t0024g0308 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.398-12972A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26982407 | ||||||
| chr4:26982913
|
T | C | 1 | a0001c0001t0041g0235 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.398-12466T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26982913 | ||||||
| chr4:26983194
|
G | A | 1 | a0001c0001t0024g0308 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.398-12185G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26983194 | ||||||
| chr4:26983383
|
G | A | 325 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.398-11996G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26983383 | ||||||
| chr4:26983668
|
A | T | 95 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0006others(92): Show | 96 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.398-11711A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26983668 | ||||||
| chr4:26983785
|
C | T | 1 | a0001c0001t0004g0231 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.398-11594C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26983785 | ||||||
| chr4:26983891
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-11488A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26983891 | ||||||
| chr4:26983981
|
A | C | 2 | a0001c0001t0003g0190a0001c0001t0003g0191 | 2 | NA19085.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.398-11398A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26983981 | ||||||
| chr4:26984019
|
A | G | 125 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0306others(122): Show | 126 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.398-11360A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26984019 | ||||||
| chr4:26984050
|
A | G | 2 | a0001c0001t0009g0328a0001c0001t0019g0150 | 2 | HG01261.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.398-11329A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26984050 | ||||||
| chr4:26984359
|
A | G | 166 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0306others(163): Show | 167 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.398-11020A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26984359 | ||||||
| chr4:26984566
|
T | C | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-10813T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26984566 | ||||||
| chr4:26984585
|
G | A | 2 | a0001c0001t0005g0014a0001c0001t0005g0015 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.398-10794G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26984585 | ||||||
| chr4:26984796
|
C | T | 1 | a0001c0001t0003g0170 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.398-10583C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26984796 | ||||||
| chr4:26984979
|
C | T | 2 | a0001c0001t0033g0144a0001c0001t0036g0016 | 2 | HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.398-10400C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26984979 | ||||||
| chr4:26985115
|
A | G | 325 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.398-10264A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26985115 | ||||||
| chr4:26985157
|
G | A | 1 | a0001c0005t0002g0088 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.398-10222G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26985157 | ||||||
| chr4:26985201
|
G | T | 1 | a0001c0001t0001g0139 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.398-10178G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26985201 | ||||||
| chr4:26985228
|
C | T | 1 | a0001c0002t0009g0114 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.398-10151C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26985228 | ||||||
| chr4:26985375
|
A | AT | 5 | a0001c0001t0005g0208a0001c0001t0005g0209a0001c0001t0005g0210others(2): Show | 5 | HG02615.hp1 HG02717.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-9998dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26985375 | |||||
| chr4:26985436
|
C | A | 5 | a0001c0001t0005g0034a0001c0001t0005g0080a0001c0001t0005g0096others(2): Show | 5 | HG01981.hp2 NA18951.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.398-9943C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26985436 | ||||||
| chr4:26985472
|
A | G | 2 | a0001c0001t0002g0089a0001c0005t0002g0088 | 2 | HG00544.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.398-9907A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26985472 | ||||||
| chr4:26985480
|
A | G | 2 | a0001c0001t0009g0328a0001c0001t0019g0150 | 2 | HG01261.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.398-9899A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26985480 | ||||||
| chr4:26985484
|
C | T | 4 | a0001c0001t0005g0206a0001c0001t0007g0203a0001c0001t0021g0204others(1): Show | 4 | HG01884.hp2 HG01891.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-9895C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26985484 | ||||||
| chr4:26985912
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.398-9467A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26985912 | ||||||
| chr4:26986017
|
C | T | 11 | a0001c0001t0002g0207a0001c0001t0002g0277a0001c0001t0002g0310others(8): Show | 11 | HG02129.hp2 NA18957.hp2 NA18965.hp1 others(8): Show |
intron_variant | MODIFIER | c.398-9362C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26986017 | ||||||
| chr4:26986039
|
G | C | 1 | a0001c0001t0002g0290 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.398-9340G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26986039 | ||||||
| chr4:26986040
|
C | T | 1 | a0001c0001t0002g0290 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.398-9339C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26986040 | ||||||
| chr4:26986139
|
A | G | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.398-9240A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26986139 | ||||||
| chr4:26986403
|
A | G | 3 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019 | 3 | HG00741.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.398-8976A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26986403 | ||||||
| chr4:26986505
|
G | A | 108 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(105): Show | 109 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.398-8874G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26986505 | ||||||
| chr4:26986515
|
A | G | 2 | a0001c0001t0003g0190a0001c0001t0003g0191 | 2 | NA19085.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.398-8864A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26986515 | ||||||
| chr4:26986635
|
C | T | 6 | a0001c0001t0011g0213a0001c0001t0011g0214a0001c0001t0016g0017others(3): Show | 6 | HG00741.hp1 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.398-8744C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26986635 | ||||||
| chr4:26986743
|
T | C | 1 | a0001c0001t0036g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.398-8636T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26986743 | ||||||
| chr4:26986847
|
A | G | 1 | a0001c0001t0009g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.398-8532A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26986847 | ||||||
| chr4:26987216
|
T | G | 2 | a0001c0001t0033g0144a0001c0001t0036g0016 | 2 | HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.398-8163T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26987216 | ||||||
| chr4:26987219
|
G | A | 7 | a0001c0001t0005g0206a0001c0001t0007g0108a0001c0001t0007g0109others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-8160G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26987219 | ||||||
| chr4:26987349
|
G | A | 1 | a0001c0001t0036g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.398-8030G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26987349 | ||||||
| chr4:26987389
|
G | A | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.398-7990G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26987389 | ||||||
| chr4:26987406
|
A | G | 118 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0006others(115): Show | 119 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.398-7973A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26987406 | ||||||
| chr4:26987462
|
T | C | 1 | a0001c0001t0035g0289 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.398-7917T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26987462 | ||||||
| chr4:26987481
|
A | G | 1 | a0001c0001t0028g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.398-7898A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26987481 | ||||||
| chr4:26987521
|
G | A | 1 | a0001c0001t0003g0158 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.398-7858G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26987521 | ||||||
| chr4:26987695
|
T | C | 1 | a0001c0001t0012g0221 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.398-7684T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26987695 | ||||||
| chr4:26987832
|
G | A | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(1): Show | 4 | HG02647.hp2 HG02723.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-7547G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26987832 | ||||||
| chr4:26988020
|
G | A | 1 | a0001c0001t0002g0314 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.398-7359G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26988020 | ||||||
| chr4:26988083
|
G | A | 1 | a0001c0001t0009g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.398-7296G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26988083 | ||||||
| chr4:26988130
|
T | C | 1 | a0001c0001t0002g0314 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.398-7249T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26988130 | ||||||
| chr4:26988186
|
A | G | 1 | a0001c0001t0005g0034 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.398-7193A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26988186 | ||||||
| chr4:26988549
|
T | G | 1 | a0001c0001t0004g0257 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.398-6830T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26988549 | ||||||
| chr4:26988629
|
G | A | 1 | a0001c0001t0003g0165 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.398-6750G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26988629 | ||||||
| chr4:26988716
|
A | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0038 | 3 | NA18612.hp1 NA18944.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.398-6663A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26988716 | ||||||
| chr4:26988951
|
G | T | 2 | a0001c0001t0005g0014a0001c0001t0005g0015 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.398-6428G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26988951 | ||||||
| chr4:26988963
|
C | T | 1 | a0001c0001t0002g0303 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.398-6416C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26988963 | ||||||
| chr4:26988966
|
A | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.398-6413A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26988966 | ||||||
| chr4:26988996
|
G | T | 24 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0024others(21): Show | 24 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.398-6383G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26988996 | ||||||
| chr4:26989006
|
C | G | 2 | a0001c0001t0009g0328a0001c0001t0019g0150 | 2 | HG01261.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.398-6373C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26989006 | ||||||
| chr4:26989056
|
T | C | 2 | a0001c0001t0013g0217a0001c0001t0013g0219 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.398-6323T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26989056 | ||||||
| chr4:26989141
|
G | T | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-6238G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26989141 | ||||||
| chr4:26989355
|
C | A | 1 | a0001c0001t0012g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.398-6024C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26989355 | ||||||
| chr4:26989507
|
C | A | 1 | a0001c0001t0002g0314 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.398-5872C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26989507 | ||||||
| chr4:26989543
|
A | C | 163 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0306others(160): Show | 164 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.398-5836A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26989543 | ||||||
| chr4:26989578
|
C | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.398-5801C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26989578 | ||||||
| chr4:26989777
|
A | C | 161 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0006others(158): Show | 162 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.398-5602A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26989777 | ||||||
| chr4:26989936
|
A | G | 3 | a0001c0001t0006g0116a0001c0001t0006g0247a0001c0001t0006g0253 | 3 | HG01074.hp2 HG01167.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.398-5443A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26989936 | ||||||
| chr4:26989968
|
A | C | 1 | a0001c0001t0004g0243 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.398-5411A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26989968 | ||||||
| chr4:26989983
|
T | C | 1 | a0001c0001t0002g0295 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.398-5396T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26989983 | ||||||
| chr4:26990151
|
AT | A | 184 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0281others(181): Show | 185 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.398-5226delT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26990151 | |||||
| chr4:26990459
|
T | G | 1 | a0001c0001t0002g0207 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.398-4920T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26990459 | ||||||
| chr4:26990554
|
G | C | 123 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0281others(120): Show | 124 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.398-4825G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26990554 | ||||||
| chr4:26990715
|
A | G | 3 | a0001c0001t0013g0218a0001c0001t0030g0195a0001c0001t0045g0183 | 3 | HG02922.hp2 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.398-4664A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26990715 | ||||||
| chr4:26990806
|
G | A | 120 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0281others(117): Show | 121 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.398-4573G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26990806 | ||||||
| chr4:26991429
|
G | A | 1 | a0001c0001t0009g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.398-3950G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26991429 | ||||||
| chr4:26991651
|
T | G | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.398-3728T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26991651 | ||||||
| chr4:26991970
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0057 | 2 | HG00621.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.398-3409G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26991970 | ||||||
| chr4:26992117
|
G | A | 325 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.398-3262G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26992117 | ||||||
| chr4:26992136
|
T | C | 3 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0007g0110 | 3 | HG02486.hp2 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.398-3243T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26992136 | ||||||
| chr4:26992172
|
A | G | 118 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0006others(115): Show | 119 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.398-3207A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26992172 | ||||||
| chr4:26992341
|
A | G | 1 | a0001c0001t0012g0222 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.398-3038A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26992341 | ||||||
| chr4:26992448
|
C | T | 1 | a0001c0002t0013g0099 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.398-2931C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26992448 | ||||||
| chr4:26992522
|
T | C | 155 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0006others(152): Show | 156 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.398-2857T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26992522 | ||||||
| chr4:26992891
|
C | A | 7 | a0001c0001t0005g0206a0001c0001t0007g0108a0001c0001t0007g0109others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-2488C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26992891 | ||||||
| chr4:26992892
|
G | A | 5 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(2): Show | 5 | HG02071.hp1 HG02083.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-2487G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26992892 | ||||||
| chr4:26992919
|
T | C | 2 | a0001c0001t0003g0190a0001c0001t0003g0191 | 2 | NA19085.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.398-2460T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26992919 | ||||||
| chr4:26993175
|
A | G | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.398-2204A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26993175 | ||||||
| chr4:26993377
|
A | G | 11 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0148others(8): Show | 11 | HG00642.hp2 HG01071.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.398-2002A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26993377 | ||||||
| chr4:26993541
|
AT | A | 325 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.398-1831delT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 26993541 | |||||
| chr4:26993821
|
A | G | 1 | a0001c0002t0026g0102 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.398-1558A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26993821 | ||||||
| chr4:26994021
|
T | A | 1 | a0001c0001t0009g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.398-1358T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26994021 | ||||||
| chr4:26994222
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.398-1157A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26994222 | ||||||
| chr4:26994279
|
G | A | 7 | a0001c0001t0003g0151a0001c0001t0003g0162a0001c0001t0003g0166others(4): Show | 7 | HG00642.hp1 HG00741.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.398-1100G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26994279 | ||||||
| chr4:26994385
|
G | A | 180 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(177): Show | 181 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.398-994G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26994385 | ||||||
| chr4:26994572
|
A | G | 3 | a0001c0001t0005g0034a0001c0001t0005g0080a0001c0001t0005g0096 | 3 | NA18951.hp1 NA19007.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.398-807A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26994572 | ||||||
| chr4:26994635
|
G | C | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(1): Show | 4 | HG02647.hp2 HG02723.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-744G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26994635 | ||||||
| chr4:26994641
|
T | C | 1 | a0001c0001t0003g0170 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.398-738T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26994641 | ||||||
| chr4:26994885
|
A | G | 6 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(3): Show | 6 | HG02027.hp1 HG02071.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.398-494A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26994885 | ||||||
| chr4:26994919
|
G | T | 11 | a0001c0001t0002g0207a0001c0001t0002g0277a0001c0001t0002g0310others(8): Show | 11 | HG02129.hp2 NA18957.hp2 NA18965.hp1 others(8): Show |
intron_variant | MODIFIER | c.398-460G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26994919 | ||||||
| chr4:26995161
|
T | A | 1 | a0001c0001t0003g0192 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.398-218T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26995161 | ||||||
| chr4:26995243
|
T | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.398-136T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26995243 | ||||||
| chr4:26995257
|
G | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.398-122G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26995257 | ||||||
| chr4:26995259
|
A | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.398-120A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26995259 | ||||||
| chr4:26995605
|
T | C | 3 | a0001c0001t0004g0251a0001c0001t0004g0265a0001c0001t0004g0266 | 3 | HG01261.hp2 HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.509+115T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26995605 | ||||||
| chr4:26995853
|
G | A | 125 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0306others(122): Show | 126 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.509+363G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26995853 | ||||||
| chr4:26995901
|
G | A | 1 | a0001c0001t0003g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.509+411G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26995901 | ||||||
| chr4:26996007
|
A | T | 6 | a0001c0001t0014g0119a0001c0001t0014g0121a0001c0001t0014g0122others(3): Show | 6 | HG00642.hp2 HG01071.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.509+517A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26996007 | ||||||
| chr4:26996276
|
T | C | 1 | a0001c0001t0011g0087 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.509+786T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26996276 | ||||||
| chr4:26996828
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.509+1338T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26996828 | ||||||
| chr4:26996837
|
A | G | 1 | a0001c0001t0002g0323 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.509+1347A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26996837 | ||||||
| chr4:26996892
|
ACAGT | A | 3 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0012g0221 | 3 | HG02280.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.509+1407_509+1410d others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 26996892 | |||||
| chr4:26996944
|
G | A | 1 | a0001c0001t0004g0260 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.509+1454G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26996944 | ||||||
| chr4:26996994
|
A | G | 1 | a0001c0001t0009g0328 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.509+1504A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26996994 | ||||||
| chr4:26997014
|
G | A | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.509+1524G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26997014 | ||||||
| chr4:26997127
|
A | G | 1 | a0001c0001t0003g0157 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.509+1637A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26997127 | ||||||
| chr4:26997232
|
A | G | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+1742A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26997232 | ||||||
| chr4:26997516
|
G | A | 1 | a0001c0001t0003g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.510-1716G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26997516 | ||||||
| chr4:26997538
|
G | A | 1 | a0001c0001t0002g0315 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.510-1694G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26997538 | ||||||
| chr4:26997546
|
T | C | 3 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019 | 3 | HG00741.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.510-1686T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26997546 | ||||||
| chr4:26997809
|
A | T | 5 | a0001c0001t0001g0319a0001c0001t0012g0215a0001c0001t0012g0222others(2): Show | 5 | HG01433.hp2 HG02145.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-1423A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26997809 | ||||||
| chr4:26997831
|
G | C | 13 | a0001c0001t0005g0206a0001c0001t0007g0108a0001c0001t0007g0109others(10): Show | 13 | HG00642.hp2 HG01071.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.510-1401G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26997831 | ||||||
| chr4:26998117
|
C | A | 1 | a0001c0001t0003g0196 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.510-1115C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26998117 | ||||||
| chr4:26998188
|
T | C | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-1044T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26998188 | ||||||
| chr4:26998252
|
C | T | 1 | a0001c0003t0001g0285 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.510-980C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26998252 | ||||||
| chr4:26998302
|
G | A | 2 | a0001c0002t0009g0114a0001c0002t0009g0115 | 2 | HG01106.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.510-930G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26998302 | ||||||
| chr4:26998303
|
T | A | 13 | a0001c0001t0005g0206a0001c0001t0007g0108a0001c0001t0007g0109others(10): Show | 13 | HG00642.hp2 HG01071.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.510-929T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26998303 | ||||||
| chr4:26998416
|
T | C | 1 | a0001c0001t0004g0252 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.510-816T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26998416 | ||||||
| chr4:26998633
|
C | T | 1 | a0001c0001t0003g0158 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.510-599C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26998633 | ||||||
| chr4:26998726
|
C | G | 1 | a0001c0001t0014g0123 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.510-506C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26998726 | ||||||
| chr4:26998753
|
A | G | 3 | a0001c0001t0005g0291a0001c0001t0005g0300a0001c0001t0005g0301 | 3 | NA18953.hp1 NA18970.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.510-479A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26998753 | ||||||
| chr4:26998773
|
G | A | 1 | a0001c0001t0004g0243 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.510-459G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26998773 | ||||||
| chr4:26998843
|
C | T | 2 | a0001c0001t0002g0127a0001c0001t0002g0128 | 2 | HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.510-389C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26998843 | ||||||
| chr4:26998911
|
C | CA | 100 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(97): Show | 101 | HG00438.hp2 HG00621.hp1 HG00733.hp2 others(98): Show |
intron_variant | MODIFIER | c.510-310dupA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 26998911 | |||||
| chr4:26998911
|
C | CAA | 46 | a0001c0001t0004g0117a0001c0001t0004g0226a0001c0001t0004g0227others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.510-311_510-310dup others(2): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 26998911 | |||||
| chr4:26998911
|
C | CAAAAA | 167 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0281others(164): Show | 168 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.510-314_510-310dup others(5): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 26998911 | |||||
| chr4:26998911
|
C | CAAAAAA | 7 | a0001c0001t0005g0206a0001c0001t0007g0203a0001c0001t0015g0330others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.510-315_510-310dup others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 26998911 | |||||
| chr4:26998913
|
A | G | 2 | a0001c0001t0009g0328a0001c0001t0019g0150 | 2 | HG01261.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.510-319A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26998913 | ||||||
| chr4:26998923
|
T | A | 2 | a0001c0001t0005g0014a0001c0001t0005g0015 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.510-309T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26998923 | ||||||
| chr4:26999111
|
A | C | 1 | a0001c0001t0008g0094 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.510-121A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26999111 | ||||||
| chr4:26999118
|
A | T | 2 | a0001c0001t0001g0098a0001c0001t0001g0148 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.510-114A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26999118 | ||||||
| chr4:26999181
|
T | C | 1 | a0001c0001t0004g0117 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.510-51T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26999181 | ||||||
| chr4:26999183
|
T | C | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-49T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 4/11 | chr4 | 26999183 | ||||||
| chr4:26999373
|
A | G | 76 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0004g0117others(73): Show | 77 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.625+26A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | chr4 | 26999373 | ||||||
| chr4:26999409
|
T | C | 1 | a0001c0001t0015g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.625+62T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | chr4 | 26999409 | ||||||
| chr4:26999556
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.625+209A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | chr4 | 26999556 | ||||||
| chr4:26999843
|
A | C | 3 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019 | 3 | HG00741.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.625+496A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | chr4 | 26999843 | ||||||
| chr4:26999940
|
G | T | 1 | a0001c0001t0002g0153 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.625+593G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | chr4 | 26999940 | ||||||
| chr4:27000052
|
GT | G | 142 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0306others(139): Show | 143 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.625+717delT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 27000052 | |||||
| chr4:27000082
|
A | G | 161 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0006others(158): Show | 162 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.625+735A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | chr4 | 27000082 | ||||||
| chr4:27000337
|
G | A | 3 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019 | 3 | HG00741.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.625+990G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | chr4 | 27000337 | ||||||
| chr4:27000454
|
G | A | 1 | a0001c0001t0004g0243 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.625+1107G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | chr4 | 27000454 | ||||||
| chr4:27000733
|
A | G | 1 | a0001c0001t0010g0100 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.625+1386A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | chr4 | 27000733 | ||||||
| chr4:27000743
|
A | G | 1 | a0001c0001t0004g0226 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.625+1396A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | chr4 | 27000743 | ||||||
| chr4:27000814
|
GT | G | 316 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(313): Show | 318 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(315): Show |
intron_variant | MODIFIER | c.626-1390delT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 27000814 | |||||
| chr4:27000869
|
C | G | 1 | a0001c0003t0001g0285 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.626-1348C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | chr4 | 27000869 | ||||||
| chr4:27000887
|
G | A | 1 | a0001c0001t0005g0003 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.626-1330G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | chr4 | 27000887 | ||||||
| chr4:27000942
|
T | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.626-1275T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | chr4 | 27000942 | ||||||
| chr4:27001021
|
G | C | 1 | a0001c0001t0002g0295 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.626-1196G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | chr4 | 27001021 | ||||||
| chr4:27001116
|
C | T | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.626-1101C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | chr4 | 27001116 | ||||||
| chr4:27001185
|
G | A | 3 | a0001c0001t0013g0218a0001c0001t0030g0195a0001c0001t0045g0183 | 3 | HG02922.hp2 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.626-1032G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | chr4 | 27001185 | ||||||
| chr4:27001212
|
G | A | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.626-1005G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | chr4 | 27001212 | ||||||
| chr4:27001330
|
G | A | 1 | a0001c0001t0034g0120 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.626-887G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | chr4 | 27001330 | ||||||
| chr4:27001374
|
C | G | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.626-843C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | chr4 | 27001374 | ||||||
| chr4:27001552
|
C | T | 1 | a0001c0001t0004g0228 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.626-665C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | chr4 | 27001552 | ||||||
| chr4:27001667
|
A | G | 1 | a0001c0001t0005g0014 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.626-550A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | chr4 | 27001667 | ||||||
| chr4:27001844
|
A | T | 2 | a0001c0001t0007g0248a0001c0001t0007g0254 | 2 | HG00597.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.626-373A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | chr4 | 27001844 | ||||||
| chr4:27001846
|
T | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.626-371T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | chr4 | 27001846 | ||||||
| chr4:27001984
|
G | A | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(1): Show | 4 | HG02647.hp2 HG02723.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.626-233G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 5/11 | chr4 | 27001984 | ||||||
| chr4:27002700
|
G | A | 1 | a0001c0001t0004g0240 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.804-227G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 6/11 | chr4 | 27002700 | ||||||
| chr4:27002799
|
T | C | 3 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0148 | 3 | HG02258.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.804-128T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 6/11 | chr4 | 27002799 | ||||||
| chr4:27002868
|
T | TA | 163 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0006others(160): Show | 164 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.804-50dupA | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 27002868 | |||||
| chr4:27003115
|
T | G | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.981+11T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27003115 | ||||||
| chr4:27003305
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.981+201A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27003305 | ||||||
| chr4:27003315
|
C | T | 5 | a0001c0001t0003g0188a0001c0001t0003g0196a0001c0001t0003g0200others(2): Show | 5 | HG00099.hp1 HG01175.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.981+211C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27003315 | ||||||
| chr4:27003317
|
C | A | 1 | a0001c0001t0036g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.981+213C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27003317 | ||||||
| chr4:27003392
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.981+288T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27003392 | ||||||
| chr4:27003613
|
A | G | 118 | a0001c0001t0002g0026a0001c0001t0002g0064a0001c0001t0002g0065others(115): Show | 119 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.981+509A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27003613 | ||||||
| chr4:27003644
|
A | G | 3 | a0001c0001t0004g0227a0001c0001t0004g0262a0001c0001t0004g0271 | 3 | HG00597.hp1 NA18747.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.981+540A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27003644 | ||||||
| chr4:27003648
|
A | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.981+544A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27003648 | ||||||
| chr4:27003693
|
C | T | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.981+589C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27003693 | ||||||
| chr4:27003804
|
A | G | 1 | a0001c0003t0001g0285 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.981+700A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27003804 | ||||||
| chr4:27003884
|
C | A | 325 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.981+780C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27003884 | ||||||
| chr4:27004133
|
A | G | 1 | a0001c0001t0002g0292 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.981+1029A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27004133 | ||||||
| chr4:27004296
|
T | C | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.981+1192T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27004296 | ||||||
| chr4:27004390
|
G | A | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0007g0254 | 3 | HG03490.hp1 HG03492.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.981+1286G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27004390 | ||||||
| chr4:27004489
|
C | A | 138 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(135): Show | 139 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.981+1385C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27004489 | ||||||
| chr4:27004510
|
A | G | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.981+1406A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27004510 | ||||||
| chr4:27004540
|
T | C | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.981+1436T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27004540 | ||||||
| chr4:27004834
|
A | C | 1 | a0001c0001t0040g0079 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.981+1730A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27004834 | ||||||
| chr4:27004954
|
C | G | 3 | a0001c0001t0007g0091a0001c0001t0007g0145a0001c0001t0007g0146 | 3 | HG01243.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.981+1850C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27004954 | ||||||
| chr4:27005029
|
T | G | 161 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0006others(158): Show | 162 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.981+1925T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27005029 | ||||||
| chr4:27005367
|
C | T | 1 | a0001c0001t0009g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.982-2166C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27005367 | ||||||
| chr4:27005773
|
T | C | 2 | a0001c0001t0014g0122a0001c0002t0023g0155 | 2 | HG00733.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.982-1760T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27005773 | ||||||
| chr4:27005883
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.982-1650T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27005883 | ||||||
| chr4:27006108
|
A | G | 2 | a0001c0001t0002g0089a0001c0005t0002g0088 | 2 | HG00544.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.982-1425A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27006108 | ||||||
| chr4:27006263
|
G | A | 1 | a0001c0001t0004g0257 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.982-1270G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27006263 | ||||||
| chr4:27006459
|
G | A | 1 | a0001c0001t0009g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.982-1074G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27006459 | ||||||
| chr4:27006468
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.982-1065G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27006468 | ||||||
| chr4:27006802
|
C | T | 4 | a0001c0001t0004g0272a0001c0001t0006g0116a0001c0001t0006g0247others(1): Show | 4 | HG01074.hp2 HG01167.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.982-731C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27006802 | ||||||
| chr4:27006902
|
G | A | 328 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(325): Show | 330 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(327): Show |
intron_variant | MODIFIER | c.982-631G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27006902 | ||||||
| chr4:27006941
|
G | C | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.982-592G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27006941 | ||||||
| chr4:27007029
|
G | A | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.982-504G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27007029 | ||||||
| chr4:27007036
|
A | T | 2 | a0001c0001t0007g0145a0001c0001t0007g0146 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.982-497A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27007036 | ||||||
| chr4:27007177
|
CT | C | 10 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(7): Show | 10 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.982-348delT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 27007177 | |||||
| chr4:27007184
|
T | C | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(1): Show | 4 | HG02647.hp2 HG02723.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.982-349T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27007184 | ||||||
| chr4:27007316
|
A | AT | 59 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(56): Show | 59 | HG00438.hp2 HG00621.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.982-201dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 27007316 | |||||
| chr4:27007502
|
C | T | 1 | a0001c0001t0035g0289 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.982-31C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 7/11 | chr4 | 27007502 | ||||||
| chr4:27007757
|
G | C | 1 | a0001c0001t0007g0110 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1149+57G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 8/11 | chr4 | 27007757 | ||||||
| chr4:27008020
|
G | A | 1 | a0001c0001t0021g0205 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1149+320G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 8/11 | chr4 | 27008020 | ||||||
| chr4:27008058
|
A | G | 2 | a0001c0001t0021g0204a0001c0001t0021g0205 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1149+358A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 8/11 | chr4 | 27008058 | ||||||
| chr4:27008070
|
C | T | 1 | a0001c0001t0006g0001 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1150-358C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 8/11 | chr4 | 27008070 | ||||||
| chr4:27008137
|
A | G | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(1): Show | 4 | HG02647.hp2 HG02723.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150-291A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 8/11 | chr4 | 27008137 | ||||||
| chr4:27008180
|
A | G | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG00733.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1150-248A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 8/11 | chr4 | 27008180 | ||||||
| chr4:27008192
|
AAG | A | 29 | a0001c0001t0003g0002a0001c0001t0003g0111a0001c0001t0003g0156others(26): Show | 30 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1150-232_1150-231d others(4): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 27008192 | |||||
| chr4:27008249
|
C | T | 1 | a0001c0001t0002g0292 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1150-179C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 8/11 | chr4 | 27008249 | ||||||
| chr4:27008398
|
T | C | 2 | a0001c0001t0033g0144a0001c0001t0036g0016 | 2 | HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1150-30T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 8/11 | chr4 | 27008398 | ||||||
| chr4:27008676
|
G | A | 3 | a0001c0001t0014g0119a0001c0001t0014g0121a0001c0001t0014g0122 | 3 | HG00642.hp2 HG03669.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1251-88G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 9/11 | chr4 | 27008676 | ||||||
| chr4:27009226
|
CACTT | C | 4 | a0001c0001t0015g0330a0001c0001t0015g0331a0001c0001t0015g0332others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1489+225_1489+228d others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27009226 | ||||||
| chr4:27009399
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1489+397A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27009399 | ||||||
| chr4:27009430
|
C | CTGA | 7 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(4): Show | 7 | HG00544.hp2 HG02015.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.1489+429_1489+431d others(5): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 27009430 | |||||
| chr4:27009600
|
A | G | 1 | a0001c0001t0004g0249 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1489+598A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27009600 | ||||||
| chr4:27009699
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0057 | 2 | HG00621.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.1489+697A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27009699 | ||||||
| chr4:27009735
|
G | A | 118 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0006others(115): Show | 119 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.1489+733G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27009735 | ||||||
| chr4:27009920
|
T | A | 118 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0006others(115): Show | 119 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.1489+918T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27009920 | ||||||
| chr4:27009946
|
T | C | 1 | a0001c0001t0034g0120 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1489+944T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27009946 | ||||||
| chr4:27009999
|
G | A | 118 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0006others(115): Show | 119 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.1489+997G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27009999 | ||||||
| chr4:27010037
|
A | C | 11 | a0001c0001t0003g0111a0001c0001t0003g0156a0001c0001t0003g0157others(8): Show | 11 | HG01361.hp2 HG01975.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.1489+1035A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27010037 | ||||||
| chr4:27010104
|
A | T | 1 | a0001c0003t0001g0285 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1489+1102A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27010104 | ||||||
| chr4:27010170
|
G | A | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1489+1168G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27010170 | ||||||
| chr4:27010179
|
C | T | 6 | a0001c0001t0014g0119a0001c0001t0014g0121a0001c0001t0014g0122others(3): Show | 6 | HG00642.hp2 HG01071.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.1489+1177C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27010179 | ||||||
| chr4:27010317
|
G | A | 1 | a0001c0001t0004g0252 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1489+1315G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27010317 | ||||||
| chr4:27010359
|
G | A | 2 | a0001c0001t0002g0127a0001c0001t0002g0128 | 2 | HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1489+1357G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27010359 | ||||||
| chr4:27010422
|
C | T | 9 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0148others(6): Show | 9 | HG00642.hp2 HG01071.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1489+1420C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27010422 | ||||||
| chr4:27010452
|
AAAAG | A | 3 | a0001c0001t0016g0017a0001c0001t0016g0018a0001c0001t0016g0019 | 3 | HG00741.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1489+1458_1489+146 others(8): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 27010452 | |||||
| chr4:27010659
|
C | A | 3 | a0001c0001t0002g0292a0001c0001t0002g0299a0001c0001t0002g0315 | 3 | HG00423.hp2 HG02056.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1489+1657C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27010659 | ||||||
| chr4:27010789
|
A | C | 1 | a0001c0003t0001g0285 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1489+1787A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27010789 | ||||||
| chr4:27010829
|
C | T | 16 | a0001c0001t0004g0252a0001c0001t0006g0001a0001c0001t0006g0129others(13): Show | 17 | HG00735.hp1 HG01071.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1489+1827C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27010829 | ||||||
| chr4:27010837
|
A | T | 1 | a0001c0001t0004g0118 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1489+1835A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27010837 | ||||||
| chr4:27010985
|
C | G | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1489+1983C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27010985 | ||||||
| chr4:27011012
|
A | T | 1 | a0001c0001t0006g0001 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1489+2010A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27011012 | ||||||
| chr4:27011111
|
A | C | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1489+2109A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27011111 | ||||||
| chr4:27011119
|
C | G | 1 | a0001c0001t0001g0077 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1489+2117C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27011119 | ||||||
| chr4:27011201
|
G | T | 320 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(317): Show | 322 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(319): Show |
intron_variant | MODIFIER | c.1489+2199G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27011201 | ||||||
| chr4:27011338
|
C | T | 6 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(3): Show | 6 | HG02027.hp1 HG02071.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.1489+2336C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27011338 | ||||||
| chr4:27011349
|
T | C | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1489+2347T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27011349 | ||||||
| chr4:27011428
|
C | G | 5 | a0001c0001t0001g0319a0001c0001t0012g0215a0001c0001t0012g0222others(2): Show | 5 | HG01433.hp2 HG02145.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1489+2426C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27011428 | ||||||
| chr4:27011494
|
A | C | 2 | a0001c0001t0002g0127a0001c0001t0002g0128 | 2 | HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1489+2492A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27011494 | ||||||
| chr4:27011654
|
G | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1489+2652G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27011654 | ||||||
| chr4:27011918
|
A | G | 333 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(330): Show | 335 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(332): Show |
intron_variant | MODIFIER | c.1489+2916A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27011918 | ||||||
| chr4:27011979
|
C | T | 1 | a0001c0001t0003g0173 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1489+2977C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27011979 | ||||||
| chr4:27012014
|
G | A | 1 | a0001c0002t0026g0102 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1489+3012G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27012014 | ||||||
| chr4:27012055
|
A | G | 1 | a0001c0001t0009g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1489+3053A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27012055 | ||||||
| chr4:27012324
|
A | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1489+3322A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27012324 | ||||||
| chr4:27012382
|
G | A | 1 | a0001c0001t0003g0276 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1489+3380G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27012382 | ||||||
| chr4:27012387
|
C | A | 146 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(143): Show | 147 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.1489+3385C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27012387 | ||||||
| chr4:27012462
|
T | TC | 320 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(317): Show | 322 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(319): Show |
intron_variant | MODIFIER | c.1489+3460_1489+346 others(5): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27012462 | ||||||
| chr4:27012750
|
A | T | 1 | a0001c0001t0009g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1489+3748A>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27012750 | ||||||
| chr4:27012765
|
C | T | 1 | a0001c0002t0019g0107 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1489+3763C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27012765 | ||||||
| chr4:27012838
|
T | C | 138 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0006others(135): Show | 139 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.1489+3836T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27012838 | ||||||
| chr4:27013151
|
C | G | 1 | a0001c0001t0004g0257 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1489+4149C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27013151 | ||||||
| chr4:27013315
|
C | T | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1489+4313C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27013315 | ||||||
| chr4:27013423
|
A | G | 3 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0148 | 3 | HG02258.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1490-4288A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27013423 | ||||||
| chr4:27013490
|
C | T | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1490-4221C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27013490 | ||||||
| chr4:27014099
|
G | A | 73 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0226others(70): Show | 74 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1490-3612G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27014099 | ||||||
| chr4:27014165
|
C | T | 1 | a0001c0001t0003g0158 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1490-3546C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27014165 | ||||||
| chr4:27014183
|
T | G | 1 | a0001c0001t0003g0188 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1490-3528T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27014183 | ||||||
| chr4:27014377
|
C | A | 1 | a0001c0002t0013g0099 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1490-3334C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27014377 | ||||||
| chr4:27014483
|
T | G | 3 | a0001c0001t0001g0081a0001c0001t0001g0281a0001c0001t0001g0282 | 3 | HG02723.hp1 HG03195.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1490-3228T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27014483 | ||||||
| chr4:27014606
|
T | C | 5 | a0001c0001t0001g0319a0001c0001t0012g0215a0001c0001t0012g0222others(2): Show | 5 | HG01433.hp2 HG02145.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1490-3105T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27014606 | ||||||
| chr4:27014611
|
C | A | 1 | a0001c0001t0004g0273 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1490-3100C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27014611 | ||||||
| chr4:27014846
|
T | C | 139 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0006others(136): Show | 140 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1490-2865T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27014846 | ||||||
| chr4:27014858
|
A | G | 1 | a0001c0001t0005g0014 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1490-2853A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27014858 | ||||||
| chr4:27015043
|
A | G | 1 | a0001c0001t0002g0314 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1490-2668A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27015043 | ||||||
| chr4:27015442
|
TC | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0052a0001c0001t0001g0053others(4): Show | 7 | HG01169.hp1 HG02027.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1490-2268delC | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27015442 | ||||||
| chr4:27015443
|
C | T | 18 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0030others(15): Show | 18 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.1490-2268C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27015443 | ||||||
| chr4:27015596
|
C | T | 1 | a0001c0001t0008g0069 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1490-2115C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27015596 | ||||||
| chr4:27015789
|
GT | G | 138 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(135): Show | 139 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.1490-1907delT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 27015789 | |||||
| chr4:27015934
|
A | C | 1 | a0001c0001t0014g0122 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1490-1777A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27015934 | ||||||
| chr4:27016321
|
C | T | 2 | a0001c0001t0005g0014a0001c0001t0005g0015 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1490-1390C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27016321 | ||||||
| chr4:27016683
|
T | C | 1 | a0001c0001t0009g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1490-1028T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27016683 | ||||||
| chr4:27016815
|
G | C | 2 | a0001c0001t0009g0328a0001c0001t0019g0150 | 2 | HG01261.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1490-896G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27016815 | ||||||
| chr4:27016862
|
C | T | 29 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0025others(26): Show | 29 | HG00438.hp2 HG00621.hp1 HG02074.hp1 others(26): Show |
intron_variant | MODIFIER | c.1490-849C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27016862 | ||||||
| chr4:27016961
|
T | C | 320 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(317): Show | 322 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(319): Show |
intron_variant | MODIFIER | c.1490-750T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27016961 | ||||||
| chr4:27017135
|
A | G | 1 | a0001c0001t0034g0120 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1490-576A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27017135 | ||||||
| chr4:27017181
|
T | A | 1 | a0001c0001t0004g0117 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1490-530T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27017181 | ||||||
| chr4:27017321
|
T | C | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1490-390T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27017321 | ||||||
| chr4:27017623
|
C | T | 1 | a0001c0001t0037g0134 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1490-88C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27017623 | ||||||
| chr4:27017705
|
T | C | 1 | a0001c0001t0003g0159 | 1 | HG02965.hp1 | splice_region_variant&intron_variant | LOW | c.1490-6T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27017705 | ||||||
| chr4:27018052
|
G | A | 1 | a0001c0001t0040g0079 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1763+68G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27018052 | ||||||
| chr4:27018168
|
C | G | 6 | a0001c0001t0017g0185a0001c0001t0017g0186a0001c0001t0017g0187others(3): Show | 6 | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1763+184C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27018168 | ||||||
| chr4:27018299
|
T | G | 1 | a0001c0001t0003g0158 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1763+315T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27018299 | ||||||
| chr4:27018316
|
C | T | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1763+332C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27018316 | ||||||
| chr4:27018697
|
T | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1763+713T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27018697 | ||||||
| chr4:27019072
|
T | C | 161 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0006others(158): Show | 162 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.1763+1088T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27019072 | ||||||
| chr4:27019097
|
G | T | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(1): Show | 4 | HG02647.hp2 HG02723.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1763+1113G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27019097 | ||||||
| chr4:27019276
|
A | G | 2 | a0001c0001t0013g0217a0001c0001t0013g0219 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1763+1292A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27019276 | ||||||
| chr4:27019596
|
GAA | G | 3 | a0001c0001t0007g0091a0001c0001t0007g0145a0001c0001t0007g0146 | 3 | HG01243.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1763+1615_1763+161 others(6): Show |
STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 27019596 | |||||
| chr4:27019607
|
T | A | 1 | a0001c0001t0003g0200 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1763+1623T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27019607 | ||||||
| chr4:27019682
|
A | AT | 146 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(143): Show | 147 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.1763+1710dupT | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 27019682 | |||||
| chr4:27019806
|
G | C | 1 | a0001c0001t0033g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1763+1822G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27019806 | ||||||
| chr4:27019976
|
T | C | 1 | a0001c0001t0009g0126 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1763+1992T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27019976 | ||||||
| chr4:27020001
|
A | G | 1 | a0001c0001t0003g0194 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1763+2017A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27020001 | ||||||
| chr4:27020047
|
A | G | 1 | a0001c0001t0003g0196 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1763+2063A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27020047 | ||||||
| chr4:27020187
|
C | T | 328 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(325): Show | 330 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(327): Show |
intron_variant | MODIFIER | c.1763+2203C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27020187 | ||||||
| chr4:27020807
|
C | G | 1 | a0001c0001t0002g0317 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1764-1712C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27020807 | ||||||
| chr4:27020833
|
G | A | 43 | a0001c0001t0002g0026a0001c0001t0002g0064a0001c0001t0002g0065others(40): Show | 43 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.1764-1686G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27020833 | ||||||
| chr4:27020843
|
C | A | 1 | a0001c0001t0002g0321 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1764-1676C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27020843 | ||||||
| chr4:27021178
|
A | G | 328 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(325): Show | 330 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(327): Show |
intron_variant | MODIFIER | c.1764-1341A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27021178 | ||||||
| chr4:27021273
|
T | G | 2 | a0001c0001t0009g0328a0001c0001t0019g0150 | 2 | HG01261.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1764-1246T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27021273 | ||||||
| chr4:27021364
|
G | T | 6 | a0001c0001t0014g0119a0001c0001t0014g0121a0001c0001t0014g0122others(3): Show | 6 | HG00642.hp2 HG01071.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.1764-1155G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27021364 | ||||||
| chr4:27021423
|
A | G | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1764-1096A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27021423 | ||||||
| chr4:27021644
|
T | A | 1 | a0001c0001t0003g0182 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1764-875T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27021644 | ||||||
| chr4:27021725
|
C | T | 12 | a0001c0001t0005g0206a0001c0001t0007g0108a0001c0001t0007g0109others(9): Show | 12 | HG00642.hp2 HG01071.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1764-794C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27021725 | ||||||
| chr4:27021891
|
G | A | 1 | a0001c0001t0004g0118 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1764-628G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27021891 | ||||||
| chr4:27021922
|
A | G | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1764-597A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27021922 | ||||||
| chr4:27021948
|
T | A | 1 | a0001c0001t0003g0199 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1764-571T>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27021948 | ||||||
| chr4:27022004
|
C | T | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1764-515C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27022004 | ||||||
| chr4:27022013
|
G | A | 1 | a0001c0001t0007g0278 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1764-506G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27022013 | ||||||
| chr4:27022029
|
T | G | 3 | a0001c0001t0014g0119a0001c0001t0014g0121a0001c0001t0014g0122 | 3 | HG00642.hp2 HG03669.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1764-490T>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27022029 | ||||||
| chr4:27022152
|
C | T | 1 | a0001c0001t0032g0298 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1764-367C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27022152 | ||||||
| chr4:27022180
|
G | T | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0009g0279others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1764-339G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 11/11 | chr4 | 27022180 |