Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 27032 |
| ensemblid | ENSG00000017260.20 |
| hgncid | 13211 |
| symbol | ATP2C1 |
| name | ATPase secretory pathway Ca2+ transporting 1 |
| refseq_nuc | NM_001378687.1 |
| refseq_prot | NP_001365616.1 |
| ensembl_nuc | ENST00000510168.6 |
| ensembl_prot | ENSP00000427461.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 130894084 |
| end | 131003150 |
| strand | + |
| ver | v1.2 |
| region | chr3:130894084-131003150 |
| region5000 | chr3:130889084-131008150 |
| regionname0 | ATP2C1_chr3_130894084_131003150 |
| regionname5000 | ATP2C1_chr3_130889084_131008150 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 919 | 374 | 83 | 60 | 181 | 14 | 34 | 143 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | MKVAR others(914): Show |
chr3 | 130889084 | 131008150 |
| a0002 | 0/0 | 919 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | MKVAR others(914): Show |
chr3 | 130889084 | 131008150 |
| a0003 | 0/0 | 919 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | MKVAR others(914): Show |
chr3 | 130889084 | 131008150 |
| a0004 | 0/0 | 919 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | MKVAR others(914): Show |
chr3 | 130889084 | 131008150 |
| a0005 | 0/0 | 919 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | MKVAR others(914): Show |
chr3 | 130889084 | 131008150 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2757 | 326 | 77 | 54 | 153 | 13 | 27 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | ATGAA others(2752): Show |
chr3 | 130889084 | 131008150 | ||
| a0001c0002 | 0/0 | 2757 | 39 | 0 | 4 | 27 | 1 | 7 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | ATGAA others(2752): Show |
chr3 | 130889084 | 131008150 | ||
| a0001c0003 | 0/0 | 2757 | 7 | 5 | 2 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | ATGAA others(2752): Show |
chr3 | 130889084 | 131008150 | ||
| a0001c0006 | 0/0 | 2757 | 2 | 1 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | ATGAA others(2752): Show |
chr3 | 130889084 | 131008150 | ||
| a0002c0004 | 0/0 | 2757 | 4 | 4 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | ATGAA others(2752): Show |
chr3 | 130889084 | 131008150 | ||
| a0003c0005 | 0/0 | 2757 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | ATGAA others(2752): Show |
chr3 | 130889084 | 131008150 | ||
| a0004c0008 | 0/0 | 2757 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | ATGAA others(2752): Show |
chr3 | 130889084 | 131008150 | ||
| a0005c0007 | 0/0 | 2757 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | ATGAA others(2752): Show |
chr3 | 130889084 | 131008150 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4994 | 313 | 72 | 53 | 147 | 13 | 26 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | AGACC others(4989): Show |
chr3 | 130889084 | 131008150 |
| a0001c0001t0002 | 0/0 | 4989 | 4 | 3 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | AGACC others(4984): Show |
chr3 | 130889084 | 131008150 |
| a0001c0001t0004 | 0/0 | 4994 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | AGACC others(4989): Show |
chr3 | 130889084 | 131008150 |
| a0001c0001t0005 | 0/0 | 4994 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | AGACC others(4989): Show |
chr3 | 130889084 | 131008150 |
| a0001c0001t0006 | 0/0 | 4994 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | AGACC others(4989): Show |
chr3 | 130889084 | 131008150 |
| a0001c0001t0007 | 0/0 | 4994 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | AGACC others(4989): Show |
chr3 | 130889084 | 131008150 |
| a0001c0001t0009 | 0/0 | 4994 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | AGACC others(4989): Show |
chr3 | 130889084 | 131008150 |
| a0001c0001t0010 | 0/0 | 4994 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | AGACC others(4989): Show |
chr3 | 130889084 | 131008150 |
| a0001c0001t0011 | 0/0 | 4994 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | AGACC others(4989): Show |
chr3 | 130889084 | 131008150 |
| a0001c0001t0012 | 0/0 | 4994 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | AGACC others(4989): Show |
chr3 | 130889084 | 131008150 |
| a0001c0002t0001 | 0/0 | 4994 | 38 | 0 | 4 | 26 | 1 | 7 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | AGACC others(4989): Show |
chr3 | 130889084 | 131008150 |
| a0001c0002t0008 | 0/0 | 4994 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | AGACC others(4989): Show |
chr3 | 130889084 | 131008150 |
| a0001c0003t0001 | 0/0 | 4994 | 7 | 5 | 2 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | AGACC others(4989): Show |
chr3 | 130889084 | 131008150 |
| a0001c0006t0001 | 0/0 | 4994 | 2 | 1 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | AGACC others(4989): Show |
chr3 | 130889084 | 131008150 |
| a0002c0004t0001 | 0/0 | 4994 | 4 | 4 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | AGACC others(4989): Show |
chr3 | 130889084 | 131008150 |
| a0003c0005t0003 | 0/0 | 4994 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | AGACC others(4989): Show |
chr3 | 130889084 | 131008150 |
| a0004c0008t0001 | 0/0 | 4994 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | AGACC others(4989): Show |
chr3 | 130889084 | 131008150 |
| a0005c0007t0001 | 0/0 | 4994 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | AGACC others(4989): Show |
chr3 | 130889084 | 131008150 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0081 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0256 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0004g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0005g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0007g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0009g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0010g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0011g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0001t0012g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0001g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0002t0008g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0003t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0003t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0003t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0003t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0003t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0006t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0001c0006t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0002c0004t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0002c0004t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0002c0004t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0002c0004t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0003c0005t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0003c0005t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0004c0008t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| a0005c0007t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | GBR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0201 | EUR | GBR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0173 | EUR | GBR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | GBR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0240 | EUR | FIN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0373 | EUR | FIN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0317 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00558 | hp2 | a0001 | c0001 | t0007 | g0185 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0360 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00733 | hp1 | a0001 | c0003 | t0001 | g0083 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0365 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0364 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0346 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0368 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0179 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01346 | hp1 | a0001 | c0003 | t0001 | g0099 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | IBS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0371 | EUR | IBS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0238 | EUR | IBS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0369 | EUR | IBS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02015 | hp2 | a0001 | c0001 | t0004 | g0316 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0326 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0335 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0366 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | CDX | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CDX | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02258 | hp2 | a0001 | c0003 | t0001 | g0100 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02280 | hp1 | a0001 | c0006 | t0001 | g0120 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0362 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0337 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0333 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0370 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02630 | hp1 | a0002 | c0004 | t0001 | g0107 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02630 | hp2 | a0001 | c0001 | t0009 | g0078 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02717 | hp1 | a0002 | c0004 | t0001 | g0106 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02723 | hp2 | a0004 | c0008 | t0001 | g0215 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0327 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0101 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0098 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0363 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0361 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0102 | AFR | ESN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02970 | hp1 | a0003 | c0005 | t0003 | g0109 | AFR | ESN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | ESN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | ESN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03041 | hp2 | a0002 | c0004 | t0001 | g0105 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0310 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03453 | hp2 | a0002 | c0004 | t0001 | g0108 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03491 | hp1 | a0001 | c0001 | t0006 | g0119 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0332 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0331 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0353 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0372 | SAS | BEB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0347 | SAS | BEB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | STU | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0319 | SAS | STU | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0374 | SAS | BEB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | STU | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | STU | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | STU | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | STU | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | STU | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0245 | SAS | STU | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | YRI | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | YRI | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0345 | EAS | CHB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | YRI | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0324 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0323 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0355 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18966 | hp2 | a0001 | c0001 | t0011 | g0290 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0329 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18973 | hp2 | a0001 | c0001 | t0012 | g0139 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0336 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0359 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0348 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0340 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0322 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | LWK | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19030 | hp2 | a0003 | c0005 | t0003 | g0110 | AFR | LWK | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | LWK | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0349 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0341 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0354 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0343 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19072 | hp1 | a0005 | c0007 | t0001 | g0227 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0352 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0339 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0358 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0357 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0342 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0351 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19088 | hp2 | a0001 | c0006 | t0001 | g0270 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19090 | hp2 | a0001 | c0002 | t0008 | g0334 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | YRI | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | YRI | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0367 | EUR | TSI | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | TSI | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | TSI | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0205 | EUR | TSI | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0338 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02486 | hp2 | a0001 | c0001 | t0010 | g0122 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0103 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | USA | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | USA | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0325 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | USA | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | USA | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0256 | REF | REF | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0081 | REF | REF | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:130955015 | G | A | 1 | a0003 | 2 | HG02970.hp1 NA19030.hp2 |
missense_variant | MODERATE | c.691G>A | p.Val231Ile | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 10/28 | 1125/4994 | 691/2760 | 231/919 | chr3 | 130955015 | |||
| chr3:130969331 | G | A | 1 | a0002 | 4 | HG02630.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
missense_variant | MODERATE | c.1348G>A | p.Ala450Thr | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/28 | 1782/4994 | 1348/2760 | 450/919 | chr3 | 130969331 | |||
| chr3:130969337 | T | C | 1 | a0005 | 1 | NA19072.hp1 | missense_variant | MODERATE | c.1354T>C | p.Tyr452His | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/28 | 1788/4994 | 1354/2760 | 452/919 | chr3 | 130969337 | |||
| chr3:130979301 | G | C | 1 | a0004 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1623G>C | p.Leu541Phe | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/28 | 2057/4994 | 1623/2760 | 541/919 | chr3 | 130979301 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:130953925 | G | A | 1 | a0001c0003 | 7 | HG00733.hp1 HG01346.hp1 HG02258.hp2 others(4): Show |
synonymous_variant | LOW | c.636G>A | p.Ser212Ser | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 9/28 | 1070/4994 | 636/2760 | 212/919 | chr3 | 130953925 | |||
| chr3:130959276 | A | G | 1 | a0003c0005 | 2 | HG02970.hp1 NA19030.hp2 |
splice_region_variant&synonymous_variant | LOW | c.834A>G | p.Gly278Gly | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/28 | 1268/4994 | 834/2760 | 278/919 | chr3 | 130959276 | |||
| chr3:130979361 | C | T | 1 | a0001c0006 | 2 | HG02280.hp1 NA19088.hp2 |
synonymous_variant | LOW | c.1683C>T | p.Ala561Ala | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/28 | 2117/4994 | 1683/2760 | 561/919 | chr3 | 130979361 | |||
| chr3:130999628 | G | A | 1 | a0001c0002 | 39 | HG00597.hp2 HG01081.hp2 HG01123.hp1 others(36): Show |
synonymous_variant | LOW | c.2598G>A | p.Lys866Lys | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/28 | 3032/4994 | 2598/2760 | 866/919 | chr3 | 130999628 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:130894172 | C | T | 1 | a0001c0001t0004 | 2 | HG00544.hp2 HG02015.hp2 |
5_prime_UTR_variant | MODIFIER | c.-346C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 1/28 | 598 | chr3 | 130894172 | ||||||
| chr3:130894190 | C | A | 1 | a0001c0001t0005 | 1 | HG01175.hp1 | 5_prime_UTR_variant | MODIFIER | c.-328C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 1/28 | 580 | chr3 | 130894190 | ||||||
| chr3:130894195 | G | T | 1 | a0001c0001t0012 | 1 | NA18973.hp2 | 5_prime_UTR_variant | MODIFIER | c.-323G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 1/28 | 575 | chr3 | 130894195 | ||||||
| chr3:130894218 | G | A | 1 | a0001c0001t0006 | 1 | HG03491.hp1 | 5_prime_UTR_variant | MODIFIER | c.-300G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 1/28 | 552 | chr3 | 130894218 | ||||||
| chr3:130894310 | C | A | 1 | a0001c0001t0007 | 1 | HG00558.hp2 | 5_prime_UTR_variant | MODIFIER | c.-208C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 1/28 | 460 | chr3 | 130894310 | ||||||
| chr3:130894717 | G | C | 1 | a0001c0002t0008 | 1 | NA19090.hp2 | 5_prime_UTR_variant | MODIFIER | c.-53G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/28 | 53 | chr3 | 130894717 | ||||||
| chr3:131001596 | G | A | 1 | a0001c0001t0009 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*246G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 28/28 | 246 | chr3 | 131001596 | ||||||
| chr3:131001597 | G | T | 1 | a0001c0001t0009 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*247G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 28/28 | 247 | chr3 | 131001597 | ||||||
| chr3:131001598 | T | A | 1 | a0001c0001t0009 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*248T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 28/28 | 248 | chr3 | 131001598 | ||||||
| chr3:131001599 | C | A | 1 | a0001c0001t0009 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*249C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 28/28 | 249 | chr3 | 131001599 | ||||||
| chr3:131001842 | TTGTAA | T | 1 | a0001c0001t0002 | 4 | HG02970.hp2 HG02976.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*498_*502delTGTAA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 28/28 | 498 | INFO_REALIGN_3_PRIME | chr3 | 131001842 | |||||
| chr3:131002036 | G | A | 1 | a0001c0001t0010 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*686G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 28/28 | 686 | chr3 | 131002036 | ||||||
| chr3:131002281 | C | G | 1 | a0001c0001t0011 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*931C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 28/28 | 931 | chr3 | 131002281 | ||||||
| chr3:131002895 | A | G | 1 | a0003c0005t0003 | 2 | HG02970.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1545A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 28/28 | 1545 | chr3 | 131002895 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:130894512 | GCTCCCGA others(20): Show |
G | 1 | a0001c0002t0001g0374 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-180-73_-180-47del others(27): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 130894512 | ||||||
| chr3:130894533 | C | T | 7 | a0001c0003t0001g0083 a0001c0003t0001g0098 a0001c0003t0001g0099 others(4): Show |
7 | HG00733.hp1 HG01346.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-180-57C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 1/27 | chr3 | 130894533 | |||||||
| chr3:130894790 | C | G | 9 | a0001c0001t0001g0365 a0001c0001t0001g0366 a0001c0001t0001g0367 others(6): Show |
9 | HG00280.hp2 HG00735.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.6+15C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130894790 | |||||||
| chr3:130895069 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG01358.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.6+294G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130895069 | |||||||
| chr3:130895186 | G | C | 1 | a0001c0002t0001g0010 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.6+411G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130895186 | |||||||
| chr3:130895306 | C | G | 45 | a0001c0001t0001g0007 a0001c0001t0001g0328 a0001c0001t0001g0330 others(42): Show |
46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.6+531C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130895306 | |||||||
| chr3:130895350 | C | T | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
307 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.6+575C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130895350 | |||||||
| chr3:130895564 | G | T | 1 | a0001c0001t0001g0321 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.6+789G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130895564 | |||||||
| chr3:130895667 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.6+892T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130895667 | |||||||
| chr3:130895809 | C | A | 371 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(368): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.6+1034C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130895809 | |||||||
| chr3:130895964 | AT | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(6): Show |
9 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+1192delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130895964 | ||||||
| chr3:130896099 | A | T | 1 | a0001c0001t0001g0320 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6+1324A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130896099 | |||||||
| chr3:130896298 | G | A | 1 | a0001c0001t0001g0321 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.6+1523G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130896298 | |||||||
| chr3:130896787 | T | C | 1 | a0001c0003t0001g0083 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.6+2012T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130896787 | |||||||
| chr3:130896820 | G | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.6+2045G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130896820 | |||||||
| chr3:130896908 | G | A | 5 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(2): Show |
5 | HG00639.hp1 HG01258.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+2133G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130896908 | |||||||
| chr3:130896998 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.6+2223G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130896998 | |||||||
| chr3:130897044 | G | C | 1 | a0001c0001t0001g0020 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.6+2269G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130897044 | |||||||
| chr3:130897117 | C | T | 1 | a0001c0001t0001g0319 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.6+2342C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130897117 | |||||||
| chr3:130897170 | A | T | 37 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(34): Show |
37 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.6+2395A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130897170 | |||||||
| chr3:130897371 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.6+2596T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130897371 | |||||||
| chr3:130897382 | C | T | 110 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(107): Show |
112 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.6+2607C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130897382 | |||||||
| chr3:130897728 | G | A | 7 | a0001c0003t0001g0083 a0001c0003t0001g0098 a0001c0003t0001g0099 others(4): Show |
7 | HG00733.hp1 HG01346.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.6+2953G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130897728 | |||||||
| chr3:130897747 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.6+2972G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130897747 | |||||||
| chr3:130897849 | G | C | 1 | a0001c0001t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6+3074G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130897849 | |||||||
| chr3:130898290 | A | T | 7 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(4): Show |
7 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+3515A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130898290 | |||||||
| chr3:130898409 | G | C | 4 | a0002c0004t0001g0105 a0002c0004t0001g0106 a0002c0004t0001g0107 others(1): Show |
4 | HG02630.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+3634G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130898409 | |||||||
| chr3:130898429 | T | C | 2 | a0003c0005t0003g0109 a0003c0005t0003g0110 |
2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.6+3654T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130898429 | |||||||
| chr3:130898439 | T | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(8): Show |
12 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.6+3664T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130898439 | |||||||
| chr3:130898623 | A | C | 45 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(42): Show |
45 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.6+3848A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130898623 | |||||||
| chr3:130898728 | C | T | 1 | a0001c0001t0005g0179 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.6+3953C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130898728 | |||||||
| chr3:130898847 | G | T | 1 | a0001c0001t0001g0149 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.6+4072G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130898847 | |||||||
| chr3:130898936 | A | T | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.6+4161A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130898936 | |||||||
| chr3:130898993 | G | A | 6 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(3): Show |
6 | HG02109.hp1 HG02723.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+4218G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130898993 | |||||||
| chr3:130899362 | A | G | 49 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(46): Show |
50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.6+4587A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130899362 | |||||||
| chr3:130899618 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.6+4843C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130899618 | |||||||
| chr3:130899680 | A | G | 1 | a0001c0001t0001g0278 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.6+4905A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130899680 | |||||||
| chr3:130899858 | T | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.6+5083T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130899858 | |||||||
| chr3:130899877 | A | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.6+5102A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130899877 | |||||||
| chr3:130899954 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.6+5179A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130899954 | |||||||
| chr3:130900015 | C | T | 3 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 |
3 | HG01243.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.6+5240C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130900015 | |||||||
| chr3:130900536 | A | T | 1 | a0001c0001t0001g0145 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.6+5761A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130900536 | |||||||
| chr3:130900870 | A | G | 4 | a0001c0001t0001g0079 a0001c0001t0001g0117 a0001c0001t0001g0118 others(1): Show |
4 | HG02451.hp2 HG02630.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+6095A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130900870 | |||||||
| chr3:130901005 | T | C | 1 | a0001c0001t0009g0078 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6+6230T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130901005 | |||||||
| chr3:130901012 | G | T | 1 | a0001c0001t0001g0274 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.6+6237G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130901012 | |||||||
| chr3:130901366 | T | C | 32 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(29): Show |
32 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.6+6591T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130901366 | |||||||
| chr3:130901376 | C | G | 1 | a0001c0001t0001g0273 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.6+6601C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130901376 | |||||||
| chr3:130901866 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.6+7091C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130901866 | |||||||
| chr3:130901917 | G | A | 1 | a0001c0001t0006g0119 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.6+7142G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130901917 | |||||||
| chr3:130901948 | A | G | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.6+7173A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130901948 | |||||||
| chr3:130901964 | A | G | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(20): Show |
23 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.6+7189A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130901964 | |||||||
| chr3:130902008 | C | T | 4 | a0001c0001t0001g0361 a0001c0001t0001g0362 a0001c0001t0001g0363 others(1): Show |
4 | HG00735.hp2 HG02280.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+7233C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902008 | |||||||
| chr3:130902114 | T | C | 23 | a0001c0001t0001g0005 a0001c0001t0001g0096 a0001c0001t0001g0180 others(20): Show |
24 | HG00544.hp1 HG00558.hp2 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.6+7339T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902114 | |||||||
| chr3:130902283 | CGTTTTTT others(6): Show |
C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0077 a0001c0001t0001g0085 others(26): Show |
30 | HG01099.hp1 HG01243.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.6+7522_6+7534delGT others(11): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902283 | ||||||
| chr3:130902284 | G | GT | 12 | a0001c0001t0001g0058 a0001c0001t0001g0124 a0001c0001t0001g0125 others(9): Show |
12 | HG00597.hp1 HG00609.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.6+7521dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | ||||||
| chr3:130902284 | G | GTT | 10 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0130 others(7): Show |
10 | HG00741.hp2 HG04184.hp1 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.6+7520_6+7521dupTT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | ||||||
| chr3:130902284 | G | GTTTTTTT others(3): Show |
1 | a0001c0003t0001g0100 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.6+7512_6+7521dupTT others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | ||||||
| chr3:130902284 | G | GTTTTTTT others(9): Show |
1 | a0001c0003t0001g0099 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.6+7521_6+7522insTT others(14): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | ||||||
| chr3:130902284 | G | GTTTTTTT others(16): Show |
1 | a0001c0003t0001g0083 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.6+7521_6+7522insTT others(21): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | ||||||
| chr3:130902284 | GTTTTTTT others(7): Show |
G | 90 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): Show |
93 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.6+7522_6+7535delGT others(12): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | ||||||
| chr3:130902284 | GTTTTTTT others(8): Show |
G | 24 | a0001c0001t0001g0004 a0001c0001t0001g0097 a0001c0001t0001g0104 others(21): Show |
24 | HG01081.hp2 HG01175.hp1 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.6+7522_6+7536delGT others(13): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | ||||||
| chr3:130902284 | GTTTTTTT others(9): Show |
G | 72 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0093 others(69): Show |
73 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.6+7522_6+7537delGT others(14): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | ||||||
| chr3:130902284 | GTTTTTTT others(10): Show |
G | 1 | a0001c0001t0001g0092 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.6+7522_6+7538delGT others(15): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | ||||||
| chr3:130902284 | GTTTTTTT others(11): Show |
G | 2 | a0001c0001t0001g0091 a0001c0001t0001g0314 |
2 | HG01891.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.6+7522_6+7539delGT others(16): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | ||||||
| chr3:130902284 | GTTTTTTT others(12): Show |
G | 35 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(32): Show |
35 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.6+7522_6+7540delGT others(17): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | ||||||
| chr3:130902284 | GTTTTTTT others(13): Show |
G | 1 | a0001c0001t0009g0078 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6+7522_6+7541delGT others(18): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | ||||||
| chr3:130902284 | GTTTTTTT others(15): Show |
G | 3 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0218 |
3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.6+7522_6+7543delGT others(20): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | ||||||
| chr3:130902285 | TTTTTTTT others(5): Show |
T | 1 | a0001c0001t0001g0084 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.6+7522_6+7533delGT others(10): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902285 | ||||||
| chr3:130902287 | TTTTTTTT others(3): Show |
T | 1 | a0001c0001t0001g0123 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.6+7522_6+7531delGT others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902287 | ||||||
| chr3:130902291 | T | G | 3 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 |
3 | HG01243.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.6+7516T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902291 | |||||||
| chr3:130902296 | TG | T | 5 | a0001c0001t0001g0117 a0001c0001t0001g0121 a0001c0001t0001g0145 others(2): Show |
5 | HG02055.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+7522delG | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902296 | |||||||
| chr3:130902297 | G | GT | 14 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(11): Show |
14 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.6+7547dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902297 | ||||||
| chr3:130902297 | G | T | 32 | a0001c0001t0001g0118 a0001c0001t0001g0124 a0001c0001t0001g0125 others(29): Show |
32 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.6+7522G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902297 | |||||||
| chr3:130902298 | T | G | 1 | a0001c0001t0001g0022 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.6+7523T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902298 | |||||||
| chr3:130902300 | T | G | 1 | a0001c0001t0006g0119 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.6+7525T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902300 | |||||||
| chr3:130902310 | T | G | 2 | a0001c0001t0001g0282 a0001c0001t0006g0119 |
2 | HG03491.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.6+7535T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902310 | |||||||
| chr3:130902312 | T | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(1): Show |
4 | HG02615.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+7537T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902312 | |||||||
| chr3:130902346 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6+7571G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902346 | |||||||
| chr3:130902370 | T | G | 19 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(16): Show |
19 | HG00609.hp1 HG02056.hp2 NA18940.hp1 others(16): Show |
intron_variant | MODIFIER | c.6+7595T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902370 | |||||||
| chr3:130902547 | C | CATTTT | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.6+7775_6+7779dupTT others(3): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902547 | ||||||
| chr3:130902637 | T | C | 7 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(4): Show |
8 | HG02717.hp2 HG02818.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+7862T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902637 | |||||||
| chr3:130902657 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.6+7882C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902657 | |||||||
| chr3:130902786 | G | A | 15 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(12): Show |
16 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.6+8011G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902786 | |||||||
| chr3:130902859 | G | A | 48 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(45): Show |
49 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.6+8084G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902859 | |||||||
| chr3:130903442 | G | T | 1 | a0001c0001t0001g0318 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.6+8667G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130903442 | |||||||
| chr3:130903504 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG03654.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.6+8729G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130903504 | |||||||
| chr3:130903611 | T | C | 9 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(6): Show |
9 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+8836T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130903611 | |||||||
| chr3:130903613 | C | T | 9 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(6): Show |
9 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+8838C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130903613 | |||||||
| chr3:130903686 | C | G | 1 | a0001c0001t0001g0070 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.6+8911C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130903686 | |||||||
| chr3:130903688 | A | C | 38 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(35): Show |
39 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.6+8913A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130903688 | |||||||
| chr3:130903693 | CCCTTTCC others(5): Show |
C | 1 | a0001c0001t0001g0168 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.6+8926_6+8937delCC others(10): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130903693 | ||||||
| chr3:130903700 | C | CCCTTT | 13 | a0001c0001t0001g0004 a0001c0001t0001g0062 a0001c0001t0001g0063 others(10): Show |
14 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.6+8958_6+8962dupTT others(3): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130903700 | ||||||
| chr3:130903700 | C | CCCTTTCC others(3): Show |
5 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(2): Show |
5 | HG02615.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+8953_6+8962dupTT others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130903700 | ||||||
| chr3:130903700 | C | CCCTTTCC others(8): Show |
2 | a0001c0001t0002g0217 a0001c0001t0002g0218 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.6+8948_6+8962dupTT others(13): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130903700 | ||||||
| chr3:130903700 | C | CCCTTTCC others(13): Show |
5 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0086 others(2): Show |
6 | HG02818.hp2 HG02895.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.6+8943_6+8962dupTT others(18): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130903700 | ||||||
| chr3:130903700 | C | CCCTTTCC others(18): Show |
4 | a0001c0001t0001g0088 a0001c0001t0001g0279 a0001c0001t0001g0280 others(1): Show |
4 | HG01884.hp2 HG02647.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+8938_6+8962dupTT others(23): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130903700 | ||||||
| chr3:130903700 | C | CCCTTTCC others(23): Show |
1 | a0001c0001t0001g0089 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.6+8933_6+8962dupTT others(28): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130903700 | ||||||
| chr3:130903700 | C | CCCTTTCC others(28): Show |
2 | a0001c0001t0001g0085 a0001c0001t0001g0090 |
2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.6+8928_6+8962dupTT others(33): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130903700 | ||||||
| chr3:130903700 | CCCTTT | C | 233 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(230): Show |
236 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.6+8958_6+8962delTT others(3): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130903700 | ||||||
| chr3:130903700 | CCCTTTCC others(3): Show |
C | 1 | a0001c0001t0001g0091 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6+8953_6+8962delTT others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130903700 | ||||||
| chr3:130903700 | CCCTTTCC others(8): Show |
C | 1 | a0001c0002t0001g0338 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.6+8948_6+8962delTT others(13): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130903700 | ||||||
| chr3:130903741 | T | C | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.6+8966T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130903741 | |||||||
| chr3:130904496 | T | C | 7 | a0001c0001t0001g0082 a0001c0001t0001g0097 a0001c0001t0001g0209 others(4): Show |
7 | NA18978.hp2 NA18988.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.6+9721T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130904496 | |||||||
| chr3:130904734 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6+9959A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130904734 | |||||||
| chr3:130905227 | G | A | 41 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(38): Show |
42 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.6+10452G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130905227 | |||||||
| chr3:130905462 | A | G | 5 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(2): Show |
5 | NA18946.hp1 NA18964.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+10687A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130905462 | |||||||
| chr3:130905572 | C | G | 1 | a0001c0001t0005g0179 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.6+10797C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130905572 | |||||||
| chr3:130905706 | A | G | 9 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(6): Show |
9 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+10931A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130905706 | |||||||
| chr3:130905739 | A | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0112 a0001c0001t0001g0113 others(3): Show |
7 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+10964A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130905739 | |||||||
| chr3:130905861 | T | C | 7 | a0001c0001t0001g0082 a0001c0001t0001g0097 a0001c0001t0001g0209 others(4): Show |
7 | NA18978.hp2 NA18988.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.6+11086T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130905861 | |||||||
| chr3:130905951 | C | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(8): Show |
12 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.6+11176C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130905951 | |||||||
| chr3:130905990 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02602.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.6+11215C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130905990 | |||||||
| chr3:130906002 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.6+11227A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130906002 | |||||||
| chr3:130906015 | T | A | 37 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(34): Show |
37 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.6+11240T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130906015 | |||||||
| chr3:130906122 | A | G | 4 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+11347A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130906122 | |||||||
| chr3:130906162 | T | G | 1 | a0001c0001t0001g0214 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.6+11387T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130906162 | |||||||
| chr3:130906230 | C | A | 1 | a0004c0008t0001g0215 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.6+11455C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130906230 | |||||||
| chr3:130906437 | G | C | 9 | a0001c0001t0001g0007 a0001c0001t0001g0328 a0001c0002t0001g0010 others(6): Show |
10 | HG02027.hp1 HG02735.hp2 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.6+11662G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130906437 | |||||||
| chr3:130906521 | T | C | 3 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0218 |
3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.6+11746T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130906521 | |||||||
| chr3:130906575 | G | A | 1 | a0001c0001t0009g0078 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6+11800G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130906575 | |||||||
| chr3:130906675 | G | GT | 95 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0089 others(92): Show |
97 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.6+11916dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130906675 | ||||||
| chr3:130906675 | GT | G | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(3): Show |
6 | HG01884.hp2 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.6+11916delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130906675 | ||||||
| chr3:130906861 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.6+12086C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130906861 | |||||||
| chr3:130906944 | C | A | 57 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0084 others(54): Show |
59 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.6+12169C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130906944 | |||||||
| chr3:130907079 | T | TAC | 72 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(69): Show |
75 | HG00408.hp1 HG00597.hp2 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.6+12326_6+12327dup others(2): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130907079 | ||||||
| chr3:130907079 | T | TACAC | 11 | a0001c0001t0001g0091 a0001c0001t0001g0111 a0001c0001t0001g0320 others(8): Show |
11 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.6+12324_6+12327dup others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130907079 | ||||||
| chr3:130907079 | TAC | T | 49 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(46): Show |
50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.6+12326_6+12327del others(2): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130907079 | ||||||
| chr3:130907080 | A | G | 2 | a0001c0001t0001g0255 a0004c0008t0001g0215 |
2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.6+12305A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130907080 | |||||||
| chr3:130907081 | C | T | 2 | a0001c0001t0001g0255 a0004c0008t0001g0215 |
2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.6+12306C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130907081 | |||||||
| chr3:130907103 | T | C | 1 | a0001c0002t0001g0326 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.6+12328T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130907103 | |||||||
| chr3:130907217 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.6+12442T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130907217 | |||||||
| chr3:130907252 | C | T | 1 | a0001c0001t0001g0318 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.6+12477C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130907252 | |||||||
| chr3:130907377 | A | G | 1 | a0001c0002t0001g0374 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.6+12602A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130907377 | |||||||
| chr3:130907487 | G | C | 2 | a0001c0001t0001g0255 a0004c0008t0001g0215 |
2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.6+12712G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130907487 | |||||||
| chr3:130907591 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.6+12816A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130907591 | |||||||
| chr3:130907722 | C | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.6+12947C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130907722 | |||||||
| chr3:130907730 | C | CT | 34 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(31): Show |
34 | HG00140.hp1 HG00639.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.6+12969dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130907730 | ||||||
| chr3:130907817 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.6+13042A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130907817 | |||||||
| chr3:130907919 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.6+13144A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130907919 | |||||||
| chr3:130908204 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.6+13429C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130908204 | |||||||
| chr3:130908434 | G | A | 6 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(3): Show |
6 | HG00639.hp1 HG01258.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+13659G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130908434 | |||||||
| chr3:130908469 | T | TA | 25 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(22): Show |
25 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.6+13706dupA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130908469 | ||||||
| chr3:130908469 | TA | T | 55 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(52): Show |
56 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.6+13706delA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130908469 | ||||||
| chr3:130908470 | A | T | 1 | a0001c0006t0001g0120 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.6+13695A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130908470 | |||||||
| chr3:130908559 | C | G | 1 | a0001c0001t0005g0179 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.6+13784C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130908559 | |||||||
| chr3:130908564 | C | G | 1 | a0001c0001t0001g0252 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.6+13789C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130908564 | |||||||
| chr3:130908597 | C | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(6): Show |
9 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+13822C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130908597 | |||||||
| chr3:130909318 | T | C | 3 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 |
3 | HG01243.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.6+14543T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130909318 | |||||||
| chr3:130909383 | T | C | 1 | a0001c0006t0001g0120 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.6+14608T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130909383 | |||||||
| chr3:130909406 | C | G | 1 | a0001c0001t0001g0252 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.6+14631C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130909406 | |||||||
| chr3:130909862 | T | A | 3 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0321 |
3 | HG01069.hp2 HG01981.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.6+15087T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130909862 | |||||||
| chr3:130909877 | T | A | 1 | a0001c0001t0001g0221 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.6+15102T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130909877 | |||||||
| chr3:130910043 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.6+15268G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910043 | |||||||
| chr3:130910070 | G | C | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG01255.hp1 HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.6+15295G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910070 | |||||||
| chr3:130910175 | C | T | 49 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(46): Show |
50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.6+15400C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910175 | |||||||
| chr3:130910496 | T | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.6+15721T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910496 | |||||||
| chr3:130910498 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.6+15723G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910498 | |||||||
| chr3:130910567 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.6+15792T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910567 | |||||||
| chr3:130910597 | C | T | 4 | a0002c0004t0001g0105 a0002c0004t0001g0106 a0002c0004t0001g0107 others(1): Show |
4 | HG02630.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+15822C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910597 | |||||||
| chr3:130910626 | A | G | 1 | a0001c0001t0006g0119 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.6+15851A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910626 | |||||||
| chr3:130910659 | C | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
275 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.6+15884C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910659 | |||||||
| chr3:130910762 | G | A | 5 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(2): Show |
5 | HG00639.hp1 HG01258.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+15987G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910762 | |||||||
| chr3:130910790 | G | A | 1 | a0001c0001t0005g0179 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.6+16015G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910790 | |||||||
| chr3:130910921 | T | G | 9 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(6): Show |
9 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+16146T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910921 | |||||||
| chr3:130910931 | C | T | 1 | a0001c0002t0001g0360 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.6+16156C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910931 | |||||||
| chr3:130911026 | G | C | 2 | a0001c0001t0001g0255 a0004c0008t0001g0215 |
2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.6+16251G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130911026 | |||||||
| chr3:130911056 | T | C | 1 | a0001c0001t0001g0264 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.6+16281T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130911056 | |||||||
| chr3:130911180 | C | A | 302 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(299): Show |
308 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.6+16405C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130911180 | |||||||
| chr3:130911199 | T | G | 49 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(46): Show |
50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.6+16424T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130911199 | |||||||
| chr3:130911326 | G | C | 30 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(27): Show |
30 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.6+16551G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130911326 | |||||||
| chr3:130911480 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6+16705G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130911480 | |||||||
| chr3:130911641 | A | G | 2 | a0001c0002t0001g0358 a0001c0002t0001g0359 |
2 | NA18984.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.6+16866A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130911641 | |||||||
| chr3:130911896 | T | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.6+17121T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130911896 | |||||||
| chr3:130912052 | T | C | 45 | a0001c0001t0001g0007 a0001c0001t0001g0328 a0001c0001t0001g0344 others(42): Show |
46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.6+17277T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912052 | |||||||
| chr3:130912237 | A | C | 4 | a0001c0001t0001g0155 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
4 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+17462A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912237 | |||||||
| chr3:130912243 | T | C | 4 | a0002c0004t0001g0105 a0002c0004t0001g0106 a0002c0004t0001g0107 others(1): Show |
4 | HG02630.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+17468T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912243 | |||||||
| chr3:130912256 | T | A | 1 | a0001c0001t0001g0159 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.6+17481T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912256 | |||||||
| chr3:130912259 | A | C | 1 | a0001c0001t0001g0159 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.6+17484A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912259 | |||||||
| chr3:130912360 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.6+17585A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912360 | |||||||
| chr3:130912396 | C | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.6+17621C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912396 | |||||||
| chr3:130912406 | GA | G | 8 | a0001c0001t0010g0122 a0001c0003t0001g0083 a0001c0003t0001g0098 others(5): Show |
8 | HG00733.hp1 HG01346.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+17638delA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130912406 | ||||||
| chr3:130912568 | A | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0145 a0001c0006t0001g0120 |
3 | HG02055.hp2 HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.6+17793A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912568 | |||||||
| chr3:130912587 | A | C | 1 | a0001c0006t0001g0120 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.6+17812A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912587 | |||||||
| chr3:130912609 | G | A | 1 | a0001c0002t0008g0334 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.7-17807G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912609 | |||||||
| chr3:130912707 | G | C | 3 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG00597.hp1 NA19000.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.7-17709G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912707 | |||||||
| chr3:130912806 | A | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-17610A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912806 | |||||||
| chr3:130912855 | A | G | 2 | a0001c0001t0002g0140 a0001c0001t0012g0139 |
2 | NA18973.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.7-17561A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912855 | |||||||
| chr3:130912858 | G | A | 102 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(99): Show |
104 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.7-17558G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912858 | |||||||
| chr3:130913024 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG00639.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.7-17392A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913024 | |||||||
| chr3:130913058 | C | T | 371 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(368): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.7-17358C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913058 | |||||||
| chr3:130913260 | AT | A | 3 | a0001c0001t0001g0154 a0001c0001t0001g0160 a0001c0001t0001g0166 |
3 | NA19011.hp1 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.7-17153delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130913260 | ||||||
| chr3:130913263 | T | A | 47 | a0001c0001t0001g0004 a0001c0001t0001g0065 a0001c0001t0001g0092 others(44): Show |
48 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.7-17153T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913263 | |||||||
| chr3:130913264 | A | T | 1 | a0001c0002t0001g0360 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.7-17152A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913264 | |||||||
| chr3:130913314 | C | T | 1 | a0001c0001t0001g0300 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.7-17102C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913314 | |||||||
| chr3:130913417 | G | T | 1 | a0001c0001t0001g0138 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.7-16999G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913417 | |||||||
| chr3:130913536 | C | A | 23 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(20): Show |
24 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.7-16880C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913536 | |||||||
| chr3:130913546 | G | T | 1 | a0001c0001t0001g0138 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.7-16870G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913546 | |||||||
| chr3:130913549 | A | G | 15 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(12): Show |
16 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.7-16867A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913549 | |||||||
| chr3:130913568 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.7-16848G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913568 | |||||||
| chr3:130913647 | T | A | 33 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(30): Show |
33 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.7-16769T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913647 | |||||||
| chr3:130913665 | C | T | 2 | a0001c0001t0004g0316 a0001c0001t0004g0317 |
2 | HG00544.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.7-16751C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913665 | |||||||
| chr3:130913846 | G | C | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.7-16570G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913846 | |||||||
| chr3:130913873 | T | C | 1 | a0001c0001t0001g0279 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.7-16543T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913873 | |||||||
| chr3:130914159 | CT | C | 51 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(48): Show |
52 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.7-16248delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130914159 | ||||||
| chr3:130914209 | A | G | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0174 |
3 | HG02055.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.7-16207A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130914209 | |||||||
| chr3:130914211 | C | T | 23 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(20): Show |
24 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.7-16205C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130914211 | |||||||
| chr3:130914224 | A | AT | 31 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(28): Show |
31 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.7-16191dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130914224 | ||||||
| chr3:130914319 | G | A | 4 | a0001c0001t0001g0361 a0001c0001t0001g0362 a0001c0001t0001g0363 others(1): Show |
4 | HG00735.hp2 HG02280.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-16097G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130914319 | |||||||
| chr3:130914323 | G | GT | 7 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(4): Show |
8 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-16083dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130914323 | ||||||
| chr3:130914457 | C | T | 8 | a0001c0001t0010g0122 a0001c0003t0001g0083 a0001c0003t0001g0098 others(5): Show |
8 | HG00733.hp1 HG01346.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-15959C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130914457 | |||||||
| chr3:130914458 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.7-15958C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130914458 | |||||||
| chr3:130914470 | A | G | 1 | a0001c0001t0001g0307 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.7-15946A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130914470 | |||||||
| chr3:130914598 | T | C | 266 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(263): Show |
272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.7-15818T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130914598 | |||||||
| chr3:130914952 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-15464C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130914952 | |||||||
| chr3:130914962 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.7-15454G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130914962 | |||||||
| chr3:130915086 | C | T | 3 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 |
3 | NA18978.hp2 NA18988.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.7-15330C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130915086 | |||||||
| chr3:130915090 | G | GT | 11 | a0001c0001t0001g0009 a0001c0001t0001g0075 a0001c0001t0001g0124 others(8): Show |
11 | HG01175.hp2 HG01358.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.7-15314dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130915090 | ||||||
| chr3:130915090 | GT | G | 11 | a0001c0001t0001g0079 a0001c0001t0001g0149 a0001c0001t0001g0229 others(8): Show |
11 | HG00741.hp2 HG01123.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.7-15314delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130915090 | ||||||
| chr3:130915102 | T | C | 1 | a0001c0001t0001g0283 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.7-15314T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130915102 | |||||||
| chr3:130915135 | C | G | 4 | a0001c0001t0001g0004 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
5 | HG01255.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-15281C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130915135 | |||||||
| chr3:130915197 | G | A | 45 | a0001c0001t0001g0007 a0001c0001t0001g0328 a0001c0001t0001g0344 others(42): Show |
46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.7-15219G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130915197 | |||||||
| chr3:130915348 | A | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-15068A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130915348 | |||||||
| chr3:130915427 | T | C | 3 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 |
3 | HG01243.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.7-14989T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130915427 | |||||||
| chr3:130915454 | A | G | 1 | a0001c0001t0001g0320 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.7-14962A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130915454 | |||||||
| chr3:130915461 | G | A | 4 | a0001c0001t0001g0361 a0001c0001t0001g0362 a0001c0001t0001g0363 others(1): Show |
4 | HG00735.hp2 HG02280.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-14955G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130915461 | |||||||
| chr3:130915528 | T | C | 8 | a0001c0001t0010g0122 a0001c0003t0001g0083 a0001c0003t0001g0098 others(5): Show |
8 | HG00733.hp1 HG01346.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-14888T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130915528 | |||||||
| chr3:130915563 | C | T | 6 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(3): Show |
6 | HG00438.hp2 HG02015.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-14853C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130915563 | |||||||
| chr3:130915900 | A | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0320 |
2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.7-14516A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130915900 | |||||||
| chr3:130916005 | C | T | 23 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(20): Show |
24 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.7-14411C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916005 | |||||||
| chr3:130916075 | A | G | 49 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(46): Show |
50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.7-14341A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916075 | |||||||
| chr3:130916170 | C | T | 1 | a0001c0002t0001g0327 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.7-14246C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916170 | |||||||
| chr3:130916244 | C | CA | 34 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(31): Show |
34 | HG00609.hp2 HG01069.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.7-14157dupA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130916244 | ||||||
| chr3:130916370 | C | T | 2 | a0003c0005t0003g0109 a0003c0005t0003g0110 |
2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.7-14046C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916370 | |||||||
| chr3:130916439 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.7-13977A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916439 | |||||||
| chr3:130916539 | A | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(1): Show |
4 | HG02615.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-13877A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916539 | |||||||
| chr3:130916670 | G | T | 7 | a0001c0001t0001g0350 a0001c0002t0001g0219 a0001c0002t0001g0351 others(4): Show |
7 | HG03710.hp1 NA18946.hp2 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.7-13746G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916670 | |||||||
| chr3:130916763 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.7-13653T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916763 | |||||||
| chr3:130916801 | A | T | 1 | a0001c0001t0001g0138 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.7-13615A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916801 | |||||||
| chr3:130916802 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.7-13614T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916802 | |||||||
| chr3:130916803 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.7-13613C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916803 | |||||||
| chr3:130916820 | A | C | 1 | a0001c0001t0001g0115 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.7-13596A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916820 | |||||||
| chr3:130916932 | A | G | 49 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(46): Show |
50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.7-13484A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916932 | |||||||
| chr3:130916934 | A | G | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.7-13482A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916934 | |||||||
| chr3:130917046 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.7-13370G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130917046 | |||||||
| chr3:130917052 | C | G | 1 | a0001c0001t0001g0154 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7-13364C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130917052 | |||||||
| chr3:130917333 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.7-13083A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130917333 | |||||||
| chr3:130917503 | A | C | 2 | a0001c0001t0002g0140 a0001c0001t0012g0139 |
2 | NA18973.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.7-12913A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130917503 | |||||||
| chr3:130917803 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.7-12613C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130917803 | |||||||
| chr3:130917822 | C | G | 3 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0218 |
3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.7-12594C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130917822 | |||||||
| chr3:130917910 | C | T | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.7-12506C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130917910 | |||||||
| chr3:130917975 | C | CT | 32 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(29): Show |
32 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.7-12431dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130917975 | ||||||
| chr3:130918000 | A | T | 1 | a0001c0001t0001g0138 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.7-12416A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918000 | |||||||
| chr3:130918001 | T | A | 1 | a0001c0001t0001g0138 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.7-12415T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918001 | |||||||
| chr3:130918099 | A | C | 1 | a0001c0001t0001g0306 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.7-12317A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918099 | |||||||
| chr3:130918275 | A | G | 2 | a0001c0001t0001g0079 a0001c0001t0009g0078 |
2 | HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.7-12141A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918275 | |||||||
| chr3:130918318 | T | C | 1 | a0001c0002t0008g0334 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.7-12098T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918318 | |||||||
| chr3:130918548 | C | T | 1 | a0001c0001t0005g0179 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.7-11868C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918548 | |||||||
| chr3:130918664 | T | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(1): Show |
4 | HG02615.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-11752T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918664 | |||||||
| chr3:130918691 | A | C | 3 | a0001c0002t0001g0324 a0001c0002t0001g0325 a0001c0002t0001g0326 |
3 | HG02027.hp1 NA18945.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.7-11725A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918691 | |||||||
| chr3:130918713 | C | A | 3 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0218 |
3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.7-11703C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918713 | |||||||
| chr3:130918720 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.7-11696G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918720 | |||||||
| chr3:130918724 | G | C | 1 | a0001c0001t0001g0367 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.7-11692G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918724 | |||||||
| chr3:130918822 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.7-11594T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918822 | |||||||
| chr3:130918875 | C | G | 1 | a0001c0001t0001g0158 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.7-11541C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918875 | |||||||
| chr3:130918921 | G | A | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.7-11495G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918921 | |||||||
| chr3:130918980 | A | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.7-11436A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918980 | |||||||
| chr3:130918986 | C | T | 4 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(1): Show |
4 | HG00639.hp1 HG01258.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-11430C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918986 | |||||||
| chr3:130919062 | G | A | 23 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(20): Show |
24 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.7-11354G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130919062 | |||||||
| chr3:130919230 | C | T | 300 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(297): Show |
306 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.7-11186C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130919230 | |||||||
| chr3:130919242 | T | C | 49 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(46): Show |
50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.7-11174T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130919242 | |||||||
| chr3:130919410 | G | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02723.hp1 HG03579.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-11006G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130919410 | |||||||
| chr3:130919547 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.7-10869A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130919547 | |||||||
| chr3:130919601 | A | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
6 | HG01255.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-10815A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130919601 | |||||||
| chr3:130919655 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.7-10761C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130919655 | |||||||
| chr3:130919706 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0145 |
2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.7-10710C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130919706 | |||||||
| chr3:130919792 | C | A | 1 | a0001c0001t0001g0082 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.7-10624C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130919792 | |||||||
| chr3:130919798 | G | T | 1 | a0001c0001t0001g0196 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.7-10618G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130919798 | |||||||
| chr3:130919804 | C | T | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(110): Show |
115 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.7-10612C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130919804 | |||||||
| chr3:130920125 | A | T | 1 | a0001c0001t0005g0179 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.7-10291A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130920125 | |||||||
| chr3:130920353 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.7-10063G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130920353 | |||||||
| chr3:130920527 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.7-9889C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130920527 | |||||||
| chr3:130920551 | A | G | 2 | a0001c0001t0001g0285 a0001c0001t0001g0299 |
2 | NA19058.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.7-9865A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130920551 | |||||||
| chr3:130920645 | G | GAT | 3 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0218 |
3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.7-9770_7-9769dupAT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130920645 | ||||||
| chr3:130920742 | G | A | 45 | a0001c0001t0001g0007 a0001c0001t0001g0328 a0001c0001t0001g0344 others(42): Show |
46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.7-9674G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130920742 | |||||||
| chr3:130920814 | G | T | 1 | a0001c0001t0001g0148 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.7-9602G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130920814 | |||||||
| chr3:130920969 | A | G | 3 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0218 |
3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.7-9447A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130920969 | |||||||
| chr3:130921024 | C | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0174 |
3 | HG02055.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.7-9392C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130921024 | |||||||
| chr3:130921079 | C | CT | 57 | a0001c0001t0001g0002 a0001c0001t0001g0058 a0001c0001t0001g0059 others(54): Show |
58 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.7-9317dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130921079 | ||||||
| chr3:130921079 | C | CTT | 13 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0091 others(10): Show |
14 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.7-9318_7-9317dupTT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130921079 | ||||||
| chr3:130921079 | CT | C | 6 | a0001c0001t0001g0082 a0001c0001t0001g0180 a0001c0001t0001g0264 others(3): Show |
6 | HG01884.hp2 HG02647.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-9317delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130921079 | ||||||
| chr3:130921084 | T | C | 48 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(45): Show |
49 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.7-9332T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130921084 | |||||||
| chr3:130921104 | C | T | 4 | a0001c0001t0001g0173 a0001c0001t0001g0303 a0001c0001t0001g0304 others(1): Show |
4 | HG00140.hp1 HG02273.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-9312C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130921104 | |||||||
| chr3:130921168 | G | A | 110 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(107): Show |
112 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.7-9248G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130921168 | |||||||
| chr3:130921195 | C | T | 102 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(99): Show |
104 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.7-9221C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130921195 | |||||||
| chr3:130921227 | GCC | G | 49 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(46): Show |
50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.7-9188_7-9187delCC | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130921227 | |||||||
| chr3:130921231 | GCCACCAC others(3): Show |
G | 49 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(46): Show |
50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.7-9184_7-9175delCC others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130921231 | |||||||
| chr3:130921864 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0072 |
3 | NA18967.hp1 NA19057.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.7-8552C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130921864 | |||||||
| chr3:130921893 | A | G | 2 | a0001c0001t0001g0255 a0004c0008t0001g0215 |
2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.7-8523A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130921893 | |||||||
| chr3:130922153 | T | C | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(110): Show |
115 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.7-8263T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130922153 | |||||||
| chr3:130922361 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.7-8055C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130922361 | |||||||
| chr3:130922594 | C | G | 1 | a0001c0001t0001g0177 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.7-7822C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130922594 | |||||||
| chr3:130922867 | A | G | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.7-7549A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130922867 | |||||||
| chr3:130922871 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.7-7545C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130922871 | |||||||
| chr3:130922872 | G | A | 1 | a0001c0002t0001g0339 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.7-7544G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130922872 | |||||||
| chr3:130923001 | A | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-7415A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130923001 | |||||||
| chr3:130923088 | G | A | 311 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(308): Show |
317 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.7-7328G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130923088 | |||||||
| chr3:130923143 | A | G | 6 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(3): Show |
6 | HG00639.hp1 HG01258.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.7-7273A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130923143 | |||||||
| chr3:130923232 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.7-7184T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130923232 | |||||||
| chr3:130923332 | T | G | 2 | a0001c0003t0001g0083 a0001c0003t0001g0099 |
2 | HG00733.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.7-7084T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130923332 | |||||||
| chr3:130923385 | C | G | 1 | a0001c0001t0001g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.7-7031C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130923385 | |||||||
| chr3:130923431 | C | G | 23 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(20): Show |
24 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.7-6985C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130923431 | |||||||
| chr3:130923479 | A | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(1): Show |
4 | HG02615.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-6937A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130923479 | |||||||
| chr3:130923555 | A | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-6861A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130923555 | |||||||
| chr3:130923587 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.7-6829G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130923587 | |||||||
| chr3:130923686 | G | A | 3 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0218 |
3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.7-6730G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130923686 | |||||||
| chr3:130923833 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.7-6583C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130923833 | |||||||
| chr3:130923864 | C | CA | 33 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(30): Show |
34 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.7-6533dupA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130923864 | ||||||
| chr3:130923864 | CA | C | 66 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(63): Show |
69 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.7-6533delA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130923864 | ||||||
| chr3:130924032 | G | A | 24 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(21): Show |
24 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.7-6384G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130924032 | |||||||
| chr3:130924147 | GT | G | 107 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(104): Show |
109 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.7-6258delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130924147 | ||||||
| chr3:130924193 | T | C | 3 | a0001c0001t0001g0121 a0001c0001t0001g0145 a0001c0006t0001g0120 |
3 | HG02055.hp2 HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.7-6223T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130924193 | |||||||
| chr3:130924235 | G | C | 1 | a0001c0001t0001g0307 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.7-6181G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130924235 | |||||||
| chr3:130924287 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.7-6129G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130924287 | |||||||
| chr3:130924394 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.7-6022A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130924394 | |||||||
| chr3:130924604 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.7-5812G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130924604 | |||||||
| chr3:130924674 | T | C | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.7-5742T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130924674 | |||||||
| chr3:130924702 | G | C | 321 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(318): Show |
327 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.7-5714G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130924702 | |||||||
| chr3:130924768 | T | A | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(20): Show |
23 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.7-5648T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130924768 | |||||||
| chr3:130924769 | A | T | 102 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(99): Show |
104 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.7-5647A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130924769 | |||||||
| chr3:130924852 | C | T | 105 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
107 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.7-5564C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130924852 | |||||||
| chr3:130925059 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.7-5357A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925059 | |||||||
| chr3:130925097 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.7-5319C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925097 | |||||||
| chr3:130925111 | A | G | 273 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(270): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.7-5305A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925111 | |||||||
| chr3:130925215 | A | G | 45 | a0001c0001t0001g0007 a0001c0001t0001g0328 a0001c0001t0001g0344 others(42): Show |
46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.7-5201A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925215 | |||||||
| chr3:130925225 | A | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-5191A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925225 | |||||||
| chr3:130925428 | G | A | 15 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(12): Show |
16 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.7-4988G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925428 | |||||||
| chr3:130925576 | T | C | 33 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(30): Show |
33 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.7-4840T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925576 | |||||||
| chr3:130925658 | G | A | 3 | a0001c0001t0001g0350 a0001c0002t0001g0219 a0001c0002t0001g0351 |
3 | NA18946.hp2 NA19055.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.7-4758G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925658 | |||||||
| chr3:130925735 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0156 |
2 | HG01109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.7-4681C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925735 | |||||||
| chr3:130925831 | T | G | 1 | a0001c0001t0001g0229 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.7-4585T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925831 | |||||||
| chr3:130925938 | A | G | 1 | a0001c0001t0009g0078 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.7-4478A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925938 | |||||||
| chr3:130925960 | C | T | 2 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | NA18948.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.7-4456C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925960 | |||||||
| chr3:130925965 | C | T | 1 | a0001c0001t0001g0373 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.7-4451C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925965 | |||||||
| chr3:130926001 | T | A | 1 | a0001c0002t0001g0322 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.7-4415T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926001 | |||||||
| chr3:130926085 | T | G | 5 | a0001c0001t0001g0221 a0001c0001t0001g0230 a0001c0001t0001g0231 others(2): Show |
5 | HG01081.hp1 HG01255.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-4331T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926085 | |||||||
| chr3:130926225 | C | G | 1 | a0001c0001t0001g0088 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.7-4191C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926225 | |||||||
| chr3:130926227 | G | C | 4 | a0001c0001t0001g0350 a0001c0002t0001g0219 a0001c0002t0001g0351 others(1): Show |
4 | NA18946.hp2 NA19055.hp2 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-4189G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926227 | |||||||
| chr3:130926323 | C | G | 1 | a0001c0001t0001g0134 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.7-4093C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926323 | |||||||
| chr3:130926574 | A | G | 33 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(30): Show |
33 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.7-3842A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926574 | |||||||
| chr3:130926618 | A | G | 1 | a0001c0001t0001g0298 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.7-3798A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926618 | |||||||
| chr3:130926698 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.7-3718A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926698 | |||||||
| chr3:130926709 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-3707C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926709 | |||||||
| chr3:130926744 | G | A | 300 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(297): Show |
306 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.7-3672G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926744 | |||||||
| chr3:130926796 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.7-3620C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926796 | |||||||
| chr3:130926798 | C | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0145 a0001c0006t0001g0120 |
3 | HG02055.hp2 HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.7-3618C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926798 | |||||||
| chr3:130926844 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.7-3572C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926844 | |||||||
| chr3:130926882 | A | G | 24 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(21): Show |
24 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.7-3534A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926882 | |||||||
| chr3:130926911 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.7-3505G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926911 | |||||||
| chr3:130926951 | G | A | 33 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(30): Show |
33 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.7-3465G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926951 | |||||||
| chr3:130926984 | C | T | 45 | a0001c0001t0001g0007 a0001c0001t0001g0328 a0001c0001t0001g0344 others(42): Show |
46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.7-3432C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926984 | |||||||
| chr3:130926988 | C | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG00099.hp1 HG00140.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.7-3428C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926988 | |||||||
| chr3:130927055 | A | T | 1 | a0001c0001t0001g0305 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.7-3361A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130927055 | |||||||
| chr3:130927320 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0133 |
2 | HG00609.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.7-3096A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130927320 | |||||||
| chr3:130927383 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.7-3033G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130927383 | |||||||
| chr3:130927423 | A | G | 2 | a0001c0001t0001g0255 a0004c0008t0001g0215 |
2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.7-2993A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130927423 | |||||||
| chr3:130927465 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG01358.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.7-2951T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130927465 | |||||||
| chr3:130927467 | T | G | 6 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(3): Show |
6 | HG02109.hp1 HG02723.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.7-2949T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130927467 | |||||||
| chr3:130927479 | G | A | 1 | a0002c0004t0001g0106 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.7-2937G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130927479 | |||||||
| chr3:130927483 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.7-2933C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130927483 | |||||||
| chr3:130927536 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.7-2880C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130927536 | |||||||
| chr3:130927636 | C | T | 102 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(99): Show |
104 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.7-2780C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130927636 | |||||||
| chr3:130927759 | A | G | 49 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(46): Show |
50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.7-2657A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130927759 | |||||||
| chr3:130927920 | C | G | 2 | a0001c0001t0001g0255 a0004c0008t0001g0215 |
2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.7-2496C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130927920 | |||||||
| chr3:130928086 | C | T | 5 | a0001c0003t0001g0098 a0001c0003t0001g0100 a0001c0003t0001g0101 others(2): Show |
5 | HG02258.hp2 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-2330C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130928086 | |||||||
| chr3:130928139 | C | T | 2 | a0001c0001t0001g0255 a0004c0008t0001g0215 |
2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.7-2277C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130928139 | |||||||
| chr3:130928467 | G | C | 1 | a0001c0001t0001g0091 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.7-1949G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130928467 | |||||||
| chr3:130928509 | A | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0075 |
3 | NA18955.hp1 NA18961.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.7-1907A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130928509 | |||||||
| chr3:130928721 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.7-1695A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130928721 | |||||||
| chr3:130928752 | A | G | 9 | a0001c0001t0001g0007 a0001c0001t0001g0328 a0001c0002t0001g0010 others(6): Show |
10 | HG02027.hp1 HG02735.hp2 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.7-1664A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130928752 | |||||||
| chr3:130929013 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.7-1403T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130929013 | |||||||
| chr3:130929076 | A | G | 110 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(107): Show |
112 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.7-1340A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130929076 | |||||||
| chr3:130929383 | A | G | 3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0176 |
3 | NA18954.hp2 NA18970.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.7-1033A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130929383 | |||||||
| chr3:130929386 | C | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.7-1030C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130929386 | |||||||
| chr3:130929428 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.7-988A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130929428 | |||||||
| chr3:130929737 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.7-679T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130929737 | |||||||
| chr3:130929758 | A | T | 3 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG00597.hp1 NA19000.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.7-658A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130929758 | |||||||
| chr3:130929954 | A | G | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(110): Show |
115 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.7-462A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130929954 | |||||||
| chr3:130930010 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.7-406G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130930010 | |||||||
| chr3:130930020 | A | C | 2 | a0001c0001t0002g0140 a0001c0001t0012g0139 |
2 | NA18973.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.7-396A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130930020 | |||||||
| chr3:130930051 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.7-365G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130930051 | |||||||
| chr3:130930062 | G | A | 299 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
305 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.7-354G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130930062 | |||||||
| chr3:130930533 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG01358.hp1 | splice_region_variant&intron_variant | LOW | c.117+7G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130930533 | |||||||
| chr3:130930702 | T | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.117+176T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130930702 | |||||||
| chr3:130930795 | A | G | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0174 |
3 | HG02055.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.117+269A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130930795 | |||||||
| chr3:130930840 | T | G | 1 | a0001c0001t0001g0274 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.117+314T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130930840 | |||||||
| chr3:130930853 | A | G | 6 | a0001c0001t0001g0228 a0001c0001t0001g0308 a0001c0001t0001g0309 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.117+327A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130930853 | |||||||
| chr3:130930962 | A | G | 45 | a0001c0001t0001g0007 a0001c0001t0001g0328 a0001c0001t0001g0344 others(42): Show |
46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.117+436A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130930962 | |||||||
| chr3:130931036 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.117+510G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931036 | |||||||
| chr3:130931044 | C | A | 1 | a0001c0002t0001g0352 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.117+518C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931044 | |||||||
| chr3:130931103 | T | C | 23 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(20): Show |
24 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.117+577T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931103 | |||||||
| chr3:130931144 | T | C | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG03579.hp2 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.117+618T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931144 | |||||||
| chr3:130931193 | T | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.117+667T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931193 | |||||||
| chr3:130931529 | A | G | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02723.hp1 HG03579.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-493A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931529 | |||||||
| chr3:130931550 | G | A | 1 | a0001c0001t0010g0122 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.118-472G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931550 | |||||||
| chr3:130931557 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.118-465C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931557 | |||||||
| chr3:130931588 | C | T | 45 | a0001c0001t0001g0007 a0001c0001t0001g0328 a0001c0001t0001g0344 others(42): Show |
46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.118-434C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931588 | |||||||
| chr3:130931685 | T | A | 2 | a0001c0001t0001g0234 a0001c0001t0001g0266 |
2 | HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.118-337T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931685 | |||||||
| chr3:130931702 | T | G | 1 | a0001c0001t0001g0201 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.118-320T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931702 | |||||||
| chr3:130931782 | A | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.118-240A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931782 | |||||||
| chr3:130931899 | A | G | 3 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0218 |
3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.118-123A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931899 | |||||||
| chr3:130932156 | C | T | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.234+18C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130932156 | |||||||
| chr3:130932216 | T | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.234+78T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130932216 | |||||||
| chr3:130932252 | T | C | 49 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(46): Show |
50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.234+114T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130932252 | |||||||
| chr3:130932396 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.234+258T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130932396 | |||||||
| chr3:130932404 | A | G | 9 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(6): Show |
9 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.234+266A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130932404 | |||||||
| chr3:130932453 | A | T | 49 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(46): Show |
50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.234+315A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130932453 | |||||||
| chr3:130932731 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.234+593A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130932731 | |||||||
| chr3:130932929 | A | G | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.234+791A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130932929 | |||||||
| chr3:130933052 | G | A | 1 | a0001c0001t0001g0034 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.234+914G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933052 | |||||||
| chr3:130933063 | G | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
5 | HG01255.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.234+925G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933063 | |||||||
| chr3:130933080 | A | G | 1 | a0001c0001t0001g0031 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.234+942A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933080 | |||||||
| chr3:130933088 | A | C | 1 | a0001c0001t0001g0242 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.234+950A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933088 | |||||||
| chr3:130933244 | C | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0145 a0001c0006t0001g0120 |
3 | HG02055.hp2 HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.234+1106C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933244 | |||||||
| chr3:130933245 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.234+1107G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933245 | |||||||
| chr3:130933266 | ATTCT | A | 136 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
139 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.234+1131_234+1134d others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr3 | 130933266 | ||||||
| chr3:130933303 | G | T | 2 | a0001c0001t0001g0255 a0004c0008t0001g0215 |
2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.234+1165G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933303 | |||||||
| chr3:130933491 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.235-1131A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933491 | |||||||
| chr3:130933549 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.235-1073C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933549 | |||||||
| chr3:130933627 | G | T | 1 | a0001c0001t0001g0006 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.235-995G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933627 | |||||||
| chr3:130933679 | G | A | 45 | a0001c0001t0001g0007 a0001c0001t0001g0328 a0001c0001t0001g0344 others(42): Show |
46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.235-943G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933679 | |||||||
| chr3:130933775 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.235-847T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933775 | |||||||
| chr3:130933920 | A | G | 4 | a0001c0001t0001g0004 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
5 | HG01255.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.235-702A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933920 | |||||||
| chr3:130934016 | G | A | 1 | a0001c0006t0001g0120 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.235-606G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130934016 | |||||||
| chr3:130934111 | C | G | 2 | a0003c0005t0003g0109 a0003c0005t0003g0110 |
2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.235-511C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130934111 | |||||||
| chr3:130934245 | A | G | 4 | a0002c0004t0001g0105 a0002c0004t0001g0106 a0002c0004t0001g0107 others(1): Show |
4 | HG02630.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-377A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130934245 | |||||||
| chr3:130934407 | A | AT | 45 | a0001c0001t0001g0007 a0001c0001t0001g0328 a0001c0001t0001g0344 others(42): Show |
46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.235-205dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr3 | 130934407 | ||||||
| chr3:130934411 | T | C | 3 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0218 |
3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.235-211T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130934411 | |||||||
| chr3:130934457 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.235-165G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130934457 | |||||||
| chr3:130934534 | C | T | 1 | a0001c0001t0011g0290 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.235-88C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130934534 | |||||||
| chr3:130934728 | A | G | 1 | a0001c0002t0001g0245 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.324+17A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130934728 | |||||||
| chr3:130934918 | C | T | 23 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(20): Show |
24 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.324+207C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130934918 | |||||||
| chr3:130935183 | G | A | 8 | a0001c0001t0010g0122 a0001c0003t0001g0083 a0001c0003t0001g0098 others(5): Show |
8 | HG00733.hp1 HG01346.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.324+472G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130935183 | |||||||
| chr3:130935343 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG03654.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.324+632C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130935343 | |||||||
| chr3:130935349 | A | G | 4 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+638A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130935349 | |||||||
| chr3:130935474 | A | T | 1 | a0001c0001t0001g0250 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.324+763A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130935474 | |||||||
| chr3:130935479 | A | C | 45 | a0001c0001t0001g0007 a0001c0001t0001g0328 a0001c0001t0001g0344 others(42): Show |
46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.324+768A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130935479 | |||||||
| chr3:130935711 | A | G | 2 | a0003c0005t0003g0109 a0003c0005t0003g0110 |
2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.324+1000A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130935711 | |||||||
| chr3:130935739 | T | G | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.324+1028T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130935739 | |||||||
| chr3:130935960 | T | G | 1 | a0001c0002t0001g0349 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.324+1249T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130935960 | |||||||
| chr3:130936119 | T | C | 4 | a0001c0002t0001g0335 a0001c0002t0001g0340 a0001c0002t0001g0341 others(1): Show |
4 | HG02129.hp1 NA18997.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-1309T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936119 | |||||||
| chr3:130936139 | C | T | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(110): Show |
115 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.325-1289C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936139 | |||||||
| chr3:130936160 | A | C | 33 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(30): Show |
33 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.325-1268A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936160 | |||||||
| chr3:130936213 | T | A | 3 | a0001c0001t0001g0020 a0001c0002t0001g0322 a0001c0002t0001g0323 |
3 | NA18948.hp1 NA19001.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.325-1215T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936213 | |||||||
| chr3:130936213 | T | TA | 12 | a0001c0001t0001g0128 a0001c0001t0001g0150 a0001c0001t0001g0151 others(9): Show |
12 | HG01943.hp1 HG02109.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.325-1205dupA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr3 | 130936213 | ||||||
| chr3:130936214 | A | T | 3 | a0001c0001t0001g0111 a0001c0001t0001g0117 a0001c0001t0001g0118 |
3 | HG02451.hp2 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.325-1214A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936214 | |||||||
| chr3:130936215 | A | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.325-1213A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936215 | |||||||
| chr3:130936231 | G | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(6): Show |
9 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.325-1197G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936231 | |||||||
| chr3:130936243 | CCTTGGGG others(14): Show |
C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | NA19066.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.325-1169_325-1149d others(23): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr3 | 130936243 | ||||||
| chr3:130936260 | G | T | 1 | a0001c0001t0001g0319 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.325-1168G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936260 | |||||||
| chr3:130936382 | C | T | 4 | a0001c0001t0001g0173 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
4 | HG00140.hp1 HG01243.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.325-1046C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936382 | |||||||
| chr3:130936383 | G | A | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.325-1045G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936383 | |||||||
| chr3:130936628 | T | C | 255 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(252): Show |
260 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.325-800T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936628 | |||||||
| chr3:130936644 | C | G | 1 | a0001c0001t0001g0201 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.325-784C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936644 | |||||||
| chr3:130936773 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0112 a0001c0001t0001g0113 others(3): Show |
7 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.325-655C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936773 | |||||||
| chr3:130936816 | C | CA | 191 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(188): Show |
194 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.325-592dupA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr3 | 130936816 | ||||||
| chr3:130936816 | C | CAA | 16 | a0001c0001t0001g0198 a0001c0001t0001g0209 a0001c0001t0001g0211 others(13): Show |
16 | HG00621.hp2 HG01175.hp2 HG03710.hp1 others(13): Show |
intron_variant | MODIFIER | c.325-593_325-592dup others(2): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr3 | 130936816 | ||||||
| chr3:130937018 | AT | A | 102 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(99): Show |
104 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.325-403delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr3 | 130937018 | ||||||
| chr3:130937135 | A | G | 1 | a0001c0002t0001g0355 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.325-293A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130937135 | |||||||
| chr3:130937144 | A | G | 4 | a0002c0004t0001g0105 a0002c0004t0001g0106 a0002c0004t0001g0107 others(1): Show |
4 | HG02630.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-284A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130937144 | |||||||
| chr3:130937485 | C | A | 1 | a0001c0001t0001g0312 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.360+22C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130937485 | |||||||
| chr3:130937682 | C | T | 49 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(46): Show |
50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.360+219C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130937682 | |||||||
| chr3:130937868 | A | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.360+405A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130937868 | |||||||
| chr3:130937873 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.360+410A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130937873 | |||||||
| chr3:130938101 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.360+638C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130938101 | |||||||
| chr3:130938289 | A | G | 33 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(30): Show |
33 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.360+826A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130938289 | |||||||
| chr3:130938350 | A | G | 1 | a0001c0001t0001g0289 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.360+887A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130938350 | |||||||
| chr3:130938379 | C | T | 1 | a0001c0001t0001g0318 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.360+916C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130938379 | |||||||
| chr3:130938632 | C | T | 27 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(24): Show |
27 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.360+1169C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130938632 | |||||||
| chr3:130938681 | G | T | 300 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(297): Show |
306 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.360+1218G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130938681 | |||||||
| chr3:130938687 | C | T | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG00738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.360+1224C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130938687 | |||||||
| chr3:130938808 | A | G | 24 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(21): Show |
24 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.360+1345A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130938808 | |||||||
| chr3:130939245 | C | A | 2 | a0001c0001t0001g0269 a0001c0001t0001g0272 |
2 | NA19002.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.361-1385C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130939245 | |||||||
| chr3:130939375 | T | A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0030 others(14): Show |
19 | HG00438.hp1 HG00673.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.361-1255T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130939375 | |||||||
| chr3:130939606 | A | G | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.361-1024A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130939606 | |||||||
| chr3:130939621 | C | A | 1 | a0001c0001t0001g0089 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.361-1009C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130939621 | |||||||
| chr3:130939640 | G | C | 15 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(12): Show |
16 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.361-990G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130939640 | |||||||
| chr3:130939701 | A | G | 1 | a0004c0008t0001g0215 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.361-929A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130939701 | |||||||
| chr3:130939752 | T | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0328 |
3 | NA18971.hp1 NA18977.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.361-878T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130939752 | |||||||
| chr3:130940002 | G | T | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(20): Show |
23 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.361-628G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130940002 | |||||||
| chr3:130940486 | G | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.361-144G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130940486 | |||||||
| chr3:130940773 | C | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(2): Show |
5 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.422+82C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130940773 | |||||||
| chr3:130940806 | A | T | 3 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0267 |
3 | HG00280.hp1 HG00733.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.422+115A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130940806 | |||||||
| chr3:130940866 | T | G | 1 | a0001c0002t0001g0353 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.422+175T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130940866 | |||||||
| chr3:130940873 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.422+182C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130940873 | |||||||
| chr3:130940905 | A | AT | 59 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(56): Show |
61 | HG00438.hp1 HG00738.hp2 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.422+242dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130940905 | ||||||
| chr3:130940905 | A | ATT | 58 | a0001c0001t0001g0018 a0001c0001t0001g0097 a0001c0001t0001g0115 others(55): Show |
58 | HG00544.hp2 HG00609.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.422+241_422+242dup others(2): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130940905 | ||||||
| chr3:130940905 | A | ATTT | 24 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0132 others(21): Show |
24 | HG00597.hp1 HG00597.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.422+240_422+242dup others(3): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130940905 | ||||||
| chr3:130940905 | A | ATTTT | 26 | a0001c0001t0001g0104 a0001c0001t0001g0153 a0001c0001t0001g0155 others(23): Show |
26 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.422+239_422+242dup others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130940905 | ||||||
| chr3:130940905 | A | ATTTTT | 12 | a0001c0001t0001g0004 a0001c0001t0001g0146 a0001c0001t0001g0147 others(9): Show |
13 | HG01069.hp2 HG01255.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.422+238_422+242dup others(5): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130940905 | ||||||
| chr3:130940905 | A | ATTTTTT | 7 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0095 others(4): Show |
7 | HG00639.hp1 HG01516.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.422+237_422+242dup others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130940905 | ||||||
| chr3:130940905 | AT | A | 6 | a0001c0001t0001g0073 a0001c0001t0001g0182 a0001c0001t0001g0183 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.422+242delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130940905 | ||||||
| chr3:130940905 | ATTTTTTT others(6): Show |
A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.422+230_422+242del others(13): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130940905 | ||||||
| chr3:130940933 | T | A | 24 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(21): Show |
24 | HG00408.hp2 HG00609.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.422+242T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130940933 | |||||||
| chr3:130940933 | T | TA | 4 | a0001c0001t0001g0282 a0001c0001t0001g0302 a0001c0001t0001g0306 others(1): Show |
4 | HG04115.hp2 NA18950.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.422+243dupA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130940933 | ||||||
| chr3:130940937 | T | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.422+246T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130940937 | |||||||
| chr3:130940938 | G | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
5 | HG01255.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.422+247G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130940938 | |||||||
| chr3:130940970 | A | G | 2 | a0001c0001t0001g0255 a0004c0008t0001g0215 |
2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.422+279A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130940970 | |||||||
| chr3:130941032 | A | AG | 102 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(99): Show |
104 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.422+342dupG | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941032 | ||||||
| chr3:130941147 | C | G | 136 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
139 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.423-444C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941147 | |||||||
| chr3:130941147 | C | T | 49 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(46): Show |
50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.423-444C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941147 | |||||||
| chr3:130941163 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.423-428C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941163 | |||||||
| chr3:130941222 | C | CTGTGTGT others(1): Show |
5 | a0001c0003t0001g0083 a0001c0003t0001g0098 a0001c0003t0001g0099 others(2): Show |
5 | HG00733.hp1 HG01346.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.423-369_423-368ins others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941222 | |||||||
| chr3:130941222 | C | CTGTGTGT others(3): Show |
1 | a0001c0003t0001g0103 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.423-369_423-368ins others(10): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941222 | |||||||
| chr3:130941222 | CAGTG | C | 4 | a0001c0001t0001g0111 a0001c0001t0001g0320 a0003c0005t0003g0109 others(1): Show |
4 | HG02970.hp1 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.423-368_423-365del others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941222 | |||||||
| chr3:130941223 | A | AGT | 24 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0046 others(21): Show |
24 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.423-327_423-326dup others(2): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941223 | ||||||
| chr3:130941223 | A | AGTGT | 6 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(3): Show |
6 | HG02559.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.423-329_423-326dup others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941223 | ||||||
| chr3:130941223 | A | AGTGTGTG others(3): Show |
1 | a0001c0001t0001g0121 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.423-335_423-326dup others(10): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941223 | ||||||
| chr3:130941223 | A | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0112 a0001c0001t0001g0113 others(13): Show |
17 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.423-368A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941223 | |||||||
| chr3:130941223 | AGT | A | 18 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0065 others(15): Show |
18 | HG00741.hp2 HG01884.hp2 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.423-327_423-326del others(2): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941223 | ||||||
| chr3:130941223 | AGTGT | A | 8 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0043 others(5): Show |
8 | HG00597.hp1 HG01167.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.423-329_423-326del others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941223 | ||||||
| chr3:130941223 | AGTGTGT | A | 18 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0025 others(15): Show |
19 | HG02027.hp1 HG02293.hp2 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.423-331_423-326del others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941223 | ||||||
| chr3:130941223 | AGTGTGTG others(1): Show |
A | 122 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(119): Show |
124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.423-333_423-326del others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941223 | ||||||
| chr3:130941223 | AGTGTGTG others(3): Show |
A | 47 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0096 others(44): Show |
47 | HG00544.hp1 HG00558.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.423-335_423-326del others(10): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941223 | ||||||
| chr3:130941223 | AGTGTGTG others(5): Show |
A | 2 | a0001c0001t0001g0182 a0001c0001t0001g0356 |
2 | NA18990.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.423-337_423-326del others(12): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941223 | ||||||
| chr3:130941223 | AGTGTGTG others(7): Show |
A | 10 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(7): Show |
11 | HG01243.hp2 HG02280.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.423-339_423-326del others(14): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941223 | ||||||
| chr3:130941223 | AGTGTGTG others(11): Show |
A | 1 | a0001c0001t0001g0060 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.423-343_423-326del others(18): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941223 | ||||||
| chr3:130941252 | G | C | 1 | a0001c0001t0001g0156 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.423-339G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941252 | |||||||
| chr3:130941252 | G | GTGTGTC | 4 | a0001c0001t0001g0154 a0001c0001t0001g0368 a0001c0001t0001g0369 others(1): Show |
4 | HG01099.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.423-334_423-333ins others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941252 | ||||||
| chr3:130941252 | G | GTGTGTCT others(23): Show |
3 | a0001c0001t0001g0004 a0001c0001t0001g0146 a0001c0001t0001g0147 |
4 | HG01255.hp1 HG02486.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.423-334_423-333ins others(30): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941252 | ||||||
| chr3:130941252 | G | GTGTGTGT others(1): Show |
32 | a0001c0001t0001g0092 a0001c0001t0001g0104 a0001c0001t0001g0150 others(29): Show |
32 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.423-332_423-331ins others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941252 | ||||||
| chr3:130941252 | G | GTGTGTGT others(3): Show |
5 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(2): Show |
5 | HG00639.hp1 HG01258.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.423-330_423-329ins others(10): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941252 | ||||||
| chr3:130941252 | G | GTGTGTGT others(7): Show |
1 | a0001c0001t0001g0321 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.423-328_423-315dup others(14): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941252 | ||||||
| chr3:130941252 | G | GTGTGTGT others(11): Show |
1 | a0001c0001t0001g0168 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.423-326_423-325ins others(18): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941252 | ||||||
| chr3:130941254 | G | GTGTGTGT others(1): Show |
8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(5): Show |
8 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.423-330_423-329ins others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941254 | ||||||
| chr3:130941254 | G | GTGTGTGT others(3): Show |
2 | a0001c0001t0001g0016 a0001c0001t0001g0019 |
2 | HG01884.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.423-328_423-327ins others(10): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941254 | ||||||
| chr3:130941266 | C | G | 4 | a0001c0001t0001g0136 a0001c0001t0001g0142 a0001c0001t0001g0160 others(1): Show |
4 | HG02486.hp2 NA18969.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.423-325C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941266 | |||||||
| chr3:130941268 | G | C | 1 | a0001c0001t0001g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.423-323G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941268 | |||||||
| chr3:130941275 | T | C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(6): Show |
10 | HG01243.hp2 HG02486.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.423-316T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941275 | |||||||
| chr3:130941283 | C | CA | 3 | a0001c0001t0001g0036 a0001c0001t0001g0065 a0001c0001t0001g0084 |
3 | HG02818.hp2 NA18940.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.423-308_423-307ins others(1): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941283 | |||||||
| chr3:130941283 | C | T | 1 | a0001c0001t0001g0328 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.423-308C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941283 | |||||||
| chr3:130941283 | CGCGCGCA others(1): Show |
C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(1): Show |
4 | HG02615.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.423-305_423-298del others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941283 | ||||||
| chr3:130941327 | C | A | 45 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(42): Show |
45 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.423-264C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941327 | |||||||
| chr3:130941431 | T | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.423-160T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941431 | |||||||
| chr3:130941709 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.531+10G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130941709 | |||||||
| chr3:130941777 | A | G | 2 | a0001c0001t0001g0255 a0004c0008t0001g0215 |
2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.531+78A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130941777 | |||||||
| chr3:130941964 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.531+265C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130941964 | |||||||
| chr3:130942041 | G | A | 1 | a0001c0001t0001g0373 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.531+342G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942041 | |||||||
| chr3:130942139 | A | G | 45 | a0001c0001t0001g0007 a0001c0001t0001g0328 a0001c0001t0001g0344 others(42): Show |
46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.531+440A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942139 | |||||||
| chr3:130942145 | A | C | 1 | a0001c0002t0001g0347 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.531+446A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942145 | |||||||
| chr3:130942164 | A | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0145 a0001c0006t0001g0120 |
3 | HG02055.hp2 HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.531+465A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942164 | |||||||
| chr3:130942259 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.531+560G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942259 | |||||||
| chr3:130942393 | T | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.531+694T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942393 | |||||||
| chr3:130942448 | C | T | 18 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0030 others(15): Show |
20 | HG00438.hp1 HG00673.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.531+749C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942448 | |||||||
| chr3:130942455 | G | T | 1 | a0001c0001t0001g0050 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.531+756G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942455 | |||||||
| chr3:130942456 | T | A | 1 | a0001c0001t0001g0050 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.531+757T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942456 | |||||||
| chr3:130942471 | C | T | 110 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(107): Show |
112 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.531+772C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942471 | |||||||
| chr3:130942528 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.531+829A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942528 | |||||||
| chr3:130942564 | G | A | 7 | a0001c0001t0001g0104 a0001c0001t0001g0156 a0001c0001t0001g0158 others(4): Show |
7 | HG01069.hp2 HG01109.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.531+865G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942564 | |||||||
| chr3:130942567 | G | C | 1 | a0001c0001t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.531+868G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942567 | |||||||
| chr3:130942758 | T | G | 1 | a0001c0001t0001g0314 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.531+1059T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942758 | |||||||
| chr3:130943123 | C | T | 1 | a0001c0001t0001g0306 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.531+1424C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130943123 | |||||||
| chr3:130943164 | G | T | 1 | a0001c0001t0001g0149 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.531+1465G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130943164 | |||||||
| chr3:130943307 | C | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG00099.hp1 HG00140.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.531+1608C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130943307 | |||||||
| chr3:130943506 | C | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG00099.hp1 HG00140.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.531+1807C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130943506 | |||||||
| chr3:130943658 | T | C | 5 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(2): Show |
5 | NA18946.hp1 NA18964.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.531+1959T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130943658 | |||||||
| chr3:130944104 | G | T | 1 | a0001c0001t0001g0079 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.531+2405G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130944104 | |||||||
| chr3:130944145 | C | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0145 a0001c0006t0001g0120 |
3 | HG02055.hp2 HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.531+2446C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130944145 | |||||||
| chr3:130944410 | A | G | 49 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(46): Show |
50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.531+2711A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130944410 | |||||||
| chr3:130944611 | G | T | 3 | a0002c0004t0001g0106 a0002c0004t0001g0107 a0002c0004t0001g0108 |
3 | HG02630.hp1 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.531+2912G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130944611 | |||||||
| chr3:130944784 | A | C | 3 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 |
3 | HG02273.hp1 NA19007.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.531+3085A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130944784 | |||||||
| chr3:130944938 | T | C | 1 | a0001c0002t0001g0339 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.531+3239T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130944938 | |||||||
| chr3:130945453 | G | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.531+3754G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130945453 | |||||||
| chr3:130945487 | TA | T | 308 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
314 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.531+3790delA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130945487 | ||||||
| chr3:130945524 | C | T | 49 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(46): Show |
50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.531+3825C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130945524 | |||||||
| chr3:130945757 | G | A | 3 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 |
3 | HG02273.hp1 NA19007.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.531+4058G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130945757 | |||||||
| chr3:130945901 | G | GT | 6 | a0001c0001t0001g0121 a0001c0001t0001g0132 a0001c0001t0001g0156 others(3): Show |
6 | HG01109.hp1 HG02027.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.531+4217dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130945901 | ||||||
| chr3:130945995 | T | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.531+4296T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130945995 | |||||||
| chr3:130946043 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.531+4344T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130946043 | |||||||
| chr3:130946255 | C | T | 49 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(46): Show |
50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.531+4556C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130946255 | |||||||
| chr3:130946502 | C | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.531+4803C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130946502 | |||||||
| chr3:130946560 | C | T | 4 | a0001c0002t0001g0335 a0001c0002t0001g0340 a0001c0002t0001g0341 others(1): Show |
4 | HG02129.hp1 NA18997.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.531+4861C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130946560 | |||||||
| chr3:130946564 | C | G | 1 | a0001c0001t0001g0048 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.531+4865C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130946564 | |||||||
| chr3:130946687 | A | G | 49 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(46): Show |
50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.531+4988A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130946687 | |||||||
| chr3:130946964 | A | T | 57 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0084 others(54): Show |
59 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.531+5265A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130946964 | |||||||
| chr3:130946979 | C | T | 49 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(46): Show |
50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.531+5280C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130946979 | |||||||
| chr3:130947015 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.531+5316T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130947015 | |||||||
| chr3:130947017 | A | G | 2 | a0001c0001t0001g0255 a0004c0008t0001g0215 |
2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.531+5318A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130947017 | |||||||
| chr3:130947060 | C | G | 1 | a0001c0001t0001g0306 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.531+5361C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130947060 | |||||||
| chr3:130947065 | C | G | 1 | a0001c0001t0001g0307 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.531+5366C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130947065 | |||||||
| chr3:130947251 | TA | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.531+5563delA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130947251 | ||||||
| chr3:130947263 | T | A | 4 | a0001c0001t0001g0222 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
4 | HG01891.hp2 HG01981.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.531+5564T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130947263 | |||||||
| chr3:130947329 | T | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG01358.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.531+5630T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130947329 | |||||||
| chr3:130947330 | T | A | 1 | a0001c0002t0001g0360 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.531+5631T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130947330 | |||||||
| chr3:130947527 | A | G | 2 | a0001c0001t0001g0131 a0001c0001t0001g0137 |
2 | HG04184.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.531+5828A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130947527 | |||||||
| chr3:130947893 | T | A | 1 | a0001c0001t0001g0213 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.532-5928T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130947893 | |||||||
| chr3:130948166 | T | A | 2 | a0001c0002t0001g0324 a0001c0002t0001g0325 |
2 | NA18945.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.532-5655T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130948166 | |||||||
| chr3:130948269 | TGTTTA | T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(12): Show |
16 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.532-5551_532-5547d others(7): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130948269 | |||||||
| chr3:130948328 | G | A | 1 | a0001c0001t0012g0139 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.532-5493G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130948328 | |||||||
| chr3:130948346 | G | GT | 10 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(7): Show |
10 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.532-5465dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130948346 | ||||||
| chr3:130948346 | GT | G | 8 | a0001c0001t0010g0122 a0001c0003t0001g0083 a0001c0003t0001g0098 others(5): Show |
8 | HG00733.hp1 HG01346.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.532-5465delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130948346 | ||||||
| chr3:130948436 | TG | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.532-5384delG | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130948436 | |||||||
| chr3:130948444 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.532-5377G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130948444 | |||||||
| chr3:130948583 | T | C | 1 | a0001c0003t0001g0100 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.532-5238T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130948583 | |||||||
| chr3:130948635 | C | T | 5 | a0001c0002t0001g0329 a0001c0002t0001g0339 a0001c0002t0001g0343 others(2): Show |
5 | HG00597.hp2 NA18968.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.532-5186C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130948635 | |||||||
| chr3:130948691 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.532-5130A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130948691 | |||||||
| chr3:130948964 | T | C | 33 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(30): Show |
33 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.532-4857T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130948964 | |||||||
| chr3:130949155 | T | C | 109 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(106): Show |
111 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.532-4666T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130949155 | |||||||
| chr3:130949273 | A | T | 1 | a0001c0001t0006g0119 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.532-4548A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130949273 | |||||||
| chr3:130949324 | C | T | 33 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(30): Show |
33 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.532-4497C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130949324 | |||||||
| chr3:130949403 | G | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.532-4418G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130949403 | |||||||
| chr3:130949409 | G | A | 1 | a0001c0001t0009g0078 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.532-4412G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130949409 | |||||||
| chr3:130949637 | AC | A | 15 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(12): Show |
16 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.532-4183delC | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130949637 | |||||||
| chr3:130949667 | C | T | 12 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(9): Show |
12 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.532-4154C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130949667 | |||||||
| chr3:130949763 | TAGTA | T | 101 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(98): Show |
103 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.532-4054_532-4051d others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130949763 | ||||||
| chr3:130949910 | G | A | 33 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(30): Show |
33 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.532-3911G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130949910 | |||||||
| chr3:130949986 | T | C | 5 | a0001c0001t0001g0221 a0001c0001t0001g0230 a0001c0001t0001g0231 others(2): Show |
5 | HG01081.hp1 HG01255.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.532-3835T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130949986 | |||||||
| chr3:130950036 | C | A | 2 | a0001c0001t0001g0184 a0001c0001t0007g0185 |
2 | HG00558.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.532-3785C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130950036 | |||||||
| chr3:130950247 | T | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.532-3574T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130950247 | |||||||
| chr3:130950429 | G | C | 1 | a0001c0001t0001g0232 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.532-3392G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130950429 | |||||||
| chr3:130950551 | T | A | 1 | a0001c0001t0001g0065 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.532-3270T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130950551 | |||||||
| chr3:130950876 | T | TA | 19 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(16): Show |
20 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.532-2934dupA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130950876 | ||||||
| chr3:130950876 | T | TAA | 7 | a0001c0003t0001g0083 a0001c0003t0001g0098 a0001c0003t0001g0099 others(4): Show |
7 | HG00733.hp1 HG01346.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.532-2935_532-2934d others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130950876 | ||||||
| chr3:130950876 | TA | T | 110 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(107): Show |
112 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.532-2934delA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130950876 | ||||||
| chr3:130951263 | A | G | 1 | a0001c0001t0001g0244 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.532-2558A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130951263 | |||||||
| chr3:130951327 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0112 a0001c0001t0001g0113 others(3): Show |
7 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.532-2494C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130951327 | |||||||
| chr3:130951367 | A | C | 2 | a0001c0002t0001g0354 a0001c0002t0001g0355 |
2 | NA18962.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.532-2454A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130951367 | |||||||
| chr3:130951521 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.532-2300C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130951521 | |||||||
| chr3:130951625 | T | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.532-2196T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130951625 | |||||||
| chr3:130951655 | G | C | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0075 |
3 | NA18955.hp1 NA18961.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.532-2166G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130951655 | |||||||
| chr3:130951827 | A | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0320 |
2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.532-1994A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130951827 | |||||||
| chr3:130951961 | T | TTA | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.532-1858_532-1857d others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130951961 | ||||||
| chr3:130951971 | C | T | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(20): Show |
23 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.532-1850C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130951971 | |||||||
| chr3:130952173 | T | C | 321 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(318): Show |
327 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.532-1648T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130952173 | |||||||
| chr3:130952195 | A | G | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.532-1626A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130952195 | |||||||
| chr3:130952318 | A | T | 1 | a0001c0001t0001g0247 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.532-1503A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130952318 | |||||||
| chr3:130952447 | G | T | 1 | a0001c0001t0001g0025 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.532-1374G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130952447 | |||||||
| chr3:130952468 | T | C | 23 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(20): Show |
24 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.532-1353T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130952468 | |||||||
| chr3:130952524 | T | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.532-1297T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130952524 | |||||||
| chr3:130952845 | C | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(8): Show |
12 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.532-976C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130952845 | |||||||
| chr3:130952896 | A | T | 3 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0218 |
3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.532-925A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130952896 | |||||||
| chr3:130953076 | C | CGTAT | 52 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0023 others(49): Show |
54 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.532-708_532-705dup others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130953076 | ||||||
| chr3:130953076 | C | CGTATGTA others(1): Show |
3 | a0001c0001t0001g0024 a0001c0001t0001g0150 a0001c0001t0001g0153 |
3 | HG02723.hp1 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.532-712_532-705dup others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130953076 | ||||||
| chr3:130953076 | C | CGTATGTA others(5): Show |
1 | a0001c0001t0001g0146 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.532-716_532-705dup others(12): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130953076 | ||||||
| chr3:130953076 | C | CGTATGTA others(9): Show |
1 | a0001c0001t0001g0147 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.532-720_532-705dup others(16): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130953076 | ||||||
| chr3:130953076 | CGTAT | C | 103 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(100): Show |
105 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.532-708_532-705del others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130953076 | ||||||
| chr3:130953076 | CGTATGTA others(1): Show |
C | 40 | a0001c0001t0001g0002 a0001c0001t0001g0079 a0001c0001t0001g0084 others(37): Show |
41 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.532-712_532-705del others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130953076 | ||||||
| chr3:130953436 | GT | G | 15 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(12): Show |
15 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.532-381delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130953436 | ||||||
| chr3:130953456 | A | G | 1 | a0001c0001t0001g0008 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.532-365A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130953456 | |||||||
| chr3:130953557 | T | G | 1 | a0001c0001t0001g0159 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.532-264T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130953557 | |||||||
| chr3:130953678 | T | G | 1 | a0001c0001t0001g0094 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.532-143T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130953678 | |||||||
| chr3:130954158 | G | A | 1 | a0001c0002t0001g0323 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.687+182G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 9/27 | chr3 | 130954158 | |||||||
| chr3:130954331 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0009g0078 |
2 | HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.687+355G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 9/27 | chr3 | 130954331 | |||||||
| chr3:130954414 | C | T | 2 | a0001c0002t0001g0333 a0001c0002t0001g0346 |
2 | HG01081.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.687+438C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 9/27 | chr3 | 130954414 | |||||||
| chr3:130954469 | G | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0267 |
2 | HG00280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.687+493G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 9/27 | chr3 | 130954469 | |||||||
| chr3:130954525 | G | A | 101 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(98): Show |
103 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.688-487G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 9/27 | chr3 | 130954525 | |||||||
| chr3:130954681 | T | C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0095 |
3 | HG00639.hp1 HG01516.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.688-331T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 9/27 | chr3 | 130954681 | |||||||
| chr3:130954733 | C | T | 23 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(20): Show |
24 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.688-279C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 9/27 | chr3 | 130954733 | |||||||
| chr3:130954765 | G | A | 1 | a0001c0001t0001g0373 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.688-247G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 9/27 | chr3 | 130954765 | |||||||
| chr3:130954861 | A | C | 1 | a0001c0001t0001g0214 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.688-151A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 9/27 | chr3 | 130954861 | |||||||
| chr3:130954898 | T | C | 2 | a0001c0003t0001g0101 a0001c0003t0001g0102 |
2 | HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.688-114T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 9/27 | chr3 | 130954898 | |||||||
| chr3:130955139 | G | A | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.756+59G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 10/27 | chr3 | 130955139 | |||||||
| chr3:130955178 | A | G | 320 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(317): Show |
326 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.756+98A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 10/27 | chr3 | 130955178 | |||||||
| chr3:130955221 | A | G | 2 | a0001c0001t0001g0158 a0001c0002t0001g0327 |
2 | HG02735.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.756+141A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 10/27 | chr3 | 130955221 | |||||||
| chr3:130955227 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.756+147G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 10/27 | chr3 | 130955227 | |||||||
| chr3:130955240 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.756+160T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 10/27 | chr3 | 130955240 | |||||||
| chr3:130955346 | T | C | 1 | a0001c0002t0001g0352 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.756+266T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 10/27 | chr3 | 130955346 | |||||||
| chr3:130955633 | G | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.757-471G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 10/27 | chr3 | 130955633 | |||||||
| chr3:130955634 | A | T | 2 | a0001c0001t0001g0301 a0001c0001t0001g0302 |
2 | NA19067.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.757-470A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 10/27 | chr3 | 130955634 | |||||||
| chr3:130955734 | A | T | 1 | a0001c0001t0001g0097 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.757-370A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 10/27 | chr3 | 130955734 | |||||||
| chr3:130956444 | T | C | 1 | a0001c0001t0001g0211 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.832+265T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130956444 | |||||||
| chr3:130956504 | A | G | 3 | a0001c0001t0001g0128 a0001c0001t0001g0130 a0001c0001t0001g0132 |
3 | NA18988.hp1 NA18991.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.832+325A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130956504 | |||||||
| chr3:130956532 | G | T | 1 | a0001c0002t0001g0325 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.832+353G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130956532 | |||||||
| chr3:130956610 | G | T | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
307 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.832+431G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130956610 | |||||||
| chr3:130956622 | A | C | 33 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(30): Show |
33 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.832+443A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130956622 | |||||||
| chr3:130956912 | G | T | 1 | a0001c0001t0001g0254 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.832+733G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130956912 | |||||||
| chr3:130956943 | A | G | 15 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(12): Show |
16 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.832+764A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130956943 | |||||||
| chr3:130957006 | T | C | 110 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(107): Show |
112 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.832+827T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130957006 | |||||||
| chr3:130957424 | T | C | 1 | a0001c0001t0001g0364 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.832+1245T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130957424 | |||||||
| chr3:130957460 | G | A | 48 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(45): Show |
49 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.832+1281G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130957460 | |||||||
| chr3:130957477 | G | A | 32 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(29): Show |
32 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.832+1298G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130957477 | |||||||
| chr3:130957478 | G | A | 32 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(29): Show |
32 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.832+1299G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130957478 | |||||||
| chr3:130957836 | T | C | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(20): Show |
23 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.833-1439T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130957836 | |||||||
| chr3:130957848 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.833-1427G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130957848 | |||||||
| chr3:130957868 | A | G | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(20): Show |
23 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.833-1407A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130957868 | |||||||
| chr3:130958041 | T | C | 1 | a0001c0001t0001g0269 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.833-1234T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130958041 | |||||||
| chr3:130958052 | G | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(6): Show |
9 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.833-1223G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130958052 | |||||||
| chr3:130958069 | A | G | 3 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 |
3 | HG01243.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.833-1206A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130958069 | |||||||
| chr3:130958174 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.833-1101A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130958174 | |||||||
| chr3:130958280 | G | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.833-995G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130958280 | |||||||
| chr3:130958329 | A | T | 2 | a0001c0002t0001g0322 a0001c0002t0001g0323 |
2 | NA18948.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.833-946A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130958329 | |||||||
| chr3:130958478 | C | A | 1 | a0001c0001t0001g0025 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.833-797C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130958478 | |||||||
| chr3:130958486 | G | A | 1 | a0001c0001t0001g0264 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.833-789G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130958486 | |||||||
| chr3:130958701 | T | C | 23 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(20): Show |
24 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.833-574T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130958701 | |||||||
| chr3:130958766 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.833-509C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130958766 | |||||||
| chr3:130958870 | A | G | 44 | a0001c0001t0001g0007 a0001c0001t0001g0328 a0001c0001t0001g0344 others(41): Show |
45 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.833-405A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130958870 | |||||||
| chr3:130958964 | A | T | 1 | a0001c0001t0001g0225 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.833-311A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130958964 | |||||||
| chr3:130959193 | G | A | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.833-82G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130959193 | |||||||
| chr3:130959209 | G | C | 1 | a0001c0001t0001g0118 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.833-66G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130959209 | |||||||
| chr3:130959419 | T | C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0084 others(54): Show |
59 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.899+78T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130959419 | |||||||
| chr3:130959584 | A | T | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(20): Show |
23 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.899+243A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130959584 | |||||||
| chr3:130959585 | T | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02602.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.899+244T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130959585 | |||||||
| chr3:130959626 | C | A | 6 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(3): Show |
6 | HG00738.hp1 HG02300.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.899+285C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130959626 | |||||||
| chr3:130959751 | A | G | 1 | a0001c0001t0001g0307 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.899+410A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130959751 | |||||||
| chr3:130960040 | A | T | 1 | a0001c0002t0001g0327 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.899+699A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130960040 | |||||||
| chr3:130960326 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.899+985C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130960326 | |||||||
| chr3:130960343 | A | G | 1 | a0001c0001t0001g0097 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.899+1002A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130960343 | |||||||
| chr3:130960480 | T | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.899+1139T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130960480 | |||||||
| chr3:130960634 | C | G | 1 | a0001c0001t0001g0229 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.899+1293C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130960634 | |||||||
| chr3:130960638 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.899+1297T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130960638 | |||||||
| chr3:130960641 | A | C | 1 | a0001c0002t0001g0342 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.899+1300A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130960641 | |||||||
| chr3:130960733 | A | G | 9 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(6): Show |
9 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.899+1392A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130960733 | |||||||
| chr3:130961116 | A | C | 1 | a0001c0001t0001g0252 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.899+1775A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130961116 | |||||||
| chr3:130961198 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0026 |
2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.899+1857T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130961198 | |||||||
| chr3:130961250 | GT | G | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(139): Show |
146 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.899+1922delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr3 | 130961250 | ||||||
| chr3:130961250 | GTT | G | 155 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0092 others(152): Show |
157 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.899+1921_899+1922d others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr3 | 130961250 | ||||||
| chr3:130961780 | T | C | 80 | a0001c0001t0001g0007 a0001c0001t0001g0117 a0001c0001t0001g0118 others(77): Show |
81 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.900-2191T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130961780 | |||||||
| chr3:130961785 | A | G | 57 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0084 others(54): Show |
59 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.900-2186A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130961785 | |||||||
| chr3:130961853 | A | AG | 5 | a0001c0003t0001g0098 a0001c0003t0001g0100 a0001c0003t0001g0101 others(2): Show |
5 | HG02258.hp2 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.900-2116dupG | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr3 | 130961853 | ||||||
| chr3:130961943 | C | A | 1 | a0001c0001t0001g0319 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.900-2028C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130961943 | |||||||
| chr3:130961968 | G | A | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.900-2003G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130961968 | |||||||
| chr3:130962302 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.900-1669A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130962302 | |||||||
| chr3:130962398 | T | C | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0174 |
3 | HG02055.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.900-1573T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130962398 | |||||||
| chr3:130962478 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.900-1493G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130962478 | |||||||
| chr3:130962492 | G | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.900-1479G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130962492 | |||||||
| chr3:130962551 | T | C | 30 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(27): Show |
30 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.900-1420T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130962551 | |||||||
| chr3:130962715 | TA | T | 252 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(249): Show |
258 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.900-1239delA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr3 | 130962715 | ||||||
| chr3:130962715 | TAA | T | 6 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(3): Show |
6 | HG01243.hp1 HG02258.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.900-1240_900-1239d others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr3 | 130962715 | ||||||
| chr3:130962738 | G | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0086 others(2): Show |
6 | HG02818.hp2 HG02895.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.900-1233G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130962738 | |||||||
| chr3:130962807 | A | G | 1 | a0001c0001t0001g0295 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.900-1164A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130962807 | |||||||
| chr3:130962849 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.900-1122A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130962849 | |||||||
| chr3:130963043 | T | C | 1 | a0001c0003t0001g0083 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.900-928T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130963043 | |||||||
| chr3:130963216 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.900-755G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130963216 | |||||||
| chr3:130963239 | G | A | 80 | a0001c0001t0001g0007 a0001c0001t0001g0117 a0001c0001t0001g0118 others(77): Show |
81 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.900-732G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130963239 | |||||||
| chr3:130963382 | T | G | 1 | a0001c0001t0001g0025 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.900-589T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130963382 | |||||||
| chr3:130963818 | A | G | 2 | a0001c0001t0001g0160 a0001c0001t0001g0177 |
2 | HG04204.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.900-153A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130963818 | |||||||
| chr3:130964132 | C | T | 34 | a0001c0001t0001g0079 a0001c0001t0001g0282 a0001c0001t0001g0283 others(31): Show |
34 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.1024+37C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 13/27 | chr3 | 130964132 | |||||||
| chr3:130964161 | C | CA | 45 | a0001c0001t0001g0007 a0001c0001t0001g0328 a0001c0001t0001g0344 others(42): Show |
46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.1024+67dupA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr3 | 130964161 | ||||||
| chr3:130964217 | A | G | 9 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(6): Show |
10 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1024+122A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 13/27 | chr3 | 130964217 | |||||||
| chr3:130964366 | A | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0145 a0001c0006t0001g0120 |
3 | HG02055.hp2 HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1024+271A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 13/27 | chr3 | 130964366 | |||||||
| chr3:130964373 | A | G | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1024+278A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 13/27 | chr3 | 130964373 | |||||||
| chr3:130964508 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1024+413A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 13/27 | chr3 | 130964508 | |||||||
| chr3:130964662 | G | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0112 a0001c0001t0001g0113 others(3): Show |
7 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1025-286G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 13/27 | chr3 | 130964662 | |||||||
| chr3:130964840 | A | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1025-108A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 13/27 | chr3 | 130964840 | |||||||
| chr3:130964901 | A | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1025-47A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 13/27 | chr3 | 130964901 | |||||||
| chr3:130965165 | T | G | 1 | a0001c0001t0001g0250 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1122+120T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130965165 | |||||||
| chr3:130965194 | C | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1122+149C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130965194 | |||||||
| chr3:130965225 | A | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1122+180A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130965225 | |||||||
| chr3:130965504 | G | A | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1122+459G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130965504 | |||||||
| chr3:130965574 | C | G | 23 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(20): Show |
24 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.1122+529C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130965574 | |||||||
| chr3:130965580 | C | T | 310 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(307): Show |
316 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.1122+535C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130965580 | |||||||
| chr3:130965769 | G | A | 80 | a0001c0001t0001g0007 a0001c0001t0001g0117 a0001c0001t0001g0118 others(77): Show |
81 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.1122+724G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130965769 | |||||||
| chr3:130965779 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1122+734G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130965779 | |||||||
| chr3:130966142 | CA | C | 3 | a0001c0001t0001g0121 a0001c0001t0001g0145 a0001c0006t0001g0120 |
3 | HG02055.hp2 HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1123-1002delA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130966142 | |||||||
| chr3:130966425 | T | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1123-720T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130966425 | |||||||
| chr3:130966560 | A | C | 2 | a0001c0001t0001g0308 a0001c0001t0001g0309 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1123-585A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130966560 | |||||||
| chr3:130966562 | T | A | 2 | a0001c0001t0001g0308 a0001c0001t0001g0309 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1123-583T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130966562 | |||||||
| chr3:130966803 | C | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1123-342C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130966803 | |||||||
| chr3:130966850 | A | C | 1 | a0001c0001t0001g0123 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1123-295A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130966850 | |||||||
| chr3:130966913 | T | C | 45 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(42): Show |
45 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.1123-232T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130966913 | |||||||
| chr3:130966946 | G | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1123-199G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130966946 | |||||||
| chr3:130966965 | A | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1123-180A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130966965 | |||||||
| chr3:130967002 | A | T | 109 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(106): Show |
111 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.1123-143A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130967002 | |||||||
| chr3:130967022 | CT | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1123-119delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr3 | 130967022 | ||||||
| chr3:130967571 | T | C | 4 | a0001c0001t0001g0350 a0001c0002t0001g0219 a0001c0002t0001g0351 others(1): Show |
4 | NA18946.hp2 NA19055.hp2 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.1308+152T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130967571 | |||||||
| chr3:130967571 | T | G | 7 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(4): Show |
8 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1308+152T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130967571 | |||||||
| chr3:130967821 | CTT | C | 5 | a0001c0003t0001g0098 a0001c0003t0001g0100 a0001c0003t0001g0101 others(2): Show |
5 | HG02258.hp2 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1308+404_1308+405d others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr3 | 130967821 | ||||||
| chr3:130967847 | C | G | 1 | a0001c0001t0001g0226 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1308+428C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130967847 | |||||||
| chr3:130967870 | G | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0145 a0001c0006t0001g0120 |
3 | HG02055.hp2 HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1308+451G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130967870 | |||||||
| chr3:130967933 | T | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0071 |
2 | HG02145.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1308+514T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130967933 | |||||||
| chr3:130968073 | C | T | 101 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(98): Show |
103 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1308+654C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130968073 | |||||||
| chr3:130968250 | G | A | 45 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(42): Show |
45 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.1308+831G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130968250 | |||||||
| chr3:130968338 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1308+919A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130968338 | |||||||
| chr3:130968388 | C | T | 8 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(5): Show |
8 | HG02027.hp2 NA18747.hp2 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.1309-904C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130968388 | |||||||
| chr3:130968627 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1309-665A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130968627 | |||||||
| chr3:130968718 | T | G | 1 | a0001c0001t0009g0078 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1309-574T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130968718 | |||||||
| chr3:130968860 | C | T | 310 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(307): Show |
316 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.1309-432C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130968860 | |||||||
| chr3:130969113 | T | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1309-179T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130969113 | |||||||
| chr3:130969472 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1413+76G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130969472 | |||||||
| chr3:130969585 | A | G | 1 | a0001c0001t0001g0306 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1413+189A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130969585 | |||||||
| chr3:130970036 | G | A | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1413+640G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970036 | |||||||
| chr3:130970050 | G | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1413+654G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970050 | |||||||
| chr3:130970055 | C | T | 1 | a0001c0001t0001g0205 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1413+659C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970055 | |||||||
| chr3:130970089 | G | A | 24 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(21): Show |
24 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1413+693G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970089 | |||||||
| chr3:130970183 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1413+787T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970183 | |||||||
| chr3:130970369 | T | TAC | 60 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0032 others(57): Show |
61 | HG00639.hp2 HG00741.hp1 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.1413+1010_1413+101 others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | ||||||
| chr3:130970369 | T | TACAC | 55 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0045 others(52): Show |
56 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1413+1008_1413+101 others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | ||||||
| chr3:130970369 | T | TACACAC | 88 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(85): Show |
90 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1413+1006_1413+101 others(10): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | ||||||
| chr3:130970369 | T | TACACACA others(1): Show |
39 | a0001c0001t0001g0003 a0001c0001t0001g0097 a0001c0001t0001g0114 others(36): Show |
40 | HG00544.hp1 HG00544.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1413+1004_1413+101 others(12): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | ||||||
| chr3:130970369 | T | TACACACA others(3): Show |
17 | a0001c0001t0001g0117 a0001c0001t0001g0135 a0001c0001t0001g0211 others(14): Show |
17 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.1413+1002_1413+101 others(14): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | ||||||
| chr3:130970369 | T | TACACACA others(5): Show |
8 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0210 others(5): Show |
8 | HG01123.hp2 HG02809.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1413+1000_1413+101 others(16): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | ||||||
| chr3:130970369 | T | TACACACA others(7): Show |
1 | a0001c0001t0001g0230 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1413+998_1413+1011 others(17): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | ||||||
| chr3:130970369 | T | TACACACA others(9): Show |
1 | a0001c0001t0001g0115 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1413+996_1413+1011 others(19): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | ||||||
| chr3:130970369 | T | TACACACA others(11): Show |
1 | a0001c0001t0001g0306 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1413+994_1413+1011 others(21): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | ||||||
| chr3:130970369 | TAC | T | 17 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0025 others(14): Show |
17 | HG01943.hp2 HG02040.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1413+1010_1413+101 others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | ||||||
| chr3:130970369 | TACAC | T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0070 a0001c0001t0001g0079 |
5 | NA18941.hp1 NA18944.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1413+1008_1413+101 others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | ||||||
| chr3:130970369 | TACACACA others(3): Show |
T | 1 | a0001c0002t0001g0245 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1413+1002_1413+101 others(14): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | ||||||
| chr3:130970369 | TACACACA others(9): Show |
T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1413+996_1413+1011 others(19): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | ||||||
| chr3:130970369 | TACACACA others(13): Show |
T | 1 | a0001c0002t0001g0347 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1413+992_1413+1011 others(23): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | ||||||
| chr3:130970406 | A | ACACACAC others(3): Show |
2 | a0001c0001t0001g0121 a0001c0001t0001g0145 |
2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1413+1011_1413+101 others(14): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970406 | ||||||
| chr3:130970407 | C | CACACA | 3 | a0001c0001t0001g0126 a0001c0001t0001g0250 a0001c0001t0001g0372 |
3 | HG01175.hp2 HG03927.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1413+1011_1413+101 others(9): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970407 | |||||||
| chr3:130970407 | C | CACACACA | 3 | a0001c0001t0001g0132 a0001c0001t0001g0254 a0001c0001t0001g0272 |
3 | NA18991.hp1 NA19006.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1413+1011_1413+101 others(11): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970407 | |||||||
| chr3:130970407 | C | CACACACA others(4): Show |
1 | a0001c0001t0001g0177 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1413+1011_1413+101 others(15): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970407 | |||||||
| chr3:130970479 | C | T | 7 | a0001c0001t0001g0104 a0001c0001t0001g0156 a0001c0001t0001g0158 others(4): Show |
7 | HG01069.hp2 HG01109.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1413+1083C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970479 | |||||||
| chr3:130970490 | A | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1413+1094A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970490 | |||||||
| chr3:130970632 | G | T | 1 | a0001c0001t0009g0078 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1413+1236G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970632 | |||||||
| chr3:130970812 | G | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02723.hp1 HG03579.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1413+1416G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970812 | |||||||
| chr3:130970845 | G | A | 23 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(20): Show |
24 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.1413+1449G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970845 | |||||||
| chr3:130970918 | A | G | 35 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0282 others(32): Show |
35 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.1413+1522A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970918 | |||||||
| chr3:130971147 | G | C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0095 |
3 | HG00639.hp1 HG01516.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1413+1751G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130971147 | |||||||
| chr3:130971220 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1413+1824T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130971220 | |||||||
| chr3:130971230 | C | T | 2 | a0001c0001t0001g0301 a0001c0001t0001g0302 |
2 | NA19067.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1413+1834C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130971230 | |||||||
| chr3:130971544 | T | C | 1 | a0001c0001t0001g0306 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1413+2148T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130971544 | |||||||
| chr3:130971729 | C | G | 1 | a0001c0001t0001g0048 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1413+2333C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130971729 | |||||||
| chr3:130971769 | T | G | 1 | a0001c0001t0001g0175 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1413+2373T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130971769 | |||||||
| chr3:130971890 | C | G | 1 | a0001c0002t0001g0352 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1413+2494C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130971890 | |||||||
| chr3:130971950 | A | G | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02723.hp1 HG03579.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1413+2554A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130971950 | |||||||
| chr3:130971991 | C | T | 3 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 |
3 | HG01243.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1413+2595C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130971991 | |||||||
| chr3:130972078 | C | T | 2 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | NA18948.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1413+2682C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972078 | |||||||
| chr3:130972092 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1413+2696A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972092 | |||||||
| chr3:130972098 | A | G | 9 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(6): Show |
9 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1413+2702A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972098 | |||||||
| chr3:130972142 | A | G | 1 | a0001c0001t0009g0078 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1413+2746A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972142 | |||||||
| chr3:130972204 | G | A | 45 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(42): Show |
45 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.1413+2808G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972204 | |||||||
| chr3:130972230 | C | T | 1 | a0001c0001t0001g0318 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1413+2834C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972230 | |||||||
| chr3:130972285 | TG | T | 3 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0218 |
3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1413+2890delG | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972285 | |||||||
| chr3:130972348 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1413+2952C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972348 | |||||||
| chr3:130972472 | C | CT | 11 | a0001c0001t0001g0125 a0001c0001t0001g0154 a0001c0002t0001g0333 others(8): Show |
11 | HG00597.hp1 HG00733.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.1414-2846dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130972472 | ||||||
| chr3:130972472 | C | CTT | 9 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(6): Show |
10 | HG01243.hp2 HG01346.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1414-2847_1414-284 others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130972472 | ||||||
| chr3:130972472 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1414-2860C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972472 | |||||||
| chr3:130972472 | CT | C | 45 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(42): Show |
45 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.1414-2846delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130972472 | ||||||
| chr3:130972485 | T | A | 3 | a0001c0001t0001g0079 a0001c0001t0001g0303 a0001c0001t0001g0304 |
3 | NA19007.hp2 NA19043.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1414-2847T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972485 | |||||||
| chr3:130972487 | A | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1414-2845A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972487 | |||||||
| chr3:130972525 | C | G | 33 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(30): Show |
33 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1414-2807C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972525 | |||||||
| chr3:130972589 | C | T | 1 | a0001c0001t0002g0140 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1414-2743C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972589 | |||||||
| chr3:130972617 | T | TC | 40 | a0001c0001t0001g0007 a0001c0001t0001g0268 a0001c0001t0001g0328 others(37): Show |
41 | HG00597.hp2 HG01081.hp2 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.1414-2710dupC | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130972617 | ||||||
| chr3:130972623 | T | TC | 28 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0036 others(25): Show |
28 | HG00639.hp1 HG00639.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.1414-2703dupC | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130972623 | ||||||
| chr3:130972628 | C | G | 11 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 others(8): Show |
11 | HG00099.hp1 HG00140.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.1414-2704C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972628 | |||||||
| chr3:130972659 | C | T | 1 | a0001c0001t0009g0078 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1414-2673C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972659 | |||||||
| chr3:130972710 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0167 |
2 | HG02451.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.1414-2622C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972710 | |||||||
| chr3:130972820 | T | C | 5 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(2): Show |
5 | NA18978.hp2 NA18989.hp2 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.1414-2512T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972820 | |||||||
| chr3:130973004 | T | C | 81 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(78): Show |
84 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.1414-2328T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130973004 | |||||||
| chr3:130973069 | T | TAAG | 120 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(117): Show |
123 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.1414-2261_1414-226 others(7): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130973069 | ||||||
| chr3:130973245 | T | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
121 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.1414-2087T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130973245 | |||||||
| chr3:130973268 | A | T | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0075 others(1): Show |
4 | NA18955.hp1 NA18961.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.1414-2064A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130973268 | |||||||
| chr3:130973341 | C | T | 3 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0218 |
3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1414-1991C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130973341 | |||||||
| chr3:130973512 | G | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG00099.hp1 HG00140.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1414-1820G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130973512 | |||||||
| chr3:130973558 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1414-1774C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130973558 | |||||||
| chr3:130973687 | T | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(6): Show |
9 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1414-1645T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130973687 | |||||||
| chr3:130973772 | A | G | 69 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(66): Show |
69 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.1414-1560A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130973772 | |||||||
| chr3:130973885 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1414-1447A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130973885 | |||||||
| chr3:130973892 | A | G | 102 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(99): Show |
104 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.1414-1440A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130973892 | |||||||
| chr3:130973966 | G | C | 1 | a0001c0001t0001g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1414-1366G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130973966 | |||||||
| chr3:130974098 | T | C | 7 | a0001c0003t0001g0083 a0001c0003t0001g0098 a0001c0003t0001g0099 others(4): Show |
7 | HG00733.hp1 HG01346.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1414-1234T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130974098 | |||||||
| chr3:130974236 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1414-1096A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130974236 | |||||||
| chr3:130974327 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1414-1005T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130974327 | |||||||
| chr3:130974329 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG00639.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.1414-1003G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130974329 | |||||||
| chr3:130974378 | A | G | 3 | a0001c0002t0001g0219 a0001c0002t0001g0351 a0001c0002t0001g0352 |
3 | NA19055.hp2 NA19072.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1414-954A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130974378 | |||||||
| chr3:130974736 | G | A | 1 | a0001c0001t0010g0122 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1414-596G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130974736 | |||||||
| chr3:130974847 | C | T | 147 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(144): Show |
150 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1414-485C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130974847 | |||||||
| chr3:130974961 | T | C | 1 | a0003c0005t0003g0110 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1414-371T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130974961 | |||||||
| chr3:130974983 | A | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1414-349A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130974983 | |||||||
| chr3:130974992 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1414-340G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130974992 | |||||||
| chr3:130975259 | C | T | 1 | a0001c0001t0001g0047 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1414-73C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130975259 | |||||||
| chr3:130975266 | T | C | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG00544.hp2 HG00621.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.1414-66T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130975266 | |||||||
| chr3:130975510 | C | T | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1570+22C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130975510 | |||||||
| chr3:130975662 | A | G | 16 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0128 others(13): Show |
16 | HG00609.hp2 HG02074.hp1 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.1570+174A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130975662 | |||||||
| chr3:130975709 | A | G | 20 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(17): Show |
21 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.1570+221A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130975709 | |||||||
| chr3:130976179 | A | C | 1 | a0002c0004t0001g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1570+691A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130976179 | |||||||
| chr3:130976334 | T | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1570+846T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130976334 | |||||||
| chr3:130976418 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0145 |
2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1570+930C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130976418 | |||||||
| chr3:130976480 | T | C | 20 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(17): Show |
21 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.1570+992T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130976480 | |||||||
| chr3:130976501 | C | G | 2 | a0001c0001t0001g0192 a0001c0001t0001g0242 |
2 | HG02129.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1570+1013C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130976501 | |||||||
| chr3:130976715 | T | C | 2 | a0003c0005t0003g0109 a0003c0005t0003g0110 |
2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1570+1227T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130976715 | |||||||
| chr3:130976755 | C | G | 1 | a0001c0001t0001g0054 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1570+1267C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130976755 | |||||||
| chr3:130976755 | C | T | 1 | a0001c0001t0001g0363 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1570+1267C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130976755 | |||||||
| chr3:130976882 | C | G | 1 | a0001c0001t0001g0178 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1570+1394C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130976882 | |||||||
| chr3:130976919 | A | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1570+1431A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130976919 | |||||||
| chr3:130976984 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1570+1496C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130976984 | |||||||
| chr3:130977006 | C | G | 1 | a0001c0001t0001g0070 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1570+1518C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977006 | |||||||
| chr3:130977118 | T | C | 104 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(101): Show |
106 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.1570+1630T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977118 | |||||||
| chr3:130977146 | A | G | 1 | a0001c0001t0010g0122 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1570+1658A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977146 | |||||||
| chr3:130977172 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1570+1684C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977172 | |||||||
| chr3:130977186 | G | A | 2 | a0001c0001t0001g0234 a0001c0001t0001g0266 |
2 | HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1570+1698G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977186 | |||||||
| chr3:130977318 | A | G | 1 | a0001c0001t0001g0251 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1570+1830A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977318 | |||||||
| chr3:130977328 | T | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1570+1840T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977328 | |||||||
| chr3:130977468 | C | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1571-1781C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977468 | |||||||
| chr3:130977539 | G | A | 24 | a0001c0002t0001g0219 a0001c0002t0001g0329 a0001c0002t0001g0331 others(21): Show |
24 | HG00597.hp2 HG01081.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.1571-1710G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977539 | |||||||
| chr3:130977665 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1571-1584A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977665 | |||||||
| chr3:130977669 | T | C | 1 | a0001c0001t0001g0246 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1571-1580T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977669 | |||||||
| chr3:130977774 | A | G | 1 | a0001c0001t0006g0119 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1571-1475A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977774 | |||||||
| chr3:130977885 | T | A | 3 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0218 |
3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1571-1364T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977885 | |||||||
| chr3:130977980 | A | T | 1 | a0001c0001t0001g0091 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1571-1269A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977980 | |||||||
| chr3:130978122 | G | T | 3 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 |
3 | HG02273.hp1 NA19007.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1571-1127G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130978122 | |||||||
| chr3:130978124 | C | T | 3 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 |
3 | HG02273.hp1 NA19007.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1571-1125C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130978124 | |||||||
| chr3:130978125 | C | G | 20 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(17): Show |
21 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.1571-1124C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130978125 | |||||||
| chr3:130978130 | C | T | 3 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 |
3 | HG02273.hp1 NA19007.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1571-1119C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130978130 | |||||||
| chr3:130978141 | A | G | 5 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(2): Show |
5 | HG02615.hp1 HG02965.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1571-1108A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130978141 | |||||||
| chr3:130978188 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1571-1061G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130978188 | |||||||
| chr3:130978358 | T | G | 6 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(3): Show |
6 | HG02109.hp1 HG02723.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1571-891T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130978358 | |||||||
| chr3:130978466 | C | T | 1 | a0001c0001t0001g0311 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1571-783C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130978466 | |||||||
| chr3:130978474 | C | A | 1 | a0001c0001t0001g0280 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1571-775C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130978474 | |||||||
| chr3:130978594 | T | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1571-655T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130978594 | |||||||
| chr3:130978920 | T | A | 3 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 |
3 | HG01243.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1571-329T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130978920 | |||||||
| chr3:130978955 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1571-294T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130978955 | |||||||
| chr3:130979082 | T | C | 1 | a0001c0001t0001g0303 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1571-167T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130979082 | |||||||
| chr3:130979172 | A | G | 1 | a0001c0002t0001g0346 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1571-77A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130979172 | |||||||
| chr3:130979178 | T | C | 4 | a0001c0001t0001g0222 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
4 | HG01891.hp2 HG01981.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1571-71T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130979178 | |||||||
| chr3:130979450 | A | G | 1 | a0001c0001t0001g0009 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1741+31A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/27 | chr3 | 130979450 | |||||||
| chr3:130979468 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG00597.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1741+49C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/27 | chr3 | 130979468 | |||||||
| chr3:130979471 | T | A | 1 | a0001c0001t0001g0149 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1741+52T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/27 | chr3 | 130979471 | |||||||
| chr3:130979541 | G | A | 1 | a0001c0002t0001g0360 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1741+122G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/27 | chr3 | 130979541 | |||||||
| chr3:130979674 | TC | T | 99 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(96): Show |
101 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.1741+256delC | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/27 | chr3 | 130979674 | |||||||
| chr3:130979683 | CA | C | 257 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(254): Show |
262 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.1741+266delA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr3 | 130979683 | ||||||
| chr3:130980070 | C | T | 1 | a0004c0008t0001g0215 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1742-512C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/27 | chr3 | 130980070 | |||||||
| chr3:130980254 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1742-328T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/27 | chr3 | 130980254 | |||||||
| chr3:130980256 | T | A | 1 | a0001c0001t0001g0123 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1742-326T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/27 | chr3 | 130980256 | |||||||
| chr3:130980282 | T | TG | 7 | a0001c0001t0001g0228 a0001c0001t0001g0252 a0001c0001t0001g0308 others(4): Show |
7 | HG01069.hp1 HG01071.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1742-299dupG | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr3 | 130980282 | ||||||
| chr3:130980313 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1742-269T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/27 | chr3 | 130980313 | |||||||
| chr3:130980345 | A | G | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG01255.hp1 HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1742-237A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/27 | chr3 | 130980345 | |||||||
| chr3:130980942 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1839+263A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130980942 | |||||||
| chr3:130980973 | A | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0328 |
3 | NA18971.hp1 NA18977.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1839+294A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130980973 | |||||||
| chr3:130981111 | A | T | 1 | a0001c0001t0001g0175 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1839+432A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130981111 | |||||||
| chr3:130981145 | G | A | 1 | a0001c0002t0001g0347 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1839+466G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130981145 | |||||||
| chr3:130981183 | G | T | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(256): Show |
264 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.1839+504G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130981183 | |||||||
| chr3:130981272 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1839+593T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130981272 | |||||||
| chr3:130981291 | T | C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
5 | HG01255.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1839+612T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130981291 | |||||||
| chr3:130981381 | T | C | 3 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 |
3 | HG02155.hp1 HG02523.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1839+702T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130981381 | |||||||
| chr3:130981428 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1839+749A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130981428 | |||||||
| chr3:130981814 | T | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0112 a0001c0001t0001g0113 others(3): Show |
7 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1839+1135T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130981814 | |||||||
| chr3:130981894 | A | G | 1 | a0001c0001t0006g0119 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1839+1215A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130981894 | |||||||
| chr3:130982097 | C | G | 4 | a0001c0001t0001g0004 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
5 | HG01255.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1839+1418C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982097 | |||||||
| chr3:130982119 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1839+1440G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982119 | |||||||
| chr3:130982214 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1839+1535G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982214 | |||||||
| chr3:130982338 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1839+1659G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982338 | |||||||
| chr3:130982346 | G | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1839+1667G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982346 | |||||||
| chr3:130982367 | A | C | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1839+1688A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982367 | |||||||
| chr3:130982420 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1839+1741C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982420 | |||||||
| chr3:130982421 | T | A | 1 | a0001c0001t0001g0225 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1839+1742T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982421 | |||||||
| chr3:130982450 | G | T | 1 | a0001c0006t0001g0270 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1839+1771G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982450 | |||||||
| chr3:130982467 | C | G | 2 | a0001c0001t0001g0079 a0001c0001t0009g0078 |
2 | HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1839+1788C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982467 | |||||||
| chr3:130982474 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1839+1795C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982474 | |||||||
| chr3:130982524 | C | T | 1 | a0001c0002t0001g0238 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1839+1845C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982524 | |||||||
| chr3:130982581 | T | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
5 | HG01255.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1839+1902T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982581 | |||||||
| chr3:130982706 | A | G | 46 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(43): Show |
46 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1839+2027A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982706 | |||||||
| chr3:130982757 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1839+2078A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982757 | |||||||
| chr3:130982763 | T | C | 45 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(42): Show |
45 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.1839+2084T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982763 | |||||||
| chr3:130982836 | G | C | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1839+2157G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982836 | |||||||
| chr3:130982967 | T | C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(18): Show |
22 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.1839+2288T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982967 | |||||||
| chr3:130983105 | T | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0145 a0001c0006t0001g0120 |
3 | HG02055.hp2 HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1839+2426T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983105 | |||||||
| chr3:130983107 | T | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
122 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.1839+2428T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983107 | |||||||
| chr3:130983109 | G | T | 8 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(5): Show |
8 | HG00639.hp1 HG01258.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.1839+2430G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983109 | |||||||
| chr3:130983218 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1839+2539G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983218 | |||||||
| chr3:130983239 | A | G | 1 | a0001c0001t0009g0078 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1839+2560A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983239 | |||||||
| chr3:130983271 | G | A | 24 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(21): Show |
24 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1839+2592G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983271 | |||||||
| chr3:130983338 | T | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1839+2659T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983338 | |||||||
| chr3:130983446 | A | G | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1839+2767A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983446 | |||||||
| chr3:130983657 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1839+2978C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983657 | |||||||
| chr3:130983747 | G | C | 6 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(3): Show |
6 | HG02109.hp1 HG02723.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1839+3068G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983747 | |||||||
| chr3:130983799 | C | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1839+3120C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983799 | |||||||
| chr3:130983886 | G | C | 1 | a0001c0006t0001g0120 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1839+3207G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983886 | |||||||
| chr3:130983908 | C | T | 9 | a0001c0001t0001g0111 a0001c0001t0001g0320 a0001c0003t0001g0083 others(6): Show |
9 | HG00733.hp1 HG01346.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1839+3229C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983908 | |||||||
| chr3:130983972 | C | G | 3 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 |
3 | HG01243.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1839+3293C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983972 | |||||||
| chr3:130984004 | C | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1839+3325C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130984004 | |||||||
| chr3:130984037 | TG | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0145 a0001c0006t0001g0120 |
3 | HG02055.hp2 HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1839+3359delG | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130984037 | |||||||
| chr3:130984243 | T | C | 2 | a0001c0001t0001g0121 a0001c0001t0001g0145 |
2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1839+3564T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130984243 | |||||||
| chr3:130984391 | C | T | 11 | a0001c0001t0001g0022 a0001c0001t0001g0030 a0001c0001t0001g0034 others(8): Show |
11 | HG00438.hp1 HG00673.hp1 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.1839+3712C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130984391 | |||||||
| chr3:130984564 | T | A | 1 | a0001c0001t0001g0155 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1839+3885T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130984564 | |||||||
| chr3:130984624 | A | G | 1 | a0001c0001t0001g0135 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1839+3945A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130984624 | |||||||
| chr3:130984767 | A | G | 1 | a0001c0001t0010g0122 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1839+4088A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130984767 | |||||||
| chr3:130984917 | CAGAA | C | 44 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(41): Show |
44 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.1839+4242_1839+424 others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130984917 | ||||||
| chr3:130985491 | G | T | 4 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0190 others(1): Show |
4 | NA18941.hp2 NA18949.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1839+4812G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130985491 | |||||||
| chr3:130985658 | C | CA | 49 | a0001c0001t0001g0093 a0001c0001t0001g0147 a0001c0001t0001g0169 others(46): Show |
49 | HG00597.hp2 HG00639.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.1839+4990dupA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130985658 | ||||||
| chr3:130985664 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1839+4985A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130985664 | |||||||
| chr3:130985698 | A | G | 3 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0218 |
3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1839+5019A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130985698 | |||||||
| chr3:130985737 | A | G | 2 | a0001c0001t0001g0090 a0001c0001t0001g0297 |
2 | HG01243.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1839+5058A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130985737 | |||||||
| chr3:130985754 | A | C | 1 | a0001c0001t0001g0321 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1839+5075A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130985754 | |||||||
| chr3:130985767 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1839+5088A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130985767 | |||||||
| chr3:130985840 | T | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1839+5161T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130985840 | |||||||
| chr3:130985864 | CG | C | 36 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(33): Show |
36 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.1839+5186delG | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130985864 | |||||||
| chr3:130986184 | C | CT | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(256): Show |
264 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.1839+5520dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986184 | ||||||
| chr3:130986184 | C | CTT | 43 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0104 others(40): Show |
43 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.1839+5519_1839+552 others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986184 | ||||||
| chr3:130986184 | C | CTTT | 7 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0157 others(4): Show |
7 | HG00639.hp1 HG01358.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1839+5518_1839+552 others(7): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986184 | ||||||
| chr3:130986233 | A | T | 292 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(289): Show |
297 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.1839+5554A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130986233 | |||||||
| chr3:130986316 | T | G | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1839+5637T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130986316 | |||||||
| chr3:130986332 | C | G | 1 | a0001c0001t0001g0274 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1839+5653C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130986332 | |||||||
| chr3:130986347 | A | G | 26 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(23): Show |
26 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.1839+5668A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130986347 | |||||||
| chr3:130986383 | C | A | 1 | a0001c0002t0001g0326 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1839+5704C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130986383 | |||||||
| chr3:130986543 | G | A | 5 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0001g0249 others(2): Show |
5 | HG00438.hp2 HG02083.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1839+5864G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130986543 | |||||||
| chr3:130986648 | A | G | 45 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(42): Show |
46 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.1839+5969A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130986648 | |||||||
| chr3:130986666 | A | G | 2 | a0001c0001t0001g0234 a0001c0001t0001g0266 |
2 | HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1839+5987A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130986666 | |||||||
| chr3:130986674 | T | C | 321 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(318): Show |
326 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1839+5995T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130986674 | |||||||
| chr3:130986864 | ATTAGT | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(42): Show |
48 | HG00438.hp1 HG00673.hp1 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.1840-6030_1840-602 others(9): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986864 | ||||||
| chr3:130986864 | ATTAGTTT others(3): Show |
A | 16 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0027 others(13): Show |
16 | HG00099.hp1 HG00140.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1840-6035_1840-602 others(14): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986864 | ||||||
| chr3:130986864 | ATTAGTTT others(8): Show |
A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0079 a0001c0001t0009g0078 |
3 | HG02630.hp2 HG02896.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1840-6040_1840-602 others(19): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986864 | ||||||
| chr3:130986864 | ATTAGTTT others(13): Show |
A | 1 | a0001c0001t0001g0043 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1840-6045_1840-602 others(24): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986864 | ||||||
| chr3:130986893 | G | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0328 |
3 | NA18971.hp1 NA18977.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1840-6058G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130986893 | |||||||
| chr3:130986893 | GTTTAGTT others(33): Show |
G | 1 | a0001c0001t0001g0111 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1840-6055_1840-601 others(44): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986893 | ||||||
| chr3:130986898 | GTTTAGTT others(28): Show |
G | 22 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0112 others(19): Show |
23 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.1840-6050_1840-601 others(39): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986898 | ||||||
| chr3:130986903 | GTTTAGTT others(23): Show |
G | 177 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(174): Show |
180 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.1840-6045_1840-601 others(34): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986903 | ||||||
| chr3:130986908 | GTTTAGTT others(18): Show |
G | 61 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0086 others(58): Show |
62 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.1840-6040_1840-601 others(29): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986908 | ||||||
| chr3:130986913 | GTTTAGTT others(13): Show |
G | 29 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0092 others(26): Show |
29 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.1840-6035_1840-601 others(24): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986913 | ||||||
| chr3:130986918 | GTTTAGTT others(8): Show |
G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0117 |
2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1840-6030_1840-601 others(19): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986918 | ||||||
| chr3:130987062 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1840-5889C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130987062 | |||||||
| chr3:130987107 | TA | T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0146 others(3): Show |
7 | HG01255.hp1 HG02056.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1840-5829delA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130987107 | ||||||
| chr3:130987292 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1840-5659G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130987292 | |||||||
| chr3:130987461 | G | A | 1 | a0001c0002t0001g0010 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1840-5490G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130987461 | |||||||
| chr3:130987550 | C | T | 9 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(6): Show |
9 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1840-5401C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130987550 | |||||||
| chr3:130987918 | A | G | 24 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(21): Show |
24 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1840-5033A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130987918 | |||||||
| chr3:130988019 | T | G | 1 | a0001c0001t0001g0001 | 3 | NA18941.hp1 NA18944.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1840-4932T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130988019 | |||||||
| chr3:130988330 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1840-4621G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130988330 | |||||||
| chr3:130988354 | G | A | 1 | a0001c0001t0006g0119 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1840-4597G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130988354 | |||||||
| chr3:130988560 | C | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1840-4391C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130988560 | |||||||
| chr3:130988590 | A | T | 2 | a0003c0005t0003g0109 a0003c0005t0003g0110 |
2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1840-4361A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130988590 | |||||||
| chr3:130988591 | T | A | 26 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(23): Show |
26 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.1840-4360T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130988591 | |||||||
| chr3:130988679 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1840-4272C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130988679 | |||||||
| chr3:130988748 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1840-4203G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130988748 | |||||||
| chr3:130988839 | G | A | 1 | a0001c0001t0004g0316 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1840-4112G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130988839 | |||||||
| chr3:130988850 | A | G | 24 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(21): Show |
24 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1840-4101A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130988850 | |||||||
| chr3:130988875 | G | A | 24 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(21): Show |
24 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1840-4076G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130988875 | |||||||
| chr3:130988971 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1840-3980G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130988971 | |||||||
| chr3:130989242 | C | T | 20 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(17): Show |
21 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.1840-3709C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989242 | |||||||
| chr3:130989245 | CTCAAAAA others(8): Show |
C | 3 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 |
3 | HG01243.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1840-3705_1840-369 others(19): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989245 | |||||||
| chr3:130989247 | C | CA | 208 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(205): Show |
212 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.1840-3690dupA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130989247 | ||||||
| chr3:130989247 | C | CAA | 9 | a0001c0001t0001g0091 a0001c0001t0001g0162 a0001c0001t0001g0193 others(6): Show |
9 | HG00280.hp1 HG01123.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1840-3691_1840-369 others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130989247 | ||||||
| chr3:130989262 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1840-3689C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989262 | |||||||
| chr3:130989266 | A | C | 1 | a0004c0008t0001g0215 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1840-3685A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989266 | |||||||
| chr3:130989270 | C | A | 1 | a0004c0008t0001g0215 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1840-3681C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989270 | |||||||
| chr3:130989447 | C | G | 1 | a0001c0001t0001g0048 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1840-3504C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989447 | |||||||
| chr3:130989489 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02602.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1840-3462C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989489 | |||||||
| chr3:130989490 | G | A | 1 | a0001c0006t0001g0120 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1840-3461G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989490 | |||||||
| chr3:130989565 | C | CA | 39 | a0001c0001t0001g0047 a0001c0001t0001g0051 a0001c0001t0001g0058 others(36): Show |
39 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1840-3368dupA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130989565 | ||||||
| chr3:130989565 | C | CAA | 7 | a0001c0001t0001g0046 a0001c0001t0001g0155 a0001c0001t0001g0156 others(4): Show |
7 | HG01109.hp1 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1840-3369_1840-336 others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130989565 | ||||||
| chr3:130989565 | C | CAAA | 7 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(4): Show |
7 | HG02027.hp2 NA18747.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.1840-3370_1840-336 others(7): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130989565 | ||||||
| chr3:130989565 | CA | C | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(205): Show |
212 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.1840-3368delA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130989565 | ||||||
| chr3:130989583 | A | C | 2 | a0001c0002t0001g0329 a0001c0002t0001g0348 |
2 | NA18968.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1840-3368A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989583 | |||||||
| chr3:130989592 | C | T | 1 | a0001c0001t0009g0078 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1840-3359C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989592 | |||||||
| chr3:130989619 | G | T | 1 | a0001c0001t0006g0119 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1840-3332G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989619 | |||||||
| chr3:130989650 | G | C | 3 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 |
3 | HG01243.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1840-3301G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989650 | |||||||
| chr3:130989793 | C | T | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1840-3158C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989793 | |||||||
| chr3:130989916 | T | C | 2 | a0001c0001t0001g0160 a0001c0001t0001g0177 |
2 | HG04204.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1840-3035T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989916 | |||||||
| chr3:130989955 | T | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0112 a0001c0001t0001g0113 others(3): Show |
7 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1840-2996T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989955 | |||||||
| chr3:130990070 | T | G | 1 | a0001c0001t0001g0226 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1840-2881T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130990070 | |||||||
| chr3:130990154 | C | A | 1 | a0001c0001t0001g0239 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1840-2797C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130990154 | |||||||
| chr3:130990272 | A | AC | 149 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(146): Show |
152 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.1840-2668dupC | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130990272 | ||||||
| chr3:130990272 | A | ACC | 45 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(42): Show |
45 | HG00621.hp2 HG00639.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1840-2669_1840-266 others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130990272 | ||||||
| chr3:130990272 | A | ACCC | 18 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0079 others(15): Show |
18 | HG00280.hp2 HG00597.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1840-2670_1840-266 others(7): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130990272 | ||||||
| chr3:130990310 | A | T | 292 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(289): Show |
297 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.1840-2641A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130990310 | |||||||
| chr3:130990372 | A | G | 2 | a0001c0001t0001g0079 a0001c0001t0009g0078 |
2 | HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1840-2579A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130990372 | |||||||
| chr3:130990412 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0009g0078 |
2 | HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1840-2539G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130990412 | |||||||
| chr3:130990504 | T | A | 30 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(27): Show |
30 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.1840-2447T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130990504 | |||||||
| chr3:130990622 | C | T | 257 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(254): Show |
262 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.1840-2329C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130990622 | |||||||
| chr3:130990730 | T | C | 1 | a0001c0001t0009g0078 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1840-2221T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130990730 | |||||||
| chr3:130990883 | A | G | 20 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(17): Show |
21 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.1840-2068A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130990883 | |||||||
| chr3:130991030 | T | C | 20 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(17): Show |
21 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.1840-1921T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130991030 | |||||||
| chr3:130991203 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1840-1748A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130991203 | |||||||
| chr3:130991364 | G | A | 1 | a0001c0001t0010g0122 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1840-1587G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130991364 | |||||||
| chr3:130991514 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1840-1437C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130991514 | |||||||
| chr3:130991628 | T | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1840-1323T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130991628 | |||||||
| chr3:130991671 | T | C | 24 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(21): Show |
24 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1840-1280T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130991671 | |||||||
| chr3:130991675 | A | G | 19 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(16): Show |
19 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1840-1276A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130991675 | |||||||
| chr3:130992005 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1840-946C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130992005 | |||||||
| chr3:130992103 | A | G | 1 | a0001c0001t0001g0320 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1840-848A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130992103 | |||||||
| chr3:130992195 | C | A | 2 | a0003c0005t0003g0109 a0003c0005t0003g0110 |
2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1840-756C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130992195 | |||||||
| chr3:130992205 | GGTACTAT others(54): Show |
G | 1 | a0001c0001t0001g0089 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1840-682_1840-622d others(63): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130992205 | ||||||
| chr3:130992341 | A | C | 1 | a0001c0001t0001g0173 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1840-610A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130992341 | |||||||
| chr3:130992613 | G | T | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1840-338G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130992613 | |||||||
| chr3:130992735 | G | A | 24 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(21): Show |
24 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1840-216G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130992735 | |||||||
| chr3:130992806 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1840-145T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130992806 | |||||||
| chr3:130993079 | A | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02602.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1890+78A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 21/27 | chr3 | 130993079 | |||||||
| chr3:130993091 | A | G | 31 | a0001c0001t0001g0005 a0001c0001t0001g0180 a0001c0001t0001g0181 others(28): Show |
32 | HG00544.hp1 HG00558.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.1890+90A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 21/27 | chr3 | 130993091 | |||||||
| chr3:130993120 | C | T | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0040 others(1): Show |
4 | HG00438.hp1 HG00673.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.1890+119C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 21/27 | chr3 | 130993120 | |||||||
| chr3:130993122 | G | GT | 7 | a0001c0001t0001g0004 a0001c0001t0001g0046 a0001c0001t0001g0146 others(4): Show |
8 | HG01255.hp1 HG02135.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1890+133dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr3 | 130993122 | ||||||
| chr3:130993123 | T | TG | 19 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0022 others(16): Show |
22 | HG00438.hp1 HG00673.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.1890+122_1890+123i others(3): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 21/27 | chr3 | 130993123 | |||||||
| chr3:130993311 | G | C | 1 | a0001c0001t0001g0223 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1890+310G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 21/27 | chr3 | 130993311 | |||||||
| chr3:130994116 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2057+18G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130994116 | |||||||
| chr3:130994138 | C | T | 1 | a0001c0001t0001g0022 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2057+40C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130994138 | |||||||
| chr3:130994370 | G | A | 2 | a0003c0005t0003g0109 a0003c0005t0003g0110 |
2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2057+272G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130994370 | |||||||
| chr3:130994494 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2057+396G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130994494 | |||||||
| chr3:130994571 | T | G | 1 | a0001c0001t0001g0361 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2057+473T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130994571 | |||||||
| chr3:130994598 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2057+500T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130994598 | |||||||
| chr3:130994599 | A | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0059 |
2 | HG02056.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.2057+501A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130994599 | |||||||
| chr3:130994601 | A | G | 2 | a0003c0005t0003g0109 a0003c0005t0003g0110 |
2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2057+503A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130994601 | |||||||
| chr3:130994648 | C | CATTT | 7 | a0001c0001t0001g0228 a0001c0001t0001g0252 a0001c0001t0001g0308 others(4): Show |
7 | HG01069.hp1 HG01071.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2057+567_2057+570d others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr3 | 130994648 | ||||||
| chr3:130994655 | T | G | 3 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG00099.hp1 HG00140.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.2057+557T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130994655 | |||||||
| chr3:130994798 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2057+700A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130994798 | |||||||
| chr3:130995059 | A | T | 26 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(23): Show |
26 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.2057+961A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130995059 | |||||||
| chr3:130995380 | G | A | 292 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(289): Show |
297 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.2058-663G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130995380 | |||||||
| chr3:130995398 | G | C | 1 | a0001c0001t0001g0205 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2058-645G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130995398 | |||||||
| chr3:130995419 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2058-624A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130995419 | |||||||
| chr3:130995637 | T | TTTTA | 20 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(17): Show |
21 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.2058-398_2058-395d others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr3 | 130995637 | ||||||
| chr3:130995744 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2058-299G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130995744 | |||||||
| chr3:130995790 | G | A | 20 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0111 others(17): Show |
21 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.2058-253G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130995790 | |||||||
| chr3:130995801 | C | T | 4 | a0002c0004t0001g0105 a0002c0004t0001g0106 a0002c0004t0001g0107 others(1): Show |
4 | HG02630.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2058-242C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130995801 | |||||||
| chr3:130995886 | C | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2058-157C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130995886 | |||||||
| chr3:130995896 | C | T | 1 | a0001c0002t0001g0010 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2058-147C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130995896 | |||||||
| chr3:130996023 | C | G | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0174 |
3 | HG02055.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2058-20C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130996023 | |||||||
| chr3:130996026 | T | C | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | HG00621.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.2058-17T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130996026 | |||||||
| chr3:130996224 | A | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2126+113A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 23/27 | chr3 | 130996224 | |||||||
| chr3:130996571 | T | G | 45 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(42): Show |
45 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.2127-109T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 23/27 | chr3 | 130996571 | |||||||
| chr3:130996612 | A | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0145 |
2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2127-68A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 23/27 | chr3 | 130996612 | |||||||
| chr3:130996904 | A | C | 31 | a0001c0002t0001g0219 a0001c0002t0001g0238 a0001c0002t0001g0329 others(28): Show |
31 | HG00597.hp2 HG01081.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.2243+108A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 24/27 | chr3 | 130996904 | |||||||
| chr3:130996931 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2243+135G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 24/27 | chr3 | 130996931 | |||||||
| chr3:130996970 | A | G | 44 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(41): Show |
44 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.2243+174A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 24/27 | chr3 | 130996970 | |||||||
| chr3:130997020 | G | A | 1 | a0001c0002t0001g0336 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2243+224G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 24/27 | chr3 | 130997020 | |||||||
| chr3:130997194 | T | A | 1 | a0001c0001t0001g0033 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2243+398T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 24/27 | chr3 | 130997194 | |||||||
| chr3:130997325 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2244-281C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 24/27 | chr3 | 130997325 | |||||||
| chr3:130997811 | CTTAG | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2391+62_2391+65del others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr3 | 130997811 | ||||||
| chr3:130997951 | C | T | 1 | a0001c0002t0001g0323 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2391+198C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 25/27 | chr3 | 130997951 | |||||||
| chr3:130998076 | A | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2392-218A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 25/27 | chr3 | 130998076 | |||||||
| chr3:130998128 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2392-166A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 25/27 | chr3 | 130998128 | |||||||
| chr3:130998148 | G | A | 1 | a0001c0001t0002g0140 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2392-146G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 25/27 | chr3 | 130998148 | |||||||
| chr3:130998677 | A | G | 7 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(4): Show |
8 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.2487+288A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 26/27 | chr3 | 130998677 | |||||||
| chr3:130998703 | T | A | 1 | a0001c0001t0001g0123 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2487+314T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 26/27 | chr3 | 130998703 | |||||||
| chr3:130998752 | A | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0145 |
2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2487+363A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 26/27 | chr3 | 130998752 | |||||||
| chr3:130998787 | C | T | 4 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2487+398C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 26/27 | chr3 | 130998787 | |||||||
| chr3:130998866 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2487+477C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 26/27 | chr3 | 130998866 | |||||||
| chr3:130999029 | A | G | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0174 |
3 | HG02055.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2488-489A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 26/27 | chr3 | 130999029 | |||||||
| chr3:130999052 | G | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
5 | HG01255.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2488-466G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 26/27 | chr3 | 130999052 | |||||||
| chr3:130999065 | T | C | 16 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0128 others(13): Show |
16 | HG00609.hp2 HG02074.hp1 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.2488-453T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 26/27 | chr3 | 130999065 | |||||||
| chr3:130999312 | A | T | 39 | a0001c0002t0001g0010 a0001c0002t0001g0219 a0001c0002t0001g0238 others(36): Show |
39 | HG00597.hp2 HG01081.hp2 HG01123.hp1 others(36): Show |
intron_variant | MODIFIER | c.2488-206A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 26/27 | chr3 | 130999312 | |||||||
| chr3:130999715 | A | C | 1 | a0001c0001t0006g0119 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2629+56A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | chr3 | 130999715 | |||||||
| chr3:131000205 | G | A | 257 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(254): Show |
262 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.2629+546G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | chr3 | 131000205 | |||||||
| chr3:131000375 | A | G | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2629+716A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | chr3 | 131000375 | |||||||
| chr3:131000391 | A | T | 2 | a0001c0001t0002g0216 a0001c0001t0002g0218 |
2 | HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2629+732A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | chr3 | 131000391 | |||||||
| chr3:131000452 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2630-768A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | chr3 | 131000452 | |||||||
| chr3:131000460 | T | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0146 a0001c0001t0001g0147 others(40): Show |
44 | HG00597.hp2 HG01081.hp2 HG01123.hp1 others(41): Show |
intron_variant | MODIFIER | c.2630-760T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | chr3 | 131000460 | |||||||
| chr3:131000529 | A | G | 1 | a0001c0002t0001g0347 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2630-691A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | chr3 | 131000529 | |||||||
| chr3:131000555 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2630-665C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | chr3 | 131000555 | |||||||
| chr3:131000595 | TA | T | 9 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(6): Show |
9 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.2630-624delA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | chr3 | 131000595 | |||||||
| chr3:131000645 | A | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2630-575A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | chr3 | 131000645 | |||||||
| chr3:131000948 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2630-272C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | chr3 | 131000948 | |||||||
| chr3:131001104 | G | GA | 206 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(203): Show |
209 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.2630-93dupA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr3 | 131001104 | ||||||
| chr3:131001104 | G | GAA | 35 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0033 others(32): Show |
37 | HG00733.hp1 HG00738.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.2630-94_2630-93dup others(2): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr3 | 131001104 | ||||||
| chr3:131001104 | G | GAAA | 12 | a0001c0001t0001g0091 a0001c0001t0001g0114 a0001c0001t0001g0121 others(9): Show |
12 | HG01169.hp1 HG01346.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.2630-95_2630-93dup others(3): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr3 | 131001104 |