Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2238 | 323 | 75 | 55 | 151 | 8 | 33 | STIM2_chr4_26855841_27030381 | STIM2 | TTGCT others(2233): Show |
chr4 | 26855841 | 27030381 | ||
| a0001c0002 | 1/0 | 2238 | 9 | 5 | 3 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | TTGCT others(2233): Show |
chr4 | 26855841 | 27030381 | ||
| a0001c0003 | 0/0 | 2238 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | TTGCT others(2233): Show |
chr4 | 26855841 | 27030381 | ||
| a0001c0004 | 0/0 | 2238 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | TTGCT others(2233): Show |
chr4 | 26855841 | 27030381 | ||
| a0001c0005 | 0/0 | 2238 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | TTGCT others(2233): Show |
chr4 | 26855841 | 27030381 | ||
| a0001c0006 | 0/0 | 2238 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | TTGCT others(2233): Show |
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 | AGAGC others(4998): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0002 | 0/0 | 5004 | 51 | 6 | 3 | 38 | 1 | 3 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4999): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0003 | 0/0 | 5004 | 45 | 6 | 11 | 22 | 2 | 4 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4999): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0004 | 0/0 | 5003 | 40 | 1 | 5 | 25 | 1 | 8 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4998): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0005 | 0/0 | 5004 | 18 | 8 | 1 | 8 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4999): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0006 | 0/0 | 5002 | 12 | 0 | 6 | 4 | 2 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4997): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0007 | 0/0 | 5005 | 11 | 7 | 1 | 3 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(5000): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0008 | 0/0 | 5003 | 10 | 0 | 0 | 10 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4998): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0009 | 0/0 | 5002 | 5 | 2 | 1 | 0 | 0 | 2 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4997): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0010 | 0/0 | 5001 | 8 | 5 | 3 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4996): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0011 | 0/0 | 5004 | 6 | 2 | 0 | 4 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4999): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0012 | 0/0 | 5001 | 5 | 5 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4996): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0013 | 0/0 | 5000 | 3 | 3 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4995): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0014 | 0/0 | 5004 | 4 | 0 | 1 | 1 | 0 | 2 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4999): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0015 | 0/0 | 5004 | 4 | 4 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4999): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0016 | 0/0 | 5003 | 3 | 2 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4998): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0017 | 0/0 | 5004 | 3 | 0 | 3 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4999): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0018 | 0/0 | 5002 | 3 | 1 | 1 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4997): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0019 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4997): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0020 | 0/0 | 5003 | 2 | 0 | 1 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4998): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0021 | 0/0 | 5004 | 2 | 2 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4999): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0022 | 0/0 | 5004 | 2 | 0 | 0 | 2 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4999): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0023 | 0/0 | 5003 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4998): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0024 | 0/0 | 5005 | 2 | 0 | 0 | 0 | 1 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(5000): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0025 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4997): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0027 | 0/0 | 5003 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4998): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0028 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4997): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0029 | 0/0 | 5001 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4996): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0030 | 0/0 | 5001 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4996): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0031 | 0/0 | 5004 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4999): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0032 | 0/0 | 5003 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4998): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0033 | 0/0 | 5005 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(5000): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0034 | 0/0 | 5004 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4999): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0035 | 0/0 | 5004 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4999): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0036 | 0/0 | 5004 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4999): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0037 | 0/0 | 5002 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4997): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0038 | 0/0 | 5002 | 1 | 0 | 0 | 0 | 1 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4997): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0040 | 0/0 | 5004 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4999): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0041 | 0/0 | 5003 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4998): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0042 | 0/0 | 5005 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(5000): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0043 | 0/0 | 5005 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(5000): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0044 | 0/0 | 5005 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(5000): Show |
chr4 | 26855841 | 27030381 |
| a0001c0001t0045 | 0/0 | 5003 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4998): Show |
chr4 | 26855841 | 27030381 |
| a0001c0002t0009 | 0/0 | 5002 | 4 | 2 | 2 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4997): Show |
chr4 | 26855841 | 27030381 |
| a0001c0002t0011 | 1/0 | 5004 | 1 | 0 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4999): Show |
chr4 | 26855841 | 27030381 |
| a0001c0002t0013 | 0/0 | 5000 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4995): Show |
chr4 | 26855841 | 27030381 |
| a0001c0002t0019 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4997): Show |
chr4 | 26855841 | 27030381 |
| a0001c0002t0023 | 0/0 | 5003 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4998): Show |
chr4 | 26855841 | 27030381 |
| a0001c0002t0026 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4997): Show |
chr4 | 26855841 | 27030381 |
| a0001c0003t0001 | 0/0 | 5003 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4998): Show |
chr4 | 26855841 | 27030381 |
| a0001c0004t0039 | 0/0 | 5004 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4999): Show |
chr4 | 26855841 | 27030381 |
| a0001c0005t0002 | 0/0 | 5004 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4999): Show |
chr4 | 26855841 | 27030381 |
| a0001c0006t0003 | 0/0 | 5004 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | AGAGC others(4999): Show |
chr4 | 26855841 | 27030381 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0022 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0027 | 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 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0037 | 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 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0040 | 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 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0291 | 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 |
| a0001c0001t0002g0294 | 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 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0302 | 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 |
| a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0319 | 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 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 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 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0003g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0004g0229 | 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 |
| a0001c0001t0004g0235 | 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 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0004g0251 | 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 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0207 | 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 |
| a0001c0001t0005g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0005g0299 | 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 |
| a0001c0001t0006g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0006g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0006g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0006g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0006g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0006g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0006g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0006g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0006g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0007g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0007g0092 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0007g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0007g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0007g0247 | 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 |
| a0001c0001t0007g0277 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0008g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0008g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0008g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0008g0072 | 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 |
| a0001c0001t0008g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0008g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0008g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0008g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0009g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0009g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0009g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0009g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0009g0327 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0010g0102 | 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 |
| a0001c0001t0010g0107 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0010g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0010g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0010g0326 | 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 |
| a0001c0001t0011g0212 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0011g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0011g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0011g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0012g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0012g0220 | 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 |
| a0001c0001t0012g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0013g0216 | 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 |
| a0001c0001t0014g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0014g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0014g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0014g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0015g0329 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0016g0018 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0016g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0017g0184 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0018g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0018g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0018g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0019g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0020g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0020g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0021g0203 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0022g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0022g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0023g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0024g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0024g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0025g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0027g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0028g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0029g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0030g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0031g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0032g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0033g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0034g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0035g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0036g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0037g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0038g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0040g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0041g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0042g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0043g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0044g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0001t0045g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0002t0009g0104 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0002t0009g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0002t0009g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0002t0011g0253 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0002t0013g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0002t0019g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0002t0023g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0002t0026g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0004t0039g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0005t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| a0001c0006t0003g0175 | 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 | g0199 | EUR | GBR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0243 | EUR | GBR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00408 | hp1 | a0001 | c0001 | t0044 | g0269 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0273 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00544 | hp1 | a0001 | c0001 | t0005 | g0073 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00544 | hp2 | a0001 | c0005 | t0002 | g0089 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0232 | 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 | g0247 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00621 | hp2 | a0001 | c0001 | t0023 | g0159 | EAS | CHS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0182 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00642 | hp2 | a0001 | c0001 | t0014 | g0122 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00733 | hp1 | a0001 | c0002 | t0023 | g0154 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00735 | hp1 | a0001 | c0001 | t0010 | g0133 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00738 | hp2 | a0001 | c0001 | t0017 | g0185 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00741 | hp1 | a0001 | c0001 | t0016 | g0018 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0179 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01071 | hp1 | a0001 | c0001 | t0042 | g0249 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01071 | hp2 | a0001 | c0001 | t0010 | g0136 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01074 | hp1 | a0001 | c0001 | t0006 | g0130 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01074 | hp2 | a0001 | c0001 | t0006 | g0252 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0138 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0225 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01106 | hp1 | a0001 | c0001 | t0029 | g0137 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01106 | hp2 | a0001 | c0002 | t0009 | g0115 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0246 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01167 | hp2 | a0001 | c0001 | t0017 | g0186 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01169 | hp2 | a0001 | c0001 | t0017 | g0184 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0195 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01243 | hp1 | a0001 | c0001 | t0007 | g0092 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01255 | hp2 | a0001 | c0002 | t0009 | g0116 | AMR | CLM | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01256 | hp1 | a0001 | c0001 | t0006 | g0134 | AMR | CLM | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0161 | AMR | CLM | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01261 | hp1 | a0001 | c0001 | t0009 | g0327 | AMR | CLM | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0250 | AMR | CLM | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01358 | hp1 | a0001 | c0001 | t0018 | g0274 | 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 | g0275 | AMR | CLM | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01433 | hp1 | a0001 | c0001 | t0010 | g0132 | AMR | CLM | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0318 | 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 | g0187 | EUR | IBS | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01517 | hp1 | a0001 | c0001 | t0038 | g0131 | 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 | g0181 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0202 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0183 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0205 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0165 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0180 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0118 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0156 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01975 | hp2 | a0001 | c0001 | t0020 | g0292 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01981 | hp2 | a0001 | c0001 | t0005 | g0098 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0168 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG01993 | hp2 | a0001 | c0001 | t0006 | g0117 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0176 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0233 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02056 | hp2 | a0001 | c0006 | t0003 | g0175 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0230 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02135 | hp2 | a0001 | c0001 | t0006 | g0238 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02145 | hp1 | a0001 | c0001 | t0012 | g0214 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0235 | EAS | CDX | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | CDX | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0150 | AMR | PEL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02280 | hp1 | a0001 | c0001 | t0012 | g0220 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02280 | hp2 | a0001 | c0001 | t0036 | g0017 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02451 | hp1 | a0001 | c0001 | t0015 | g0332 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0170 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | KHV | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02572 | hp1 | a0001 | c0001 | t0010 | g0102 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02572 | hp2 | a0001 | c0001 | t0028 | g0283 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0151 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0242 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0211 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0111 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02622 | hp2 | a0001 | c0001 | t0010 | g0107 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02630 | hp2 | a0001 | c0001 | t0016 | g0020 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02647 | hp2 | a0001 | c0001 | t0012 | g0279 | 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 | g0157 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0207 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0167 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0313 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0285 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02809 | hp1 | a0001 | c0001 | t0027 | g0105 | 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 | g0139 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02896 | hp1 | a0001 | c0002 | t0009 | g0148 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0002 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0119 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0002 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02922 | hp1 | a0001 | c0002 | t0013 | g0100 | AFR | ESN | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02922 | hp2 | a0001 | c0001 | t0030 | g0194 | AFR | ESN | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | ESN | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02965 | hp2 | a0001 | c0001 | t0015 | g0329 | AFR | ESN | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03041 | hp1 | a0001 | c0002 | t0019 | g0108 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03041 | hp2 | a0001 | c0001 | t0012 | g0222 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0278 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03130 | hp1 | a0001 | c0001 | t0019 | g0149 | AFR | ESN | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0210 | AFR | ESN | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0208 | AFR | ESN | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03139 | hp2 | a0001 | c0001 | t0012 | g0221 | AFR | ESN | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ESN | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0209 | AFR | ESN | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03209 | hp2 | a0001 | c0001 | t0016 | g0019 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03225 | hp2 | a0001 | c0001 | t0011 | g0212 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0191 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03239 | hp2 | a0001 | c0001 | t0009 | g0127 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03453 | hp1 | a0001 | c0002 | t0026 | g0103 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03453 | hp2 | a0001 | c0001 | t0013 | g0217 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03486 | hp1 | a0001 | c0001 | t0011 | g0213 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03486 | hp2 | a0001 | c0001 | t0010 | g0326 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0245 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0244 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0306 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03669 | hp1 | a0001 | c0001 | t0014 | g0123 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0333 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | STU | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03688 | hp2 | a0001 | c0001 | t0009 | g0215 | SAS | STU | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03704 | hp1 | a0001 | c0001 | t0043 | g0311 | 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 | g0172 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0200 | SAS | BEB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0004 | SAS | BEB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03834 | hp2 | a0001 | c0004 | t0039 | g0160 | SAS | BEB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0241 | SAS | BEB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03927 | hp2 | a0001 | c0001 | t0014 | g0120 | SAS | BEB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG04115 | hp1 | a0001 | c0001 | t0037 | g0135 | SAS | STU | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0251 | SAS | STU | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0109 | AFR | YRI | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18522 | hp2 | a0001 | c0001 | t0021 | g0204 | AFR | YRI | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | CHB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0226 | EAS | CHB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | CHB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18906 | hp1 | a0001 | c0001 | t0013 | g0216 | AFR | YRI | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18906 | hp2 | a0001 | c0002 | t0009 | g0104 | AFR | YRI | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18944 | hp2 | a0001 | c0001 | t0011 | g0228 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18948 | hp1 | a0001 | c0001 | t0008 | g0077 | 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 | g0316 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18949 | hp2 | a0001 | c0001 | t0031 | g0010 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18950 | hp2 | a0001 | c0001 | t0008 | g0067 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18951 | hp1 | a0001 | c0001 | t0005 | g0036 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18953 | hp1 | a0001 | c0001 | t0005 | g0300 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18954 | hp2 | a0001 | c0001 | t0008 | g0030 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0206 | 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 | g0086 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18968 | hp2 | a0001 | c0001 | t0014 | g0124 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0229 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18970 | hp2 | a0001 | c0001 | t0005 | g0299 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18973 | hp1 | a0001 | c0001 | t0011 | g0240 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18973 | hp2 | a0001 | c0001 | t0006 | g0063 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18980 | hp1 | a0001 | c0001 | t0032 | g0296 | 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 | g0231 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0008 | 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 | g0290 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18985 | hp2 | a0001 | c0003 | t0001 | g0284 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18989 | hp1 | a0001 | c0001 | t0005 | g0141 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0045 | 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 | g0095 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18993 | hp2 | a0001 | c0001 | t0041 | g0234 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18994 | hp1 | a0001 | c0001 | t0008 | g0074 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18995 | hp2 | a0001 | c0001 | t0008 | g0031 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18997 | hp1 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0153 | 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 | g0294 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0270 | 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 | g0097 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19011 | hp1 | a0001 | c0001 | t0040 | g0080 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19030 | hp1 | a0001 | c0001 | t0021 | g0203 | AFR | LWK | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19030 | hp2 | a0001 | c0001 | t0033 | g0145 | AFR | LWK | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19058 | hp2 | a0001 | c0001 | t0022 | g0317 | 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 | g0081 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19063 | hp1 | a0001 | c0001 | t0008 | g0146 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19063 | hp2 | a0001 | c0001 | t0020 | g0005 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19068 | hp1 | a0001 | c0001 | t0022 | g0301 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19070 | hp1 | a0001 | c0001 | t0008 | g0072 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0239 | 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 | g0064 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0312 | 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 | g0025 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19078 | hp2 | a0001 | c0001 | t0011 | g0286 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19080 | hp2 | a0001 | c0001 | t0008 | g0029 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0248 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19086 | hp1 | a0001 | c0001 | t0008 | g0075 | 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 | g0062 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19090 | hp1 | a0001 | c0001 | t0006 | g0066 | 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 | g0236 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19091 | hp2 | a0001 | c0001 | t0035 | g0288 | EAS | JPT | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0277 | AFR | YRI | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA19240 | hp2 | a0001 | c0001 | t0010 | g0106 | AFR | YRI | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA20805 | hp1 | a0001 | c0001 | t0024 | g0307 | EUR | TSI | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0289 | EUR | TSI | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | GIH | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA20905 | hp2 | a0001 | c0001 | t0024 | g0308 | SAS | GIH | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02109 | hp1 | a0001 | c0001 | t0015 | g0330 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0201 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02486 | hp1 | a0001 | c0001 | t0010 | g0101 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0110 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02559 | hp1 | a0001 | c0001 | t0013 | g0218 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG02559 | hp2 | a0001 | c0001 | t0009 | g0282 | AFR | ACB | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG06807 | hp1 | a0001 | c0001 | t0045 | g0171 | AFR | USA | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| HG06807 | hp2 | a0001 | c0001 | t0034 | g0121 | AFR | USA | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA20300 | hp1 | a0001 | c0001 | t0015 | g0331 | AFR | USA | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| NA20300 | hp2 | a0001 | c0001 | t0025 | g0219 | AFR | USA | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0022 | REF | REF | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0011 | g0253 | REF | REF | STIM2_chr4_26855841_27030381 | STIM2 | chr4 | 26855841 | 27030381 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:27007598 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:27002389 | G | A | 5 | a0001c0001 a0001c0003 a0001c0004 others(2): Show |
326 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(323): 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:26860921 | C | A | 2 | a0001c0001t0019 a0001c0002t0019 |
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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(25): Show |
234 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(231): 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 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0019 others(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 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0025 others(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 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0018 others(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 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0018 others(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 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(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 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(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 | a0001c0001t0014 a0001c0001t0042 |
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 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0017 others(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 | a0001c0001t0015 a0001c0001t0025 a0001c0001t0033 |
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 | a0001c0001t0016 a0001c0001t0028 |
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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:26861414 | G | GACCTCT | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(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 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 |
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 | a0001c0001t0003g0333 | 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 | a0001c0001t0001g0014 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0002g0276 others(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 | a0001c0001t0001g0305 a0001c0001t0001g0318 a0001c0001t0002g0006 others(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 | 105 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(102): Show |
106 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(103): 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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0016g0018 others(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 | a0001c0001t0004g0119 | 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 | 278 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(275): Show |
281 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(278): 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0009g0215 a0001c0001t0012g0214 a0001c0001t0012g0220 others(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 | a0001c0001t0014g0120 | 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 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0002g0128 others(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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0012g0222 | 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 | a0001c0001t0001g0224 a0001c0001t0002g0328 a0001c0001t0004g0270 others(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 | a0001c0001t0001g0305 a0001c0001t0002g0006 a0001c0001t0002g0007 others(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 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0125 others(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 | 88 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(85): Show |
90 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(87): 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 | a0001c0001t0002g0013 | 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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0009g0215 a0001c0001t0009g0327 a0001c0001t0012g0214 others(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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0018g0274 | 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 | a0001c0001t0009g0327 | 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 | a0001c0001t0005g0205 a0001c0001t0007g0202 a0001c0001t0021g0203 others(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 | a0001c0001t0043g0311 | 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 | a0001c0001t0009g0215 a0001c0001t0009g0327 a0001c0001t0012g0214 others(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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0006g0130 others(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 | a0001c0001t0002g0094 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0007g0109 a0001c0001t0007g0110 a0001c0001t0007g0111 |
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 | 271 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(268): Show |
274 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(271): Show |
intron_variant | MODIFIER | c.151+3720T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26865089 | |||||||
| chr4:26865125 | TTC | T | 2 | a0001c0001t0007g0002 a0001c0001t0007g0092 |
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 | 109 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(106): Show |
110 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.151+3772C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26865141 | |||||||
| chr4:26865178 | T | G | 2 | a0001c0001t0007g0002 a0001c0001t0007g0092 |
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 | a0001c0001t0002g0310 | 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 | a0001c0001t0003g0150 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0223 a0001c0001t0001g0224 others(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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | a0001c0001t0033g0145 | 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 | 2 | a0001c0001t0007g0002 a0001c0001t0007g0092 |
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 | a0001c0001t0001g0305 a0001c0001t0001g0318 a0001c0001t0002g0006 others(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 | a0001c0001t0004g0227 a0001c0001t0004g0229 a0001c0001t0004g0230 others(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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0205 others(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 | |||||||
| chr4:26866037 | A | G | 1 | a0001c0001t0001g0091 | 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 | a0001c0001t0007g0277 | 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 | a0001c0001t0007g0109 a0001c0001t0007g0110 a0001c0001t0007g0111 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 others(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 | a0001c0001t0004g0231 a0001c0001t0004g0232 a0001c0001t0004g0233 others(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 | a0001c0001t0001g0023 | 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 | 9 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0205 others(6): 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 | a0001c0002t0023g0154 | 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 | a0001c0001t0007g0109 a0001c0001t0007g0110 a0001c0001t0007g0111 |
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 | a0001c0002t0013g0100 | 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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0009g0127 |
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 | a0001c0001t0033g0145 | 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 | a0001c0001t0006g0138 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0305 a0001c0001t0001g0318 others(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 | a0001c0001t0005g0205 a0001c0001t0007g0202 a0001c0001t0021g0203 others(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 | a0001c0001t0002g0090 a0001c0005t0002g0089 |
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 | a0001c0001t0001g0305 a0001c0001t0001g0318 a0001c0001t0002g0006 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0011g0087 |
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 | a0001c0001t0033g0145 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0003g0200 a0001c0001t0003g0201 |
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 | a0001c0001t0009g0282 | 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 | a0001c0001t0010g0326 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0139 |
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 | 2 | a0001c0001t0007g0002 a0001c0001t0007g0092 |
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 | a0001c0001t0005g0205 a0001c0001t0007g0202 a0001c0001t0009g0327 others(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 | 188 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(185): Show |
190 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(187): 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 | a0001c0001t0003g0199 | 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 | 2 | a0001c0001t0007g0002 a0001c0001t0007g0092 |
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 | a0001c0001t0018g0274 | 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 | a0001c0001t0005g0205 | 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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0036g0017 |
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 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0031 others(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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0205 others(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 | a0001c0001t0012g0214 a0001c0001t0012g0220 a0001c0001t0012g0221 others(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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0002g0153 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0003g0158 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0036g0017 |
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 | a0001c0001t0005g0205 a0001c0001t0007g0202 a0001c0001t0021g0203 others(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 | 22 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0205 others(19): 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 | a0001c0001t0028g0283 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | 115 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(112): Show |
117 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(114): 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0008g0095 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0086 a0001c0001t0002g0287 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0012g0279 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
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 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
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 | a0001c0001t0034g0121 | 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 | a0001c0001t0009g0327 | 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 | a0001c0001t0004g0230 | 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 | a0001c0001t0009g0327 | 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 | a0001c0001t0004g0265 a0001c0001t0004g0266 |
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 | 160 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(157): Show |
162 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(159): 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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0001g0014 | 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 | 180 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(177): Show |
182 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(179): 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 | a0001c0001t0001g0035 | 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 | a0001c0001t0002g0011 a0001c0001t0002g0012 |
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 | a0001c0001t0014g0120 a0001c0001t0014g0122 a0001c0001t0014g0123 |
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 | a0001c0001t0004g0229 a0001c0001t0004g0231 a0001c0001t0004g0232 others(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 | a0001c0001t0001g0083 | 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 | a0001c0001t0002g0128 a0001c0001t0002g0129 |
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 | 120 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(117): Show |
121 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.151+11415G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26872784 | |||||||
| chr4:26872814 | T | C | 120 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(117): Show |
121 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(118): 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0002g0153 | 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0012g0214 a0001c0001t0012g0220 a0001c0001t0012g0221 others(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 | a0001c0001t0004g0265 a0001c0001t0004g0266 |
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 | a0001c0001t0004g0236 a0001c0001t0004g0237 a0001c0001t0006g0238 |
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 | a0001c0001t0014g0120 a0001c0001t0014g0122 a0001c0001t0014g0123 others(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 | a0001c0001t0009g0327 | 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 | a0001c0001t0003g0155 | 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 | a0001c0001t0002g0090 a0001c0005t0002g0089 |
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 | 229 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(226): Show |
232 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(229): Show |
intron_variant | MODIFIER | c.151+12275A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26873644 | |||||||
| chr4:26873833 | C | T | 86 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(83): Show |
87 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(84): 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 | a0001c0001t0012g0279 | 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 | a0001c0001t0003g0197 a0001c0001t0003g0198 |
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 | a0001c0001t0019g0149 a0001c0002t0019g0108 |
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 | a0001c0001t0004g0226 a0001c0001t0004g0262 |
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 | a0001c0001t0001g0096 | 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 | 52 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0280 others(49): 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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | a0001c0001t0005g0081 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0018g0274 | 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 | a0001c0001t0001g0147 | 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 | 277 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(274): Show |
280 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(277): 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 | a0001c0001t0012g0221 | 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 | a0001c0001t0005g0036 a0001c0001t0005g0081 a0001c0001t0005g0097 others(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 | a0001c0001t0005g0205 a0001c0001t0007g0202 a0001c0001t0021g0203 others(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 | a0001c0001t0009g0327 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0040g0080 | 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 | a0001c0001t0007g0109 a0001c0001t0007g0110 a0001c0001t0007g0111 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(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 | a0001c0001t0005g0205 a0001c0001t0007g0202 a0001c0001t0014g0120 others(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 | a0001c0001t0003g0196 | 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 | a0001c0001t0019g0149 a0001c0002t0019g0108 |
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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0009g0327 a0001c0001t0044g0269 |
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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0003g0195 others(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 | a0001c0001t0001g0305 a0001c0001t0001g0318 a0001c0001t0002g0006 others(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 | a0001c0001t0004g0226 | 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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | a0001c0001t0003g0114 a0001c0001t0003g0193 |
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 | a0001c0001t0006g0130 a0001c0001t0038g0131 |
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 | a0001c0001t0028g0283 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0005g0205 a0001c0001t0007g0202 |
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 | a0001c0001t0007g0109 a0001c0001t0007g0110 a0001c0001t0007g0111 |
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 | a0001c0001t0003g0192 | 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 | a0001c0001t0003g0161 | 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 | a0001c0001t0034g0121 | 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 | a0001c0001t0001g0021 a0001c0001t0003g0003 a0001c0001t0003g0113 others(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 | a0001c0001t0001g0318 a0001c0001t0002g0006 a0001c0001t0002g0007 others(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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0036g0017 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0010g0326 | 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 | a0001c0001t0002g0153 | 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 | a0001c0001t0002g0153 | 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 | a0001c0001t0002g0153 | 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 | a0001c0001t0012g0214 a0001c0001t0012g0220 a0001c0001t0012g0221 others(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 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 |
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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0036g0017 |
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 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
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 | 2 | a0001c0001t0007g0002 a0001c0001t0007g0092 |
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 | 121 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(118): Show |
122 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(119): 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 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0041 others(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 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0003g0162 others(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 | a0001c0001t0002g0013 a0001c0002t0026g0103 |
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 | a0001c0001t0038g0131 | 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 | a0001c0001t0033g0145 | 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0003g0191 | 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 | a0001c0001t0005g0211 | 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 | a0001c0001t0003g0188 | 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 | a0001c0001t0003g0333 | 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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 |
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 | 2 | a0001c0001t0007g0002 a0001c0001t0007g0092 |
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 | a0001c0001t0002g0153 | 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 | a0001c0001t0002g0153 | 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 | a0001c0001t0009g0327 | 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 | a0001c0001t0010g0106 | 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 | a0001c0001t0001g0035 a0001c0001t0001g0043 |
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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0002g0153 | 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 | a0001c0001t0009g0327 | 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 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0147 others(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 | 84 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(81): Show |
85 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(82): 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 | a0001c0004t0039g0160 | 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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0005g0205 a0001c0001t0007g0202 |
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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | 257 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(254): Show |
260 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(257): 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 | a0001c0001t0001g0021 a0001c0001t0001g0096 a0001c0001t0001g0099 others(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 | a0001c0001t0009g0278 | 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 | 178 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(175): Show |
180 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(177): 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 | 69 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0280 others(66): 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 | a0001c0001t0012g0214 a0001c0001t0012g0220 a0001c0001t0012g0221 others(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 | 79 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0280 others(76): 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 | a0001c0001t0002g0153 | 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 | a0001c0001t0002g0153 | 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 | a0001c0001t0038g0131 | 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 | a0001c0001t0001g0305 | 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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0036g0017 |
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 | a0001c0001t0007g0109 a0001c0001t0007g0110 a0001c0001t0007g0111 |
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 | 257 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(254): Show |
260 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(257): 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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0036g0017 | 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 | 113 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(110): Show |
115 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(112): 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 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0033 others(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 | a0001c0001t0002g0153 | 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 | a0001c0001t0009g0127 | 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 | a0001c0001t0007g0109 a0001c0001t0007g0110 a0001c0001t0007g0111 others(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 | a0001c0001t0017g0184 a0001c0001t0017g0185 a0001c0001t0017g0186 |
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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0001g0305 | 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 | a0001c0001t0014g0122 | 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 | 2 | a0001c0001t0007g0002 a0001c0001t0007g0092 |
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 | 122 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(119): Show |
123 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(120): 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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | a0001c0001t0001g0023 | 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 | a0001c0001t0001g0099 | 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 | a0001c0001t0006g0130 a0001c0001t0006g0134 a0001c0001t0006g0138 others(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 | a0001c0001t0004g0273 | 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 | 100 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(97): Show |
101 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.151+23305C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26884674 | |||||||
| chr4:26885043 | T | C | 2 | a0001c0001t0007g0002 a0001c0001t0007g0092 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0059 a0001c0001t0001g0060 others(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 | a0001c0001t0007g0202 | 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 | a0001c0002t0009g0115 a0001c0002t0009g0116 |
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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0001g0281 a0001c0001t0004g0235 a0001c0001t0004g0250 others(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 | a0001c0001t0001g0280 a0001c0001t0004g0225 a0001c0001t0004g0226 others(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 | a0001c0001t0004g0230 a0001c0001t0004g0231 a0001c0001t0006g0246 others(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 | a0001c0001t0004g0242 a0001c0001t0004g0243 a0001c0001t0004g0244 others(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 | a0001c0001t0004g0241 a0001c0001t0004g0270 a0001c0001t0007g0202 others(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 | a0001c0001t0004g0119 a0001c0001t0004g0263 a0001c0001t0006g0117 others(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 | a0001c0001t0004g0239 | 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 | a0001c0001t0002g0153 a0001c0001t0004g0227 a0001c0001t0004g0257 others(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 | a0001c0001t0005g0205 a0001c0001t0006g0130 a0001c0001t0010g0326 others(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 | a0001c0001t0004g0236 a0001c0001t0004g0237 a0001c0001t0004g0259 others(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 | a0001c0001t0004g0118 a0001c0001t0004g0260 a0001c0002t0026g0103 |
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 | a0001c0001t0029g0137 | 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 | a0001c0001t0006g0238 a0001c0001t0015g0331 a0001c0001t0021g0204 |
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 | a0001c0001t0019g0149 a0001c0001t0044g0269 a0001c0002t0013g0100 others(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 | a0001c0001t0001g0058 a0001c0001t0006g0138 |
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 | a0001c0001t0033g0145 | 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 | a0001c0001t0003g0114 a0001c0001t0011g0228 |
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 | 13 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0003g0155 others(10): 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 | a0001c0001t0001g0021 a0001c0001t0001g0305 a0001c0001t0001g0318 others(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 | a0001c0001t0014g0122 | 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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0002g0070 | 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 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
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 | a0001c0001t0011g0212 | 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 | a0001c0001t0005g0211 | 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 | a0001c0001t0005g0210 | 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 | a0001c0001t0002g0040 a0001c0001t0008g0067 |
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 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0139 | 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 |
4 | a0001c0001t0001g0054 a0001c0001t0001g0091 a0001c0001t0005g0098 others(1): Show |
4 | HG01981.hp2 HG02004.hp1 HG03688.hp1 others(1): 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 | a0001c0001t0002g0065 | 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 | a0001c0001t0001g0039 | 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 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0009g0127 |
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 | a0001c0005t0002g0089 | 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 | a0001c0001t0001g0043 | 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 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0144 a0001c0001t0002g0071 |
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 | a0001c0001t0001g0014 a0001c0001t0002g0064 |
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 | a0001c0001t0008g0029 a0001c0001t0008g0095 |
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 | a0001c0001t0005g0097 | 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 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0049 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
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 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
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 | a0001c0001t0001g0024 | 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 | a0001c0001t0002g0094 | 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 | a0001c0001t0005g0073 | 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 | a0001c0001t0001g0088 a0001c0001t0002g0028 a0001c0001t0008g0074 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0142 a0001c0001t0008g0031 others(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 | a0001c0001t0008g0030 | 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 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0047 a0001c0001t0006g0001 |
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 | a0001c0001t0006g0025 | 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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0027 a0001c0001t0001g0068 |
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 | a0001c0001t0001g0086 a0001c0001t0002g0084 a0001c0001t0008g0075 others(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 | a0001c0001t0001g0126 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0057 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
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 | a0001c0001t0001g0042 a0001c0001t0001g0093 |
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 | a0001c0001t0006g0066 | 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 | a0001c0001t0001g0044 a0001c0001t0002g0090 |
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 | a0001c0001t0012g0220 | 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 | a0001c0001t0002g0085 | 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 | a0001c0001t0005g0081 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0058 others(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 | a0001c0001t0005g0207 | 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 | a0001c0001t0005g0208 a0001c0001t0005g0209 |
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 | a0001c0001t0014g0120 a0001c0001t0014g0122 |
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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0014g0120 a0001c0001t0014g0122 a0001c0001t0016g0018 others(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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0003g0195 | 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 | a0001c0001t0004g0233 | 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 | a0001c0001t0010g0132 a0001c0001t0010g0133 a0001c0001t0010g0136 others(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 | a0001c0001t0001g0058 | 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 | a0001c0001t0009g0215 a0001c0001t0028g0283 |
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 | a0001c0001t0004g0244 a0001c0001t0004g0245 |
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 | 234 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(231): Show |
237 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(234): 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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0036g0017 |
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 | a0001c0001t0031g0010 | 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 | a0001c0001t0002g0304 | 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 | a0001c0001t0002g0007 | 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 | 94 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(91): Show |
95 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(92): 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 | a0001c0001t0005g0205 a0001c0001t0007g0202 a0001c0001t0021g0203 others(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 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0002g0152 others(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 | 185 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(182): Show |
187 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(184): 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 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0006g0001 |
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 | 231 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(228): Show |
234 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(231): 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 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0147 |
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 | a0001c0001t0009g0215 a0001c0001t0028g0283 |
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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | 124 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(121): Show |
125 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.151+26332G>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26887701 | |||||||
| chr4:26887702 | T | C | 7 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0007g0002 others(4): 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 | a0001c0001t0018g0274 | 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 | a0001c0001t0001g0091 | 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 | a0001c0001t0004g0251 | 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 | a0001c0001t0003g0188 | 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 | a0001c0001t0009g0215 | 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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0033g0145 | 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 | a0001c0003t0001g0284 | 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 | 191 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(188): Show |
193 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(190): 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0001g0091 | 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 | a0001c0001t0002g0303 | 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 | a0001c0001t0008g0077 | 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 | a0001c0001t0019g0149 a0001c0002t0019g0108 |
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 | a0001c0001t0010g0102 | 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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | a0001c0001t0005g0073 | 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 | a0001c0001t0002g0128 a0001c0001t0002g0129 |
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 | a0001c0001t0001g0093 | 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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0001g0059 | 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 | a0001c0001t0006g0117 a0001c0001t0006g0246 a0001c0001t0006g0252 |
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 | a0001c0001t0001g0305 a0001c0001t0001g0318 a0001c0001t0002g0006 others(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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 |
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 | a0001c0001t0004g0225 | 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 | 80 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0280 others(77): 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 | a0001c0001t0006g0130 | 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 | 246 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(243): Show |
249 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(246): 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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0004g0226 | 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 | a0001c0001t0008g0031 a0001c0001t0008g0146 |
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 | a0001c0001t0004g0251 | 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 | a0001c0001t0012g0214 a0001c0001t0012g0221 a0001c0001t0012g0222 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0057 a0001c0001t0001g0096 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0082 a0001c0001t0002g0302 others(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 | a0001c0001t0009g0327 | 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 | 137 | a0001c0001t0001g0021 a0001c0001t0001g0223 a0001c0001t0001g0224 others(134): 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 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | |||||||
| chr4:26891350 | T | C | 57 | a0001c0001t0001g0305 a0001c0001t0001g0318 a0001c0001t0002g0006 others(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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0004g0118 a0001c0001t0004g0119 a0001c0001t0004g0241 others(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 | a0001c0001t0004g0261 a0001c0001t0010g0102 a0001c0001t0011g0240 others(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 | a0001c0001t0002g0291 a0001c0001t0005g0015 a0001c0001t0005g0207 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0305 a0001c0001t0002g0006 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0058 a0001c0001t0001g0096 others(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 | 92 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0026 others(89): Show |
93 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(90): 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 | a0001c0001t0001g0048 a0001c0001t0015g0329 a0001c0001t0015g0330 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0001c0003t0001g0284 | 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 | 2 | a0001c0001t0007g0002 a0001c0001t0007g0092 |
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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 others(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 | a0001c0001t0004g0232 | 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 | a0001c0001t0002g0006 a0001c0001t0002g0009 |
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 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0147 |
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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0033g0145 | 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 | a0001c0001t0009g0215 | 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 | a0001c0002t0019g0108 | 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 | a0001c0001t0004g0244 a0001c0001t0004g0245 |
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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0012g0214 others(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 | a0001c0001t0004g0251 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0002g0306 | 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 | 45 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0305 others(42): 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 | 109 | a0001c0001t0001g0021 a0001c0001t0001g0223 a0001c0001t0001g0224 others(106): 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 | a0001c0001t0021g0203 a0001c0001t0021g0204 |
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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0006g0252 | 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 | a0001c0001t0005g0210 | 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 | a0001c0001t0037g0135 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0009g0215 a0001c0001t0028g0283 |
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 | 2 | a0001c0001t0007g0002 a0001c0001t0007g0092 |
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 | 231 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(228): Show |
234 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(231): 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0009g0215 others(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 | a0001c0001t0002g0008 | 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0006g0130 others(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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0059 a0001c0001t0001g0060 others(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 | 119 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(116): Show |
120 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(117): 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0012g0214 others(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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0003g0155 | 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 | a0001c0001t0002g0006 a0001c0001t0002g0153 a0001c0001t0002g0293 others(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 | a0001c0001t0007g0109 a0001c0001t0007g0110 a0001c0001t0007g0111 |
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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 |
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 | a0001c0001t0013g0218 | 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 | a0001c0001t0004g0242 a0001c0001t0042g0249 |
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 | a0001c0001t0015g0330 | 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 | a0001c0001t0003g0166 a0001c0001t0005g0015 a0001c0001t0005g0016 others(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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0021g0204 | 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 | 329 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(326): Show |
332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.152-24081A>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26895423 | |||||||
| chr4:26895424 | A | G | 329 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(326): Show |
332 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.152-24080A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 1/11 | chr4 | 26895424 | |||||||
| chr4:26895436 | C | T | 122 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(119): Show |
123 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(120): 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 | a0001c0002t0009g0148 | 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 | a0001c0001t0013g0217 | 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 | a0001c0001t0002g0310 a0001c0001t0005g0290 a0001c0001t0005g0299 others(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 | a0001c0001t0003g0113 a0001c0001t0003g0155 |
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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | a0001c0001t0003g0167 | 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 | 122 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(119): Show |
123 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(120): 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 | a0001c0001t0009g0327 | 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 | a0001c0001t0005g0205 a0001c0001t0007g0202 |
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 | 2 | a0001c0001t0007g0002 a0001c0001t0007g0092 |
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 | a0001c0001t0009g0278 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(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 | a0001c0001t0021g0204 | 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 | a0001c0001t0002g0151 | 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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0005g0015 | 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 | a0001c0001t0003g0187 | 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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0205 others(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 | a0001c0001t0001g0093 | 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 | a0001c0001t0003g0157 | 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 | a0001c0001t0004g0251 | 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 | a0001c0001t0012g0279 | 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 | 87 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(84): Show |
88 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(85): 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 | a0001c0001t0002g0009 | 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 | a0001c0001t0006g0138 | 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 | a0001c0001t0037g0135 | 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 | a0001c0001t0024g0308 | 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 | a0001c0001t0009g0215 a0001c0001t0028g0283 |
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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | a0001c0001t0001g0021 a0001c0001t0003g0003 a0001c0001t0003g0113 others(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 | a0001c0001t0001g0021 a0001c0001t0003g0003 a0001c0001t0003g0113 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0009g0127 |
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 | a0001c0001t0027g0105 | 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 | a0001c0001t0011g0228 | 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 | a0001c0001t0009g0282 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | 179 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(176): Show |
181 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(178): 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 | a0001c0001t0002g0151 a0001c0001t0002g0152 |
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 | a0001c0001t0002g0064 a0001c0001t0002g0065 |
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 | a0001c0001t0004g0231 a0001c0001t0004g0232 a0001c0001t0004g0233 others(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 | a0001c0001t0028g0283 | 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 | a0001c0001t0001g0305 a0001c0001t0001g0318 a0001c0001t0002g0006 others(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 | a0001c0001t0006g0066 | 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 | a0001c0001t0007g0109 a0001c0001t0007g0110 a0001c0001t0007g0111 |
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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0002g0007 | 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 | 37 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0032 others(34): Show |
38 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(35): 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 | a0001c0001t0036g0017 | 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 | a0001c0001t0007g0109 | 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 | 94 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(91): Show |
95 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(92): 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 | a0001c0001t0008g0031 | 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 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(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 | 122 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(119): Show |
123 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(120): 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 | a0001c0001t0014g0120 a0001c0001t0014g0122 a0001c0001t0014g0123 others(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 | a0001c0001t0004g0272 | 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 | a0001c0001t0008g0067 | 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 | a0001c0001t0005g0015 a0001c0001t0005g0016 |
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 | a0001c0001t0009g0327 | 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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | a0001c0001t0001g0039 a0001c0001t0002g0040 |
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 | a0001c0001t0041g0234 | 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 | a0001c0001t0005g0098 | 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 | a0001c0001t0001g0041 | 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 | a0001c0001t0005g0205 a0001c0001t0007g0109 a0001c0001t0007g0110 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0054 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0001g0318 a0001c0001t0002g0006 a0001c0001t0002g0007 others(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 | a0001c0001t0009g0327 | 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 | a0001c0001t0009g0327 | 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 | a0001c0001t0001g0038 | 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 | a0001c0001t0009g0278 | 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 | 231 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(228): Show |
234 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(231): 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 | a0001c0001t0037g0135 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0005g0205 a0001c0001t0007g0202 |
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 | a0001c0001t0015g0329 | 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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0036g0017 |
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 | 277 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(274): Show |
280 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(277): 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 | a0001c0001t0001g0068 | 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 | a0001c0001t0003g0199 | 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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 |
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 | a0001c0001t0009g0215 a0001c0001t0028g0283 |
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 | 125 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(122): Show |
127 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(124): 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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 |
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 | 155 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(152): Show |
158 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(155): 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 | a0001c0001t0001g0033 a0001c0001t0001g0062 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0280 others(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 | a0001c0001t0004g0225 | 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 | 223 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(220): Show |
226 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(223): 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 | a0001c0001t0002g0309 a0001c0001t0003g0177 a0001c0001t0003g0196 others(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 | a0001c0001t0003g0182 | 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 | a0001c0002t0013g0100 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0017g0184 a0001c0001t0017g0185 a0001c0001t0017g0186 |
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 | a0001c0001t0002g0151 a0001c0001t0002g0152 |
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 | a0001c0001t0014g0123 | 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 | 167 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(164): Show |
169 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(166): 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 | a0001c0001t0002g0314 | 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 | a0001c0002t0023g0154 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0036g0017 |
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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0012g0214 others(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 | a0001c0001t0002g0153 a0001c0001t0002g0287 a0001c0001t0002g0289 others(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 | a0001c0001t0017g0184 a0001c0001t0017g0185 a0001c0001t0017g0186 |
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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 |
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 | a0001c0001t0005g0208 | 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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0036g0017 |
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 | a0001c0001t0021g0203 a0001c0001t0021g0204 |
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 | a0001c0001t0003g0188 | 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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0280 others(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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0006g0130 a0001c0001t0006g0134 a0001c0001t0006g0138 others(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 | 39 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0026 others(36): Show |
40 | HG00544.hp2 HG00621.hp1 HG00733.hp2 others(37): 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 | a0001c0001t0005g0081 | 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 | 149 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(146): Show |
152 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(149): 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0305 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0147 |
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 | a0001c0001t0014g0120 a0001c0001t0014g0122 a0001c0001t0014g0123 others(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 | a0001c0001t0009g0215 a0001c0001t0028g0283 |
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 | a0001c0001t0005g0073 | 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 | a0001c0001t0002g0291 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0002t0026g0103 | 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 | 169 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(166): Show |
172 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(169): 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 | a0001c0001t0009g0278 a0001c0001t0009g0282 |
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 | a0001c0001t0001g0014 | 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 | a0001c0001t0024g0308 a0001c0001t0043g0311 |
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 | a0001c0001t0002g0297 | 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 | a0001c0001t0010g0326 | 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 | a0001c0001t0003g0176 | 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0280 others(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 | a0001c0001t0006g0130 a0001c0001t0006g0134 a0001c0001t0006g0138 others(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 | a0001c0001t0034g0121 | 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 | a0001c0001t0044g0269 | 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 | 183 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(180): Show |
186 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(183): 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 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0002g0153 others(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 | a0001c0004t0039g0160 | 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 | a0001c0001t0009g0282 | 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 | a0001c0001t0012g0214 a0001c0001t0012g0221 a0001c0001t0012g0222 others(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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 |
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 | a0001c0001t0036g0017 | 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 | a0001c0001t0004g0119 | 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 | a0001c0001t0009g0215 | 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 | a0001c0001t0024g0307 | 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 | 187 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(184): Show |
190 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(187): 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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | 235 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(232): Show |
238 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(235): 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 | a0001c0001t0001g0021 a0001c0001t0003g0003 a0001c0001t0003g0113 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0068 a0001c0001t0001g0069 |
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 | a0001c0001t0004g0229 a0001c0001t0011g0228 |
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 | a0001c0001t0001g0044 | 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 | a0001c0001t0008g0029 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0012g0214 others(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 | a0001c0001t0001g0305 a0001c0001t0001g0318 a0001c0001t0002g0006 others(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 | a0001c0001t0001g0045 | 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 | a0001c0001t0002g0306 | 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 | a0001c0001t0005g0205 a0001c0001t0007g0202 |
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 | a0001c0001t0009g0215 a0001c0001t0028g0283 |
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 | a0001c0001t0033g0145 | 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0280 others(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 | a0001c0001t0002g0319 | 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 | a0001c0001t0014g0120 a0001c0001t0014g0122 a0001c0001t0014g0123 others(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 | a0001c0001t0002g0310 a0001c0001t0005g0290 a0001c0001t0005g0299 |
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 | 88 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(85): Show |
89 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(86): 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0012g0279 |
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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 |
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 | a0001c0001t0001g0082 | 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 | a0001c0001t0003g0178 | 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 | a0001c0006t0003g0175 | 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 | a0001c0001t0003g0195 | 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 | a0001c0001t0002g0321 | 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 | 33 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0032 others(30): Show |
34 | HG00544.hp2 HG00621.hp1 HG00733.hp2 others(31): 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 | a0001c0001t0007g0109 a0001c0001t0007g0110 a0001c0001t0007g0111 |
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 | a0001c0001t0003g0156 a0001c0001t0003g0168 a0001c0001t0003g0176 others(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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0009g0282 a0001c0001t0012g0279 |
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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | 280 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(277): Show |
283 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(280): 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0002g0084 | 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 | 2 | a0001c0001t0007g0002 a0001c0001t0007g0092 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0305 a0001c0001t0001g0318 others(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 | 93 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(90): Show |
94 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(91): 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | 93 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(90): Show |
94 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(91): 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 | a0001c0001t0002g0322 a0001c0001t0002g0328 |
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 | a0001c0001t0001g0014 a0001c0001t0001g0068 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0021 a0001c0001t0002g0064 a0001c0001t0003g0113 others(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 | a0001c0001t0004g0226 a0001c0001t0004g0262 |
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 | a0001c0001t0003g0195 | 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 | a0001c0001t0002g0007 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0009g0278 | 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 | 91 | a0001c0001t0001g0021 a0001c0001t0001g0305 a0001c0001t0001g0318 others(88): 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 | a0001c0001t0001g0280 | 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 | a0001c0001t0003g0169 | 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 | a0001c0001t0003g0158 a0001c0001t0003g0170 a0001c0001t0018g0112 others(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 | a0001c0001t0003g0156 a0001c0001t0003g0168 a0001c0001t0003g0176 others(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 | a0001c0001t0009g0327 | 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 | a0001c0001t0033g0145 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0282 others(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 | a0001c0001t0003g0195 | 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 | a0001c0001t0036g0017 | 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 | a0001c0001t0012g0214 a0001c0001t0012g0221 a0001c0001t0012g0222 others(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 | 110 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0280 others(107): 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 | 111 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(108): Show |
112 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(109): 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 | a0001c0001t0004g0285 | 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 | a0001c0001t0003g0195 | 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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0036g0017 |
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 | a0001c0001t0003g0187 a0001c0001t0003g0199 a0001c0001t0003g0200 others(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 | a0001c0001t0005g0036 a0001c0001t0005g0097 |
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 | 2 | a0001c0001t0007g0002 a0001c0001t0007g0092 |
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 | a0001c0002t0019g0108 | 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 | 108 | a0001c0001t0001g0021 a0001c0001t0001g0223 a0001c0001t0001g0224 others(105): 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 | a0001c0001t0003g0150 a0001c0001t0003g0161 a0001c0001t0003g0165 others(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 | a0001c0001t0003g0164 | 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 | a0001c0001t0010g0326 | 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 | a0001c0001t0033g0145 | 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 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0147 |
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 | a0001c0001t0002g0007 | 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 | a0001c0001t0004g0230 | 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 | a0001c0004t0039g0160 | 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 | a0001c0001t0005g0208 a0001c0001t0005g0209 |
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 | a0001c0001t0009g0282 | 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 | 108 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(105): Show |
109 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(106): 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 | a0001c0001t0009g0327 | 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 | a0001c0001t0005g0205 a0001c0001t0007g0202 a0001c0001t0021g0203 others(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 | 107 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(104): Show |
108 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.282+2781delG | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26922414 | |||||||
| chr4:26922710 | G | C | 1 | a0001c0001t0001g0099 | 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 | 107 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(104): Show |
108 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(105): 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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0003g0195 | 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 | a0001c0001t0014g0120 a0001c0001t0014g0122 a0001c0001t0014g0123 others(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 | a0001c0001t0009g0215 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0002g0294 a0001c0001t0005g0300 |
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 | a0001c0001t0005g0208 a0001c0001t0005g0209 |
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 | a0001c0001t0005g0208 a0001c0001t0005g0209 |
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 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0033 others(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 | a0001c0001t0004g0259 a0001c0001t0004g0260 a0001c0001t0011g0240 |
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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | 2 | a0001c0001t0007g0002 a0001c0001t0007g0092 |
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 | a0001c0001t0002g0028 | 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 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0147 |
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 | a0001c0001t0018g0172 | 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 | 264 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(261): Show |
267 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(264): 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 | a0001c0001t0002g0298 | 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 | a0001c0001t0005g0205 a0001c0001t0007g0202 a0001c0001t0021g0203 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0005g0015 others(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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0305 a0001c0001t0001g0318 others(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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | 264 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(261): Show |
267 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(264): 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 | a0001c0001t0005g0015 a0001c0001t0005g0016 |
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 | a0001c0001t0005g0205 | 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 | a0001c0001t0001g0023 | 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 | a0001c0001t0012g0214 a0001c0001t0012g0221 a0001c0001t0012g0222 others(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 | a0001c0001t0012g0214 a0001c0001t0012g0221 a0001c0001t0012g0222 others(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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0009g0282 | 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 | a0001c0001t0002g0306 | 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 | a0001c0001t0009g0215 | 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 | a0001c0001t0003g0156 a0001c0001t0003g0168 a0001c0001t0003g0176 others(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 | a0001c0001t0005g0208 a0001c0001t0005g0209 |
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 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
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 | 122 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(119): Show |
123 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(120): 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 | a0001c0001t0003g0174 a0001c0006t0003g0175 |
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 | 122 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(119): Show |
123 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(120): Show |
intron_variant | MODIFIER | c.282+5574G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26925208 | |||||||
| chr4:26925296 | C | T | 94 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(91): Show |
95 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(92): 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 | a0001c0001t0007g0202 | 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 | a0001c0001t0012g0214 a0001c0001t0012g0221 a0001c0001t0012g0222 others(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 | a0001c0001t0006g0134 | 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 | 328 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(325): Show |
331 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(328): 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 | a0001c0001t0003g0168 | 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 | a0001c0001t0033g0145 | 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 | 242 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(239): Show |
245 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(242): 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
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 | a0001c0001t0002g0287 | 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 | a0001c0001t0001g0027 | 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 | a0001c0001t0002g0151 a0001c0001t0002g0152 |
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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0009g0215 others(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 | 264 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(261): Show |
267 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(264): 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 | a0001c0001t0019g0149 | 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 | 112 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(109): Show |
114 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(111): 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0012g0214 others(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 | a0001c0001t0021g0204 | 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 | a0001c0001t0003g0188 a0001c0001t0005g0073 |
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 | 236 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(233): Show |
239 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(236): 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 | a0001c0001t0003g0199 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0003g0201 | 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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0009g0327 | 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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0001g0305 a0001c0001t0001g0318 a0001c0001t0002g0006 others(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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0002g0312 | 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 | a0001c0001t0012g0214 a0001c0001t0012g0221 a0001c0001t0012g0222 others(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 | a0001c0001t0005g0015 | 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 | a0001c0001t0009g0282 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0003g0182 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0002g0313 | 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 | a0001c0001t0007g0109 a0001c0001t0007g0110 a0001c0001t0007g0111 |
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 | a0001c0001t0021g0203 a0001c0001t0021g0204 |
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 | a0001c0001t0033g0145 | 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 | 2 | a0001c0001t0007g0002 a0001c0001t0007g0092 |
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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0004g0236 | 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 | a0001c0001t0002g0310 a0001c0001t0005g0290 a0001c0001t0005g0299 others(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 | a0001c0001t0003g0157 | 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 | a0001c0001t0014g0120 a0001c0001t0014g0122 a0001c0001t0014g0123 others(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 | a0001c0001t0019g0149 | 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 | a0001c0001t0019g0149 | 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 | a0001c0001t0019g0149 | 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 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0147 |
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 | 65 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0093 others(62): 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 | a0001c0001t0001g0142 a0001c0001t0002g0028 a0001c0001t0002g0295 others(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 | 46 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0026 others(43): Show |
47 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(44): 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 | a0001c0001t0001g0021 a0001c0001t0001g0305 a0001c0001t0001g0318 others(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 | a0001c0001t0002g0129 a0001c0001t0003g0158 a0001c0001t0003g0170 others(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 | a0001c0001t0002g0319 | 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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(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 | a0001c0001t0015g0329 | 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 | 103 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(100): Show |
104 | HG00438.hp2 HG00733.hp2 HG00735.hp2 others(101): 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 | 42 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0051 others(39): 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 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0319 |
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 | a0001c0001t0001g0014 | 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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0007g0109 a0001c0001t0007g0110 a0001c0001t0007g0111 |
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 | a0001c0001t0001g0093 | 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 | a0001c0001t0002g0310 | 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 | a0001c0001t0012g0220 | 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 | a0001c0001t0005g0015 a0001c0001t0005g0016 |
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 | a0001c0001t0003g0165 | 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 | a0001c0001t0005g0073 | 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 | a0001c0001t0003g0162 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0305 a0001c0001t0001g0318 others(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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0019g0149 a0001c0002t0019g0108 |
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 | a0001c0001t0002g0303 | 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 | a0001c0001t0014g0120 a0001c0001t0014g0122 a0001c0001t0014g0123 others(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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | a0001c0001t0004g0244 a0001c0001t0004g0245 |
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 | a0001c0001t0003g0003 a0001c0001t0003g0113 a0001c0001t0003g0114 others(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 | a0001c0001t0002g0295 | 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 | a0001c0001t0005g0004 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0012g0214 a0001c0001t0012g0221 a0001c0001t0012g0222 others(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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 others(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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 others(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 | a0001c0001t0009g0278 | 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 | 170 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(167): Show |
173 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(170): 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0007g0109 a0001c0001t0007g0110 a0001c0001t0007g0111 others(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 | 219 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(216): Show |
222 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(219): 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 | a0001c0001t0004g0225 | 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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | a0001c0001t0029g0137 | 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 | a0001c0001t0002g0321 a0001c0001t0002g0325 |
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 | a0001c0001t0001g0318 | 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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 others(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 | a0001c0001t0009g0327 | 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 | 233 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(230): Show |
236 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(233): 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 | a0001c0001t0002g0319 | 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 | a0001c0001t0024g0307 | 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 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0147 |
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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0002g0008 others(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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0036g0017 |
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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0305 others(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 | a0001c0001t0002g0306 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0002t0013g0100 | 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 | a0001c0001t0012g0214 a0001c0001t0012g0221 a0001c0001t0012g0222 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0069 a0001c0001t0001g0280 others(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 | a0001c0001t0002g0094 a0001c0001t0005g0205 a0001c0001t0007g0202 others(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 | a0001c0001t0002g0206 a0001c0001t0005g0004 a0001c0001t0014g0120 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0002g0084 others(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 | a0001c0001t0033g0145 | 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 | a0001c0001t0009g0215 | 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 | 235 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(232): Show |
238 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(235): 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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0012g0214 a0001c0001t0012g0221 a0001c0001t0012g0222 others(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 | a0001c0001t0004g0270 | 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 | a0001c0001t0005g0205 a0001c0001t0007g0202 a0001c0001t0021g0203 others(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 | a0001c0006t0003g0175 | 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 | 232 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(229): Show |
235 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(232): 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 | a0001c0001t0002g0206 | 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 | 135 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(132): Show |
137 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(134): 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 | a0001c0001t0001g0223 a0001c0001t0001g0280 a0001c0001t0001g0281 others(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 | 108 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0024 others(105): Show |
110 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(107): 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 | a0001c0001t0001g0088 | 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 | a0001c0001t0005g0015 a0001c0001t0005g0016 |
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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0002g0028 a0001c0001t0002g0064 a0001c0001t0002g0065 others(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 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0147 |
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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 |
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 | a0001c0001t0001g0142 | 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 | a0001c0001t0005g0016 | 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 | 236 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(233): Show |
239 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(236): 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 | a0001c0001t0001g0024 a0001c0001t0001g0139 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0002g0153 | 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 | a0001c0001t0001g0024 | 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 | 261 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(258): Show |
264 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(261): Show |
intron_variant | MODIFIER | c.282+17396T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26937030 | |||||||
| chr4:26937139 | G | C | 127 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(124): Show |
129 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(126): 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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0002t0009g0115 a0001c0002t0009g0116 |
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 | a0001c0001t0012g0214 a0001c0001t0012g0221 a0001c0001t0012g0222 others(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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0009g0278 | 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 | a0001c0001t0005g0205 a0001c0001t0007g0202 a0001c0001t0021g0203 others(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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0004g0260 a0001c0001t0010g0101 a0001c0001t0010g0102 others(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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0030g0194 | 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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0036g0017 |
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 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0034 others(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 | a0001c0001t0011g0212 | 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 | a0001c0001t0004g0259 a0001c0001t0004g0260 a0001c0001t0011g0240 |
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 | a0001c0002t0013g0100 | 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 | 99 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(96): Show |
101 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(98): 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 | a0001c0001t0003g0193 | 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0002g0294 a0001c0001t0005g0300 |
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 | a0001c0002t0009g0116 | 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 | a0001c0001t0002g0302 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0305 a0001c0001t0001g0318 others(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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0002t0009g0148 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
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 | a0001c0001t0003g0168 | 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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 |
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 | |||||||
| chr4:26939547 | A | T | 4 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0002g0306 | 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0003g0182 | 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 | a0001c0001t0004g0271 | 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 | a0001c0001t0009g0327 | 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 | a0001c0001t0003g0190 | 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 | a0001c0001t0012g0214 a0001c0001t0012g0221 a0001c0001t0012g0222 others(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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0036g0017 |
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 | 2 | a0001c0001t0007g0002 a0001c0001t0007g0092 |
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 | a0001c0001t0001g0021 | 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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 |
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 | a0001c0001t0013g0216 a0001c0001t0013g0217 a0001c0001t0013g0218 |
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 | 232 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(229): Show |
235 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(232): Show |
intron_variant | MODIFIER | c.283-16486C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26941126 | |||||||
| chr4:26941127 | C | G | 234 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(231): Show |
237 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(234): 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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | a0001c0001t0002g0151 a0001c0001t0002g0152 |
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 | a0001c0001t0001g0042 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(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 | a0001c0001t0021g0203 a0001c0001t0021g0204 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0009g0215 | 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 | a0001c0001t0003g0162 | 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 | a0001c0001t0004g0250 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0006g0001 |
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 | 87 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(84): Show |
88 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(85): 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 | a0001c0001t0011g0240 | 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 | 280 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(277): Show |
283 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(280): 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 | a0001c0001t0009g0278 | 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 | a0001c0001t0007g0109 a0001c0001t0007g0110 a0001c0001t0007g0111 |
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 | 89 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(86): Show |
91 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(88): 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 | a0001c0001t0004g0265 a0001c0001t0004g0266 |
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 | a0001c0001t0009g0215 a0001c0001t0028g0283 |
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 | a0001c0001t0001g0050 | 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 | 216 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(213): Show |
219 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(216): 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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | 232 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(229): Show |
235 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(232): 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 | a0001c0001t0002g0291 | 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 | a0001c0001t0004g0230 | 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 | a0001c0002t0013g0100 | 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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0147 |
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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0044g0269 | 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 | a0001c0001t0009g0215 | 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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0001g0042 | 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 | a0001c0001t0033g0145 | 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 | a0001c0001t0028g0283 | 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 | a0001c0001t0014g0120 a0001c0001t0014g0122 a0001c0001t0014g0123 others(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 | 328 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(325): Show |
331 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(328): 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0009g0215 others(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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0028g0283 | 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 | a0001c0001t0003g0003 a0001c0001t0003g0113 a0001c0001t0003g0114 others(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 | a0001c0001t0013g0216 a0001c0001t0013g0217 a0001c0001t0013g0218 |
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 | a0001c0001t0003g0003 a0001c0001t0003g0113 a0001c0001t0003g0114 others(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 | a0001c0001t0012g0279 | 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 | a0001c0001t0003g0158 a0001c0001t0003g0170 a0001c0001t0018g0112 |
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 | a0001c0001t0007g0109 a0001c0001t0007g0110 a0001c0001t0007g0111 |
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 | a0001c0001t0044g0269 | 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 | a0001c0001t0003g0189 a0001c0001t0003g0190 |
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 | a0001c0001t0025g0219 | 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 | a0001c0001t0005g0205 a0001c0001t0007g0202 a0001c0001t0021g0203 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0004g0251 | 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 | a0001c0001t0004g0263 a0001c0001t0004g0264 |
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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | 97 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(94): Show |
98 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(95): 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 | a0001c0001t0014g0120 a0001c0001t0014g0122 a0001c0001t0014g0123 others(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 | 97 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(94): Show |
98 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(95): 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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | 230 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(227): Show |
233 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(230): 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0004g0250 | 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 | a0001c0001t0003g0188 a0001c0001t0005g0073 |
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 | a0001c0001t0001g0079 | 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 | a0001c0002t0013g0100 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0305 a0001c0001t0001g0318 a0001c0001t0002g0006 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0280 a0001c0001t0001g0281 others(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 | a0001c0001t0012g0220 | 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 | a0001c0001t0012g0220 | 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 | a0001c0002t0023g0154 | 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 | a0001c0001t0001g0140 a0001c0001t0005g0141 |
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 | 97 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(94): Show |
98 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(95): 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 | a0001c0001t0001g0039 a0001c0001t0002g0040 |
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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | a0001c0001t0001g0021 | 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 | a0001c0001t0006g0138 | 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 | a0001c0001t0001g0086 | 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 | a0001c0001t0020g0005 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0003g0158 | 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 | a0001c0001t0003g0158 | 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 | a0001c0001t0003g0156 a0001c0001t0003g0168 a0001c0001t0003g0176 others(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 | a0001c0001t0001g0305 a0001c0001t0001g0318 a0001c0001t0002g0006 others(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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | a0001c0001t0007g0247 | 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 | a0001c0001t0001g0305 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0005g0004 | 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 | a0001c0001t0002g0314 | 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 | a0001c0001t0006g0134 | 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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | 96 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(93): Show |
97 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(94): 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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0012g0279 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0012g0214 others(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 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0147 |
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 | a0001c0001t0020g0292 | 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 | a0001c0001t0009g0327 | 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 | a0001c0001t0002g0090 a0001c0005t0002g0089 |
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 | a0001c0001t0003g0162 | 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 | a0001c0001t0009g0327 | 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0016g0018 | 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 | a0001c0001t0001g0058 | 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 | a0001c0001t0036g0017 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
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 | a0001c0001t0001g0035 a0001c0001t0001g0093 a0001c0001t0001g0142 others(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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0005g0015 others(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 | a0001c0001t0002g0206 | 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 | a0001c0001t0010g0101 a0001c0001t0010g0106 a0001c0001t0010g0107 others(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 | 238 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(235): Show |
241 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(238): Show |
intron_variant | MODIFIER | c.283-2470T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26955142 | |||||||
| chr4:26955309 | C | T | 99 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(96): Show |
101 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.283-2303C>T | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 2/11 | chr4 | 26955309 | |||||||
| chr4:26955376 | G | A | 111 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(108): Show |
113 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(110): 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 | a0001c0001t0007g0277 | 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 | a0001c0001t0010g0101 a0001c0001t0010g0106 a0001c0001t0010g0107 others(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 | a0001c0001t0001g0140 | 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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 |
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 | a0001c0001t0001g0091 | 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 | a0001c0001t0012g0214 a0001c0001t0012g0221 a0001c0001t0012g0222 others(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 | a0001c0001t0004g0235 a0001c0001t0004g0259 a0001c0001t0011g0212 others(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 | a0001c0001t0010g0101 a0001c0001t0010g0102 a0001c0001t0010g0106 others(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 | a0001c0001t0002g0306 | 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 | 2 | a0001c0001t0007g0002 a0001c0001t0007g0092 |
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 | 90 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(87): Show |
92 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(89): 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | 97 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(94): Show |
99 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(96): 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 | a0001c0001t0013g0216 a0001c0001t0013g0217 a0001c0001t0013g0218 |
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 | a0001c0001t0043g0311 | 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 | a0001c0001t0004g0244 a0001c0001t0004g0245 a0001c0001t0004g0261 |
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 | a0001c0001t0008g0095 | 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 | a0001c0001t0005g0205 a0001c0001t0007g0202 a0001c0001t0021g0203 others(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 | a0001c0001t0002g0319 | 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 | a0001c0001t0035g0288 | 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 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0002g0151 others(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 | a0001c0001t0003g0162 | 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 | a0001c0001t0030g0194 | 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0005g0015 others(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 | 301 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(298): Show |
304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): 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 | a0001c0001t0004g0270 | 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 | a0001c0002t0026g0103 | 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 | a0001c0001t0021g0203 a0001c0001t0021g0204 |
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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0002g0153 others(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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0009g0215 others(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 | a0001c0002t0023g0154 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0005t0002g0089 | 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 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0006g0001 |
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 | a0001c0001t0004g0226 a0001c0001t0004g0262 a0001c0001t0004g0270 |
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 | 316 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(313): Show |
319 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(316): 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 | a0001c0001t0004g0250 a0001c0001t0004g0265 a0001c0001t0004g0266 |
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 | a0001c0001t0002g0293 | 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 | a0001c0001t0013g0217 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0147 others(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 | a0001c0001t0001g0058 a0001c0001t0001g0305 a0001c0001t0002g0006 others(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 | a0001c0001t0001g0033 a0001c0001t0002g0070 a0001c0001t0002g0151 others(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 | a0001c0001t0005g0205 | 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 | a0001c0001t0002g0011 | 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 | a0001c0001t0005g0205 a0001c0001t0009g0327 a0001c0001t0016g0018 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0059 a0001c0001t0001g0061 others(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 | a0001c0001t0006g0238 | 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 | a0001c0001t0012g0214 a0001c0001t0012g0221 a0001c0001t0012g0222 others(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 | a0001c0001t0001g0318 a0001c0001t0012g0214 a0001c0001t0012g0221 others(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 | a0001c0001t0009g0282 | 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 | a0001c0001t0028g0283 | 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 | a0001c0001t0003g0189 a0001c0001t0003g0190 a0001c0001t0005g0290 others(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 | a0001c0001t0006g0134 | 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 | a0001c0001t0001g0305 | 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 | a0001c0001t0004g0270 | 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0280 others(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 | a0001c0001t0002g0007 a0001c0001t0003g0192 a0001c0001t0004g0258 others(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 | a0001c0001t0002g0071 a0001c0001t0002g0084 a0001c0001t0002g0085 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0059 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0026 others(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 | 6 | a0001c0001t0001g0046 a0001c0001t0001g0053 a0001c0001t0010g0133 others(3): Show |
6 | HG00735.hp1 HG00735.hp2 HG01071.hp2 others(3): 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 | a0001c0001t0001g0043 a0001c0001t0001g0078 a0001c0001t0004g0250 others(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 | a0001c0001t0007g0277 | 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 | a0001c0001t0007g0277 | 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 | a0001c0001t0003g0187 a0001c0006t0003g0175 |
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 | a0001c0001t0003g0164 a0001c0001t0003g0174 a0001c0001t0014g0123 |
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 | a0001c0001t0003g0187 a0001c0006t0003g0175 |
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 | a0001c0001t0005g0205 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0003g0164 a0001c0001t0003g0174 a0001c0001t0014g0123 |
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 | 105 | a0001c0001t0001g0305 a0001c0001t0002g0006 a0001c0001t0002g0007 others(102): 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 | a0001c0001t0005g0205 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0205 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | 323 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(320): Show |
326 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(323): 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 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0033 others(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 | a0001c0001t0009g0215 | 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 | a0001c0001t0009g0278 | 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 | a0001c0001t0007g0277 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 |
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 | a0001c0001t0004g0251 a0001c0001t0006g0001 a0001c0001t0006g0130 others(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 | 323 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(320): Show |
326 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(323): 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 | a0001c0001t0009g0215 | 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 | a0001c0001t0001g0042 | 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 | a0001c0001t0003g0158 a0001c0001t0003g0170 a0001c0001t0007g0277 |
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 | a0001c0001t0003g0189 a0001c0001t0003g0190 |
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 | 194 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(191): Show |
196 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(193): 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 | a0001c0001t0003g0197 a0001c0001t0003g0198 |
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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0001g0318 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.397+6811T>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26964537 | |||||||
| chr4:26964655 | A | G | 54 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(51): Show |
54 | HG00438.hp2 HG00621.hp1 HG00733.hp2 others(51): 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 | a0001c0001t0009g0215 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0014g0120 a0001c0001t0014g0122 a0001c0001t0014g0123 others(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 | a0001c0001t0003g0174 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0086 a0001c0001t0001g0088 others(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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0002g0040 a0001c0001t0003g0003 a0001c0001t0003g0113 others(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 | 26 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0026 others(23): Show |
26 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(23): 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 | a0001c0001t0002g0304 | 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 | a0001c0001t0009g0215 | 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 | a0001c0001t0004g0270 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | 165 | a0001c0001t0001g0041 a0001c0001t0001g0086 a0001c0001t0001g0088 others(162): 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 | a0001c0001t0003g0165 a0001c0001t0003g0180 |
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 | a0001c0001t0033g0145 | 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 | a0001c0001t0009g0215 | 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 | a0001c0001t0002g0287 a0001c0001t0002g0291 a0001c0001t0002g0295 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0086 a0001c0001t0001g0088 others(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 | a0001c0001t0002g0151 a0001c0001t0002g0152 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0086 a0001c0001t0001g0088 others(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 | a0001c0001t0002g0151 a0001c0001t0002g0152 |
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 | a0001c0001t0001g0091 | 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 | a0001c0001t0005g0300 | 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 | a0001c0001t0002g0306 | 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 | a0001c0002t0013g0100 | 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 | a0001c0001t0009g0215 | 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 | a0001c0001t0009g0327 a0001c0001t0019g0149 |
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 | a0001c0001t0003g0180 | 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 | 165 | a0001c0001t0001g0041 a0001c0001t0001g0086 a0001c0001t0001g0088 others(162): 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 | a0001c0001t0003g0155 | 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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 |
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 | a0001c0001t0009g0327 a0001c0001t0019g0149 |
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 | a0001c0001t0004g0118 a0001c0001t0004g0119 a0001c0001t0004g0225 others(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 | a0001c0001t0009g0215 | 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 | a0001c0001t0005g0205 a0001c0001t0007g0109 a0001c0001t0007g0110 others(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 | a0001c0001t0003g0188 | 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 | a0001c0001t0001g0014 | 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 | a0001c0001t0014g0120 a0001c0001t0014g0122 a0001c0001t0014g0123 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0086 a0001c0001t0001g0088 others(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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0001g0305 a0001c0001t0002g0006 a0001c0001t0002g0007 others(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 | a0001c0001t0004g0235 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0012g0279 |
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 | a0001c0001t0033g0145 | 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 | a0001c0002t0026g0103 | 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 | 111 | a0001c0001t0001g0305 a0001c0001t0002g0006 a0001c0001t0002g0007 others(108): 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 | a0001c0001t0005g0205 a0001c0001t0007g0109 a0001c0001t0007g0110 others(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 | a0001c0001t0001g0305 | 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 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0002g0291 others(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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0009g0215 |
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 | a0001c0001t0001g0082 a0001c0001t0034g0121 |
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 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0047 others(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 | 74 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(71): Show |
75 | HG00438.hp2 HG00621.hp1 HG00733.hp2 others(72): 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 | a0001c0001t0001g0224 a0001c0001t0002g0028 a0001c0001t0002g0064 others(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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0021g0203 others(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 | 61 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0027 others(58): Show |
61 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(58): 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 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0043 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0056 others(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 | a0001c0001t0009g0327 a0001c0001t0011g0213 a0001c0001t0013g0217 others(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 | a0001c0001t0001g0318 | 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 | a0001c0001t0045g0171 | 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 | a0001c0001t0012g0214 a0001c0001t0012g0222 a0001c0001t0025g0219 |
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 | a0001c0001t0003g0189 a0001c0001t0003g0190 a0001c0001t0005g0290 others(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 | a0001c0001t0007g0002 a0001c0001t0007g0092 a0001c0002t0026g0103 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0215 others(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 | a0001c0001t0001g0082 a0001c0001t0034g0121 a0001c0002t0013g0100 |
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 | a0001c0001t0033g0145 | 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 | a0001c0001t0002g0276 a0001c0001t0002g0309 a0001c0001t0002g0320 others(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 | a0001c0001t0034g0121 | 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 | a0001c0001t0033g0145 | 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 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(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 | 231 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(228): Show |
233 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(230): 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 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0147 |
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 | a0001c0001t0012g0214 | 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 | 323 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(320): Show |
326 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(323): Show |
intron_variant | MODIFIER | c.397+12683C>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26970409 | |||||||
| chr4:26970932 | G | A | 312 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(312): 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 | a0001c0001t0009g0327 a0001c0001t0019g0149 |
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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0003g0166 a0001c0001t0003g0177 |
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 | a0001c0001t0003g0166 a0001c0001t0003g0177 |
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 | a0001c0001t0005g0205 a0001c0001t0007g0109 a0001c0001t0007g0110 others(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 | a0001c0001t0001g0318 a0001c0001t0012g0214 a0001c0001t0012g0221 others(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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0005g0015 a0001c0001t0005g0016 |
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 | a0001c0001t0009g0327 a0001c0001t0019g0149 |
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 | a0001c0001t0005g0205 a0001c0001t0007g0109 a0001c0001t0007g0110 others(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 | a0001c0001t0002g0151 a0001c0001t0002g0152 |
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 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0147 others(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 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0147 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0009g0215 |
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 | a0001c0001t0004g0244 a0001c0001t0004g0245 a0001c0001t0004g0261 others(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 | a0001c0001t0025g0219 | 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0009g0215 |
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 | a0001c0001t0001g0069 | 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 | a0001c0001t0003g0333 | 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 | a0001c0001t0003g0333 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0002t0019g0108 | 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 | a0001c0001t0014g0120 a0001c0001t0014g0122 a0001c0001t0014g0123 others(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 | a0001c0001t0004g0119 | 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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 |
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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0009 |
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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0001g0305 | 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 | a0001c0001t0001g0318 a0001c0001t0012g0214 a0001c0001t0012g0221 others(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 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0147 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0086 a0001c0001t0001g0088 others(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 | a0001c0001t0003g0200 a0001c0001t0003g0201 |
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 | a0001c0001t0002g0314 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0014g0123 | 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 | a0001c0001t0007g0277 | 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 | a0001c0001t0001g0318 a0001c0001t0012g0214 a0001c0001t0012g0221 others(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 | 177 | a0001c0001t0001g0041 a0001c0001t0001g0086 a0001c0001t0001g0088 others(174): 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 | a0001c0001t0028g0283 | 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 | a0001c0001t0005g0036 a0001c0001t0005g0081 a0001c0001t0005g0097 |
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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0002t0019g0108 | 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 | a0001c0001t0014g0120 a0001c0001t0014g0122 a0001c0001t0014g0123 others(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 | a0001c0001t0009g0215 | 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 | a0001c0002t0026g0103 | 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 | a0001c0002t0026g0103 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0003g0173 | 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 | 323 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(320): Show |
326 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(323): 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 | a0001c0001t0004g0225 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0009g0215 | 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 | a0001c0001t0002g0289 | 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 | a0001c0001t0010g0326 | 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 | a0001c0001t0009g0327 a0001c0001t0019g0149 |
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 | a0001c0001t0004g0251 a0001c0001t0006g0001 a0001c0001t0006g0130 others(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 | a0001c0001t0001g0305 a0001c0001t0002g0006 a0001c0001t0002g0007 others(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 | a0001c0001t0014g0120 a0001c0001t0014g0122 a0001c0001t0014g0123 others(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 | a0001c0001t0002g0152 | 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 | 125 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(122): Show |
127 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(124): 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 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0004g0267 others(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 | a0001c0001t0001g0318 a0001c0001t0012g0214 a0001c0001t0012g0221 others(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 | a0001c0001t0033g0145 | 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 | a0001c0002t0019g0108 | 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 | 323 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(320): Show |
326 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(323): 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 | a0001c0001t0004g0251 | 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 | a0001c0001t0001g0042 | 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 | a0001c0001t0012g0221 | 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 | a0001c0001t0017g0184 a0001c0001t0017g0185 a0001c0001t0017g0186 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0048 a0001c0001t0001g0054 |
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 | a0001c0001t0009g0215 | 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 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0147 |
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 | a0001c0001t0001g0043 | 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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 |
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 | a0001c0001t0001g0318 a0001c0001t0012g0214 a0001c0001t0012g0221 others(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 | a0001c0001t0009g0215 | 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 | 323 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(320): Show |
326 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(323): 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 | a0001c0001t0009g0327 a0001c0001t0019g0149 |
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 | 323 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(320): Show |
326 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(323): Show |
intron_variant | MODIFIER | c.398-17307A>G | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26978072 | |||||||
| chr4:26978091 | G | A | 323 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(320): Show |
326 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(323): Show |
intron_variant | MODIFIER | c.398-17288G>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 3/11 | chr4 | 26978091 | |||||||
| chr4:26978399 | A | G | 59 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(56): Show |
59 | HG00438.hp2 HG00621.hp1 HG00733.hp2 others(56): 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 | a0001c0001t0012g0279 | 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 | a0001c0001t0009g0215 | 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 | a0001c0001t0005g0073 | 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 | a0001c0001t0033g0145 a0001c0001t0036g0017 |
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 | a0001c0001t0003g0192 | 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 | a0001c0001t0005g0015 a0001c0001t0005g0016 |
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 | a0001c0001t0004g0231 | 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 | a0001c0001t0036g0017 | 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 | a0001c0001t0003g0158 | 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 | 326 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(323): Show |
329 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(326): 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0008g0031 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0003g0170 | 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 | a0001c0001t0007g0277 | 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 | a0001c0001t0006g0117 | 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 | a0001c0001t0003g0200 | 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 | a0001c0001t0033g0145 a0001c0001t0036g0017 |
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 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0049 |
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 | a0001c0001t0002g0007 | 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 | a0001c0001t0013g0217 a0001c0001t0030g0194 a0001c0001t0045g0171 |
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 | a0001c0001t0007g0109 a0001c0001t0007g0110 a0001c0001t0007g0111 |
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 | a0001c0001t0010g0326 | 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 | 323 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(320): Show |
326 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(323): 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 | a0001c0001t0024g0307 | 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 | a0001c0001t0012g0279 | 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 | a0001c0001t0001g0091 | 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 | a0001c0001t0012g0214 a0001c0001t0012g0221 a0001c0001t0012g0222 others(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 | a0001c0001t0009g0282 | 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 | a0001c0001t0001g0024 | 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 | a0001c0001t0002g0316 | 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 | a0001c0001t0003g0156 | 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 | 182 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(179): Show |
184 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(181): 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0280 others(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 | a0001c0001t0001g0318 a0001c0001t0012g0214 a0001c0001t0012g0221 others(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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 others(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 | a0001c0001t0024g0307 | 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 | a0001c0001t0041g0234 | 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 | a0001c0001t0024g0307 | 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 | 323 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(320): Show |
326 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(323): 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 | a0001c0001t0001g0305 a0001c0001t0002g0006 a0001c0001t0002g0007 others(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 | a0001c0001t0004g0230 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0003g0189 a0001c0001t0003g0190 |
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 | 124 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0305 others(121): 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 | a0001c0001t0009g0327 a0001c0001t0019g0149 |
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 | 165 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0305 others(162): 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0005g0015 a0001c0001t0005g0016 |
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 | a0001c0001t0003g0169 | 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 | a0001c0001t0033g0145 a0001c0001t0036g0017 |
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 | 323 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(320): Show |
326 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(323): 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 | a0001c0005t0002g0089 | 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 | a0001c0001t0001g0140 | 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 | a0001c0002t0009g0115 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0036 a0001c0001t0005g0081 a0001c0001t0005g0097 others(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 | a0001c0001t0002g0090 a0001c0005t0002g0089 |
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 | a0001c0001t0009g0327 a0001c0001t0019g0149 |
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 | a0001c0001t0005g0205 a0001c0001t0007g0202 a0001c0001t0021g0203 others(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 | a0001c0001t0001g0140 | 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 | a0001c0001t0002g0206 a0001c0001t0002g0276 a0001c0001t0002g0309 others(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 | a0001c0001t0002g0289 | 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 | a0001c0001t0002g0289 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 |
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 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(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 | a0001c0001t0003g0189 a0001c0001t0003g0190 |
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 | a0001c0001t0011g0212 a0001c0001t0011g0213 a0001c0001t0016g0018 others(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 | a0001c0001t0036g0017 | 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 | a0001c0001t0009g0215 | 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 | a0001c0001t0033g0145 a0001c0001t0036g0017 |
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 | a0001c0001t0005g0205 a0001c0001t0007g0109 a0001c0001t0007g0110 others(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 | a0001c0001t0036g0017 | 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 | a0001c0001t0033g0145 | 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 | 117 | a0001c0001t0001g0305 a0001c0001t0002g0006 a0001c0001t0002g0007 others(114): 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 | a0001c0001t0035g0288 | 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 | a0001c0001t0028g0283 | 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 | a0001c0001t0003g0157 | 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 | a0001c0001t0012g0220 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0002g0313 | 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 | a0001c0001t0009g0215 | 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 | a0001c0001t0002g0313 | 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 | a0001c0001t0005g0036 | 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 | a0001c0001t0004g0258 | 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 | a0001c0001t0003g0164 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 |
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 | a0001c0001t0005g0015 a0001c0001t0005g0016 |
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 | a0001c0001t0002g0302 | 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | 23 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0026 others(20): Show |
23 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(20): 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 | a0001c0001t0009g0327 a0001c0001t0019g0149 |
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 | a0001c0001t0013g0216 a0001c0001t0013g0218 |
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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0012g0279 | 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 | a0001c0001t0002g0313 | 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 | 162 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0305 others(159): 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | 160 | a0001c0001t0001g0305 a0001c0001t0002g0006 a0001c0001t0002g0007 others(157): 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 | a0001c0001t0006g0117 a0001c0001t0006g0246 a0001c0001t0006g0252 |
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 | a0001c0001t0004g0242 | 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 | a0001c0001t0002g0293 | 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0280 others(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 | a0001c0001t0002g0206 | 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 | 122 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0280 others(119): 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 | a0001c0001t0013g0217 a0001c0001t0030g0194 a0001c0001t0045g0171 |
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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0280 others(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 | a0001c0001t0009g0215 | 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 | a0001c0001t0033g0145 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0058 |
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 | 323 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(320): Show |
326 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(323): 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 | a0001c0001t0007g0109 a0001c0001t0007g0110 a0001c0001t0007g0111 |
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 | 117 | a0001c0001t0001g0305 a0001c0001t0002g0006 a0001c0001t0002g0007 others(114): 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 | a0001c0001t0012g0221 | 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 | a0001c0002t0013g0100 | 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 | 154 | a0001c0001t0001g0305 a0001c0001t0002g0006 a0001c0001t0002g0007 others(151): 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 | a0001c0001t0005g0205 a0001c0001t0007g0109 a0001c0001t0007g0110 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0001c0001t0003g0189 a0001c0001t0003g0190 |
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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0147 others(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 | 323 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(320): Show |
326 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(323): 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 | a0001c0002t0026g0103 | 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 | a0001c0001t0009g0215 | 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 | a0001c0001t0001g0027 | 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 | a0001c0001t0003g0150 a0001c0001t0003g0161 a0001c0001t0003g0165 others(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 | 179 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(176): Show |
180 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(177): 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 | a0001c0001t0005g0036 a0001c0001t0005g0081 a0001c0001t0005g0097 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0003g0169 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0051 others(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 | a0001c0001t0002g0206 a0001c0001t0002g0276 a0001c0001t0002g0309 others(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 | a0001c0001t0003g0191 | 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0004g0250 a0001c0001t0004g0265 a0001c0001t0004g0266 |
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 | 124 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0305 others(121): 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 | a0001c0001t0003g0155 | 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 | a0001c0001t0014g0120 a0001c0001t0014g0122 a0001c0001t0014g0123 others(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 | a0001c0001t0001g0140 | 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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0012g0220 |
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 | a0001c0001t0009g0327 | 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 | a0001c0001t0033g0145 | 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 | a0001c0001t0003g0156 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0003g0155 | 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 | a0001c0001t0002g0314 | 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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 |
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 | a0001c0001t0001g0318 a0001c0001t0012g0214 a0001c0001t0012g0221 others(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 | a0001c0001t0005g0205 a0001c0001t0007g0109 a0001c0001t0007g0110 others(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 | a0001c0001t0003g0195 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0003t0001g0284 | 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 | a0001c0002t0009g0115 a0001c0002t0009g0116 |
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 | a0001c0001t0005g0205 a0001c0001t0007g0109 a0001c0001t0007g0110 others(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 | a0001c0001t0004g0251 | 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 | a0001c0001t0003g0157 | 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 | a0001c0001t0014g0124 | 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 | a0001c0001t0005g0290 a0001c0001t0005g0299 a0001c0001t0005g0300 |
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 | a0001c0001t0004g0242 | 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 | a0001c0001t0002g0128 a0001c0001t0002g0129 |
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 | 99 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(96): Show |
100 | HG00438.hp2 HG00621.hp1 HG00733.hp2 others(97): 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 | a0001c0001t0004g0118 a0001c0001t0004g0225 a0001c0001t0004g0226 others(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 | 166 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0280 others(163): 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 | a0001c0001t0005g0205 a0001c0001t0007g0202 a0001c0001t0015g0329 others(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 | a0001c0001t0009g0327 a0001c0001t0019g0149 |
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 | a0001c0001t0005g0015 a0001c0001t0005g0016 |
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 | a0001c0001t0008g0095 | 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 | a0001c0001t0001g0099 a0001c0001t0001g0147 |
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 | a0001c0001t0004g0118 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0004g0118 others(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 | a0001c0001t0015g0332 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 |
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 | a0001c0001t0002g0152 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0305 others(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 | 160 | a0001c0001t0001g0305 a0001c0001t0002g0006 a0001c0001t0002g0007 others(157): 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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 |
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 | a0001c0001t0004g0242 | 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 | a0001c0001t0010g0101 | 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 | a0001c0001t0004g0225 | 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 | 314 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(311): Show |
317 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(314): 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 | a0001c0003t0001g0284 | 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 | a0001c0001t0005g0004 | 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0002g0293 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0013g0217 a0001c0001t0030g0194 a0001c0001t0045g0171 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0034g0121 | 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0004g0227 | 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 | a0001c0001t0005g0015 | 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 | a0001c0001t0007g0247 a0001c0001t0007g0254 |
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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0004g0239 | 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 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0147 |
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 | 162 | a0001c0001t0001g0305 a0001c0001t0002g0006 a0001c0001t0002g0007 others(159): 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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | a0001c0001t0001g0139 | 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 | a0001c0001t0003g0187 a0001c0001t0003g0195 a0001c0001t0003g0199 others(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 | a0001c0001t0036g0017 | 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 | a0001c0001t0001g0083 | 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 | a0001c0001t0002g0028 a0001c0001t0002g0064 a0001c0001t0002g0065 others(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 | a0001c0001t0004g0226 a0001c0001t0004g0262 a0001c0001t0004g0270 |
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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | a0001c0003t0001g0284 | 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 | 323 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(320): Show |
326 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(323): 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 | a0001c0001t0002g0291 | 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0007g0254 |
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 | 137 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(134): Show |
138 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(135): 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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0040g0080 | 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 | 2 | a0001c0001t0007g0002 a0001c0001t0007g0092 |
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 | 160 | a0001c0001t0001g0305 a0001c0001t0002g0006 a0001c0001t0002g0007 others(157): 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 | a0001c0001t0009g0215 | 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 | a0001c0001t0014g0123 a0001c0002t0023g0154 |
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 | a0001c0001t0001g0058 | 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 | a0001c0001t0002g0090 a0001c0005t0002g0089 |
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 | a0001c0001t0004g0258 | 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 | a0001c0001t0009g0282 | 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0004g0271 a0001c0001t0006g0117 a0001c0001t0006g0246 others(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 | 326 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(323): Show |
329 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(326): 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 | a0001c0001t0033g0145 | 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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | 1 | a0001c0001t0007g0002 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | 58 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(55): Show |
58 | HG00438.hp2 HG00621.hp1 HG00733.hp2 others(55): 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 | a0001c0001t0035g0288 | 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 | a0001c0001t0007g0111 | 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 | a0001c0001t0021g0204 | 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 | a0001c0001t0021g0203 a0001c0001t0021g0204 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
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 | a0001c0001t0003g0003 a0001c0001t0003g0113 a0001c0001t0003g0155 others(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 | a0001c0001t0002g0291 | 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 | a0001c0001t0033g0145 a0001c0001t0036g0017 |
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 | a0001c0001t0014g0120 a0001c0001t0014g0122 a0001c0001t0014g0123 |
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 | a0001c0001t0015g0329 a0001c0001t0015g0330 a0001c0001t0015g0331 others(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 | a0001c0001t0001g0140 | 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 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0004g0248 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0058 |
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 | 117 | a0001c0001t0001g0305 a0001c0001t0002g0006 a0001c0001t0002g0007 others(114): 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 | 117 | a0001c0001t0001g0305 a0001c0001t0002g0006 a0001c0001t0002g0007 others(114): 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 | a0001c0001t0034g0121 | 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 | 117 | a0001c0001t0001g0305 a0001c0001t0002g0006 a0001c0001t0002g0007 others(114): 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 | a0001c0001t0003g0113 a0001c0001t0003g0155 a0001c0001t0003g0156 others(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 | a0001c0003t0001g0284 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0014g0120 a0001c0001t0014g0122 a0001c0001t0014g0123 others(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 | a0001c0001t0004g0251 | 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 | a0001c0001t0002g0128 a0001c0001t0002g0129 |
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 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0147 others(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 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0020 |
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 | a0001c0001t0002g0291 a0001c0001t0002g0297 a0001c0001t0002g0314 |
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 | a0001c0003t0001g0284 | 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 | a0001c0001t0004g0251 a0001c0001t0006g0001 a0001c0001t0006g0130 others(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 | a0001c0001t0004g0119 | 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0001g0078 | 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 | 318 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(315): Show |
321 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(318): 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 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0001g0318 a0001c0001t0012g0214 a0001c0001t0012g0221 others(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 | a0001c0001t0002g0128 a0001c0001t0002g0129 |
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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1489+2652G>C | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27011654 | |||||||
| chr4:27011979 | C | T | 1 | a0001c0001t0003g0174 | 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 | a0001c0002t0026g0103 | 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 | a0001c0001t0009g0282 | 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0003g0275 | 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 | 145 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(142): Show |
146 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.1489+3385C>A | STIM2 | ENSG00000109689.20 | transcript | ENST00000467087.7 | protein_coding | 10/11 | chr4 | 27012387 | |||||||
| chr4:27012462 | T | TC | 318 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(315): Show |
321 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(318): 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 | a0001c0001t0009g0282 | 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 | a0001c0002t0019g0108 | 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 | a0001c0001t0001g0305 a0001c0001t0002g0006 a0001c0001t0002g0007 others(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 | a0001c0001t0004g0258 | 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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0147 |
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 | a0001c0001t0033g0145 | 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 | a0001c0001t0004g0118 a0001c0001t0004g0119 a0001c0001t0004g0225 others(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 | a0001c0001t0003g0157 | 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 | a0001c0001t0003g0187 | 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 | a0001c0002t0013g0100 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0280 a0001c0001t0001g0281 |
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 | a0001c0001t0001g0318 a0001c0001t0012g0214 a0001c0001t0012g0221 others(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 | a0001c0001t0004g0272 | 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 | a0001c0001t0001g0305 a0001c0001t0002g0006 a0001c0001t0002g0007 others(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 | a0001c0001t0005g0015 | 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 | a0001c0001t0002g0313 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0047 others(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 | 17 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0032 others(14): Show |
17 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(14): 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 | a0001c0001t0008g0072 | 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 | 137 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(134): Show |
138 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(135): 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 | a0001c0001t0014g0123 | 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 | a0001c0001t0005g0015 a0001c0001t0005g0016 |
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 | a0001c0001t0009g0282 | 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 | a0001c0001t0009g0327 a0001c0001t0019g0149 |
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 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0027 others(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 | 318 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(315): Show |
321 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(318): 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 | a0001c0001t0034g0121 | 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 | a0001c0001t0004g0118 | 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 | a0001c0001t0033g0145 | 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 | a0001c0001t0037g0135 | 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 | a0001c0001t0003g0158 | 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 | a0001c0001t0040g0080 | 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 | a0001c0001t0017g0184 a0001c0001t0017g0185 a0001c0001t0017g0186 others(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 | a0001c0001t0003g0157 | 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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0001g0305 a0001c0001t0002g0006 a0001c0001t0002g0007 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0013g0216 a0001c0001t0013g0218 |
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 | 2 | a0001c0001t0007g0002 a0001c0001t0007g0092 |
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 | a0001c0001t0003g0199 | 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 | 144 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(141): Show |
146 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(143): 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 | a0001c0001t0033g0145 | 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 | a0001c0001t0009g0127 | 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 | a0001c0001t0003g0193 | 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 | a0001c0001t0003g0195 | 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 | 326 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(323): Show |
329 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(326): 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 | a0001c0001t0002g0316 | 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 | a0001c0001t0002g0028 a0001c0001t0002g0064 a0001c0001t0002g0065 others(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 | a0001c0001t0002g0320 | 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 | 326 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(323): Show |
329 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(326): 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 | a0001c0001t0009g0327 a0001c0001t0019g0149 |
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 | a0001c0001t0014g0120 a0001c0001t0014g0122 a0001c0001t0014g0123 others(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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | a0001c0001t0003g0170 | 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 | a0001c0001t0005g0205 a0001c0001t0007g0109 a0001c0001t0007g0110 others(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 | a0001c0001t0004g0119 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 | a0001c0001t0003g0198 | 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 | a0001c0001t0011g0212 a0001c0001t0011g0213 |
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 | a0001c0001t0007g0277 | 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 | a0001c0001t0014g0120 a0001c0001t0014g0122 a0001c0001t0014g0123 |
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 | a0001c0001t0032g0296 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0009g0278 others(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 |