Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 488 |
| ensemblid | ENSG00000174437.18 |
| hgncid | 812 |
| symbol | ATP2A2 |
| name | ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2 |
| refseq_nuc | NM_170665.4 |
| refseq_prot | NP_733765.1 |
| ensembl_nuc | ENST00000539276.7 |
| ensembl_prot | ENSP00000440045.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 110281247 |
| end | 110351093 |
| strand | + |
| ver | v1.2 |
| region | chr12:110281247-110351093 |
| region5000 | chr12:110276247-110356093 |
| regionname0 | ATP2A2_chr12_110281247_110351093 |
| regionname5000 | ATP2A2_chr12_110276247_110356093 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1042 | 225 | 88 | 61 | 34 | 16 | 24 | 28 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | MENAH others(1037): Show |
chr12 | 110276247 | 110356093 |
| a0002 | 0/0 | 1042 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | MENAH others(1037): Show |
chr12 | 110276247 | 110356093 |
| a0003 | 0/0 | 1042 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | MENAH others(1037): Show |
chr12 | 110276247 | 110356093 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3126 | 211 | 82 | 58 | 33 | 13 | 23 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATGGA others(3121): Show |
chr12 | 110276247 | 110356093 | ||
| a0001c0002 | 0/0 | 3126 | 4 | 0 | 1 | 0 | 3 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATGGA others(3121): Show |
chr12 | 110276247 | 110356093 | ||
| a0001c0003 | 0/0 | 3126 | 4 | 4 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATGGA others(3121): Show |
chr12 | 110276247 | 110356093 | ||
| a0001c0005 | 0/0 | 3126 | 2 | 0 | 2 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATGGA others(3121): Show |
chr12 | 110276247 | 110356093 | ||
| a0001c0006 | 0/0 | 3126 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATGGA others(3121): Show |
chr12 | 110276247 | 110356093 | ||
| a0001c0007 | 0/0 | 3126 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATGGA others(3121): Show |
chr12 | 110276247 | 110356093 | ||
| a0001c0008 | 0/0 | 3126 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATGGA others(3121): Show |
chr12 | 110276247 | 110356093 | ||
| a0001c0010 | 0/0 | 3126 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATGGA others(3121): Show |
chr12 | 110276247 | 110356093 | ||
| a0002c0004 | 0/0 | 3126 | 2 | 0 | 0 | 0 | 0 | 2 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATGGA others(3121): Show |
chr12 | 110276247 | 110356093 | ||
| a0003c0009 | 0/0 | 3126 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATGGA others(3121): Show |
chr12 | 110276247 | 110356093 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 8295 | 103 | 42 | 22 | 20 | 5 | 13 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0002 | 0/0 | 8299 | 26 | 14 | 3 | 5 | 1 | 3 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8294): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0003 | 0/1 | 8295 | 27 | 1 | 18 | 0 | 5 | 2 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0004 | 0/0 | 8299 | 9 | 8 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8294): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0005 | 0/0 | 8295 | 8 | 1 | 4 | 0 | 1 | 2 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0006 | 0/0 | 8295 | 6 | 5 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0007 | 0/0 | 8295 | 5 | 0 | 4 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0008 | 0/0 | 8295 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0010 | 0/0 | 8295 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0011 | 0/0 | 8299 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8294): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0012 | 0/0 | 8299 | 2 | 1 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8294): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0013 | 0/0 | 8295 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0014 | 0/0 | 8295 | 2 | 1 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0015 | 0/0 | 8295 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0016 | 0/0 | 8295 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0017 | 0/0 | 8299 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8294): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0018 | 0/0 | 8299 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8294): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0019 | 0/0 | 8299 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8294): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0021 | 0/0 | 8295 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0022 | 0/0 | 8295 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0023 | 0/0 | 8295 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0024 | 0/0 | 8295 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0025 | 0/0 | 8295 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0026 | 0/0 | 8295 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0027 | 0/0 | 8295 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0028 | 0/0 | 8295 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0001c0001t0029 | 0/0 | 8295 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0001c0002t0001 | 0/0 | 8295 | 4 | 0 | 1 | 0 | 3 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0001c0003t0002 | 0/0 | 8299 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8294): Show |
chr12 | 110276247 | 110356093 |
| a0001c0003t0004 | 0/0 | 8299 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8294): Show |
chr12 | 110276247 | 110356093 |
| a0001c0003t0020 | 0/0 | 8299 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8294): Show |
chr12 | 110276247 | 110356093 |
| a0001c0005t0009 | 0/0 | 8295 | 2 | 0 | 2 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0001c0006t0001 | 0/0 | 8295 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0001c0007t0002 | 0/0 | 8299 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8294): Show |
chr12 | 110276247 | 110356093 |
| a0001c0008t0030 | 0/0 | 8295 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0001c0010t0001 | 0/0 | 8295 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0002c0004t0003 | 0/0 | 8295 | 2 | 0 | 0 | 0 | 0 | 2 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| a0003c0009t0001 | 0/0 | 8295 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | ATTAG others(8290): Show |
chr12 | 110276247 | 110356093 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0063 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0005g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0005g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0006g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0006g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0007g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0007g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0007g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0007g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0007g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0008g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0008g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0010g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0010g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0011g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0011g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0012g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0012g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0013g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0013g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0014g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0014g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0015g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0015g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0016g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0017g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0018g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0019g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0021g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0022g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0023g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0024g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0025g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0026g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0027g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0028g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0029g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0003t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0003t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0003t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0003t0020g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0005t0009g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0005t0009g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0006t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0007t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0008t0030g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0010t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0002c0004t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0002c0004t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0003c0009t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | GBR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0139 | EUR | GBR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0208 | EUR | FIN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0047 | EUR | FIN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0191 | EUR | FIN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00423 | hp1 | a0001 | c0001 | t0023 | g0148 | EAS | CHS | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0187 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0209 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00738 | hp1 | a0001 | c0005 | t0009 | g0219 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0125 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01069 | hp1 | a0001 | c0001 | t0007 | g0049 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01069 | hp2 | a0001 | c0005 | t0009 | g0220 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01071 | hp1 | a0001 | c0001 | t0007 | g0051 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0189 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0154 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01074 | hp2 | a0001 | c0001 | t0028 | g0206 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01099 | hp1 | a0001 | c0001 | t0012 | g0222 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01109 | hp1 | a0001 | c0001 | t0014 | g0176 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0169 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0161 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0180 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0184 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0119 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0194 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0224 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01346 | hp1 | a0001 | c0001 | t0029 | g0197 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0202 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0186 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | IBS | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0117 | EUR | IBS | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0116 | EUR | IBS | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0199 | EUR | IBS | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0175 | EUR | IBS | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0115 | EUR | IBS | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01884 | hp1 | a0001 | c0001 | t0015 | g0077 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01891 | hp2 | a0001 | c0003 | t0020 | g0019 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0185 | AMR | PEL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01928 | hp2 | a0001 | c0001 | t0026 | g0113 | AMR | PEL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0190 | AMR | PEL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01943 | hp1 | a0001 | c0001 | t0006 | g0017 | AMR | PEL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01943 | hp2 | a0001 | c0001 | t0007 | g0048 | AMR | PEL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0196 | AMR | PEL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0178 | AMR | PEL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0192 | AMR | PEL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02145 | hp1 | a0001 | c0001 | t0012 | g0223 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02145 | hp2 | a0001 | c0008 | t0030 | g0183 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02257 | hp2 | a0001 | c0001 | t0018 | g0026 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0173 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02293 | hp1 | a0001 | c0001 | t0007 | g0050 | AMR | PEL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | PEL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0122 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02615 | hp1 | a0001 | c0001 | t0021 | g0029 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0168 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0167 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0013 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0218 | SAS | PJL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02717 | hp2 | a0001 | c0007 | t0002 | g0025 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02735 | hp2 | a0001 | c0001 | t0005 | g0109 | SAS | PJL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0170 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02922 | hp1 | a0001 | c0003 | t0002 | g0020 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02970 | hp1 | a0001 | c0001 | t0015 | g0076 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02970 | hp2 | a0001 | c0001 | t0011 | g0056 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02976 | hp2 | a0001 | c0001 | t0017 | g0004 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0014 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0174 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03195 | hp1 | a0001 | c0003 | t0002 | g0021 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03490 | hp2 | a0002 | c0004 | t0003 | g0181 | SAS | PJL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03492 | hp1 | a0002 | c0004 | t0003 | g0182 | SAS | PJL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03516 | hp1 | a0001 | c0001 | t0011 | g0058 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | STU | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | STU | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG04115 | hp2 | a0001 | c0001 | t0016 | g0215 | SAS | STU | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0193 | SAS | BEB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0044 | SAS | BEB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG04199 | hp2 | a0001 | c0001 | t0025 | g0074 | SAS | STU | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG04204 | hp1 | a0001 | c0001 | t0027 | g0201 | SAS | STU | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | STU | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | STU | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG04228 | hp2 | a0001 | c0010 | t0001 | g0106 | SAS | STU | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | YRI | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | YRI | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | YRI | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18946 | hp1 | a0001 | c0001 | t0013 | g0085 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18946 | hp2 | a0001 | c0001 | t0008 | g0163 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18959 | hp2 | a0001 | c0001 | t0013 | g0083 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18973 | hp1 | a0001 | c0001 | t0022 | g0134 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18995 | hp1 | a0001 | c0006 | t0001 | g0162 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18998 | hp1 | a0001 | c0001 | t0008 | g0165 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | LWK | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | LWK | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19062 | hp2 | a0001 | c0001 | t0010 | g0138 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19077 | hp2 | a0001 | c0001 | t0010 | g0140 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | YRI | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ASW | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0203 | EUR | TSI | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | TSI | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA20805 | hp1 | a0001 | c0001 | t0007 | g0052 | EUR | TSI | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0126 | EUR | TSI | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | GIH | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0108 | SAS | GIH | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01123 | hp1 | a0003 | c0009 | t0001 | g0066 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0195 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02109 | hp2 | a0001 | c0001 | t0014 | g0177 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02486 | hp1 | a0001 | c0003 | t0004 | g0216 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03471 | hp1 | a0001 | c0001 | t0019 | g0045 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA21309 | hp1 | a0001 | c0001 | t0024 | g0092 | AFR | LWK | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0179 | REF | REF | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0063 | REF | REF | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110332597 | A | G | 1 | a0003 | 1 | HG01123.hp1 | missense_variant&splice_region_variant | MODERATE | c.1096A>G | p.Met366Val | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 9/20 | 1639/8295 | 1096/3129 | 366/1042 | chr12 | 110332597 | |||
| chr12:110346405 | A | G | 1 | a0002 | 2 | HG03490.hp2 HG03492.hp1 |
missense_variant | MODERATE | c.3064A>G | p.Ile1022Val | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 3607/8295 | 3064/3129 | 1022/1042 | chr12 | 110346405 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110281870 | A | G | 1 | a0001c0005 | 2 | HG00738.hp1 HG01069.hp2 |
synonymous_variant | LOW | c.81A>G | p.Glu27Glu | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/20 | 624/8295 | 81/3129 | 27/1042 | chr12 | 110281870 | |||
| chr12:110296601 | A | G | 1 | a0001c0005 | 2 | HG00738.hp1 HG01069.hp2 |
splice_region_variant&synonymous_variant | LOW | c.327A>G | p.Glu109Glu | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/20 | 870/8295 | 327/3129 | 109/1042 | chr12 | 110296601 | |||
| chr12:110326424 | C | T | 1 | a0001c0010 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.579C>T | p.Pro193Pro | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 7/20 | 1122/8295 | 579/3129 | 193/1042 | chr12 | 110326424 | |||
| chr12:110342302 | G | A | 1 | a0001c0002 | 4 | HG01261.hp2 HG01515.hp2 HG01516.hp1 others(1): Show |
synonymous_variant | LOW | c.2172G>A | p.Ala724Ala | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 15/20 | 2715/8295 | 2172/3129 | 724/1042 | chr12 | 110342302 | |||
| chr12:110342440 | A | G | 1 | a0001c0008 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.2310A>G | p.Glu770Glu | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 15/20 | 2853/8295 | 2310/3129 | 770/1042 | chr12 | 110342440 | |||
| chr12:110345269 | A | G | 1 | a0001c0003 | 4 | HG01891.hp2 HG02486.hp1 HG02922.hp1 others(1): Show |
synonymous_variant | LOW | c.2628A>G | p.Lys876Lys | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 18/20 | 3171/8295 | 2628/3129 | 876/1042 | chr12 | 110345269 | |||
| chr12:110346007 | C | T | 1 | a0001c0007 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.2748C>T | p.Ser916Ser | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 19/20 | 3291/8295 | 2748/3129 | 916/1042 | chr12 | 110346007 | |||
| chr12:110346266 | C | G | 1 | a0001c0006 | 1 | NA18995.hp1 | synonymous_variant | LOW | c.2925C>G | p.Pro975Pro | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 3468/8295 | 2925/3129 | 975/1042 | chr12 | 110346266 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110281270 | G | C | 1 | a0001c0001t0008 | 2 | NA18946.hp2 NA18998.hp1 |
5_prime_UTR_variant | MODIFIER | c.-520G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/20 | 520 | chr12 | 110281270 | ||||||
| chr12:110281290 | T | C | 1 | a0001c0005t0009 | 2 | HG00738.hp1 HG01069.hp2 |
5_prime_UTR_variant | MODIFIER | c.-500T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/20 | 500 | chr12 | 110281290 | ||||||
| chr12:110281387 | C | G | 6 | a0001c0001t0003 a0001c0001t0027 a0001c0001t0028 others(3): Show |
32 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(29): Show |
5_prime_UTR_variant | MODIFIER | c.-403C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/20 | 403 | chr12 | 110281387 | ||||||
| chr12:110281516 | G | C | 2 | a0001c0001t0008 a0001c0001t0010 |
4 | NA18946.hp2 NA18998.hp1 NA19062.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-274G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/20 | 274 | chr12 | 110281516 | ||||||
| chr12:110281550 | G | A | 1 | a0001c0001t0016 | 1 | HG04115.hp2 | 5_prime_UTR_variant | MODIFIER | c.-240G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/20 | 240 | chr12 | 110281550 | ||||||
| chr12:110281569 | A | G | 1 | a0001c0001t0026 | 1 | HG01928.hp2 | 5_prime_UTR_variant | MODIFIER | c.-221A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/20 | 221 | chr12 | 110281569 | ||||||
| chr12:110281780 | C | G | 1 | a0001c0005t0009 | 2 | HG00738.hp1 HG01069.hp2 |
5_prime_UTR_variant | MODIFIER | c.-10C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/20 | 10 | chr12 | 110281780 | ||||||
| chr12:110346773 | T | C | 1 | a0001c0001t0005 | 8 | HG00738.hp2 HG01074.hp1 HG01175.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*303T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 303 | chr12 | 110346773 | ||||||
| chr12:110346847 | T | C | 1 | a0001c0001t0027 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*377T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 377 | chr12 | 110346847 | ||||||
| chr12:110347055 | G | A | 1 | a0001c0001t0011 | 2 | HG02970.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*585G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 585 | chr12 | 110347055 | ||||||
| chr12:110347102 | C | CATCA | 11 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0011 others(8): Show |
47 | HG00323.hp1 HG01081.hp1 HG01099.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*633_*636dupATCA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 637 | INFO_REALIGN_3_PRIME | chr12 | 110347102 | |||||
| chr12:110347162 | C | G | 1 | a0001c0001t0025 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*692C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 692 | chr12 | 110347162 | ||||||
| chr12:110347254 | A | T | 1 | a0001c0001t0012 | 2 | HG01099.hp1 HG02145.hp1 |
3_prime_UTR_variant | MODIFIER | c.*784A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 784 | chr12 | 110347254 | ||||||
| chr12:110347557 | G | A | 1 | a0001c0001t0028 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1087G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 1087 | chr12 | 110347557 | ||||||
| chr12:110347704 | G | A | 3 | a0001c0001t0004 a0001c0001t0017 a0001c0003t0004 |
11 | HG01167.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1234G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 1234 | chr12 | 110347704 | ||||||
| chr12:110347755 | G | A | 1 | a0001c0001t0013 | 2 | NA18946.hp1 NA18959.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1285G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 1285 | chr12 | 110347755 | ||||||
| chr12:110348131 | G | A | 1 | a0001c0001t0014 | 2 | HG01109.hp1 HG02109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1661G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 1661 | chr12 | 110348131 | ||||||
| chr12:110348237 | G | A | 2 | a0001c0001t0017 a0001c0001t0021 |
2 | HG02615.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1767G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 1767 | chr12 | 110348237 | ||||||
| chr12:110348249 | C | T | 1 | a0001c0001t0007 | 5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1779C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 1779 | chr12 | 110348249 | ||||||
| chr12:110348411 | C | G | 1 | a0001c0005t0009 | 2 | HG00738.hp1 HG01069.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1941C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 1941 | chr12 | 110348411 | ||||||
| chr12:110348445 | C | T | 1 | a0001c0001t0006 | 6 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1975C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 1975 | chr12 | 110348445 | ||||||
| chr12:110348750 | G | T | 1 | a0001c0008t0030 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2280G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 2280 | chr12 | 110348750 | ||||||
| chr12:110348804 | G | A | 1 | a0001c0005t0009 | 2 | HG00738.hp1 HG01069.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2334G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 2334 | chr12 | 110348804 | ||||||
| chr12:110348832 | A | T | 1 | a0001c0005t0009 | 2 | HG00738.hp1 HG01069.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2362A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 2362 | chr12 | 110348832 | ||||||
| chr12:110349070 | G | C | 1 | a0001c0001t0022 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2600G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 2600 | chr12 | 110349070 | ||||||
| chr12:110349170 | G | A | 1 | a0001c0001t0029 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2700G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 2700 | chr12 | 110349170 | ||||||
| chr12:110349170 | G | C | 1 | a0001c0001t0015 | 2 | HG01884.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2700G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 2700 | chr12 | 110349170 | ||||||
| chr12:110349507 | T | G | 1 | a0001c0001t0018 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3037T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 3037 | chr12 | 110349507 | ||||||
| chr12:110349778 | G | A | 1 | a0001c0001t0019 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3308G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 3308 | chr12 | 110349778 | ||||||
| chr12:110350028 | C | G | 1 | a0001c0001t0022 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3558C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 3558 | chr12 | 110350028 | ||||||
| chr12:110350072 | C | T | 1 | a0001c0001t0007 | 5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3602C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 3602 | chr12 | 110350072 | ||||||
| chr12:110350517 | A | G | 1 | a0001c0005t0009 | 2 | HG00738.hp1 HG01069.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4047A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 4047 | chr12 | 110350517 | ||||||
| chr12:110350582 | C | T | 1 | a0001c0003t0020 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4112C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 4112 | chr12 | 110350582 | ||||||
| chr12:110350673 | A | G | 1 | a0001c0001t0024 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4203A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 4203 | chr12 | 110350673 | ||||||
| chr12:110350941 | G | A | 1 | a0001c0001t0023 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4471G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 4471 | chr12 | 110350941 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110282363 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.119-241C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/19 | chr12 | 110282363 | |||||||
| chr12:110282390 | A | C | 1 | a0001c0002t0001g0224 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.119-214A>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/19 | chr12 | 110282390 | |||||||
| chr12:110282421 | C | T | 2 | a0001c0001t0012g0222 a0001c0001t0012g0223 |
2 | HG01099.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.119-183C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/19 | chr12 | 110282421 | |||||||
| chr12:110282508 | G | A | 2 | a0001c0001t0012g0222 a0001c0001t0012g0223 |
2 | HG01099.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.119-96G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/19 | chr12 | 110282508 | |||||||
| chr12:110282517 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.119-87A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/19 | chr12 | 110282517 | |||||||
| chr12:110282522 | A | G | 3 | a0001c0001t0001g0221 a0001c0005t0009g0219 a0001c0005t0009g0220 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.119-82A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/19 | chr12 | 110282522 | |||||||
| chr12:110282538 | GTC | G | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.119-58_119-57delCT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 110282538 | ||||||
| chr12:110282917 | T | C | 1 | a0001c0001t0017g0004 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.219+122T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110282917 | |||||||
| chr12:110282970 | A | G | 1 | a0001c0001t0003g0218 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.219+175A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110282970 | |||||||
| chr12:110283698 | G | A | 1 | a0001c0001t0004g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.219+903G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110283698 | |||||||
| chr12:110283801 | A | G | 2 | a0001c0001t0001g0217 a0001c0003t0004g0216 |
2 | HG02486.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.219+1006A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110283801 | |||||||
| chr12:110283957 | G | A | 1 | a0001c0001t0002g0006 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.219+1162G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110283957 | |||||||
| chr12:110284107 | G | A | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.219+1312G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110284107 | |||||||
| chr12:110284147 | T | C | 1 | a0001c0001t0001g0007 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.219+1352T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110284147 | |||||||
| chr12:110284342 | A | G | 1 | a0001c0001t0016g0215 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.219+1547A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110284342 | |||||||
| chr12:110284387 | C | T | 2 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.219+1592C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110284387 | |||||||
| chr12:110284494 | T | G | 1 | a0001c0001t0001g0008 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219+1699T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110284494 | |||||||
| chr12:110284530 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(1): Show |
4 | HG02717.hp1 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+1735T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110284530 | |||||||
| chr12:110284583 | A | G | 3 | a0001c0001t0002g0210 a0001c0001t0002g0211 a0001c0001t0002g0212 |
3 | HG02055.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.219+1788A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110284583 | |||||||
| chr12:110284827 | A | G | 40 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(37): Show |
41 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.219+2032A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110284827 | |||||||
| chr12:110285123 | GACTT | G | 9 | a0001c0001t0004g0005 a0001c0001t0004g0167 a0001c0001t0004g0168 others(6): Show |
9 | HG01167.hp1 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.219+2333_219+2336d others(6): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr12 | 110285123 | ||||||
| chr12:110285169 | T | A | 6 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0015 others(3): Show |
6 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.219+2374T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110285169 | |||||||
| chr12:110285345 | C | A | 3 | a0001c0003t0002g0020 a0001c0003t0002g0021 a0001c0003t0020g0019 |
3 | HG01891.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219+2550C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110285345 | |||||||
| chr12:110285397 | G | A | 1 | a0001c0001t0006g0013 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.219+2602G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110285397 | |||||||
| chr12:110285398 | T | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(110): Show |
115 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.219+2603T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110285398 | |||||||
| chr12:110285440 | C | T | 77 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0094 others(74): Show |
77 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.219+2645C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110285440 | |||||||
| chr12:110285915 | C | CT | 32 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(29): Show |
32 | HG00423.hp2 HG00558.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.219+3140dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr12 | 110285915 | ||||||
| chr12:110285915 | CT | C | 8 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0094 others(5): Show |
8 | HG00738.hp1 HG01069.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.219+3140delT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr12 | 110285915 | ||||||
| chr12:110285936 | A | T | 1 | a0001c0001t0002g0061 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.219+3141A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110285936 | |||||||
| chr12:110285993 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.219+3198G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110285993 | |||||||
| chr12:110286118 | T | A | 1 | a0001c0001t0001g0096 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.219+3323T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110286118 | |||||||
| chr12:110286193 | G | T | 1 | a0001c0001t0004g0174 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.219+3398G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110286193 | |||||||
| chr12:110286246 | A | G | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.219+3451A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110286246 | |||||||
| chr12:110286316 | A | T | 7 | a0001c0001t0002g0057 a0001c0001t0002g0059 a0001c0001t0002g0210 others(4): Show |
7 | HG02055.hp2 HG02809.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.219+3521A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110286316 | |||||||
| chr12:110286394 | T | C | 4 | a0001c0001t0002g0006 a0001c0001t0002g0027 a0001c0001t0018g0026 others(1): Show |
4 | HG02257.hp2 HG02559.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+3599T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110286394 | |||||||
| chr12:110286467 | C | T | 53 | a0001c0001t0001g0221 a0001c0001t0002g0006 a0001c0001t0002g0023 others(50): Show |
53 | HG00323.hp1 HG00738.hp1 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.219+3672C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110286467 | |||||||
| chr12:110286614 | A | G | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.219+3819A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110286614 | |||||||
| chr12:110286700 | T | TA | 9 | a0001c0001t0002g0060 a0001c0001t0006g0013 a0001c0001t0006g0014 others(6): Show |
9 | HG01081.hp1 HG01099.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.219+3920dupA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr12 | 110286700 | ||||||
| chr12:110286701 | A | T | 1 | a0001c0001t0002g0055 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.219+3906A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110286701 | |||||||
| chr12:110286868 | A | G | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.219+4073A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110286868 | |||||||
| chr12:110286910 | G | C | 1 | a0001c0001t0001g0097 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.219+4115G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110286910 | |||||||
| chr12:110287050 | C | T | 1 | a0001c0001t0002g0055 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.219+4255C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110287050 | |||||||
| chr12:110287262 | T | A | 3 | a0001c0001t0001g0221 a0001c0005t0009g0219 a0001c0005t0009g0220 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.219+4467T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110287262 | |||||||
| chr12:110287300 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.219+4505G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110287300 | |||||||
| chr12:110287613 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.220-4407C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110287613 | |||||||
| chr12:110287749 | G | A | 3 | a0001c0003t0002g0020 a0001c0003t0002g0021 a0001c0003t0020g0019 |
3 | HG01891.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.220-4271G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110287749 | |||||||
| chr12:110287764 | A | G | 3 | a0001c0001t0001g0221 a0001c0005t0009g0219 a0001c0005t0009g0220 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.220-4256A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110287764 | |||||||
| chr12:110287865 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.220-4155C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110287865 | |||||||
| chr12:110287978 | G | A | 1 | a0001c0001t0002g0055 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.220-4042G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110287978 | |||||||
| chr12:110288101 | C | CT | 93 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0030 others(90): Show |
94 | HG00323.hp1 HG00558.hp1 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.220-3895dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr12 | 110288101 | ||||||
| chr12:110288101 | C | CTT | 11 | a0001c0001t0001g0073 a0001c0001t0001g0091 a0001c0001t0002g0006 others(8): Show |
11 | HG00423.hp2 HG01175.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-3896_220-3895d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr12 | 110288101 | ||||||
| chr12:110288174 | G | A | 1 | a0001c0001t0002g0055 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.220-3846G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110288174 | |||||||
| chr12:110288266 | T | TA | 9 | a0001c0001t0002g0006 a0001c0001t0002g0027 a0001c0001t0002g0037 others(6): Show |
9 | HG01099.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.220-3745dupA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr12 | 110288266 | ||||||
| chr12:110288276 | T | A | 37 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0038 others(34): Show |
37 | HG00323.hp1 HG01167.hp1 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.220-3744T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110288276 | |||||||
| chr12:110288404 | C | CT | 6 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(3): Show |
6 | HG00558.hp1 HG00738.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.220-3603dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr12 | 110288404 | ||||||
| chr12:110288415 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.220-3605T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110288415 | |||||||
| chr12:110288438 | C | G | 1 | a0001c0001t0001g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.220-3582C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110288438 | |||||||
| chr12:110288497 | C | T | 2 | a0001c0001t0002g0047 a0001c0001t0002g0054 |
2 | HG00323.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.220-3523C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110288497 | |||||||
| chr12:110288653 | C | A | 1 | a0001c0001t0002g0061 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.220-3367C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110288653 | |||||||
| chr12:110288741 | A | G | 3 | a0001c0003t0002g0020 a0001c0003t0002g0021 a0001c0003t0020g0019 |
3 | HG01891.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.220-3279A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110288741 | |||||||
| chr12:110288860 | G | A | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.220-3160G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110288860 | |||||||
| chr12:110289012 | A | G | 1 | a0001c0006t0001g0162 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.220-3008A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110289012 | |||||||
| chr12:110289386 | T | C | 2 | a0001c0001t0001g0099 a0001c0001t0001g0149 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.220-2634T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110289386 | |||||||
| chr12:110289450 | C | T | 1 | a0001c0001t0003g0208 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.220-2570C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110289450 | |||||||
| chr12:110289608 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.220-2412G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110289608 | |||||||
| chr12:110289615 | A | G | 2 | a0001c0001t0002g0046 a0001c0001t0002g0053 |
2 | NA18952.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.220-2405A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110289615 | |||||||
| chr12:110289805 | G | T | 6 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0015 others(3): Show |
6 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.220-2215G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110289805 | |||||||
| chr12:110290044 | A | G | 17 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0081 others(14): Show |
17 | HG00423.hp2 HG00558.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.220-1976A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110290044 | |||||||
| chr12:110290196 | C | G | 38 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(35): Show |
39 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.220-1824C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110290196 | |||||||
| chr12:110290294 | C | G | 7 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(4): Show |
7 | HG01099.hp1 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.220-1726C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110290294 | |||||||
| chr12:110290391 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.220-1629T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110290391 | |||||||
| chr12:110290560 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.220-1460A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110290560 | |||||||
| chr12:110290700 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.220-1320G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110290700 | |||||||
| chr12:110291002 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0002g0055 |
2 | HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.220-1018G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110291002 | |||||||
| chr12:110291034 | G | C | 1 | a0001c0001t0003g0178 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.220-986G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110291034 | |||||||
| chr12:110291044 | G | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0031 others(5): Show |
9 | HG01168.hp2 HG01169.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.220-976G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110291044 | |||||||
| chr12:110291204 | G | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0030 others(6): Show |
10 | HG01168.hp2 HG01169.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.220-816G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110291204 | |||||||
| chr12:110291328 | C | T | 2 | a0001c0001t0003g0003 a0001c0001t0028g0206 |
3 | HG00741.hp1 HG01074.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.220-692C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110291328 | |||||||
| chr12:110291593 | A | C | 1 | a0001c0001t0001g0205 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.220-427A>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110291593 | |||||||
| chr12:110291640 | CT | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(139): Show |
143 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.220-360delT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr12 | 110291640 | ||||||
| chr12:110291640 | CTT | C | 11 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0225 others(8): Show |
11 | HG00323.hp1 HG01169.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-361_220-360del others(2): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr12 | 110291640 | ||||||
| chr12:110291808 | A | G | 3 | a0001c0001t0001g0221 a0001c0005t0009g0219 a0001c0005t0009g0220 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.220-212A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110291808 | |||||||
| chr12:110291942 | C | CG | 10 | a0001c0001t0001g0068 a0001c0001t0004g0005 a0001c0001t0004g0167 others(7): Show |
10 | HG01167.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.220-76dupG | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr12 | 110291942 | ||||||
| chr12:110292273 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.324+149A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110292273 | |||||||
| chr12:110292808 | C | T | 6 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0015 others(3): Show |
6 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+684C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110292808 | |||||||
| chr12:110292903 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.324+779A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110292903 | |||||||
| chr12:110292904 | A | G | 5 | a0001c0001t0007g0048 a0001c0001t0007g0049 a0001c0001t0007g0050 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+780A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110292904 | |||||||
| chr12:110293046 | G | A | 1 | a0001c0001t0002g0054 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.324+922G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293046 | |||||||
| chr12:110293367 | C | CT | 19 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0068 others(16): Show |
19 | HG00423.hp1 HG00558.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.324+1264dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293367 | ||||||
| chr12:110293367 | CTT | C | 5 | a0001c0001t0007g0048 a0001c0001t0007g0049 a0001c0001t0007g0050 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+1263_324+1264d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293367 | ||||||
| chr12:110293373 | T | G | 3 | a0001c0001t0001g0010 a0001c0001t0003g0178 a0001c0001t0003g0218 |
3 | HG01978.hp2 HG02683.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.324+1249T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293373 | |||||||
| chr12:110293377 | T | G | 35 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(32): Show |
36 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.324+1253T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293377 | |||||||
| chr12:110293378 | TTTTTTTT others(4): Show |
T | 1 | a0001c0001t0001g0100 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.324+1258_324+1268d others(13): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293378 | ||||||
| chr12:110293381 | T | G | 40 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(37): Show |
41 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.324+1257T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293381 | |||||||
| chr12:110293385 | T | G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(41): Show |
45 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.324+1261T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293385 | |||||||
| chr12:110293385 | T | TTTTG | 6 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(3): Show |
6 | HG01168.hp2 HG01169.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+1285_324+1288d others(6): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293385 | ||||||
| chr12:110293386 | TTTG | T | 14 | a0001c0001t0002g0047 a0001c0001t0004g0005 a0001c0001t0004g0168 others(11): Show |
14 | HG00323.hp1 HG01167.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.324+1265_324+1267d others(5): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293386 | ||||||
| chr12:110293387 | TTG | T | 17 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0038 others(14): Show |
17 | HG01175.hp2 HG02630.hp1 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.324+1265_324+1266d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293387 | ||||||
| chr12:110293388 | TG | T | 23 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(20): Show |
23 | HG00140.hp1 HG01069.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.324+1265delG | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293388 | |||||||
| chr12:110293389 | G | T | 59 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0094 others(56): Show |
59 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.324+1265G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293389 | |||||||
| chr12:110293393 | G | T | 3 | a0001c0001t0001g0127 a0001c0005t0009g0219 a0001c0005t0009g0220 |
3 | HG00738.hp1 HG01069.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.324+1269G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293393 | |||||||
| chr12:110293475 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.324+1351A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293475 | |||||||
| chr12:110293485 | C | G | 6 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0015 others(3): Show |
6 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+1361C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293485 | |||||||
| chr12:110293570 | C | T | 48 | a0001c0001t0001g0221 a0001c0001t0002g0006 a0001c0001t0002g0023 others(45): Show |
48 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.324+1446C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293570 | |||||||
| chr12:110293619 | T | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0151 |
2 | HG01934.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.324+1495T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293619 | |||||||
| chr12:110293657 | A | G | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.324+1533A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293657 | |||||||
| chr12:110293680 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.324+1556G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293680 | |||||||
| chr12:110293691 | C | T | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.324+1567C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293691 | |||||||
| chr12:110293819 | CAT | C | 3 | a0001c0001t0001g0094 a0001c0001t0001g0157 a0001c0001t0003g0202 |
3 | HG01167.hp2 HG01169.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.324+1702_324+1703d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293819 | ||||||
| chr12:110293824 | A | ATGTGTG | 2 | a0001c0001t0001g0071 a0001c0001t0001g0091 |
2 | HG00423.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.324+1701_324+1702i others(8): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293824 | ||||||
| chr12:110293826 | A | ATG | 34 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(31): Show |
35 | HG00558.hp2 HG00741.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.324+1740_324+1741d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293826 | ||||||
| chr12:110293826 | A | ATGTG | 28 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0031 others(25): Show |
29 | HG00558.hp1 HG00738.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.324+1738_324+1741d others(6): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293826 | ||||||
| chr12:110293826 | A | ATGTGTG | 23 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0036 others(20): Show |
23 | HG00423.hp1 HG01099.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.324+1736_324+1741d others(8): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293826 | ||||||
| chr12:110293826 | A | ATGTGTGT others(1): Show |
5 | a0001c0001t0001g0072 a0001c0001t0001g0078 a0001c0001t0004g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.324+1734_324+1741d others(10): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293826 | ||||||
| chr12:110293826 | A | ATGTGTGT others(3): Show |
2 | a0001c0001t0001g0146 a0001c0001t0006g0017 |
2 | HG01934.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.324+1732_324+1741d others(12): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293826 | ||||||
| chr12:110293826 | A | ATGTGTGT others(5): Show |
2 | a0001c0001t0001g0079 a0001c0001t0002g0037 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.324+1730_324+1741d others(14): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293826 | ||||||
| chr12:110293826 | A | G | 10 | a0001c0001t0001g0071 a0001c0001t0001g0091 a0001c0001t0001g0132 others(7): Show |
10 | HG00423.hp2 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.324+1702A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293826 | |||||||
| chr12:110293826 | ATG | A | 9 | a0001c0001t0001g0099 a0001c0001t0001g0102 a0001c0001t0001g0103 others(6): Show |
9 | HG00140.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.324+1740_324+1741d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293826 | ||||||
| chr12:110293826 | ATGTG | A | 5 | a0001c0001t0001g0101 a0001c0001t0002g0006 a0001c0001t0002g0047 others(2): Show |
5 | HG00323.hp1 HG02922.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+1738_324+1741d others(6): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293826 | ||||||
| chr12:110293826 | ATGTGTG | A | 4 | a0001c0001t0002g0055 a0001c0001t0018g0026 a0001c0001t0022g0134 others(1): Show |
4 | HG02257.hp2 HG02717.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+1736_324+1741d others(8): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293826 | ||||||
| chr12:110293826 | ATGTGTGT others(3): Show |
A | 1 | a0001c0001t0001g0088 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.324+1732_324+1741d others(12): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293826 | ||||||
| chr12:110293826 | ATGTGTGT others(7): Show |
A | 1 | a0001c0001t0001g0204 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.324+1728_324+1741d others(16): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293826 | ||||||
| chr12:110293850 | G | GTATATAT others(13): Show |
1 | a0001c0005t0009g0219 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.324+1727_324+1728i others(22): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293850 | ||||||
| chr12:110293852 | G | A | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.324+1728G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293852 | |||||||
| chr12:110293854 | G | A | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.324+1730G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293854 | |||||||
| chr12:110293856 | G | A | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.324+1732G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293856 | |||||||
| chr12:110293858 | G | A | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.324+1734G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293858 | |||||||
| chr12:110293860 | G | A | 18 | a0001c0001t0002g0023 a0001c0001t0002g0041 a0001c0001t0002g0042 others(15): Show |
18 | HG00738.hp1 HG01069.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.324+1736G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293860 | |||||||
| chr12:110293862 | G | A | 21 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0041 others(18): Show |
21 | HG00738.hp1 HG01069.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.324+1738G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293862 | |||||||
| chr12:110293864 | G | A | 27 | a0001c0001t0002g0006 a0001c0001t0002g0023 a0001c0001t0002g0024 others(24): Show |
27 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.324+1740G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293864 | |||||||
| chr12:110293864 | G | GTGTGTGT others(1): Show |
2 | a0001c0001t0004g0167 a0001c0001t0004g0168 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.324+1741_324+1742i others(10): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293864 | ||||||
| chr12:110293864 | G | GTGTGTGT others(7): Show |
1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.324+1741_324+1742i others(16): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293864 | ||||||
| chr12:110293866 | A | G | 1 | a0001c0001t0027g0201 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.324+1742A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293866 | |||||||
| chr12:110293870 | A | AT | 7 | a0001c0001t0001g0008 a0001c0001t0001g0101 a0001c0001t0001g0121 others(4): Show |
7 | HG01175.hp1 HG02698.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+1771dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293870 | ||||||
| chr12:110293870 | A | ATT | 7 | a0001c0001t0004g0005 a0001c0001t0004g0169 a0001c0001t0004g0170 others(4): Show |
7 | HG01167.hp1 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.324+1770_324+1771d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293870 | ||||||
| chr12:110293870 | A | T | 1 | a0001c0001t0001g0139 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.324+1746A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293870 | |||||||
| chr12:110293870 | AT | A | 13 | a0001c0001t0001g0091 a0001c0001t0001g0095 a0001c0001t0001g0137 others(10): Show |
13 | HG00423.hp2 HG01071.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.324+1771delT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293870 | ||||||
| chr12:110293870 | ATT | A | 22 | a0001c0001t0001g0022 a0001c0001t0001g0072 a0001c0001t0001g0081 others(19): Show |
22 | HG00558.hp1 HG01943.hp1 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.324+1770_324+1771d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293870 | ||||||
| chr12:110293870 | ATTT | A | 18 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0041 others(15): Show |
18 | HG01074.hp2 HG01175.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.324+1769_324+1771d others(5): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293870 | ||||||
| chr12:110293871 | T | TA | 9 | a0001c0001t0001g0080 a0001c0001t0001g0221 a0001c0001t0003g0195 others(6): Show |
9 | HG01099.hp1 HG01109.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.324+1747_324+1748i others(3): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293871 | |||||||
| chr12:110293871 | T | TATATATA others(12): Show |
1 | a0001c0005t0009g0220 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.324+1747_324+1748i others(21): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293871 | |||||||
| chr12:110293872 | T | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(54): Show |
59 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.324+1748T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293872 | |||||||
| chr12:110293873 | T | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0221 |
2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.324+1749T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293873 | |||||||
| chr12:110293874 | T | A | 14 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0031 others(11): Show |
15 | HG00323.hp1 HG01168.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.324+1750T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293874 | |||||||
| chr12:110293875 | T | A | 7 | a0001c0001t0001g0221 a0001c0001t0002g0024 a0001c0001t0002g0041 others(4): Show |
7 | HG03579.hp1 NA18948.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+1751T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293875 | |||||||
| chr12:110293877 | T | A | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.324+1753T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293877 | |||||||
| chr12:110293940 | G | A | 9 | a0001c0001t0001g0096 a0001c0001t0001g0114 a0001c0001t0001g0121 others(6): Show |
9 | HG01261.hp2 HG01515.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.324+1816G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293940 | |||||||
| chr12:110294056 | T | C | 1 | a0001c0001t0002g0043 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.324+1932T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294056 | |||||||
| chr12:110294201 | G | A | 6 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0015 others(3): Show |
6 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+2077G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294201 | |||||||
| chr12:110294233 | C | T | 6 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0015 others(3): Show |
6 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+2109C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294233 | |||||||
| chr12:110294244 | C | T | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.324+2120C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294244 | |||||||
| chr12:110294311 | G | A | 4 | a0001c0001t0001g0164 a0001c0001t0002g0038 a0001c0001t0002g0039 others(1): Show |
4 | HG02280.hp2 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+2187G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294311 | |||||||
| chr12:110294321 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.324+2197G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294321 | |||||||
| chr12:110294571 | C | A | 1 | a0001c0001t0002g0055 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.325-2028C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294571 | |||||||
| chr12:110294635 | C | T | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.325-1964C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294635 | |||||||
| chr12:110294652 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.325-1947A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294652 | |||||||
| chr12:110294663 | C | T | 4 | a0001c0001t0001g0094 a0001c0001t0001g0155 a0001c0001t0001g0157 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-1936C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294663 | |||||||
| chr12:110294686 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.325-1913C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294686 | |||||||
| chr12:110294976 | C | T | 20 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0075 others(17): Show |
20 | HG00423.hp2 HG00558.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.325-1623C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294976 | |||||||
| chr12:110294977 | G | A | 1 | a0001c0001t0002g0061 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.325-1622G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294977 | |||||||
| chr12:110295063 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.325-1536C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110295063 | |||||||
| chr12:110295313 | C | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.325-1286C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110295313 | |||||||
| chr12:110295374 | G | C | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.325-1225G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110295374 | |||||||
| chr12:110295540 | C | G | 7 | a0001c0001t0002g0060 a0001c0001t0006g0013 a0001c0001t0006g0014 others(4): Show |
7 | HG01081.hp1 HG01943.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.325-1059C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110295540 | |||||||
| chr12:110295546 | T | C | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.325-1053T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110295546 | |||||||
| chr12:110295547 | G | C | 1 | a0001c0001t0002g0027 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.325-1052G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110295547 | |||||||
| chr12:110295718 | A | G | 1 | a0001c0007t0002g0025 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.325-881A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110295718 | |||||||
| chr12:110296080 | G | T | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | HG00558.hp1 NA18948.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.325-519G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110296080 | |||||||
| chr12:110296127 | G | GT | 5 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(2): Show |
5 | HG01884.hp2 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-465dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110296127 | ||||||
| chr12:110296208 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.325-391G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110296208 | |||||||
| chr12:110296413 | C | T | 31 | a0001c0001t0003g0003 a0001c0001t0003g0175 a0001c0001t0003g0178 others(28): Show |
32 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.325-186C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110296413 | |||||||
| chr12:110296414 | G | A | 1 | a0001c0010t0001g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.325-185G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110296414 | |||||||
| chr12:110296568 | C | G | 7 | a0001c0001t0002g0060 a0001c0001t0006g0013 a0001c0001t0006g0014 others(4): Show |
7 | HG01081.hp1 HG01943.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.325-31C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110296568 | |||||||
| chr12:110296578 | C | A | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.325-21C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110296578 | |||||||
| chr12:110297132 | A | G | 1 | a0001c0001t0017g0004 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.463+395A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110297132 | |||||||
| chr12:110297205 | C | T | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+468C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110297205 | |||||||
| chr12:110297238 | G | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.463+501G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110297238 | |||||||
| chr12:110297292 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.463+555G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110297292 | |||||||
| chr12:110297327 | T | C | 6 | a0001c0001t0001g0072 a0001c0001t0001g0081 a0001c0001t0001g0086 others(3): Show |
6 | HG04115.hp2 NA18946.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.463+590T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110297327 | |||||||
| chr12:110297394 | C | T | 6 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0171 others(3): Show |
6 | HG01167.hp1 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.463+657C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110297394 | |||||||
| chr12:110297434 | C | CA | 26 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0030 others(23): Show |
27 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.463+715dupA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110297434 | ||||||
| chr12:110297434 | CA | C | 22 | a0001c0001t0001g0133 a0001c0001t0002g0006 a0001c0001t0002g0027 others(19): Show |
22 | HG00735.hp1 HG01099.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.463+715delA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110297434 | ||||||
| chr12:110297446 | A | C | 1 | a0001c0001t0001g0112 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.463+709A>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110297446 | |||||||
| chr12:110297474 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.463+737T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110297474 | |||||||
| chr12:110297870 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.463+1133G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110297870 | |||||||
| chr12:110297892 | GGTGTGCC others(8): Show |
G | 1 | a0001c0001t0001g0135 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.463+1156_463+1170d others(17): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110297892 | |||||||
| chr12:110298010 | G | A | 3 | a0001c0001t0001g0221 a0001c0005t0009g0219 a0001c0005t0009g0220 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.463+1273G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110298010 | |||||||
| chr12:110298299 | A | G | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+1562A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110298299 | |||||||
| chr12:110298300 | A | G | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+1563A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110298300 | |||||||
| chr12:110298323 | T | TGTGTGTA others(4): Show |
6 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0015 others(3): Show |
6 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.463+1593_463+1603d others(13): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110298323 | ||||||
| chr12:110298814 | G | C | 5 | a0001c0001t0007g0048 a0001c0001t0007g0049 a0001c0001t0007g0050 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+2077G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110298814 | |||||||
| chr12:110298874 | T | C | 7 | a0001c0001t0002g0060 a0001c0001t0006g0013 a0001c0001t0006g0014 others(4): Show |
7 | HG01081.hp1 HG01943.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.463+2137T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110298874 | |||||||
| chr12:110298875 | C | A | 7 | a0001c0001t0002g0060 a0001c0001t0006g0013 a0001c0001t0006g0014 others(4): Show |
7 | HG01081.hp1 HG01943.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.463+2138C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110298875 | |||||||
| chr12:110298987 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.463+2250G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110298987 | |||||||
| chr12:110299037 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.463+2300A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110299037 | |||||||
| chr12:110299086 | C | CAG | 12 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0097 others(9): Show |
12 | HG00735.hp1 HG01106.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.463+2350_463+2351d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110299086 | ||||||
| chr12:110299361 | T | C | 1 | a0001c0001t0006g0015 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.463+2624T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110299361 | |||||||
| chr12:110299612 | C | T | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.463+2875C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110299612 | |||||||
| chr12:110299650 | G | A | 1 | a0001c0001t0002g0055 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.463+2913G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110299650 | |||||||
| chr12:110299975 | C | T | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+3238C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110299975 | |||||||
| chr12:110300002 | C | T | 1 | a0001c0001t0004g0174 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.463+3265C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110300002 | |||||||
| chr12:110300008 | A | G | 2 | a0001c0001t0001g0144 a0001c0006t0001g0162 |
2 | NA18995.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.463+3271A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110300008 | |||||||
| chr12:110300031 | C | T | 35 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(32): Show |
36 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.463+3294C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110300031 | |||||||
| chr12:110300052 | G | A | 1 | a0001c0001t0003g0003 | 2 | HG00741.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.463+3315G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110300052 | |||||||
| chr12:110300092 | G | GTCCT | 7 | a0001c0001t0001g0028 a0001c0001t0006g0013 a0001c0001t0006g0014 others(4): Show |
7 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.463+3368_463+3371d others(6): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300092 | ||||||
| chr12:110300116 | T | TCCCTC | 27 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0084 others(24): Show |
27 | HG00423.hp2 HG00558.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.463+3406_463+3410d others(7): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300116 | ||||||
| chr12:110300116 | T | TCCCTCCC others(3): Show |
8 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0031 others(5): Show |
9 | HG01168.hp2 HG01169.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.463+3401_463+3410d others(12): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300116 | ||||||
| chr12:110300116 | TCCCTC | T | 17 | a0001c0001t0001g0221 a0001c0001t0004g0005 a0001c0001t0004g0167 others(14): Show |
17 | HG00738.hp1 HG01069.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.463+3406_463+3410d others(7): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300116 | ||||||
| chr12:110300141 | C | A | 1 | a0001c0001t0001g0112 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.463+3404C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110300141 | |||||||
| chr12:110300176 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.463+3439C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110300176 | |||||||
| chr12:110300179 | T | G | 1 | a0001c0001t0001g0100 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.463+3442T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110300179 | |||||||
| chr12:110300184 | C | CT | 55 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(52): Show |
57 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.463+3467dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300184 | ||||||
| chr12:110300184 | C | CTT | 22 | a0001c0001t0001g0068 a0001c0001t0001g0078 a0001c0001t0001g0079 others(19): Show |
22 | HG00423.hp2 HG00558.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.463+3466_463+3467d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300184 | ||||||
| chr12:110300184 | CT | C | 35 | a0001c0001t0001g0118 a0001c0001t0001g0136 a0001c0001t0001g0144 others(32): Show |
35 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.463+3467delT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300184 | ||||||
| chr12:110300184 | CTT | C | 17 | a0001c0001t0002g0043 a0001c0001t0002g0055 a0001c0001t0004g0005 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.463+3466_463+3467d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300184 | ||||||
| chr12:110300340 | A | G | 1 | a0001c0001t0005g0154 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.463+3603A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110300340 | |||||||
| chr12:110300351 | C | CT | 120 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(117): Show |
122 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.463+3634dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300351 | ||||||
| chr12:110300351 | C | CTT | 10 | a0001c0001t0003g0193 a0001c0001t0003g0194 a0001c0001t0003g0208 others(7): Show |
10 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.463+3633_463+3634d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300351 | ||||||
| chr12:110300377 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.463+3640C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110300377 | |||||||
| chr12:110300423 | C | T | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.463+3686C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110300423 | |||||||
| chr12:110300440 | C | T | 2 | a0001c0001t0014g0176 a0001c0001t0014g0177 |
2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.463+3703C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110300440 | |||||||
| chr12:110300643 | C | CT | 28 | a0001c0001t0001g0086 a0001c0001t0002g0006 a0001c0001t0002g0023 others(25): Show |
28 | HG00323.hp1 HG01175.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.463+3925dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300643 | ||||||
| chr12:110300643 | C | CTT | 6 | a0001c0001t0001g0221 a0001c0001t0012g0222 a0001c0001t0012g0223 others(3): Show |
6 | HG01099.hp1 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.463+3924_463+3925d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300643 | ||||||
| chr12:110300643 | CT | C | 9 | a0001c0001t0001g0107 a0001c0001t0001g0133 a0001c0001t0001g0137 others(6): Show |
9 | HG00735.hp1 HG01069.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.463+3925delT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300643 | ||||||
| chr12:110300643 | CTTTTTT | C | 12 | a0001c0001t0002g0055 a0001c0001t0004g0005 a0001c0001t0004g0167 others(9): Show |
12 | HG01167.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.463+3920_463+3925d others(8): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300643 | ||||||
| chr12:110300849 | A | G | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.463+4112A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110300849 | |||||||
| chr12:110301041 | T | A | 3 | a0001c0001t0001g0221 a0001c0005t0009g0219 a0001c0005t0009g0220 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.463+4304T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110301041 | |||||||
| chr12:110301072 | G | A | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.463+4335G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110301072 | |||||||
| chr12:110301174 | G | A | 2 | a0001c0001t0011g0056 a0001c0001t0011g0058 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.463+4437G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110301174 | |||||||
| chr12:110301199 | T | C | 4 | a0001c0003t0002g0020 a0001c0003t0002g0021 a0001c0003t0004g0216 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.463+4462T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110301199 | |||||||
| chr12:110301289 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.463+4552C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110301289 | |||||||
| chr12:110301461 | A | AT | 5 | a0001c0001t0002g0006 a0001c0001t0002g0027 a0001c0001t0003g0192 others(2): Show |
5 | HG02004.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.463+4730dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110301461 | ||||||
| chr12:110301461 | AT | A | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.463+4730delT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110301461 | ||||||
| chr12:110301473 | C | G | 1 | a0001c0001t0001g0143 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.463+4736C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110301473 | |||||||
| chr12:110301562 | T | C | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+4825T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110301562 | |||||||
| chr12:110301610 | G | T | 1 | a0001c0001t0003g0191 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.463+4873G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110301610 | |||||||
| chr12:110301642 | C | T | 1 | a0001c0001t0014g0176 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.463+4905C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110301642 | |||||||
| chr12:110301722 | C | T | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+4985C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110301722 | |||||||
| chr12:110302013 | A | G | 3 | a0001c0001t0001g0107 a0001c0001t0001g0118 a0001c0001t0001g0120 |
3 | HG03491.hp2 HG03492.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.463+5276A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110302013 | |||||||
| chr12:110302228 | CT | C | 3 | a0001c0001t0001g0221 a0001c0005t0009g0219 a0001c0005t0009g0220 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.463+5495delT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110302228 | ||||||
| chr12:110302357 | C | T | 2 | a0001c0001t0002g0006 a0001c0001t0002g0027 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.463+5620C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110302357 | |||||||
| chr12:110302567 | AATTTTTA others(5): Show |
A | 2 | a0001c0001t0001g0068 a0001c0001t0024g0092 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.463+5834_463+5845d others(14): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110302567 | ||||||
| chr12:110302581 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0024g0092 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.463+5844T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110302581 | |||||||
| chr12:110302584 | C | CTAT | 105 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(102): Show |
106 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.463+5871_463+5873d others(5): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110302584 | ||||||
| chr12:110302584 | C | CTATTAT | 14 | a0001c0001t0001g0008 a0001c0001t0001g0104 a0001c0001t0001g0105 others(11): Show |
14 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.463+5868_463+5873d others(8): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110302584 | ||||||
| chr12:110302584 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0024g0092 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.463+5847C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110302584 | |||||||
| chr12:110302584 | CTAT | C | 64 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0022 others(61): Show |
65 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.463+5871_463+5873d others(5): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110302584 | ||||||
| chr12:110302665 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.463+5928T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110302665 | |||||||
| chr12:110303039 | T | C | 2 | a0001c0001t0001g0099 a0001c0001t0001g0149 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.463+6302T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110303039 | |||||||
| chr12:110303350 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.463+6613C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110303350 | |||||||
| chr12:110303551 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(214): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.463+6814T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110303551 | |||||||
| chr12:110303567 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.463+6830C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110303567 | |||||||
| chr12:110303705 | C | T | 5 | a0001c0001t0007g0048 a0001c0001t0007g0049 a0001c0001t0007g0050 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+6968C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110303705 | |||||||
| chr12:110303840 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.463+7103C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110303840 | |||||||
| chr12:110303936 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.463+7199G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110303936 | |||||||
| chr12:110304082 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0005g0126 |
2 | HG02818.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.463+7345A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110304082 | |||||||
| chr12:110304273 | C | T | 2 | a0001c0001t0013g0083 a0001c0001t0013g0085 |
2 | NA18946.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.463+7536C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110304273 | |||||||
| chr12:110304291 | T | G | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+7554T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110304291 | |||||||
| chr12:110304297 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.463+7560A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110304297 | |||||||
| chr12:110304353 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.463+7616G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110304353 | |||||||
| chr12:110304459 | G | C | 2 | a0001c0001t0012g0222 a0001c0001t0012g0223 |
2 | HG01099.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.463+7722G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110304459 | |||||||
| chr12:110304510 | C | A | 2 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.463+7773C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110304510 | |||||||
| chr12:110304590 | A | C | 5 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(2): Show |
5 | HG01884.hp2 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.463+7853A>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110304590 | |||||||
| chr12:110304605 | A | G | 3 | a0001c0001t0001g0221 a0001c0005t0009g0219 a0001c0005t0009g0220 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.463+7868A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110304605 | |||||||
| chr12:110304952 | C | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0207 |
3 | HG02559.hp2 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.463+8215C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110304952 | |||||||
| chr12:110304988 | G | A | 1 | a0001c0001t0005g0126 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.463+8251G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110304988 | |||||||
| chr12:110305112 | T | G | 1 | a0001c0001t0001g0008 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.463+8375T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110305112 | |||||||
| chr12:110305120 | A | G | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+8383A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110305120 | |||||||
| chr12:110305176 | C | T | 1 | a0001c0001t0001g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.463+8439C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110305176 | |||||||
| chr12:110305186 | A | G | 61 | a0001c0001t0001g0221 a0001c0001t0001g0225 a0001c0001t0002g0006 others(58): Show |
61 | HG00323.hp1 HG00738.hp1 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.463+8449A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110305186 | |||||||
| chr12:110305598 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.463+8861G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110305598 | |||||||
| chr12:110305632 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.463+8895G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110305632 | |||||||
| chr12:110305765 | G | A | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+9028G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110305765 | |||||||
| chr12:110305856 | A | T | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+9119A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110305856 | |||||||
| chr12:110305872 | T | G | 11 | a0001c0001t0002g0006 a0001c0001t0002g0027 a0001c0001t0002g0038 others(8): Show |
11 | HG01099.hp1 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.463+9135T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110305872 | |||||||
| chr12:110305873 | T | G | 8 | a0001c0001t0002g0006 a0001c0001t0002g0027 a0001c0001t0002g0213 others(5): Show |
8 | HG01099.hp1 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.463+9136T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110305873 | |||||||
| chr12:110305882 | G | GT | 8 | a0001c0001t0002g0024 a0001c0001t0002g0041 a0001c0001t0002g0042 others(5): Show |
8 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.463+9157dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110305882 | ||||||
| chr12:110305882 | GT | G | 11 | a0001c0001t0001g0073 a0001c0001t0001g0094 a0001c0001t0001g0152 others(8): Show |
11 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.463+9157delT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110305882 | ||||||
| chr12:110305931 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.463+9194T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110305931 | |||||||
| chr12:110305970 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.463+9233G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110305970 | |||||||
| chr12:110306179 | G | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(190): Show |
195 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.463+9442G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110306179 | |||||||
| chr12:110306184 | G | A | 1 | a0001c0001t0017g0004 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.463+9447G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110306184 | |||||||
| chr12:110306200 | A | G | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+9463A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110306200 | |||||||
| chr12:110306239 | C | T | 19 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0041 others(16): Show |
19 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.463+9502C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110306239 | |||||||
| chr12:110306253 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.463+9516A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110306253 | |||||||
| chr12:110306464 | AGAT | A | 2 | a0001c0001t0012g0222 a0001c0001t0012g0223 |
2 | HG01099.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.463+9733_463+9735d others(5): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110306464 | ||||||
| chr12:110306877 | C | T | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+10140C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110306877 | |||||||
| chr12:110306950 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.463+10213G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110306950 | |||||||
| chr12:110307004 | C | A | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+10267C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110307004 | |||||||
| chr12:110307017 | C | T | 1 | a0001c0001t0018g0026 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.463+10280C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110307017 | |||||||
| chr12:110307067 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.463+10330T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110307067 | |||||||
| chr12:110307100 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.463+10363G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110307100 | |||||||
| chr12:110307222 | C | CT | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(181): Show |
187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.463+10502dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110307222 | ||||||
| chr12:110307222 | C | CTT | 27 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0068 others(24): Show |
27 | HG00558.hp1 HG01243.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.463+10501_463+1050 others(6): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110307222 | ||||||
| chr12:110307240 | C | T | 8 | a0001c0001t0001g0099 a0001c0001t0001g0102 a0001c0001t0001g0129 others(5): Show |
8 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.463+10503C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110307240 | |||||||
| chr12:110307241 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.463+10504T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110307241 | |||||||
| chr12:110307271 | G | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0207 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.463+10534G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110307271 | |||||||
| chr12:110307716 | A | G | 2 | a0001c0001t0002g0046 a0001c0001t0002g0053 |
2 | NA18952.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.463+10979A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110307716 | |||||||
| chr12:110307792 | AG | A | 38 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(35): Show |
39 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.463+11057delG | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110307792 | ||||||
| chr12:110307810 | G | T | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+11073G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110307810 | |||||||
| chr12:110307967 | C | T | 2 | a0001c0002t0001g0115 a0001c0002t0001g0117 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.463+11230C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110307967 | |||||||
| chr12:110308227 | C | T | 6 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0171 others(3): Show |
6 | HG01167.hp1 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.463+11490C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110308227 | |||||||
| chr12:110308242 | A | C | 2 | a0001c0003t0002g0021 a0001c0003t0020g0019 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.463+11505A>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110308242 | |||||||
| chr12:110308303 | G | A | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.463+11566G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110308303 | |||||||
| chr12:110308347 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.463+11610G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110308347 | |||||||
| chr12:110308427 | G | A | 3 | a0001c0001t0005g0108 a0001c0001t0005g0109 a0001c0001t0005g0119 |
3 | HG01255.hp2 HG02735.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.463+11690G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110308427 | |||||||
| chr12:110308627 | C | T | 2 | a0001c0001t0002g0006 a0001c0001t0002g0027 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.463+11890C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110308627 | |||||||
| chr12:110308639 | T | G | 2 | a0001c0001t0014g0176 a0001c0001t0014g0177 |
2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.463+11902T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110308639 | |||||||
| chr12:110308759 | G | A | 1 | a0001c0001t0002g0055 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.463+12022G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110308759 | |||||||
| chr12:110308776 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.463+12039C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110308776 | |||||||
| chr12:110309004 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.463+12267T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110309004 | |||||||
| chr12:110309021 | A | T | 1 | a0001c0001t0003g0191 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.463+12284A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110309021 | |||||||
| chr12:110309083 | T | C | 1 | a0001c0003t0004g0216 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.463+12346T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110309083 | |||||||
| chr12:110309133 | G | A | 1 | a0001c0001t0003g0180 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.463+12396G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110309133 | |||||||
| chr12:110309139 | A | T | 2 | a0001c0001t0003g0175 a0001c0001t0003g0199 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.463+12402A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110309139 | |||||||
| chr12:110309140 | A | AT | 35 | a0001c0001t0001g0010 a0001c0001t0001g0064 a0001c0001t0001g0067 others(32): Show |
35 | HG00558.hp2 HG00642.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.463+12438dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | ||||||
| chr12:110309140 | A | ATT | 23 | a0001c0001t0001g0062 a0001c0001t0001g0065 a0001c0001t0001g0081 others(20): Show |
23 | HG00323.hp2 HG01361.hp1 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.463+12437_463+1243 others(6): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | ||||||
| chr12:110309140 | A | ATTT | 14 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0078 others(11): Show |
14 | HG00558.hp1 HG01081.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.463+12436_463+1243 others(7): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | ||||||
| chr12:110309140 | A | ATTTT | 9 | a0001c0001t0001g0090 a0001c0001t0001g0217 a0001c0001t0002g0024 others(6): Show |
9 | HG00423.hp1 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.463+12435_463+1243 others(8): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | ||||||
| chr12:110309140 | A | ATTTTTTT others(4): Show |
1 | a0001c0008t0030g0183 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.463+12428_463+1243 others(15): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | ||||||
| chr12:110309140 | A | ATTTTTTT others(7): Show |
2 | a0001c0001t0003g0188 a0001c0001t0003g0195 |
2 | HG01081.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.463+12425_463+1243 others(18): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | ||||||
| chr12:110309140 | A | ATTTTTTT others(8): Show |
1 | a0001c0001t0003g0189 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.463+12424_463+1243 others(19): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | ||||||
| chr12:110309140 | A | ATTTTTTT others(9): Show |
5 | a0001c0001t0003g0192 a0001c0001t0003g0203 a0001c0001t0028g0206 others(2): Show |
5 | HG01074.hp2 HG02004.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+12423_463+1243 others(20): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | ||||||
| chr12:110309140 | A | ATTTTTTT others(12): Show |
2 | a0001c0001t0003g0190 a0001c0001t0003g0202 |
2 | HG01358.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.463+12420_463+1243 others(23): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | ||||||
| chr12:110309140 | A | ATTTTTTT others(14): Show |
2 | a0001c0001t0003g0196 a0001c0001t0029g0197 |
2 | HG01346.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.463+12418_463+1243 others(25): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | ||||||
| chr12:110309140 | A | ATTTTTTT others(17): Show |
1 | a0001c0001t0027g0201 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.463+12415_463+1243 others(28): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | ||||||
| chr12:110309140 | A | T | 2 | a0001c0001t0003g0175 a0001c0001t0003g0199 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.463+12403A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110309140 | |||||||
| chr12:110309140 | AT | A | 37 | a0001c0001t0001g0008 a0001c0001t0001g0097 a0001c0001t0001g0100 others(34): Show |
37 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.463+12438delT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | ||||||
| chr12:110309140 | ATTTTTTT others(2): Show |
A | 6 | a0001c0001t0003g0218 a0001c0001t0007g0048 a0001c0001t0007g0049 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.463+12430_463+1243 others(13): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | ||||||
| chr12:110309140 | ATTTTTTT others(3): Show |
A | 5 | a0001c0001t0001g0094 a0001c0001t0001g0157 a0001c0001t0002g0038 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+12429_463+1243 others(14): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | ||||||
| chr12:110309140 | ATTTTTTT others(5): Show |
A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0032 others(9): Show |
13 | HG01169.hp2 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.463+12427_463+1243 others(16): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | ||||||
| chr12:110309140 | ATTTTTTT others(6): Show |
A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0221 a0001c0001t0003g0184 |
3 | HG01168.hp2 HG01255.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.463+12426_463+1243 others(17): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | ||||||
| chr12:110309140 | ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0018g0026 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.463+12425_463+1243 others(18): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | ||||||
| chr12:110309140 | ATTTTTTT others(9): Show |
A | 1 | a0001c0001t0001g0204 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.463+12423_463+1243 others(20): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | ||||||
| chr12:110309567 | G | A | 2 | a0001c0001t0014g0176 a0001c0001t0014g0177 |
2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.463+12830G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110309567 | |||||||
| chr12:110309614 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(107): Show |
112 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.463+12877G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110309614 | |||||||
| chr12:110309638 | C | T | 5 | a0001c0001t0007g0048 a0001c0001t0007g0049 a0001c0001t0007g0050 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+12901C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110309638 | |||||||
| chr12:110309882 | G | C | 1 | a0001c0001t0017g0004 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.464-13110G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110309882 | |||||||
| chr12:110309908 | CA | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(70): Show |
75 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.464-13070delA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309908 | ||||||
| chr12:110309908 | CAA | C | 34 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0041 others(31): Show |
34 | HG00323.hp1 HG01167.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.464-13071_464-1307 others(6): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309908 | ||||||
| chr12:110310282 | C | T | 1 | a0001c0001t0002g0060 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.464-12710C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110310282 | |||||||
| chr12:110310283 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0151 |
2 | HG01934.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.464-12709G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110310283 | |||||||
| chr12:110310337 | C | G | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-12655C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110310337 | |||||||
| chr12:110310369 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.464-12623T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110310369 | |||||||
| chr12:110310458 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.464-12534A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110310458 | |||||||
| chr12:110310647 | G | C | 1 | a0001c0001t0001g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.464-12345G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110310647 | |||||||
| chr12:110310658 | T | TTAACA | 3 | a0001c0001t0001g0221 a0001c0005t0009g0219 a0001c0005t0009g0220 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.464-12331_464-1233 others(9): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110310658 | ||||||
| chr12:110310759 | C | T | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | HG00558.hp1 NA18948.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.464-12233C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110310759 | |||||||
| chr12:110310831 | G | A | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-12161G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110310831 | |||||||
| chr12:110310930 | G | C | 19 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0041 others(16): Show |
19 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.464-12062G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110310930 | |||||||
| chr12:110310981 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.464-12011A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110310981 | |||||||
| chr12:110310982 | T | C | 1 | a0001c0003t0004g0216 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.464-12010T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110310982 | |||||||
| chr12:110311310 | A | G | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.464-11682A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110311310 | |||||||
| chr12:110311535 | G | A | 1 | a0001c0001t0010g0140 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.464-11457G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110311535 | |||||||
| chr12:110311551 | G | A | 7 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0007g0048 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.464-11441G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110311551 | |||||||
| chr12:110311552 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.464-11440C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110311552 | |||||||
| chr12:110311595 | C | CA | 32 | a0001c0001t0001g0007 a0001c0001t0001g0030 a0001c0001t0001g0035 others(29): Show |
32 | HG00423.hp1 HG01109.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.464-11370dupA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110311595 | ||||||
| chr12:110311595 | C | CAA | 17 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(14): Show |
18 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.464-11371_464-1137 others(6): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110311595 | ||||||
| chr12:110311595 | C | CAAA | 19 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(16): Show |
19 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.464-11372_464-1137 others(7): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110311595 | ||||||
| chr12:110311595 | C | CAAAA | 15 | a0001c0001t0001g0204 a0001c0001t0003g0178 a0001c0001t0003g0180 others(12): Show |
15 | HG01074.hp2 HG01081.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.464-11373_464-1137 others(8): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110311595 | ||||||
| chr12:110311595 | CA | C | 30 | a0001c0001t0001g0095 a0001c0001t0001g0103 a0001c0001t0001g0105 others(27): Show |
30 | HG00642.hp1 HG00738.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.464-11370delA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110311595 | ||||||
| chr12:110311595 | CAAAAA | C | 6 | a0001c0001t0002g0044 a0001c0001t0002g0053 a0001c0001t0002g0054 others(3): Show |
6 | HG01099.hp1 HG01175.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.464-11374_464-1137 others(9): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110311595 | ||||||
| chr12:110311595 | CAAAAAA | C | 14 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0041 others(11): Show |
14 | HG00323.hp1 HG01361.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.464-11375_464-1137 others(10): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110311595 | ||||||
| chr12:110311611 | A | C | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-11381A>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110311611 | |||||||
| chr12:110311613 | A | AC | 19 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0075 others(16): Show |
19 | HG00558.hp1 HG01884.hp1 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.464-11379_464-1137 others(5): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110311613 | |||||||
| chr12:110311732 | TA | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(91): Show |
96 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.464-11243delA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110311732 | ||||||
| chr12:110311732 | TAA | T | 17 | a0001c0001t0002g0043 a0001c0001t0002g0213 a0001c0001t0002g0214 others(14): Show |
17 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.464-11244_464-1124 others(6): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110311732 | ||||||
| chr12:110311828 | A | G | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.464-11164A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110311828 | |||||||
| chr12:110311962 | C | A | 1 | a0001c0001t0002g0055 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.464-11030C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110311962 | |||||||
| chr12:110312073 | G | A | 1 | a0001c0001t0028g0206 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.464-10919G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110312073 | |||||||
| chr12:110312113 | G | A | 48 | a0001c0001t0001g0221 a0001c0001t0002g0006 a0001c0001t0002g0023 others(45): Show |
48 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.464-10879G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110312113 | |||||||
| chr12:110312289 | T | A | 5 | a0001c0001t0007g0048 a0001c0001t0007g0049 a0001c0001t0007g0050 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-10703T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110312289 | |||||||
| chr12:110312498 | T | G | 1 | a0001c0001t0001g0082 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.464-10494T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110312498 | |||||||
| chr12:110312553 | G | A | 3 | a0001c0001t0001g0221 a0001c0005t0009g0219 a0001c0005t0009g0220 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.464-10439G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110312553 | |||||||
| chr12:110312706 | C | T | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-10286C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110312706 | |||||||
| chr12:110312753 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.464-10239G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110312753 | |||||||
| chr12:110312849 | C | CA | 7 | a0001c0001t0001g0022 a0001c0001t0001g0095 a0001c0001t0001g0141 others(4): Show |
7 | HG00735.hp2 HG01106.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-10127dupA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110312849 | ||||||
| chr12:110312866 | G | C | 3 | a0001c0001t0001g0097 a0001c0001t0013g0083 a0001c0001t0013g0085 |
3 | HG02622.hp1 NA18946.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.464-10126G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110312866 | |||||||
| chr12:110313062 | A | C | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.464-9930A>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110313062 | |||||||
| chr12:110313206 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.464-9786G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110313206 | |||||||
| chr12:110313213 | T | C | 2 | a0001c0003t0002g0021 a0001c0003t0020g0019 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.464-9779T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110313213 | |||||||
| chr12:110313223 | AG | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0031 others(5): Show |
9 | HG01168.hp2 HG01169.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.464-9767delG | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110313223 | ||||||
| chr12:110313310 | C | CT | 96 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(93): Show |
98 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.464-9660dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110313310 | ||||||
| chr12:110313310 | C | CTT | 5 | a0001c0001t0001g0008 a0001c0001t0001g0102 a0001c0001t0003g0180 others(2): Show |
5 | HG01192.hp1 HG01258.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.464-9661_464-9660d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110313310 | ||||||
| chr12:110313310 | C | CTTT | 5 | a0001c0001t0007g0048 a0001c0001t0007g0049 a0001c0001t0007g0050 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-9662_464-9660d others(5): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110313310 | ||||||
| chr12:110313310 | CTTTT | C | 24 | a0001c0001t0001g0221 a0001c0001t0002g0006 a0001c0001t0002g0027 others(21): Show |
24 | HG01099.hp1 HG01167.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.464-9663_464-9660d others(6): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110313310 | ||||||
| chr12:110313310 | CTTTTT | C | 21 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0041 others(18): Show |
21 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.464-9664_464-9660d others(7): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110313310 | ||||||
| chr12:110313314 | T | C | 1 | a0001c0001t0012g0223 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.464-9678T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110313314 | |||||||
| chr12:110313339 | G | A | 1 | a0001c0001t0002g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.464-9653G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110313339 | |||||||
| chr12:110313344 | G | A | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-9648G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110313344 | |||||||
| chr12:110313501 | G | C | 1 | a0001c0001t0017g0004 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.464-9491G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110313501 | |||||||
| chr12:110313569 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.464-9423C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110313569 | |||||||
| chr12:110313705 | C | CT | 8 | a0001c0001t0001g0100 a0001c0001t0001g0159 a0001c0001t0001g0166 others(5): Show |
8 | HG00738.hp1 HG01069.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.464-9265dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110313705 | ||||||
| chr12:110313705 | CT | C | 41 | a0001c0001t0001g0031 a0001c0001t0001g0103 a0001c0001t0001g0118 others(38): Show |
41 | HG00558.hp2 HG01071.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.464-9265delT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110313705 | ||||||
| chr12:110313705 | CTT | C | 16 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0097 others(13): Show |
16 | HG00735.hp1 HG01106.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.464-9266_464-9265d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110313705 | ||||||
| chr12:110313856 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.464-9136G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110313856 | |||||||
| chr12:110313883 | A | AT | 7 | a0001c0001t0001g0221 a0001c0001t0006g0013 a0001c0001t0006g0014 others(4): Show |
7 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-9099dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110313883 | ||||||
| chr12:110314094 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.464-8898C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110314094 | |||||||
| chr12:110314127 | G | A | 2 | a0001c0001t0027g0201 a0001c0001t0029g0197 |
2 | HG01346.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.464-8865G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110314127 | |||||||
| chr12:110314283 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.464-8709G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110314283 | |||||||
| chr12:110314336 | G | GA | 127 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(124): Show |
129 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.464-8641dupA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110314336 | ||||||
| chr12:110314336 | G | GAA | 6 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0002g0006 others(3): Show |
6 | HG01884.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.464-8642_464-8641d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110314336 | ||||||
| chr12:110314598 | C | T | 1 | a0001c0001t0004g0169 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.464-8394C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110314598 | |||||||
| chr12:110314674 | G | A | 3 | a0001c0003t0002g0020 a0001c0003t0002g0021 a0001c0003t0020g0019 |
3 | HG01891.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.464-8318G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110314674 | |||||||
| chr12:110314708 | G | C | 1 | a0001c0001t0003g0189 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.464-8284G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110314708 | |||||||
| chr12:110314750 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.464-8242T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110314750 | |||||||
| chr12:110314820 | G | A | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.464-8172G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110314820 | |||||||
| chr12:110314918 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.464-8074G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110314918 | |||||||
| chr12:110314952 | C | T | 2 | a0001c0001t0006g0016 a0001c0001t0006g0017 |
2 | HG01943.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.464-8040C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110314952 | |||||||
| chr12:110315011 | C | T | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-7981C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110315011 | |||||||
| chr12:110315079 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.464-7913G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110315079 | |||||||
| chr12:110315119 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.464-7873G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110315119 | |||||||
| chr12:110315129 | G | T | 1 | a0001c0001t0002g0038 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.464-7863G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110315129 | |||||||
| chr12:110315150 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.464-7842G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110315150 | |||||||
| chr12:110315161 | C | T | 2 | a0001c0001t0003g0202 a0001c0001t0003g0203 |
2 | HG01358.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.464-7831C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110315161 | |||||||
| chr12:110315393 | T | C | 22 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0075 others(19): Show |
22 | HG00423.hp2 HG00558.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.464-7599T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110315393 | |||||||
| chr12:110315519 | G | A | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-7473G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110315519 | |||||||
| chr12:110315627 | G | A | 1 | a0001c0001t0019g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.464-7365G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110315627 | |||||||
| chr12:110315908 | C | T | 2 | a0002c0004t0003g0181 a0002c0004t0003g0182 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.464-7084C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110315908 | |||||||
| chr12:110316216 | A | G | 4 | a0001c0001t0003g0178 a0001c0001t0003g0180 a0001c0001t0003g0186 others(1): Show |
4 | HG01192.hp1 HG01433.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-6776A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110316216 | |||||||
| chr12:110316292 | A | G | 23 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0075 others(20): Show |
23 | HG00423.hp2 HG00558.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.464-6700A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110316292 | |||||||
| chr12:110316561 | A | G | 1 | a0001c0001t0002g0060 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.464-6431A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110316561 | |||||||
| chr12:110316887 | G | A | 4 | a0001c0001t0008g0163 a0001c0001t0008g0165 a0001c0001t0010g0138 others(1): Show |
4 | NA18946.hp2 NA18998.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-6105G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110316887 | |||||||
| chr12:110317097 | C | T | 2 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.464-5895C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110317097 | |||||||
| chr12:110317299 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.464-5693C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110317299 | |||||||
| chr12:110317420 | G | GT | 43 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(40): Show |
44 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.464-5564dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110317420 | ||||||
| chr12:110317432 | A | G | 1 | a0001c0001t0002g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.464-5560A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110317432 | |||||||
| chr12:110317593 | G | T | 1 | a0001c0001t0001g0098 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.464-5399G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110317593 | |||||||
| chr12:110317679 | G | C | 5 | a0001c0001t0007g0048 a0001c0001t0007g0049 a0001c0001t0007g0050 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-5313G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110317679 | |||||||
| chr12:110318067 | A | G | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-4925A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110318067 | |||||||
| chr12:110318170 | C | T | 2 | a0001c0001t0013g0083 a0001c0001t0013g0085 |
2 | NA18946.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.464-4822C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110318170 | |||||||
| chr12:110318534 | C | T | 2 | a0001c0001t0014g0176 a0001c0001t0014g0177 |
2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.464-4458C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110318534 | |||||||
| chr12:110318608 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.464-4384G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110318608 | |||||||
| chr12:110318737 | G | C | 1 | a0001c0001t0017g0004 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.464-4255G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110318737 | |||||||
| chr12:110318754 | A | G | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-4238A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110318754 | |||||||
| chr12:110318763 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.464-4229C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110318763 | |||||||
| chr12:110318764 | G | A | 34 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0041 others(31): Show |
34 | HG00323.hp1 HG01167.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.464-4228G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110318764 | |||||||
| chr12:110318859 | C | G | 1 | a0001c0001t0001g0145 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.464-4133C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110318859 | |||||||
| chr12:110318933 | A | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0031 others(5): Show |
9 | HG01168.hp2 HG01169.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.464-4059A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110318933 | |||||||
| chr12:110319215 | T | TA | 4 | a0001c0001t0007g0048 a0001c0001t0007g0049 a0001c0001t0007g0050 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-3771dupA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110319215 | ||||||
| chr12:110319222 | T | A | 1 | a0001c0001t0007g0052 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.464-3770T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110319222 | |||||||
| chr12:110319223 | G | GA | 7 | a0001c0001t0001g0022 a0001c0001t0001g0123 a0001c0001t0001g0144 others(4): Show |
7 | HG01891.hp1 HG02293.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.464-3746dupA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110319223 | ||||||
| chr12:110319223 | G | T | 1 | a0001c0001t0007g0052 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.464-3769G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110319223 | |||||||
| chr12:110319223 | GA | G | 108 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0028 others(105): Show |
108 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.464-3746delA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110319223 | ||||||
| chr12:110319223 | GAA | G | 7 | a0001c0001t0001g0087 a0001c0001t0001g0105 a0001c0001t0001g0127 others(4): Show |
7 | HG01106.hp2 HG02572.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-3747_464-3746d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110319223 | ||||||
| chr12:110319223 | GAAAAAAA others(4): Show |
G | 1 | a0001c0008t0030g0183 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.464-3756_464-3746d others(13): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110319223 | ||||||
| chr12:110319224 | A | G | 1 | a0001c0001t0007g0052 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.464-3768A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110319224 | |||||||
| chr12:110319496 | A | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0217 |
2 | HG02698.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.464-3496A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110319496 | |||||||
| chr12:110319679 | T | C | 1 | a0001c0001t0002g0053 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.464-3313T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110319679 | |||||||
| chr12:110319780 | A | G | 20 | a0001c0001t0001g0007 a0001c0001t0001g0095 a0001c0001t0001g0098 others(17): Show |
20 | HG00140.hp1 HG00738.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.464-3212A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110319780 | |||||||
| chr12:110320237 | T | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0031 others(5): Show |
9 | HG01168.hp2 HG01169.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.464-2755T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110320237 | |||||||
| chr12:110320276 | T | A | 19 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0041 others(16): Show |
19 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.464-2716T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110320276 | |||||||
| chr12:110320337 | C | T | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-2655C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110320337 | |||||||
| chr12:110320393 | C | T | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-2599C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110320393 | |||||||
| chr12:110320409 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.464-2583A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110320409 | |||||||
| chr12:110320428 | G | C | 2 | a0001c0001t0002g0023 a0001c0001t0002g0044 |
2 | HG03491.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.464-2564G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110320428 | |||||||
| chr12:110320546 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.464-2446G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110320546 | |||||||
| chr12:110320719 | G | A | 1 | a0001c0002t0001g0224 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.464-2273G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110320719 | |||||||
| chr12:110320777 | TGA | T | 5 | a0001c0001t0001g0103 a0001c0001t0001g0110 a0001c0001t0001g0111 others(2): Show |
5 | HG02647.hp1 HG03516.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.464-2212_464-2211d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110320777 | ||||||
| chr12:110320950 | T | C | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-2042T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110320950 | |||||||
| chr12:110321114 | G | A | 3 | a0001c0001t0005g0108 a0001c0001t0005g0109 a0001c0001t0005g0119 |
3 | HG01255.hp2 HG02735.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.464-1878G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110321114 | |||||||
| chr12:110321145 | T | C | 3 | a0001c0001t0001g0105 a0001c0001t0001g0127 a0001c0001t0001g0133 |
3 | HG00735.hp1 HG01106.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.464-1847T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110321145 | |||||||
| chr12:110321277 | A | G | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.464-1715A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110321277 | |||||||
| chr12:110321387 | T | G | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-1605T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110321387 | |||||||
| chr12:110321475 | A | G | 5 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(2): Show |
5 | HG01884.hp2 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.464-1517A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110321475 | |||||||
| chr12:110321544 | C | T | 1 | a0001c0001t0017g0004 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.464-1448C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110321544 | |||||||
| chr12:110321550 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.464-1442A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110321550 | |||||||
| chr12:110321632 | G | A | 1 | a0001c0005t0009g0219 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.464-1360G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110321632 | |||||||
| chr12:110322034 | A | T | 2 | a0001c0001t0012g0222 a0001c0001t0012g0223 |
2 | HG01099.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.464-958A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110322034 | |||||||
| chr12:110322038 | T | G | 19 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0041 others(16): Show |
19 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.464-954T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110322038 | |||||||
| chr12:110322054 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0021g0029 |
2 | HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.464-938G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110322054 | |||||||
| chr12:110322076 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.464-916C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110322076 | |||||||
| chr12:110322268 | G | A | 2 | a0001c0001t0004g0167 a0001c0001t0004g0168 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.464-724G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110322268 | |||||||
| chr12:110322305 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.464-687T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110322305 | |||||||
| chr12:110323196 | T | C | 2 | a0001c0001t0012g0222 a0001c0001t0012g0223 |
2 | HG01099.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.544+124T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110323196 | |||||||
| chr12:110323216 | G | A | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.544+144G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110323216 | |||||||
| chr12:110323246 | G | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0030 others(6): Show |
10 | HG01168.hp2 HG01169.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.544+174G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110323246 | |||||||
| chr12:110323255 | G | T | 6 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0015 others(3): Show |
6 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.544+183G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110323255 | |||||||
| chr12:110323270 | C | T | 2 | a0001c0001t0002g0047 a0001c0001t0002g0054 |
2 | HG00323.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.544+198C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110323270 | |||||||
| chr12:110323524 | A | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0150 others(1): Show |
4 | HG02615.hp1 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.544+452A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110323524 | |||||||
| chr12:110324038 | A | G | 2 | a0001c0002t0001g0115 a0001c0002t0001g0117 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.544+966A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110324038 | |||||||
| chr12:110324181 | A | G | 1 | a0001c0001t0012g0222 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.544+1109A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110324181 | |||||||
| chr12:110324254 | T | TG | 3 | a0001c0001t0001g0221 a0001c0005t0009g0219 a0001c0005t0009g0220 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.544+1184dupG | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 110324254 | ||||||
| chr12:110324288 | A | G | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.544+1216A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110324288 | |||||||
| chr12:110324426 | A | T | 2 | a0002c0004t0003g0181 a0002c0004t0003g0182 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.544+1354A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110324426 | |||||||
| chr12:110324427 | T | A | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.544+1355T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110324427 | |||||||
| chr12:110324452 | C | T | 2 | a0001c0001t0002g0006 a0001c0001t0002g0027 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.544+1380C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110324452 | |||||||
| chr12:110324570 | C | T | 6 | a0001c0001t0002g0006 a0001c0001t0002g0027 a0001c0001t0012g0222 others(3): Show |
6 | HG01099.hp1 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.544+1498C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110324570 | |||||||
| chr12:110324601 | T | A | 1 | a0001c0007t0002g0025 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.544+1529T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110324601 | |||||||
| chr12:110324611 | G | A | 1 | a0001c0001t0005g0108 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.544+1539G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110324611 | |||||||
| chr12:110324704 | A | T | 2 | a0001c0001t0001g0068 a0001c0001t0024g0092 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.544+1632A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110324704 | |||||||
| chr12:110324803 | C | A | 15 | a0001c0001t0002g0055 a0001c0001t0004g0005 a0001c0001t0004g0167 others(12): Show |
15 | HG01167.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.545-1587C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110324803 | |||||||
| chr12:110324828 | C | CT | 7 | a0001c0001t0001g0022 a0001c0001t0001g0128 a0001c0001t0002g0038 others(4): Show |
7 | HG02622.hp2 HG02630.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.545-1545dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 110324828 | ||||||
| chr12:110324951 | A | G | 62 | a0001c0001t0001g0221 a0001c0001t0001g0225 a0001c0001t0002g0006 others(59): Show |
62 | HG00323.hp1 HG00738.hp1 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.545-1439A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110324951 | |||||||
| chr12:110325303 | C | T | 2 | a0001c0001t0002g0211 a0001c0001t0002g0212 |
2 | HG02055.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.545-1087C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110325303 | |||||||
| chr12:110325409 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(1): Show |
4 | HG02717.hp1 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.545-981G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110325409 | |||||||
| chr12:110325449 | A | G | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.545-941A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110325449 | |||||||
| chr12:110325549 | G | C | 22 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0075 others(19): Show |
22 | HG00423.hp2 HG00558.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.545-841G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110325549 | |||||||
| chr12:110325552 | C | T | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.545-838C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110325552 | |||||||
| chr12:110325632 | A | C | 1 | a0001c0001t0002g0055 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.545-758A>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110325632 | |||||||
| chr12:110326120 | C | G | 2 | a0001c0001t0027g0201 a0001c0001t0029g0197 |
2 | HG01346.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.545-270C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110326120 | |||||||
| chr12:110326229 | G | A | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.545-161G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110326229 | |||||||
| chr12:110326313 | G | A | 1 | a0001c0001t0006g0016 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.545-77G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110326313 | |||||||
| chr12:110326317 | G | T | 1 | a0001c0001t0001g0114 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.545-73G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110326317 | |||||||
| chr12:110327193 | C | A | 2 | a0001c0001t0002g0023 a0001c0001t0002g0044 |
2 | HG03491.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.631-360C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 7/19 | chr12 | 110327193 | |||||||
| chr12:110327255 | C | CTA | 46 | a0001c0001t0002g0006 a0001c0001t0002g0023 a0001c0001t0002g0024 others(43): Show |
46 | HG00323.hp1 HG01099.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.631-294_631-293dup others(2): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr12 | 110327255 | ||||||
| chr12:110327349 | C | G | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.631-204C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 7/19 | chr12 | 110327349 | |||||||
| chr12:110327495 | G | A | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.631-58G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 7/19 | chr12 | 110327495 | |||||||
| chr12:110328361 | C | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(108): Show |
113 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.1095+344C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110328361 | |||||||
| chr12:110328423 | T | C | 1 | a0001c0001t0010g0138 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1095+406T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110328423 | |||||||
| chr12:110328458 | A | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0021g0029 |
3 | HG02615.hp1 HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1095+441A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110328458 | |||||||
| chr12:110328460 | T | G | 1 | a0001c0001t0001g0103 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1095+443T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110328460 | |||||||
| chr12:110328516 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1095+499C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110328516 | |||||||
| chr12:110328714 | T | C | 1 | a0001c0001t0003g0196 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1095+697T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110328714 | |||||||
| chr12:110328740 | A | AT | 5 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(2): Show |
5 | HG01884.hp2 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1095+732dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr12 | 110328740 | ||||||
| chr12:110328912 | T | C | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1095+895T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110328912 | |||||||
| chr12:110328962 | A | G | 19 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0041 others(16): Show |
19 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.1095+945A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110328962 | |||||||
| chr12:110329224 | T | C | 2 | a0001c0001t0014g0176 a0001c0001t0014g0177 |
2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1095+1207T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110329224 | |||||||
| chr12:110329848 | G | A | 3 | a0001c0003t0002g0020 a0001c0003t0002g0021 a0001c0003t0020g0019 |
3 | HG01891.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1095+1831G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110329848 | |||||||
| chr12:110329887 | G | A | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | HG00558.hp1 NA18948.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1095+1870G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110329887 | |||||||
| chr12:110329902 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1095+1885T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110329902 | |||||||
| chr12:110329916 | T | A | 48 | a0001c0001t0001g0221 a0001c0001t0002g0006 a0001c0001t0002g0023 others(45): Show |
48 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.1095+1899T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110329916 | |||||||
| chr12:110330147 | G | T | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1095+2130G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110330147 | |||||||
| chr12:110330380 | A | C | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1096-2217A>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110330380 | |||||||
| chr12:110330422 | G | C | 10 | a0001c0001t0004g0005 a0001c0001t0004g0167 a0001c0001t0004g0168 others(7): Show |
10 | HG01167.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1096-2175G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110330422 | |||||||
| chr12:110330571 | TAAGCCAT others(5): Show |
T | 3 | a0001c0001t0001g0221 a0001c0005t0009g0219 a0001c0005t0009g0220 |
3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1096-2011_1096-200 others(16): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr12 | 110330571 | ||||||
| chr12:110330575 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1096-2022C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110330575 | |||||||
| chr12:110330637 | A | T | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | HG00558.hp1 NA18948.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1096-1960A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110330637 | |||||||
| chr12:110331192 | C | T | 1 | a0001c0007t0002g0025 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1096-1405C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110331192 | |||||||
| chr12:110331208 | A | G | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1096-1389A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110331208 | |||||||
| chr12:110331221 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1096-1376G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110331221 | |||||||
| chr12:110331496 | C | T | 45 | a0001c0001t0002g0006 a0001c0001t0002g0023 a0001c0001t0002g0024 others(42): Show |
45 | HG00323.hp1 HG01099.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.1096-1101C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110331496 | |||||||
| chr12:110332291 | A | G | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1096-306A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110332291 | |||||||
| chr12:110332581 | C | T | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1096-16C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110332581 | |||||||
| chr12:110332585 | C | G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0091 |
2 | HG00423.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.1096-12C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110332585 | |||||||
| chr12:110332783 | T | C | 11 | a0001c0001t0002g0006 a0001c0001t0002g0027 a0001c0001t0002g0038 others(8): Show |
11 | HG01099.hp1 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1184+98T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 9/19 | chr12 | 110332783 | |||||||
| chr12:110332792 | A | G | 11 | a0001c0001t0002g0006 a0001c0001t0002g0027 a0001c0001t0002g0038 others(8): Show |
11 | HG01099.hp1 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1184+107A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 9/19 | chr12 | 110332792 | |||||||
| chr12:110333051 | T | C | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1185-130T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 9/19 | chr12 | 110333051 | |||||||
| chr12:110333107 | CG | C | 13 | a0001c0001t0002g0006 a0001c0001t0002g0027 a0001c0001t0002g0213 others(10): Show |
13 | HG00738.hp1 HG01069.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.1185-67delG | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 110333107 | ||||||
| chr12:110333134 | A | G | 1 | a0001c0001t0003g0187 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1185-47A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 9/19 | chr12 | 110333134 | |||||||
| chr12:110333370 | C | G | 1 | a0001c0001t0018g0026 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1287+87C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 10/19 | chr12 | 110333370 | |||||||
| chr12:110333458 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1287+175G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 10/19 | chr12 | 110333458 | |||||||
| chr12:110333559 | A | G | 9 | a0001c0001t0002g0006 a0001c0001t0002g0027 a0001c0001t0002g0037 others(6): Show |
9 | HG01099.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1287+276A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 10/19 | chr12 | 110333559 | |||||||
| chr12:110333624 | T | A | 5 | a0001c0001t0007g0048 a0001c0001t0007g0049 a0001c0001t0007g0050 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1287+341T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 10/19 | chr12 | 110333624 | |||||||
| chr12:110333707 | C | G | 1 | a0001c0001t0001g0130 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1288-305C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 10/19 | chr12 | 110333707 | |||||||
| chr12:110333783 | A | G | 1 | a0001c0001t0001g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1288-229A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 10/19 | chr12 | 110333783 | |||||||
| chr12:110333861 | T | C | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1288-151T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 10/19 | chr12 | 110333861 | |||||||
| chr12:110333890 | A | AAATGGCC others(15): Show |
2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1288-120_1288-99du others(23): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr12 | 110333890 | ||||||
| chr12:110333940 | A | G | 1 | a0001c0001t0002g0043 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1288-72A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 10/19 | chr12 | 110333940 | |||||||
| chr12:110334486 | C | T | 6 | a0001c0001t0002g0006 a0001c0001t0002g0027 a0001c0001t0012g0222 others(3): Show |
6 | HG01099.hp1 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1419+343C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110334486 | |||||||
| chr12:110334586 | C | CT | 69 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0028 others(66): Show |
69 | HG00140.hp1 HG00140.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.1419+463dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr12 | 110334586 | ||||||
| chr12:110334586 | C | CTT | 15 | a0001c0001t0001g0103 a0001c0001t0001g0110 a0001c0001t0001g0111 others(12): Show |
15 | HG01081.hp1 HG01099.hp1 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.1419+462_1419+463d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr12 | 110334586 | ||||||
| chr12:110334586 | CTTTTTTT others(4): Show |
C | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1419+453_1419+463d others(13): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr12 | 110334586 | ||||||
| chr12:110334621 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1419+478C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110334621 | |||||||
| chr12:110334651 | G | A | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1419+508G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110334651 | |||||||
| chr12:110334831 | G | A | 3 | a0001c0001t0005g0108 a0001c0001t0005g0109 a0001c0001t0005g0119 |
3 | HG01255.hp2 HG02735.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1419+688G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110334831 | |||||||
| chr12:110335040 | T | C | 1 | a0001c0001t0015g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1419+897T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110335040 | |||||||
| chr12:110335432 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1419+1289G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110335432 | |||||||
| chr12:110335529 | G | A | 2 | a0001c0001t0002g0046 a0001c0001t0002g0053 |
2 | NA18952.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1419+1386G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110335529 | |||||||
| chr12:110335765 | T | C | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1419+1622T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110335765 | |||||||
| chr12:110335798 | T | C | 2 | a0001c0001t0012g0222 a0001c0001t0012g0223 |
2 | HG01099.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1419+1655T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110335798 | |||||||
| chr12:110335933 | T | A | 1 | a0001c0001t0002g0027 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1419+1790T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110335933 | |||||||
| chr12:110336013 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0024g0092 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1419+1870C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110336013 | |||||||
| chr12:110336015 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1419+1872C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110336015 | |||||||
| chr12:110336030 | G | A | 1 | a0001c0001t0002g0061 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1419+1887G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110336030 | |||||||
| chr12:110336206 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0111 |
2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1419+2063G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110336206 | |||||||
| chr12:110336363 | GA | G | 2 | a0001c0001t0014g0176 a0001c0001t0014g0177 |
2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1419+2221delA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110336363 | |||||||
| chr12:110336428 | T | G | 1 | a0001c0001t0001g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1419+2285T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110336428 | |||||||
| chr12:110336751 | A | G | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1420-2530A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110336751 | |||||||
| chr12:110337256 | T | C | 1 | a0001c0001t0002g0054 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1420-2025T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110337256 | |||||||
| chr12:110337439 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1420-1842A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110337439 | |||||||
| chr12:110337567 | T | C | 7 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0171 others(4): Show |
7 | HG01167.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1420-1714T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110337567 | |||||||
| chr12:110337775 | CT | C | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1420-1504delT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr12 | 110337775 | ||||||
| chr12:110337804 | T | C | 50 | a0001c0001t0001g0221 a0001c0001t0001g0225 a0001c0001t0002g0006 others(47): Show |
50 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.1420-1477T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110337804 | |||||||
| chr12:110337805 | G | A | 19 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0041 others(16): Show |
19 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.1420-1476G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110337805 | |||||||
| chr12:110337816 | G | A | 2 | a0001c0001t0010g0138 a0001c0001t0010g0140 |
2 | NA19062.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1420-1465G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110337816 | |||||||
| chr12:110337969 | A | C | 22 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0075 others(19): Show |
22 | HG00423.hp2 HG00558.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1420-1312A>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110337969 | |||||||
| chr12:110338141 | A | G | 10 | a0001c0001t0004g0005 a0001c0001t0004g0167 a0001c0001t0004g0168 others(7): Show |
10 | HG01167.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1420-1140A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110338141 | |||||||
| chr12:110338184 | A | G | 4 | a0001c0001t0005g0122 a0001c0001t0005g0125 a0001c0001t0005g0126 others(1): Show |
4 | HG00738.hp2 HG01175.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-1097A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110338184 | |||||||
| chr12:110338191 | C | G | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1420-1090C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110338191 | |||||||
| chr12:110338275 | G | A | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1420-1006G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110338275 | |||||||
| chr12:110338397 | C | T | 1 | a0001c0001t0002g0061 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1420-884C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110338397 | |||||||
| chr12:110338443 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1420-838C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110338443 | |||||||
| chr12:110338456 | C | T | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1420-825C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110338456 | |||||||
| chr12:110338758 | T | C | 1 | a0001c0001t0002g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1420-523T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110338758 | |||||||
| chr12:110338978 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1420-303G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110338978 | |||||||
| chr12:110339219 | T | G | 9 | a0001c0001t0002g0006 a0001c0001t0002g0027 a0001c0001t0002g0037 others(6): Show |
9 | HG01099.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1420-62T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110339219 | |||||||
| chr12:110339273 | C | G | 7 | a0001c0001t0002g0060 a0001c0001t0006g0013 a0001c0001t0006g0014 others(4): Show |
7 | HG01081.hp1 HG01943.hp1 HG02647.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1420-8C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110339273 | |||||||
| chr12:110340004 | A | G | 1 | a0001c0001t0025g0074 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1761+283A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 13/19 | chr12 | 110340004 | |||||||
| chr12:110340577 | A | G | 1 | a0001c0001t0002g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1762-82A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 13/19 | chr12 | 110340577 | |||||||
| chr12:110340578 | A | G | 34 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0041 others(31): Show |
34 | HG00323.hp1 HG01167.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.1762-81A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 13/19 | chr12 | 110340578 | |||||||
| chr12:110341229 | A | G | 5 | a0001c0001t0002g0023 a0001c0001t0002g0044 a0001c0001t0002g0047 others(2): Show |
5 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.2097+235A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 14/19 | chr12 | 110341229 | |||||||
| chr12:110341611 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2097+617T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 14/19 | chr12 | 110341611 | |||||||
| chr12:110341824 | C | T | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.2098-404C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 14/19 | chr12 | 110341824 | |||||||
| chr12:110341846 | C | A | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.2098-382C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 14/19 | chr12 | 110341846 | |||||||
| chr12:110342135 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2098-93A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 14/19 | chr12 | 110342135 | |||||||
| chr12:110342496 | G | A | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.2318+48G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 15/19 | chr12 | 110342496 | |||||||
| chr12:110342649 | T | C | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.2318+201T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 15/19 | chr12 | 110342649 | |||||||
| chr12:110342735 | A | T | 31 | a0001c0001t0003g0003 a0001c0001t0003g0175 a0001c0001t0003g0178 others(28): Show |
32 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.2318+287A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 15/19 | chr12 | 110342735 | |||||||
| chr12:110342787 | C | T | 7 | a0001c0001t0002g0060 a0001c0001t0006g0013 a0001c0001t0006g0014 others(4): Show |
7 | HG01081.hp1 HG01943.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2318+339C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 15/19 | chr12 | 110342787 | |||||||
| chr12:110342807 | G | A | 19 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0041 others(16): Show |
19 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2318+359G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 15/19 | chr12 | 110342807 | |||||||
| chr12:110342864 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2319-368G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 15/19 | chr12 | 110342864 | |||||||
| chr12:110342977 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2319-255C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 15/19 | chr12 | 110342977 | |||||||
| chr12:110343100 | A | G | 46 | a0001c0001t0002g0006 a0001c0001t0002g0023 a0001c0001t0002g0024 others(43): Show |
46 | HG00323.hp1 HG01099.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.2319-132A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 15/19 | chr12 | 110343100 | |||||||
| chr12:110343124 | AGTT | A | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2319-102_2319-100d others(5): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr12 | 110343124 | ||||||
| chr12:110343159 | T | G | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.2319-73T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 15/19 | chr12 | 110343159 | |||||||
| chr12:110343823 | G | A | 19 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0041 others(16): Show |
19 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2521+389G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 16/19 | chr12 | 110343823 | |||||||
| chr12:110344188 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2522-698C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 16/19 | chr12 | 110344188 | |||||||
| chr12:110344222 | T | C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0031 others(5): Show |
9 | HG01168.hp2 HG01169.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.2522-664T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 16/19 | chr12 | 110344222 | |||||||
| chr12:110344394 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2522-492C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 16/19 | chr12 | 110344394 | |||||||
| chr12:110344644 | A | G | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.2522-242A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 16/19 | chr12 | 110344644 | |||||||
| chr12:110344727 | C | T | 19 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0041 others(16): Show |
19 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2522-159C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 16/19 | chr12 | 110344727 | |||||||
| chr12:110344736 | G | C | 3 | a0001c0003t0002g0020 a0001c0003t0002g0021 a0001c0003t0020g0019 |
3 | HG01891.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2522-150G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 16/19 | chr12 | 110344736 | |||||||
| chr12:110345070 | G | A | 2 | a0001c0005t0009g0219 a0001c0005t0009g0220 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.2607+99G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 17/19 | chr12 | 110345070 | |||||||
| chr12:110345412 | G | A | 1 | a0001c0001t0006g0015 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2741+30G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 18/19 | chr12 | 110345412 | |||||||
| chr12:110345436 | G | A | 40 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(37): Show |
41 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.2741+54G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 18/19 | chr12 | 110345436 | |||||||
| chr12:110345883 | G | A | 1 | a0001c0003t0004g0216 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2742-118G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 18/19 | chr12 | 110345883 | |||||||
| chr12:110345885 | G | A | 6 | a0001c0001t0002g0006 a0001c0001t0002g0027 a0001c0001t0012g0222 others(3): Show |
6 | HG01099.hp1 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2742-116G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 18/19 | chr12 | 110345885 | |||||||
| chr12:110345899 | T | G | 9 | a0001c0001t0004g0005 a0001c0001t0004g0167 a0001c0001t0004g0168 others(6): Show |
9 | HG01167.hp1 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2742-102T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 18/19 | chr12 | 110345899 | |||||||
| chr12:110345917 | A | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0157 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2742-84A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 18/19 | chr12 | 110345917 | |||||||
| chr12:110346180 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0217 |
2 | HG02698.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2860-21C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 19/19 | chr12 | 110346180 | |||||||
| chr12:110346190 | CTG | C | 6 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0171 others(3): Show |
6 | HG01167.hp1 HG02280.hp1 HG02622.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.2860-5_2860-4delGT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr12 | 110346190 |