Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57113 |
| ensemblid | ENSG00000069018.19 |
| hgncid | 20754 |
| symbol | TRPC7 |
| name | transient receptor potential cation channel subfamily C member 7 |
| refseq_nuc | NM_020389.3 |
| refseq_prot | NP_065122.1 |
| ensembl_nuc | ENST00000513104.6 |
| ensembl_prot | ENSP00000426070.2 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 136212745 |
| end | 136365545 |
| strand | - |
| ver | v1.2 |
| region | chr5:136212745-136365545 |
| region5000 | chr5:136207745-136370545 |
| regionname0 | TRPC7_chr5_136212745_136365545 |
| regionname5000 | TRPC7_chr5_136207745_136370545 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 862 | 255 | 72 | 42 | 101 | 14 | 24 | 77 | TRPC7_chr5_136207745_136370545 | TRPC7 | MLRNS others(857): Show |
chr5 | 136207745 | 136370545 |
| a0002 | 0/0 | 862 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | MLRNS others(857): Show |
chr5 | 136207745 | 136370545 |
| a0003 | 0/0 | 862 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | MLRNS others(857): Show |
chr5 | 136207745 | 136370545 |
| a0004 | 0/0 | 862 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRPC7_chr5_136207745_136370545 | TRPC7 | MLRNS others(857): Show |
chr5 | 136207745 | 136370545 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2586 | 181 | 47 | 28 | 71 | 11 | 22 | TRPC7_chr5_136207745_136370545 | TRPC7 | ATGTT others(2581): Show |
chr5 | 136207745 | 136370545 | ||
| a0001c0002 | 0/0 | 2586 | 71 | 24 | 12 | 30 | 3 | 2 | TRPC7_chr5_136207745_136370545 | TRPC7 | ATGTT others(2581): Show |
chr5 | 136207745 | 136370545 | ||
| a0001c0003 | 0/0 | 2586 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | ATGTT others(2581): Show |
chr5 | 136207745 | 136370545 | ||
| a0001c0007 | 0/0 | 2586 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | ATGTT others(2581): Show |
chr5 | 136207745 | 136370545 | ||
| a0001c0008 | 0/0 | 2586 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | ATGTT others(2581): Show |
chr5 | 136207745 | 136370545 | ||
| a0002c0004 | 0/0 | 2586 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | ATGTT others(2581): Show |
chr5 | 136207745 | 136370545 | ||
| a0003c0006 | 0/0 | 2586 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | ATGTT others(2581): Show |
chr5 | 136207745 | 136370545 | ||
| a0004c0005 | 0/0 | 2586 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | ATGTT others(2581): Show |
chr5 | 136207745 | 136370545 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3570 | 176 | 47 | 28 | 68 | 9 | 22 | TRPC7_chr5_136207745_136370545 | TRPC7 | ACTCT others(3565): Show |
chr5 | 136207745 | 136370545 |
| a0001c0001t0002 | 0/0 | 3570 | 2 | 0 | 0 | 2 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | ACTCT others(3565): Show |
chr5 | 136207745 | 136370545 |
| a0001c0001t0006 | 0/0 | 3570 | 2 | 0 | 0 | 0 | 2 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | ACTCT others(3565): Show |
chr5 | 136207745 | 136370545 |
| a0001c0001t0008 | 0/0 | 3570 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | ACTCT others(3565): Show |
chr5 | 136207745 | 136370545 |
| a0001c0002t0001 | 0/0 | 3570 | 3 | 2 | 0 | 0 | 1 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | ACTCT others(3565): Show |
chr5 | 136207745 | 136370545 |
| a0001c0002t0002 | 0/0 | 3570 | 60 | 20 | 11 | 25 | 2 | 2 | TRPC7_chr5_136207745_136370545 | TRPC7 | ACTCT others(3565): Show |
chr5 | 136207745 | 136370545 |
| a0001c0002t0003 | 0/0 | 3567 | 3 | 0 | 1 | 2 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | ACTCT others(3562): Show |
chr5 | 136207745 | 136370545 |
| a0001c0002t0004 | 0/0 | 3570 | 3 | 0 | 0 | 3 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | ACTCT others(3565): Show |
chr5 | 136207745 | 136370545 |
| a0001c0002t0005 | 0/0 | 3570 | 2 | 2 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | ACTCT others(3565): Show |
chr5 | 136207745 | 136370545 |
| a0001c0003t0001 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | ACTCT others(3565): Show |
chr5 | 136207745 | 136370545 |
| a0001c0007t0002 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | ACTCT others(3565): Show |
chr5 | 136207745 | 136370545 |
| a0001c0008t0007 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | ACTCT others(3565): Show |
chr5 | 136207745 | 136370545 |
| a0002c0004t0001 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | ACTCT others(3565): Show |
chr5 | 136207745 | 136370545 |
| a0003c0006t0001 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | ACTCT others(3565): Show |
chr5 | 136207745 | 136370545 |
| a0004c0005t0001 | 0/0 | 3570 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | ACTCT others(3565): Show |
chr5 | 136207745 | 136370545 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0084 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0109 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0006g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0006g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0001t0008g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0002t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0003t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0007t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0001c0008t0007g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0002c0004t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0003c0006t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| a0004c0005t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0191 | EUR | GBR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | GBR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | FIN | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | FIN | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0210 | EAS | CHS | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG00621 | hp1 | a0001 | c0002 | t0003 | g0248 | EAS | CHS | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0193 | AMR | PUR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0169 | AMR | PUR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | CHS | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0187 | AMR | PUR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0192 | AMR | PUR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0216 | AMR | PUR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01069 | hp1 | a0001 | c0007 | t0002 | g0189 | AMR | PUR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0212 | AMR | PUR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0201 | AMR | PUR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0198 | AMR | PUR | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01258 | hp1 | a0001 | c0002 | t0003 | g0238 | AMR | CLM | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0230 | AMR | CLM | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | IBS | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0190 | EUR | IBS | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01516 | hp1 | a0001 | c0001 | t0006 | g0064 | EUR | IBS | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | IBS | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01517 | hp1 | a0001 | c0001 | t0006 | g0063 | EUR | IBS | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | IBS | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0197 | AFR | ACB | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0245 | AMR | PEL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0232 | AMR | PEL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0214 | EAS | KHV | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0220 | EAS | KHV | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0213 | EAS | KHV | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0224 | EAS | KHV | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0252 | EAS | KHV | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0199 | AFR | ACB | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0244 | AMR | PEL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | ACB | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0204 | AFR | ACB | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0239 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0202 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0234 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02809 | hp2 | a0002 | c0004 | t0001 | g0175 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0219 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02886 | hp2 | a0003 | c0006 | t0001 | g0026 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0237 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0218 | AFR | ESN | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0200 | AFR | ESN | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0209 | AFR | ESN | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03130 | hp1 | a0001 | c0002 | t0005 | g0028 | AFR | ESN | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0208 | SAS | PJL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0203 | SAS | PJL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0188 | AFR | GWD | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0231 | AFR | MSL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03579 | hp2 | a0001 | c0008 | t0007 | g0006 | AFR | MSL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | STU | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | STU | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | STU | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18522 | hp1 | a0001 | c0002 | t0005 | g0025 | AFR | YRI | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | YRI | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18940 | hp2 | a0001 | c0002 | t0004 | g0205 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18944 | hp1 | a0001 | c0001 | t0008 | g0128 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18956 | hp2 | a0001 | c0002 | t0003 | g0246 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0243 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18984 | hp1 | a0004 | c0005 | t0001 | g0091 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0253 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0233 | AFR | LWK | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0236 | AFR | LWK | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19056 | hp2 | a0001 | c0002 | t0004 | g0207 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19070 | hp1 | a0001 | c0002 | t0004 | g0206 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0194 | AFR | ASW | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ASW | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | TSI | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0114 | EUR | TSI | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | TSI | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | TSI | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | ACB | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0196 | AFR | ACB | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0195 | AFR | ACB | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | USA | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0235 | AFR | USA | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0211 | AFR | LWK | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0109 | REF | REF | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0084 | REF | REF | TRPC7_chr5_136207745_136370545 | TRPC7 | chr5 | 136207745 | 136370545 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:136251715 | G | C | 1 | a0004 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.1513C>G | p.Gln505Glu | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/12 | 1804/3570 | 1513/2589 | 505/862 | chr5 | 136251715 | |||
| chr5:136251829 | C | T | 1 | a0002 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1399G>A | p.Val467Met | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/12 | 1690/3570 | 1399/2589 | 467/862 | chr5 | 136251829 | |||
| chr5:136266279 | A | G | 1 | a0003 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.1286T>C | p.Phe429Ser | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/12 | 1577/3570 | 1286/2589 | 429/862 | chr5 | 136266279 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:136216213 | G | A | 1 | a0001c0008 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.2406C>T | p.Asp802Asp | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/12 | 2697/3570 | 2406/2589 | 802/862 | chr5 | 136216213 | |||
| chr5:136247689 | C | T | 1 | a0001c0007 | 1 | HG01069.hp1 | synonymous_variant | LOW | c.1626G>A | p.Gly542Gly | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/12 | 1917/3570 | 1626/2589 | 542/862 | chr5 | 136247689 | |||
| chr5:136356887 | G | A | 4 | a0001c0002 a0001c0007 a0001c0008 others(1): Show |
74 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(71): Show |
synonymous_variant | LOW | c.501C>T | p.Pro167Pro | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/12 | 792/3570 | 501/2589 | 167/862 | chr5 | 136356887 | |||
| chr5:136356965 | C | T | 1 | a0001c0003 | 1 | HG00642.hp2 | synonymous_variant | LOW | c.423G>A | p.Pro141Pro | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/12 | 714/3570 | 423/2589 | 141/862 | chr5 | 136356965 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:136212836 | TTTG | T | 1 | a0001c0002t0003 | 3 | HG00621.hp1 HG01258.hp1 NA18956.hp2 |
3_prime_UTR_variant | MODIFIER | c.*596_*598delCAA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 12/12 | 596 | chr5 | 136212836 | ||||||
| chr5:136213006 | G | A | 1 | a0001c0001t0008 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*429C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 12/12 | 429 | chr5 | 136213006 | ||||||
| chr5:136213185 | G | A | 1 | a0001c0002t0004 | 3 | NA18940.hp2 NA19056.hp2 NA19070.hp1 |
3_prime_UTR_variant | MODIFIER | c.*250C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 12/12 | 250 | chr5 | 136213185 | ||||||
| chr5:136213233 | A | G | 1 | a0001c0001t0006 | 2 | HG01516.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*202T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 12/12 | 202 | chr5 | 136213233 | ||||||
| chr5:136213355 | C | T | 1 | a0001c0002t0005 | 2 | HG03130.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*80G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 12/12 | 80 | chr5 | 136213355 | ||||||
| chr5:136365425 | T | G | 6 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0003 others(3): Show |
70 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(67): Show |
5_prime_UTR_variant | MODIFIER | c.-171A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/12 | 171 | chr5 | 136365425 | ||||||
| chr5:136365531 | C | G | 1 | a0001c0008t0007 | 1 | HG03579.hp2 | 5_prime_UTR_variant | MODIFIER | c.-277G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/12 | 277 | chr5 | 136365531 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:136213642 | G | A | 2 | a0001c0002t0002g0237 a0001c0002t0002g0239 |
2 | HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2420-38C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136213642 | |||||||
| chr5:136213651 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2420-47G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136213651 | |||||||
| chr5:136213747 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2420-143C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136213747 | |||||||
| chr5:136213817 | C | T | 1 | a0001c0002t0002g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2420-213G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136213817 | |||||||
| chr5:136213893 | G | C | 1 | a0001c0002t0002g0249 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2420-289C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136213893 | |||||||
| chr5:136213991 | C | A | 11 | a0001c0001t0001g0021 a0001c0001t0001g0032 a0001c0001t0001g0033 others(8): Show |
11 | HG02280.hp2 HG02572.hp1 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.2420-387G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136213991 | |||||||
| chr5:136214023 | G | A | 2 | a0001c0001t0001g0021 a0001c0002t0002g0204 |
2 | HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2420-419C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136214023 | |||||||
| chr5:136214036 | A | G | 1 | a0001c0002t0002g0235 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2420-432T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136214036 | |||||||
| chr5:136214045 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2420-441A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136214045 | |||||||
| chr5:136214071 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0105 |
2 | NA18942.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.2420-467C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136214071 | |||||||
| chr5:136214178 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0171 others(4): Show |
8 | HG01884.hp1 HG02615.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.2420-574G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136214178 | |||||||
| chr5:136214194 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0112 a0002c0004t0001g0175 |
4 | HG02717.hp2 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2420-590C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136214194 | |||||||
| chr5:136214206 | C | T | 3 | a0001c0001t0001g0021 a0001c0002t0002g0204 a0001c0008t0007g0006 |
3 | HG02280.hp2 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2420-602G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136214206 | |||||||
| chr5:136214230 | A | T | 3 | a0001c0001t0001g0034 a0001c0002t0002g0230 a0001c0002t0002g0231 |
3 | HG01496.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2420-626T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136214230 | |||||||
| chr5:136214297 | A | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0132 |
2 | NA18979.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.2420-693T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136214297 | |||||||
| chr5:136214677 | T | G | 2 | a0001c0002t0005g0025 a0001c0002t0005g0028 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2420-1073A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136214677 | |||||||
| chr5:136214710 | G | A | 1 | a0001c0008t0007g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2420-1106C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136214710 | |||||||
| chr5:136214913 | T | C | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2419+1287A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136214913 | |||||||
| chr5:136214991 | G | A | 1 | a0001c0008t0007g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2419+1209C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136214991 | |||||||
| chr5:136215073 | G | T | 3 | a0001c0001t0001g0034 a0001c0002t0002g0230 a0001c0002t0002g0231 |
3 | HG01496.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2419+1127C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136215073 | |||||||
| chr5:136215137 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2419+1063C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136215137 | |||||||
| chr5:136215367 | G | A | 3 | a0001c0002t0002g0216 a0001c0002t0002g0218 a0001c0002t0002g0219 |
3 | HG00741.hp2 HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2419+833C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136215367 | |||||||
| chr5:136215425 | C | G | 1 | a0001c0002t0002g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2419+775G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136215425 | |||||||
| chr5:136215492 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0171 others(4): Show |
8 | HG01884.hp1 HG02615.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.2419+708C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136215492 | |||||||
| chr5:136215548 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0075 |
3 | HG03130.hp2 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2419+652G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136215548 | |||||||
| chr5:136215558 | C | A | 6 | a0001c0002t0002g0236 a0001c0002t0004g0205 a0001c0002t0004g0206 others(3): Show |
6 | HG03130.hp1 NA18522.hp1 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.2419+642G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136215558 | |||||||
| chr5:136215598 | G | A | 3 | a0001c0001t0001g0134 a0001c0001t0001g0161 a0001c0002t0002g0244 |
3 | HG01261.hp2 HG01952.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.2419+602C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136215598 | |||||||
| chr5:136215769 | G | C | 3 | a0001c0002t0004g0205 a0001c0002t0004g0206 a0001c0002t0004g0207 |
3 | NA18940.hp2 NA19056.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.2419+431C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136215769 | |||||||
| chr5:136215822 | C | CA | 147 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(144): Show |
148 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.2419+377dupT | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136215822 | |||||||
| chr5:136215822 | C | CAA | 6 | a0001c0001t0001g0004 a0001c0001t0001g0075 a0001c0001t0001g0163 others(3): Show |
7 | HG02886.hp2 HG02970.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2419+376_2419+377d others(4): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136215822 | |||||||
| chr5:136215860 | A | G | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0236 others(6): Show |
9 | HG02572.hp1 HG03130.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.2419+340T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136215860 | |||||||
| chr5:136215924 | A | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0051 others(6): Show |
10 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.2419+276T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136215924 | |||||||
| chr5:136216156 | GTGT | G | 9 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0051 others(6): Show |
10 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.2419+41_2419+43del others(3): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 11/11 | chr5 | 136216156 | |||||||
| chr5:136216305 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2344-30G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136216305 | |||||||
| chr5:136216370 | C | T | 2 | a0001c0002t0003g0246 a0001c0002t0003g0248 |
2 | HG00621.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.2344-95G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136216370 | |||||||
| chr5:136216396 | G | T | 1 | a0001c0001t0001g0068 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2344-121C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136216396 | |||||||
| chr5:136216535 | C | A | 1 | a0002c0004t0001g0175 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2344-260G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136216535 | |||||||
| chr5:136216584 | A | ATACTGGA others(6): Show |
135 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(132): Show |
137 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.2344-310_2344-309i others(15): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136216584 | |||||||
| chr5:136216868 | A | G | 1 | a0001c0008t0007g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2344-593T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136216868 | |||||||
| chr5:136216974 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2344-699C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136216974 | |||||||
| chr5:136217018 | T | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | NA19057.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.2344-743A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136217018 | |||||||
| chr5:136217202 | C | T | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2344-927G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136217202 | |||||||
| chr5:136217341 | T | C | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0236 others(6): Show |
9 | HG02572.hp1 HG03130.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.2344-1066A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136217341 | |||||||
| chr5:136217662 | C | T | 1 | a0001c0002t0002g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2344-1387G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136217662 | |||||||
| chr5:136217663 | G | A | 1 | a0001c0002t0002g0208 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2344-1388C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136217663 | |||||||
| chr5:136218017 | CA | C | 12 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0129 others(9): Show |
12 | HG02015.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.2344-1743delT | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136218017 | |||||||
| chr5:136218056 | A | AATATATA others(29): Show |
1 | a0001c0001t0001g0059 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2344-1817_2344-178 others(40): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136218056 | |||||||
| chr5:136218135 | A | G | 2 | a0001c0001t0001g0021 a0001c0002t0002g0204 |
2 | HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2344-1860T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136218135 | |||||||
| chr5:136218325 | A | T | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0236 others(6): Show |
9 | HG02572.hp1 HG03130.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.2344-2050T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136218325 | |||||||
| chr5:136218499 | A | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | NA19057.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.2344-2224T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136218499 | |||||||
| chr5:136218508 | G | A | 1 | a0002c0004t0001g0175 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2344-2233C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136218508 | |||||||
| chr5:136219028 | G | T | 98 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.2344-2753C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136219028 | |||||||
| chr5:136219090 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0051 others(6): Show |
10 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.2344-2815C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136219090 | |||||||
| chr5:136219220 | A | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2344-2945T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136219220 | |||||||
| chr5:136219242 | G | C | 2 | a0001c0002t0002g0209 a0003c0006t0001g0026 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2344-2967C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136219242 | |||||||
| chr5:136219402 | C | T | 2 | a0001c0002t0005g0025 a0001c0002t0005g0028 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2344-3127G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136219402 | |||||||
| chr5:136219820 | T | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0024 others(5): Show |
9 | HG01069.hp2 HG01071.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2344-3545A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136219820 | |||||||
| chr5:136219923 | G | A | 1 | a0001c0002t0002g0212 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2344-3648C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136219923 | |||||||
| chr5:136219935 | G | C | 6 | a0001c0002t0002g0236 a0001c0002t0004g0205 a0001c0002t0004g0206 others(3): Show |
6 | HG03130.hp1 NA18522.hp1 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.2344-3660C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136219935 | |||||||
| chr5:136219936 | C | T | 4 | a0001c0002t0002g0196 a0001c0002t0004g0205 a0001c0002t0004g0206 others(1): Show |
4 | HG02486.hp1 NA18940.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.2344-3661G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136219936 | |||||||
| chr5:136219967 | G | A | 98 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.2344-3692C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136219967 | |||||||
| chr5:136219983 | G | C | 1 | a0001c0002t0002g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2344-3708C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136219983 | |||||||
| chr5:136220163 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2344-3888C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136220163 | |||||||
| chr5:136220280 | G | C | 113 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(110): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.2344-4005C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136220280 | |||||||
| chr5:136220402 | T | G | 1 | a0001c0001t0001g0118 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2344-4127A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136220402 | |||||||
| chr5:136220500 | T | A | 1 | a0001c0002t0002g0253 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2344-4225A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136220500 | |||||||
| chr5:136220500 | T | G | 6 | a0001c0001t0001g0007 a0001c0001t0001g0078 a0001c0001t0001g0094 others(3): Show |
6 | HG02135.hp1 NA18955.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.2344-4225A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136220500 | |||||||
| chr5:136220563 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2344-4288C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136220563 | |||||||
| chr5:136220645 | TTTTGCCC others(19): Show |
T | 1 | a0001c0001t0001g0122 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2344-4396_2344-437 others(30): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136220645 | |||||||
| chr5:136220683 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0105 |
2 | NA18942.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.2344-4408G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136220683 | |||||||
| chr5:136220737 | A | G | 2 | a0001c0002t0005g0025 a0001c0002t0005g0028 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2344-4462T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136220737 | |||||||
| chr5:136220861 | G | A | 31 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0037 others(28): Show |
31 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.2343+4413C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136220861 | |||||||
| chr5:136221107 | A | ATG | 3 | a0001c0002t0004g0205 a0001c0002t0004g0206 a0001c0002t0004g0207 |
3 | NA18940.hp2 NA19056.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.2343+4165_2343+416 others(6): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136221107 | |||||||
| chr5:136221113 | C | CTG | 118 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(115): Show |
119 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.2343+4159_2343+416 others(6): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136221113 | |||||||
| chr5:136221113 | C | CTGTG | 3 | a0001c0001t0001g0030 a0001c0001t0001g0100 a0001c0002t0002g0203 |
3 | HG00099.hp2 HG03209.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.2343+4157_2343+416 others(8): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136221113 | |||||||
| chr5:136221113 | C | G | 4 | a0001c0002t0002g0236 a0001c0002t0004g0205 a0001c0002t0004g0206 others(1): Show |
4 | NA18940.hp2 NA19030.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.2343+4161G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136221113 | |||||||
| chr5:136221113 | CTG | C | 5 | a0001c0001t0001g0023 a0001c0001t0001g0130 a0001c0001t0001g0140 others(2): Show |
5 | HG00408.hp1 HG01071.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.2343+4159_2343+416 others(6): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136221113 | |||||||
| chr5:136221379 | A | G | 3 | a0001c0001t0001g0034 a0001c0002t0002g0230 a0001c0002t0002g0231 |
3 | HG01496.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2343+3895T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136221379 | |||||||
| chr5:136221664 | A | C | 12 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0053 others(9): Show |
12 | HG00609.hp2 NA18944.hp2 NA18983.hp1 others(9): Show |
intron_variant | MODIFIER | c.2343+3610T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136221664 | |||||||
| chr5:136221743 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2343+3531A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136221743 | |||||||
| chr5:136221769 | G | A | 1 | a0002c0004t0001g0175 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2343+3505C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136221769 | |||||||
| chr5:136221906 | C | T | 1 | a0001c0002t0002g0201 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2343+3368G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136221906 | |||||||
| chr5:136222018 | G | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0171 others(4): Show |
8 | HG01884.hp1 HG02615.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.2343+3256C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136222018 | |||||||
| chr5:136222049 | T | C | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2343+3225A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136222049 | |||||||
| chr5:136222156 | GA | G | 29 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0031 others(26): Show |
30 | HG00733.hp1 HG01069.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.2343+3117delT | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136222156 | |||||||
| chr5:136222283 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2343+2991G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136222283 | |||||||
| chr5:136222424 | G | A | 2 | a0001c0002t0005g0025 a0001c0002t0005g0028 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2343+2850C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136222424 | |||||||
| chr5:136222539 | A | G | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0236 others(6): Show |
9 | HG02572.hp1 HG03130.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.2343+2735T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136222539 | |||||||
| chr5:136222772 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2343+2502C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136222772 | |||||||
| chr5:136222777 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2343+2497C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136222777 | |||||||
| chr5:136222783 | G | A | 1 | a0001c0002t0002g0228 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2343+2491C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136222783 | |||||||
| chr5:136222904 | G | A | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0236 others(6): Show |
9 | HG02572.hp1 HG03130.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.2343+2370C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136222904 | |||||||
| chr5:136222915 | G | A | 1 | a0002c0004t0001g0175 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2343+2359C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136222915 | |||||||
| chr5:136223345 | G | T | 1 | a0001c0002t0001g0027 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2343+1929C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136223345 | |||||||
| chr5:136223352 | G | T | 4 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
4 | HG00735.hp1 HG01981.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.2343+1922C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136223352 | |||||||
| chr5:136223364 | A | G | 2 | a0001c0002t0002g0210 a0001c0002t0002g0215 |
2 | HG00408.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.2343+1910T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136223364 | |||||||
| chr5:136223412 | G | C | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0236 others(6): Show |
9 | HG02572.hp1 HG03130.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.2343+1862C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136223412 | |||||||
| chr5:136223557 | G | A | 1 | a0001c0002t0002g0245 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2343+1717C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136223557 | |||||||
| chr5:136223921 | C | T | 1 | a0001c0002t0002g0185 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2343+1353G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136223921 | |||||||
| chr5:136223957 | G | A | 11 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0072 others(8): Show |
11 | HG00733.hp1 HG01099.hp1 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.2343+1317C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136223957 | |||||||
| chr5:136224245 | G | A | 1 | a0001c0002t0002g0243 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2343+1029C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136224245 | |||||||
| chr5:136224304 | G | A | 1 | a0002c0004t0001g0175 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2343+970C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136224304 | |||||||
| chr5:136224332 | G | C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0157 |
2 | HG00408.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.2343+942C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136224332 | |||||||
| chr5:136224566 | G | T | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.2343+708C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136224566 | |||||||
| chr5:136224715 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2343+559G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136224715 | |||||||
| chr5:136224896 | C | G | 6 | a0001c0002t0002g0236 a0001c0002t0004g0205 a0001c0002t0004g0206 others(3): Show |
6 | HG03130.hp1 NA18522.hp1 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.2343+378G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136224896 | |||||||
| chr5:136225152 | T | G | 1 | a0001c0008t0007g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2343+122A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 10/11 | chr5 | 136225152 | |||||||
| chr5:136225370 | A | G | 10 | a0001c0001t0001g0031 a0001c0001t0001g0072 a0001c0001t0001g0073 others(7): Show |
10 | HG00733.hp1 HG01099.hp1 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.2263-16T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 9/11 | chr5 | 136225370 | |||||||
| chr5:136225445 | C | T | 98 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.2263-91G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 9/11 | chr5 | 136225445 | |||||||
| chr5:136225530 | G | GCTCTGTA others(303): Show |
7 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0171 others(4): Show |
8 | HG01884.hp1 HG02615.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.2263-177_2263-176i others(312): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 9/11 | chr5 | 136225530 | |||||||
| chr5:136225610 | C | A | 1 | a0001c0002t0002g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2263-256G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 9/11 | chr5 | 136225610 | |||||||
| chr5:136225655 | C | T | 1 | a0001c0002t0002g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2263-301G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 9/11 | chr5 | 136225655 | |||||||
| chr5:136225727 | G | C | 1 | a0001c0002t0002g0203 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2262+307C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 9/11 | chr5 | 136225727 | |||||||
| chr5:136225867 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2262+167C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 9/11 | chr5 | 136225867 | |||||||
| chr5:136225934 | CATGGGGT others(16): Show |
C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2262+77_2262+99del others(23): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 9/11 | chr5 | 136225934 | |||||||
| chr5:136225996 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2262+38C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 9/11 | chr5 | 136225996 | |||||||
| chr5:136226501 | C | T | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.2041-246G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136226501 | |||||||
| chr5:136226558 | G | T | 1 | a0001c0002t0002g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2041-303C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136226558 | |||||||
| chr5:136226626 | G | T | 113 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(110): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.2041-371C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136226626 | |||||||
| chr5:136226756 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2041-501A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136226756 | |||||||
| chr5:136226857 | G | A | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0002t0001g0029 |
3 | HG02109.hp1 HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2041-602C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136226857 | |||||||
| chr5:136226987 | G | A | 1 | a0001c0002t0004g0207 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2041-732C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136226987 | |||||||
| chr5:136227462 | G | A | 1 | a0002c0004t0001g0175 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2041-1207C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136227462 | |||||||
| chr5:136227698 | G | C | 1 | a0001c0008t0007g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2041-1443C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136227698 | |||||||
| chr5:136227792 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2041-1537C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136227792 | |||||||
| chr5:136228310 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2041-2055A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136228310 | |||||||
| chr5:136228436 | C | CT | 118 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(115): Show |
119 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.2041-2182dupA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136228436 | |||||||
| chr5:136228436 | C | CTT | 6 | a0001c0001t0001g0057 a0001c0001t0001g0061 a0001c0001t0001g0177 others(3): Show |
6 | HG01496.hp1 HG03579.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.2041-2183_2041-218 others(6): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136228436 | |||||||
| chr5:136228436 | CT | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(2): Show |
6 | HG01069.hp2 HG01071.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2041-2182delA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136228436 | |||||||
| chr5:136228574 | A | G | 2 | a0001c0002t0005g0025 a0001c0002t0005g0028 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2041-2319T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136228574 | |||||||
| chr5:136228602 | G | C | 7 | a0001c0002t0002g0236 a0001c0002t0004g0205 a0001c0002t0004g0206 others(4): Show |
7 | HG03130.hp1 HG03579.hp2 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.2041-2347C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136228602 | |||||||
| chr5:136228635 | G | A | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0236 others(6): Show |
9 | HG02572.hp1 HG03130.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.2041-2380C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136228635 | |||||||
| chr5:136228664 | G | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02257.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.2041-2409C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136228664 | |||||||
| chr5:136228837 | G | A | 3 | a0001c0002t0004g0205 a0001c0002t0004g0206 a0001c0002t0004g0207 |
3 | NA18940.hp2 NA19056.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.2040+2517C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136228837 | |||||||
| chr5:136228860 | C | T | 3 | a0001c0001t0001g0104 a0001c0002t0002g0222 a0001c0002t0002g0223 |
3 | NA18966.hp1 NA19007.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.2040+2494G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136228860 | |||||||
| chr5:136228875 | G | A | 2 | a0001c0002t0002g0209 a0003c0006t0001g0026 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2040+2479C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136228875 | |||||||
| chr5:136229049 | G | A | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0236 others(6): Show |
9 | HG02572.hp1 HG03130.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.2040+2305C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136229049 | |||||||
| chr5:136229104 | A | G | 1 | a0001c0002t0003g0238 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2040+2250T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136229104 | |||||||
| chr5:136229136 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2040+2218C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136229136 | |||||||
| chr5:136229358 | G | C | 3 | a0001c0002t0004g0205 a0001c0002t0004g0206 a0001c0002t0004g0207 |
3 | NA18940.hp2 NA19056.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.2040+1996C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136229358 | |||||||
| chr5:136229402 | G | T | 2 | a0001c0002t0002g0209 a0003c0006t0001g0026 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2040+1952C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136229402 | |||||||
| chr5:136229539 | G | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG03669.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2040+1815C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136229539 | |||||||
| chr5:136229727 | A | C | 1 | a0001c0001t0001g0176 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2040+1627T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136229727 | |||||||
| chr5:136229818 | GGTGCACC others(11): Show |
G | 1 | a0001c0001t0001g0061 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2040+1518_2040+153 others(22): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136229818 | |||||||
| chr5:136229824 | C | A | 3 | a0001c0002t0004g0205 a0001c0002t0004g0206 a0001c0002t0004g0207 |
3 | NA18940.hp2 NA19056.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.2040+1530G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136229824 | |||||||
| chr5:136229854 | T | TTC | 10 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0001g0027 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.2040+1498_2040+149 others(6): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136229854 | |||||||
| chr5:136230183 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2040+1171A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136230183 | |||||||
| chr5:136230341 | C | T | 1 | a0001c0002t0002g0225 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2040+1013G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136230341 | |||||||
| chr5:136230467 | A | G | 1 | a0001c0001t0001g0003 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2040+887T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136230467 | |||||||
| chr5:136230584 | C | A | 1 | a0001c0001t0001g0111 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2040+770G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136230584 | |||||||
| chr5:136230704 | A | G | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0236 others(6): Show |
9 | HG02572.hp1 HG03130.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.2040+650T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136230704 | |||||||
| chr5:136230740 | C | T | 4 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(1): Show |
4 | HG01952.hp2 HG03834.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.2040+614G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136230740 | |||||||
| chr5:136230794 | C | T | 2 | a0001c0002t0002g0192 a0001c0002t0002g0193 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.2040+560G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136230794 | |||||||
| chr5:136230962 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2040+392G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136230962 | |||||||
| chr5:136231023 | G | A | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0176 others(4): Show |
7 | HG00673.hp2 HG02040.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2040+331C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136231023 | |||||||
| chr5:136231314 | A | C | 1 | a0001c0001t0001g0144 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2040+40T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 8/11 | chr5 | 136231314 | |||||||
| chr5:136231760 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0051 others(6): Show |
10 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1845-211C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136231760 | |||||||
| chr5:136232062 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1845-513A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136232062 | |||||||
| chr5:136232076 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1845-527A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136232076 | |||||||
| chr5:136232726 | A | G | 5 | a0001c0002t0002g0236 a0001c0002t0004g0205 a0001c0002t0004g0206 others(2): Show |
5 | HG03579.hp2 NA18940.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1845-1177T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136232726 | |||||||
| chr5:136232780 | C | T | 3 | a0001c0002t0004g0205 a0001c0002t0004g0206 a0001c0002t0004g0207 |
3 | NA18940.hp2 NA19056.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1845-1231G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136232780 | |||||||
| chr5:136232863 | CT | C | 5 | a0001c0001t0001g0020 a0001c0002t0001g0027 a0001c0002t0002g0233 others(2): Show |
5 | HG01258.hp1 HG02280.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1845-1315delA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136232863 | |||||||
| chr5:136232875 | C | T | 2 | a0001c0002t0005g0025 a0001c0002t0005g0028 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1845-1326G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136232875 | |||||||
| chr5:136233000 | C | T | 1 | a0001c0002t0002g0195 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1845-1451G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136233000 | |||||||
| chr5:136233051 | C | T | 2 | a0001c0002t0002g0236 a0001c0008t0007g0006 |
2 | HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1845-1502G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136233051 | |||||||
| chr5:136233053 | C | T | 2 | a0001c0002t0002g0233 a0001c0002t0002g0234 |
2 | HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1845-1504G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136233053 | |||||||
| chr5:136233103 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1845-1554A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136233103 | |||||||
| chr5:136233345 | G | C | 3 | a0001c0002t0004g0205 a0001c0002t0004g0206 a0001c0002t0004g0207 |
3 | NA18940.hp2 NA19056.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1845-1796C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136233345 | |||||||
| chr5:136233530 | G | A | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0236 others(6): Show |
9 | HG02572.hp1 HG03130.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.1845-1981C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136233530 | |||||||
| chr5:136233672 | G | C | 3 | a0001c0002t0004g0205 a0001c0002t0004g0206 a0001c0002t0004g0207 |
3 | NA18940.hp2 NA19056.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1845-2123C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136233672 | |||||||
| chr5:136233776 | C | T | 99 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(96): Show |
100 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.1845-2227G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136233776 | |||||||
| chr5:136233817 | T | C | 2 | a0001c0002t0005g0025 a0001c0002t0005g0028 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1845-2268A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136233817 | |||||||
| chr5:136233864 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1845-2315T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136233864 | |||||||
| chr5:136234050 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1845-2501T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136234050 | |||||||
| chr5:136234060 | G | A | 1 | a0001c0008t0007g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1845-2511C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136234060 | |||||||
| chr5:136234092 | T | C | 15 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0053 others(12): Show |
15 | HG00558.hp1 HG00609.hp2 NA18944.hp2 others(12): Show |
intron_variant | MODIFIER | c.1845-2543A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136234092 | |||||||
| chr5:136234106 | T | G | 1 | a0001c0001t0001g0082 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1845-2557A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136234106 | |||||||
| chr5:136234267 | G | A | 2 | a0001c0002t0002g0236 a0001c0008t0007g0006 |
2 | HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1845-2718C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136234267 | |||||||
| chr5:136234391 | C | T | 15 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0053 others(12): Show |
15 | HG00558.hp1 HG00609.hp2 NA18944.hp2 others(12): Show |
intron_variant | MODIFIER | c.1845-2842G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136234391 | |||||||
| chr5:136234407 | T | C | 2 | a0001c0001t0001g0177 a0001c0001t0001g0180 |
2 | NA18954.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1845-2858A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136234407 | |||||||
| chr5:136234459 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1845-2910C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136234459 | |||||||
| chr5:136234824 | A | G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0051 others(8): Show |
12 | HG01496.hp1 HG01884.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1845-3275T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136234824 | |||||||
| chr5:136234833 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1845-3284A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136234833 | |||||||
| chr5:136234879 | A | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(164): Show |
170 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.1845-3330T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136234879 | |||||||
| chr5:136235210 | T | A | 1 | a0001c0001t0001g0122 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1845-3661A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136235210 | |||||||
| chr5:136235299 | T | G | 114 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(111): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1845-3750A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136235299 | |||||||
| chr5:136235330 | C | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
169 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.1845-3781G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136235330 | |||||||
| chr5:136235423 | G | A | 1 | a0001c0002t0002g0223 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1845-3874C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136235423 | |||||||
| chr5:136235442 | A | G | 2 | a0001c0002t0002g0209 a0003c0006t0001g0026 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1845-3893T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136235442 | |||||||
| chr5:136235530 | T | C | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0236 others(6): Show |
9 | HG02572.hp1 HG03130.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.1845-3981A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136235530 | |||||||
| chr5:136235567 | T | C | 1 | a0001c0002t0002g0196 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1845-4018A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136235567 | |||||||
| chr5:136235968 | G | T | 1 | a0001c0001t0001g0033 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1845-4419C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136235968 | |||||||
| chr5:136235970 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(160): Show |
166 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1845-4421A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136235970 | |||||||
| chr5:136235985 | T | A | 1 | a0001c0001t0001g0153 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1845-4436A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136235985 | |||||||
| chr5:136236240 | G | GT | 5 | a0001c0001t0001g0007 a0001c0001t0001g0094 a0001c0001t0001g0097 others(2): Show |
5 | NA18955.hp2 NA18959.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.1845-4692dupA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136236240 | |||||||
| chr5:136236321 | T | C | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0236 others(6): Show |
9 | HG02572.hp1 HG03130.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.1845-4772A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136236321 | |||||||
| chr5:136236470 | C | A | 1 | a0001c0002t0005g0028 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1845-4921G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136236470 | |||||||
| chr5:136236653 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1845-5104C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136236653 | |||||||
| chr5:136236748 | G | A | 1 | a0001c0008t0007g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1845-5199C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136236748 | |||||||
| chr5:136237108 | C | T | 2 | a0001c0002t0005g0025 a0001c0002t0005g0028 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1845-5559G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136237108 | |||||||
| chr5:136237222 | C | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(164): Show |
170 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.1845-5673G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136237222 | |||||||
| chr5:136237738 | C | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0108 |
2 | HG00733.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1845-6189G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136237738 | |||||||
| chr5:136237769 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1845-6220G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136237769 | |||||||
| chr5:136237824 | T | C | 10 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0236 others(7): Show |
10 | HG02572.hp1 HG02809.hp2 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.1845-6275A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136237824 | |||||||
| chr5:136237892 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1845-6343T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136237892 | |||||||
| chr5:136237987 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1845-6438A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136237987 | |||||||
| chr5:136237990 | T | G | 1 | a0001c0001t0001g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1845-6441A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136237990 | |||||||
| chr5:136237991 | C | A | 1 | a0001c0001t0001g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1845-6442G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136237991 | |||||||
| chr5:136237992 | C | G | 1 | a0001c0001t0001g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1845-6443G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136237992 | |||||||
| chr5:136237993 | C | G | 1 | a0001c0001t0001g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1845-6444G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136237993 | |||||||
| chr5:136238081 | T | C | 10 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0236 others(7): Show |
10 | HG02572.hp1 HG02809.hp2 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.1845-6532A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136238081 | |||||||
| chr5:136238283 | C | T | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1845-6734G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136238283 | |||||||
| chr5:136238380 | G | A | 3 | a0001c0002t0004g0205 a0001c0002t0004g0206 a0001c0002t0004g0207 |
3 | NA18940.hp2 NA19056.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1845-6831C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136238380 | |||||||
| chr5:136238423 | C | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
162 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.1845-6874G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136238423 | |||||||
| chr5:136238601 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1845-7052T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136238601 | |||||||
| chr5:136238621 | CT | C | 114 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(111): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1845-7073delA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136238621 | |||||||
| chr5:136238652 | A | G | 3 | a0001c0002t0004g0205 a0001c0002t0004g0206 a0001c0002t0004g0207 |
3 | NA18940.hp2 NA19056.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1845-7103T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136238652 | |||||||
| chr5:136238689 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1845-7140A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136238689 | |||||||
| chr5:136238761 | A | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02559.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1845-7212T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136238761 | |||||||
| chr5:136238979 | C | T | 3 | a0001c0001t0001g0010 a0001c0002t0002g0213 a0001c0002t0002g0217 |
3 | HG02129.hp1 NA18969.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1845-7430G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136238979 | |||||||
| chr5:136239121 | C | T | 7 | a0001c0002t0002g0236 a0001c0002t0004g0205 a0001c0002t0004g0206 others(4): Show |
7 | HG03130.hp1 HG03579.hp2 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.1845-7572G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136239121 | |||||||
| chr5:136239287 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1845-7738C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136239287 | |||||||
| chr5:136239599 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1844+7872C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136239599 | |||||||
| chr5:136239606 | A | G | 137 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(134): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1844+7865T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136239606 | |||||||
| chr5:136240141 | C | A | 23 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(20): Show |
24 | HG00733.hp1 HG01069.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1844+7330G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136240141 | |||||||
| chr5:136240339 | G | T | 10 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0236 others(7): Show |
10 | HG02572.hp1 HG02809.hp2 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.1844+7132C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136240339 | |||||||
| chr5:136240554 | T | C | 1 | a0002c0004t0001g0175 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1844+6917A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136240554 | |||||||
| chr5:136240567 | C | A | 1 | a0001c0001t0001g0081 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1844+6904G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136240567 | |||||||
| chr5:136240923 | T | C | 1 | a0001c0008t0007g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1844+6548A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136240923 | |||||||
| chr5:136240967 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1844+6504A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136240967 | |||||||
| chr5:136241000 | G | T | 114 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(111): Show |
115 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1844+6471C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136241000 | |||||||
| chr5:136241150 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0171 others(4): Show |
8 | HG01884.hp1 HG02615.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1844+6321G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136241150 | |||||||
| chr5:136241226 | T | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1844+6245A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136241226 | |||||||
| chr5:136241348 | A | G | 6 | a0001c0001t0001g0139 a0001c0001t0001g0146 a0001c0001t0001g0165 others(3): Show |
6 | HG00741.hp1 HG01109.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1844+6123T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136241348 | |||||||
| chr5:136241355 | A | T | 3 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 |
3 | HG01496.hp1 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1844+6116T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136241355 | |||||||
| chr5:136241409 | G | A | 7 | a0001c0002t0002g0236 a0001c0002t0004g0205 a0001c0002t0004g0206 others(4): Show |
7 | HG03130.hp1 HG03579.hp2 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.1844+6062C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136241409 | |||||||
| chr5:136241504 | A | G | 1 | a0001c0002t0002g0222 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1844+5967T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136241504 | |||||||
| chr5:136241562 | CT | C | 7 | a0001c0001t0001g0139 a0001c0001t0001g0146 a0001c0001t0001g0154 others(4): Show |
7 | HG00423.hp1 HG00741.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1844+5908delA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136241562 | |||||||
| chr5:136241644 | C | G | 1 | a0001c0001t0001g0184 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1844+5827G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136241644 | |||||||
| chr5:136241736 | A | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0002c0004t0001g0175 |
3 | HG02572.hp1 HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1844+5735T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136241736 | |||||||
| chr5:136242197 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1844+5274G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136242197 | |||||||
| chr5:136242211 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1844+5260T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136242211 | |||||||
| chr5:136242263 | C | A | 1 | a0001c0001t0001g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1844+5208G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136242263 | |||||||
| chr5:136242276 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1844+5195G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136242276 | |||||||
| chr5:136242305 | G | A | 1 | a0001c0002t0002g0212 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1844+5166C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136242305 | |||||||
| chr5:136242508 | G | C | 1 | a0001c0002t0002g0209 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1844+4963C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136242508 | |||||||
| chr5:136242986 | G | A | 23 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(20): Show |
24 | HG00733.hp1 HG01069.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1844+4485C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136242986 | |||||||
| chr5:136243192 | G | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1844+4279C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136243192 | |||||||
| chr5:136243332 | G | C | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0236 others(6): Show |
9 | HG02572.hp1 HG03130.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.1844+4139C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136243332 | |||||||
| chr5:136243364 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1844+4107G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136243364 | |||||||
| chr5:136243413 | G | A | 5 | a0001c0001t0001g0020 a0001c0002t0001g0027 a0001c0002t0002g0233 others(2): Show |
5 | HG01258.hp1 HG02280.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1844+4058C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136243413 | |||||||
| chr5:136243435 | A | C | 1 | a0001c0002t0002g0216 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1844+4036T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136243435 | |||||||
| chr5:136243644 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1844+3827G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136243644 | |||||||
| chr5:136243668 | C | CT | 5 | a0001c0001t0001g0053 a0001c0001t0001g0117 a0001c0001t0001g0119 others(2): Show |
5 | HG04115.hp2 NA18978.hp2 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.1844+3802dupA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136243668 | |||||||
| chr5:136243716 | A | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(41): Show |
46 | HG00733.hp1 HG01069.hp1 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.1844+3755T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136243716 | |||||||
| chr5:136243734 | G | A | 116 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): Show |
117 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.1844+3737C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136243734 | |||||||
| chr5:136243893 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1844+3578G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136243893 | |||||||
| chr5:136244095 | G | A | 1 | a0001c0001t0001g0008 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1844+3376C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136244095 | |||||||
| chr5:136244268 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1844+3203C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136244268 | |||||||
| chr5:136244434 | G | C | 6 | a0001c0002t0002g0230 a0001c0002t0002g0231 a0001c0002t0004g0205 others(3): Show |
6 | HG01496.hp1 HG03579.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1844+3037C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136244434 | |||||||
| chr5:136244627 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0075 |
3 | HG03130.hp2 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1844+2844C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136244627 | |||||||
| chr5:136244633 | T | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1844+2838A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136244633 | |||||||
| chr5:136244775 | T | C | 1 | a0001c0008t0007g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1844+2696A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136244775 | |||||||
| chr5:136244902 | G | C | 2 | a0001c0002t0004g0205 a0001c0002t0004g0206 |
2 | NA18940.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1844+2569C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136244902 | |||||||
| chr5:136245030 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1844+2441C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136245030 | |||||||
| chr5:136245194 | A | G | 2 | a0001c0002t0002g0230 a0001c0002t0002g0231 |
2 | HG01496.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1844+2277T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136245194 | |||||||
| chr5:136245383 | G | A | 8 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(5): Show |
8 | HG02280.hp2 HG02572.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1844+2088C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136245383 | |||||||
| chr5:136245540 | A | C | 19 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0032 others(16): Show |
20 | HG01496.hp1 HG01884.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1844+1931T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136245540 | |||||||
| chr5:136245861 | C | T | 2 | a0001c0002t0005g0025 a0001c0002t0005g0028 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1844+1610G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136245861 | |||||||
| chr5:136245905 | G | A | 22 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0032 others(19): Show |
23 | HG01496.hp1 HG01884.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1844+1566C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136245905 | |||||||
| chr5:136245971 | G | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(19): Show |
23 | HG00733.hp1 HG01069.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.1844+1500C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136245971 | |||||||
| chr5:136246079 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1844+1392A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136246079 | |||||||
| chr5:136246095 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1844+1376C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136246095 | |||||||
| chr5:136246264 | G | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1844+1207C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136246264 | |||||||
| chr5:136246284 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1844+1187T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136246284 | |||||||
| chr5:136246401 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1844+1070G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136246401 | |||||||
| chr5:136246438 | A | T | 18 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0032 others(15): Show |
19 | HG01496.hp1 HG01884.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.1844+1033T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136246438 | |||||||
| chr5:136246455 | A | G | 18 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0032 others(15): Show |
19 | HG01496.hp1 HG01884.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.1844+1016T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136246455 | |||||||
| chr5:136246525 | A | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0183 |
3 | HG02717.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1844+946T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136246525 | |||||||
| chr5:136246541 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1844+930C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136246541 | |||||||
| chr5:136246754 | C | T | 22 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0032 others(19): Show |
23 | HG01496.hp1 HG01884.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1844+717G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136246754 | |||||||
| chr5:136246762 | G | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1844+709C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136246762 | |||||||
| chr5:136246778 | C | T | 18 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0032 others(15): Show |
19 | HG01496.hp1 HG01884.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.1844+693G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136246778 | |||||||
| chr5:136246789 | A | AT | 26 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0031 others(23): Show |
27 | HG00733.hp1 HG01099.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.1844+681dupA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136246789 | |||||||
| chr5:136246796 | T | C | 1 | a0001c0001t0001g0055 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1844+675A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136246796 | |||||||
| chr5:136246843 | C | G | 18 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0032 others(15): Show |
19 | HG01496.hp1 HG01884.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.1844+628G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136246843 | |||||||
| chr5:136246967 | C | G | 1 | a0001c0002t0002g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1844+504G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136246967 | |||||||
| chr5:136247026 | TACC | T | 18 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0032 others(15): Show |
19 | HG01496.hp1 HG01884.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.1844+442_1844+444d others(5): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136247026 | |||||||
| chr5:136247224 | A | AT | 123 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(120): Show |
124 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1844+246dupA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136247224 | |||||||
| chr5:136247224 | AT | A | 18 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0032 others(15): Show |
19 | HG01496.hp1 HG01884.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.1844+246delA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136247224 | |||||||
| chr5:136247330 | A | C | 1 | a0002c0004t0001g0175 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1844+141T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 7/11 | chr5 | 136247330 | |||||||
| chr5:136247764 | G | A | 18 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0032 others(15): Show |
19 | HG01496.hp1 HG01884.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.1580-29C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136247764 | |||||||
| chr5:136247890 | T | G | 3 | a0001c0001t0001g0022 a0001c0002t0002g0209 a0003c0006t0001g0026 |
3 | HG02257.hp2 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1580-155A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136247890 | |||||||
| chr5:136247891 | C | A | 1 | a0001c0002t0002g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1580-156G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136247891 | |||||||
| chr5:136248001 | C | G | 1 | a0001c0002t0002g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1580-266G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136248001 | |||||||
| chr5:136248029 | CG | C | 18 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0032 others(15): Show |
19 | HG01496.hp1 HG01884.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.1580-295delC | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136248029 | |||||||
| chr5:136248181 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1580-446G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136248181 | |||||||
| chr5:136248224 | C | T | 39 | a0001c0001t0001g0010 a0001c0001t0001g0037 a0001c0001t0001g0047 others(36): Show |
39 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1580-489G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136248224 | |||||||
| chr5:136248557 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1580-822C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136248557 | |||||||
| chr5:136248808 | C | T | 2 | a0001c0002t0005g0025 a0001c0002t0005g0028 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1580-1073G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136248808 | |||||||
| chr5:136248879 | C | G | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1580-1144G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136248879 | |||||||
| chr5:136249199 | G | A | 3 | a0001c0002t0002g0236 a0001c0002t0005g0025 a0001c0002t0005g0028 |
3 | HG03130.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1580-1464C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136249199 | |||||||
| chr5:136249280 | A | G | 1 | a0001c0002t0002g0247 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1580-1545T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136249280 | |||||||
| chr5:136249345 | T | C | 5 | a0001c0001t0001g0020 a0001c0002t0001g0027 a0001c0002t0002g0233 others(2): Show |
5 | HG01258.hp1 HG02280.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1580-1610A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136249345 | |||||||
| chr5:136249408 | A | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0034 a0001c0002t0002g0230 others(4): Show |
7 | HG01496.hp1 HG03195.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1580-1673T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136249408 | |||||||
| chr5:136249549 | C | T | 2 | a0001c0002t0002g0209 a0003c0006t0001g0026 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1580-1814G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136249549 | |||||||
| chr5:136249550 | G | A | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1580-1815C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136249550 | |||||||
| chr5:136249615 | A | G | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1580-1880T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136249615 | |||||||
| chr5:136249706 | T | C | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1579+1943A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136249706 | |||||||
| chr5:136249734 | G | A | 4 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0204 others(1): Show |
4 | HG02280.hp2 HG02572.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1579+1915C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136249734 | |||||||
| chr5:136249754 | T | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0083 |
2 | HG01496.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1579+1895A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136249754 | |||||||
| chr5:136249762 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1579+1887A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136249762 | |||||||
| chr5:136249765 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1579+1884G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136249765 | |||||||
| chr5:136249766 | C | T | 2 | a0001c0002t0002g0209 a0003c0006t0001g0026 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1579+1883G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136249766 | |||||||
| chr5:136249803 | T | G | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1579+1846A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136249803 | |||||||
| chr5:136249832 | G | A | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1579+1817C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136249832 | |||||||
| chr5:136249838 | A | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0171 others(4): Show |
8 | HG01884.hp1 HG02615.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1579+1811T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136249838 | |||||||
| chr5:136249930 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1579+1719G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136249930 | |||||||
| chr5:136249964 | T | C | 5 | a0001c0002t0002g0230 a0001c0002t0002g0231 a0001c0002t0004g0205 others(2): Show |
5 | HG01496.hp1 HG03579.hp1 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.1579+1685A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136249964 | |||||||
| chr5:136250063 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1579+1586T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136250063 | |||||||
| chr5:136250104 | T | TG | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1579+1544_1579+154 others(5): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136250104 | |||||||
| chr5:136250414 | T | C | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1579+1235A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136250414 | |||||||
| chr5:136250470 | T | C | 1 | a0001c0002t0002g0214 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1579+1179A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136250470 | |||||||
| chr5:136250488 | T | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0132 others(2): Show |
5 | HG00423.hp1 NA18959.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.1579+1161A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136250488 | |||||||
| chr5:136250608 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1579+1041T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136250608 | |||||||
| chr5:136250713 | AC | A | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1579+935delG | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136250713 | |||||||
| chr5:136250749 | T | C | 5 | a0001c0001t0001g0020 a0001c0002t0001g0027 a0001c0002t0002g0233 others(2): Show |
5 | HG01258.hp1 HG02280.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1579+900A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136250749 | |||||||
| chr5:136250859 | C | T | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1579+790G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136250859 | |||||||
| chr5:136250866 | A | G | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1579+783T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136250866 | |||||||
| chr5:136250889 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1579+760C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136250889 | |||||||
| chr5:136250898 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1579+751C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136250898 | |||||||
| chr5:136251066 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1579+583G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136251066 | |||||||
| chr5:136251089 | A | G | 5 | a0001c0001t0001g0020 a0001c0002t0001g0027 a0001c0002t0002g0233 others(2): Show |
5 | HG01258.hp1 HG02280.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1579+560T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136251089 | |||||||
| chr5:136251303 | G | C | 44 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0045 others(41): Show |
44 | HG00099.hp2 HG00558.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.1579+346C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136251303 | |||||||
| chr5:136251462 | G | C | 1 | a0001c0001t0001g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1579+187C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136251462 | |||||||
| chr5:136251524 | G | A | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1579+125C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136251524 | |||||||
| chr5:136251558 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1579+91T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136251558 | |||||||
| chr5:136251562 | C | T | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1579+87G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136251562 | |||||||
| chr5:136251628 | G | T | 1 | a0001c0002t0002g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1579+21C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 6/11 | chr5 | 136251628 | |||||||
| chr5:136251892 | AAGG | A | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-13_1346-11del others(3): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136251892 | |||||||
| chr5:136251917 | G | C | 1 | a0001c0001t0001g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1346-35C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136251917 | |||||||
| chr5:136251964 | G | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0065 |
2 | NA18990.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1346-82C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136251964 | |||||||
| chr5:136252017 | A | G | 1 | a0001c0002t0002g0188 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1346-135T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136252017 | |||||||
| chr5:136252059 | C | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0019 others(20): Show |
24 | HG00323.hp1 HG00639.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.1346-177G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136252059 | |||||||
| chr5:136252084 | G | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0204 |
3 | HG02280.hp2 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1346-202C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136252084 | |||||||
| chr5:136252100 | C | G | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-218G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136252100 | |||||||
| chr5:136252109 | A | T | 1 | a0001c0001t0001g0147 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1346-227T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136252109 | |||||||
| chr5:136252293 | T | G | 1 | a0001c0002t0002g0250 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1346-411A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136252293 | |||||||
| chr5:136252327 | GT | G | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-446delA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136252327 | |||||||
| chr5:136252352 | TTTTTG | T | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-475_1346-471d others(7): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136252352 | |||||||
| chr5:136252375 | T | C | 1 | a0001c0002t0002g0202 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1346-493A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136252375 | |||||||
| chr5:136252465 | T | C | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-583A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136252465 | |||||||
| chr5:136252773 | C | G | 1 | a0001c0001t0001g0090 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1346-891G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136252773 | |||||||
| chr5:136252879 | C | T | 5 | a0001c0001t0001g0020 a0001c0002t0001g0027 a0001c0002t0002g0233 others(2): Show |
5 | HG01258.hp1 HG02280.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1346-997G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136252879 | |||||||
| chr5:136252880 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1346-998C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136252880 | |||||||
| chr5:136252922 | G | A | 2 | a0001c0002t0002g0230 a0001c0002t0002g0231 |
2 | HG01496.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1346-1040C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136252922 | |||||||
| chr5:136252951 | C | A | 1 | a0001c0002t0001g0027 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1346-1069G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136252951 | |||||||
| chr5:136252968 | G | A | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-1086C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136252968 | |||||||
| chr5:136252994 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1346-1112A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136252994 | |||||||
| chr5:136253181 | C | T | 1 | a0001c0002t0002g0185 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1346-1299G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136253181 | |||||||
| chr5:136253276 | A | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0171 others(4): Show |
8 | HG01884.hp1 HG02615.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1346-1394T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136253276 | |||||||
| chr5:136253310 | TATTTAA | T | 5 | a0001c0002t0002g0230 a0001c0002t0002g0231 a0001c0002t0004g0205 others(2): Show |
5 | HG01496.hp1 HG03579.hp1 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.1346-1434_1346-142 others(10): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136253310 | |||||||
| chr5:136253332 | C | T | 1 | a0001c0002t0002g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1346-1450G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136253332 | |||||||
| chr5:136253432 | A | G | 3 | a0001c0001t0001g0079 a0001c0001t0001g0087 a0001c0001t0001g0113 |
3 | HG02698.hp2 HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1346-1550T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136253432 | |||||||
| chr5:136253439 | C | T | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-1557G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136253439 | |||||||
| chr5:136253794 | TTGC | T | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-1915_1346-191 others(7): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136253794 | |||||||
| chr5:136254004 | G | A | 24 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(21): Show |
25 | HG01258.hp1 HG01496.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1346-2122C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136254004 | |||||||
| chr5:136254171 | A | T | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-2289T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136254171 | |||||||
| chr5:136254174 | C | T | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-2292G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136254174 | |||||||
| chr5:136254352 | C | A | 1 | a0001c0002t0002g0247 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1346-2470G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136254352 | |||||||
| chr5:136254373 | A | C | 1 | a0001c0001t0001g0171 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1346-2491T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136254373 | |||||||
| chr5:136254501 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0034 |
2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1346-2619C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136254501 | |||||||
| chr5:136254521 | A | G | 7 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(4): Show |
7 | HG00673.hp2 HG02040.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1346-2639T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136254521 | |||||||
| chr5:136254524 | C | T | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-2642G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136254524 | |||||||
| chr5:136254539 | C | A | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-2657G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136254539 | |||||||
| chr5:136254676 | G | A | 2 | a0001c0002t0005g0025 a0001c0002t0005g0028 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1346-2794C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136254676 | |||||||
| chr5:136254745 | G | A | 24 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(21): Show |
25 | HG01258.hp1 HG01496.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1346-2863C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136254745 | |||||||
| chr5:136254773 | G | T | 1 | a0001c0003t0001g0169 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1346-2891C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136254773 | |||||||
| chr5:136254808 | G | GA | 7 | a0001c0001t0001g0021 a0001c0001t0001g0034 a0001c0002t0002g0230 others(4): Show |
7 | HG01496.hp1 HG03195.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1346-2927dupT | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136254808 | |||||||
| chr5:136254832 | G | A | 7 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(4): Show |
7 | HG00673.hp2 HG02040.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1346-2950C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136254832 | |||||||
| chr5:136254840 | T | A | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1346-2958A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136254840 | |||||||
| chr5:136255315 | T | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0204 |
3 | HG02280.hp2 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1346-3433A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136255315 | |||||||
| chr5:136255375 | G | C | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-3493C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136255375 | |||||||
| chr5:136255513 | T | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02559.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346-3631A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136255513 | |||||||
| chr5:136255652 | A | G | 6 | a0001c0001t0001g0021 a0001c0002t0002g0230 a0001c0002t0002g0231 others(3): Show |
6 | HG01496.hp1 HG03195.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-3770T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136255652 | |||||||
| chr5:136255760 | A | G | 1 | a0001c0002t0002g0247 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1346-3878T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136255760 | |||||||
| chr5:136256050 | A | T | 2 | a0001c0002t0002g0192 a0001c0002t0002g0193 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1346-4168T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136256050 | |||||||
| chr5:136256061 | C | T | 3 | a0001c0002t0002g0216 a0001c0002t0002g0218 a0001c0002t0002g0219 |
3 | HG00741.hp2 HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1346-4179G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136256061 | |||||||
| chr5:136256119 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1346-4237T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136256119 | |||||||
| chr5:136256165 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1346-4283C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136256165 | |||||||
| chr5:136256348 | C | G | 1 | a0001c0001t0001g0068 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1346-4466G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136256348 | |||||||
| chr5:136256403 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1346-4521G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136256403 | |||||||
| chr5:136256405 | T | C | 2 | a0001c0002t0005g0025 a0001c0002t0005g0028 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1346-4523A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136256405 | |||||||
| chr5:136256511 | C | T | 1 | a0001c0002t0002g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1346-4629G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136256511 | |||||||
| chr5:136256605 | C | A | 1 | a0001c0001t0001g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1346-4723G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136256605 | |||||||
| chr5:136256864 | G | T | 1 | a0001c0001t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1346-4982C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136256864 | |||||||
| chr5:136256929 | TA | T | 24 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(21): Show |
25 | HG01258.hp1 HG01496.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1346-5048delT | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136256929 | |||||||
| chr5:136257075 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1346-5193A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136257075 | |||||||
| chr5:136257081 | G | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0034 a0001c0002t0002g0230 others(4): Show |
7 | HG01496.hp1 HG03195.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1346-5199C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136257081 | |||||||
| chr5:136257116 | T | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0204 |
3 | HG02280.hp2 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1346-5234A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136257116 | |||||||
| chr5:136257170 | A | T | 5 | a0001c0002t0002g0209 a0001c0002t0002g0236 a0001c0002t0005g0025 others(2): Show |
5 | HG02886.hp2 HG02970.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1346-5288T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136257170 | |||||||
| chr5:136257245 | C | T | 1 | a0001c0002t0002g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1346-5363G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136257245 | |||||||
| chr5:136257254 | C | T | 2 | a0001c0002t0005g0025 a0001c0002t0005g0028 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1346-5372G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136257254 | |||||||
| chr5:136257371 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0106 a0001c0001t0001g0107 |
3 | HG03139.hp1 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1346-5489G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136257371 | |||||||
| chr5:136257446 | G | A | 2 | a0001c0002t0002g0230 a0001c0002t0002g0231 |
2 | HG01496.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1346-5564C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136257446 | |||||||
| chr5:136257465 | GCCA | G | 6 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0041 others(3): Show |
6 | NA18940.hp1 NA18960.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-5586_1346-558 others(7): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136257465 | |||||||
| chr5:136257474 | T | G | 1 | a0001c0001t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1346-5592A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136257474 | |||||||
| chr5:136257861 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1346-5979T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136257861 | |||||||
| chr5:136258256 | A | G | 11 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0002t0001g0027 others(8): Show |
11 | HG01258.hp1 HG02280.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.1346-6374T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136258256 | |||||||
| chr5:136258334 | T | G | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1346-6452A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136258334 | |||||||
| chr5:136258721 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0171 others(4): Show |
8 | HG01884.hp1 HG02615.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1346-6839G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136258721 | |||||||
| chr5:136258781 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1346-6899C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136258781 | |||||||
| chr5:136258813 | G | T | 1 | a0001c0002t0001g0029 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1346-6931C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136258813 | |||||||
| chr5:136258961 | A | G | 19 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(16): Show |
20 | HG01258.hp1 HG01496.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1346-7079T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136258961 | |||||||
| chr5:136259267 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0171 others(4): Show |
8 | HG01884.hp1 HG02615.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1345+6953G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136259267 | |||||||
| chr5:136259321 | C | G | 1 | a0001c0001t0001g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1345+6899G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136259321 | |||||||
| chr5:136259455 | A | G | 1 | a0001c0002t0002g0186 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1345+6765T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136259455 | |||||||
| chr5:136259470 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1345+6750G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136259470 | |||||||
| chr5:136259735 | C | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0171 others(4): Show |
8 | HG01884.hp1 HG02615.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1345+6485G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136259735 | |||||||
| chr5:136259764 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1345+6456C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136259764 | |||||||
| chr5:136260017 | G | A | 1 | a0001c0008t0007g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1345+6203C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136260017 | |||||||
| chr5:136260102 | A | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0204 |
3 | HG02280.hp2 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1345+6118T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136260102 | |||||||
| chr5:136260763 | T | C | 2 | a0001c0002t0002g0230 a0001c0002t0002g0231 |
2 | HG01496.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1345+5457A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136260763 | |||||||
| chr5:136260861 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1345+5359C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136260861 | |||||||
| chr5:136260903 | G | A | 5 | a0001c0001t0001g0020 a0001c0002t0001g0027 a0001c0002t0002g0233 others(2): Show |
5 | HG01258.hp1 HG02280.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1345+5317C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136260903 | |||||||
| chr5:136260988 | C | T | 1 | a0001c0002t0002g0212 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1345+5232G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136260988 | |||||||
| chr5:136261077 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1345+5143A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136261077 | |||||||
| chr5:136261283 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1345+4937C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136261283 | |||||||
| chr5:136261406 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1345+4814G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136261406 | |||||||
| chr5:136261426 | C | T | 2 | a0001c0002t0002g0230 a0001c0002t0002g0231 |
2 | HG01496.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1345+4794G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136261426 | |||||||
| chr5:136261890 | A | G | 4 | a0001c0002t0002g0209 a0001c0002t0005g0025 a0001c0002t0005g0028 others(1): Show |
4 | HG02886.hp2 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1345+4330T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136261890 | |||||||
| chr5:136261930 | C | G | 1 | a0001c0001t0001g0150 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1345+4290G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136261930 | |||||||
| chr5:136262115 | C | T | 2 | a0001c0002t0002g0209 a0003c0006t0001g0026 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1345+4105G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136262115 | |||||||
| chr5:136262179 | A | G | 5 | a0001c0001t0001g0020 a0001c0002t0001g0027 a0001c0002t0002g0233 others(2): Show |
5 | HG01258.hp1 HG02280.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1345+4041T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136262179 | |||||||
| chr5:136262642 | G | A | 16 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(13): Show |
17 | HG01258.hp1 HG01884.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1345+3578C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136262642 | |||||||
| chr5:136262718 | A | G | 5 | a0001c0001t0001g0020 a0001c0002t0001g0027 a0001c0002t0002g0233 others(2): Show |
5 | HG01258.hp1 HG02280.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1345+3502T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136262718 | |||||||
| chr5:136263150 | G | A | 2 | a0001c0002t0002g0209 a0003c0006t0001g0026 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1345+3070C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136263150 | |||||||
| chr5:136263319 | A | C | 1 | a0001c0001t0001g0131 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1345+2901T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136263319 | |||||||
| chr5:136263325 | G | A | 2 | a0001c0002t0002g0230 a0001c0002t0002g0231 |
2 | HG01496.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1345+2895C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136263325 | |||||||
| chr5:136263407 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1345+2813G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136263407 | |||||||
| chr5:136263740 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0204 |
3 | HG02280.hp2 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1345+2480C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136263740 | |||||||
| chr5:136263910 | T | C | 1 | a0001c0008t0007g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1345+2310A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136263910 | |||||||
| chr5:136264152 | G | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0023 others(5): Show |
9 | HG01069.hp2 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1345+2068C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136264152 | |||||||
| chr5:136264217 | T | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02559.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1345+2003A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136264217 | |||||||
| chr5:136264317 | G | C | 1 | a0001c0001t0001g0105 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1345+1903C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136264317 | |||||||
| chr5:136264387 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1345+1833G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136264387 | |||||||
| chr5:136264447 | C | T | 1 | a0001c0002t0002g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1345+1773G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136264447 | |||||||
| chr5:136264512 | C | T | 2 | a0001c0002t0005g0025 a0001c0002t0005g0028 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1345+1708G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136264512 | |||||||
| chr5:136264544 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1345+1676G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136264544 | |||||||
| chr5:136264595 | T | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0204 |
3 | HG02280.hp2 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1345+1625A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136264595 | |||||||
| chr5:136264596 | G | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0204 |
3 | HG02280.hp2 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1345+1624C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136264596 | |||||||
| chr5:136264685 | T | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0204 |
3 | HG02280.hp2 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1345+1535A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136264685 | |||||||
| chr5:136264695 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1345+1525G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136264695 | |||||||
| chr5:136264890 | C | T | 2 | a0001c0002t0002g0209 a0003c0006t0001g0026 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1345+1330G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136264890 | |||||||
| chr5:136265018 | T | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0171 others(4): Show |
8 | HG01884.hp1 HG02615.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1345+1202A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136265018 | |||||||
| chr5:136265162 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1345+1058G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136265162 | |||||||
| chr5:136265333 | T | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0204 |
3 | HG02280.hp2 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1345+887A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136265333 | |||||||
| chr5:136265356 | C | A | 1 | a0001c0002t0002g0242 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1345+864G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136265356 | |||||||
| chr5:136265565 | T | C | 5 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0002t0001g0114 others(2): Show |
5 | HG00733.hp2 HG01099.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.1345+655A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136265565 | |||||||
| chr5:136265566 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0204 |
3 | HG02280.hp2 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1345+654G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136265566 | |||||||
| chr5:136265688 | A | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0204 |
3 | HG02280.hp2 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1345+532T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136265688 | |||||||
| chr5:136265750 | A | C | 1 | a0001c0002t0002g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1345+470T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136265750 | |||||||
| chr5:136265800 | C | CTATGAA | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0204 |
3 | HG02280.hp2 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1345+414_1345+419d others(8): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136265800 | |||||||
| chr5:136266007 | G | A | 3 | a0001c0002t0004g0205 a0001c0002t0004g0206 a0001c0002t0004g0207 |
3 | NA18940.hp2 NA19056.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1345+213C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136266007 | |||||||
| chr5:136266062 | A | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02559.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1345+158T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136266062 | |||||||
| chr5:136266071 | T | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0171 others(4): Show |
8 | HG01884.hp1 HG02615.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1345+149A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 5/11 | chr5 | 136266071 | |||||||
| chr5:136266665 | G | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0204 |
3 | HG02280.hp2 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1129-229C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136266665 | |||||||
| chr5:136266711 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1129-275T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136266711 | |||||||
| chr5:136266797 | C | A | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1129-361G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136266797 | |||||||
| chr5:136266797 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1129-361G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136266797 | |||||||
| chr5:136266974 | A | G | 2 | a0001c0002t0002g0230 a0001c0002t0002g0231 |
2 | HG01496.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1129-538T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136266974 | |||||||
| chr5:136267332 | A | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0055 |
2 | HG03225.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1129-896T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136267332 | |||||||
| chr5:136267347 | G | A | 1 | a0001c0002t0002g0249 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1129-911C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136267347 | |||||||
| chr5:136267361 | C | A | 1 | a0001c0001t0001g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1129-925G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136267361 | |||||||
| chr5:136267767 | G | T | 1 | a0001c0001t0001g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1129-1331C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136267767 | |||||||
| chr5:136267821 | G | T | 1 | a0001c0001t0001g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1129-1385C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136267821 | |||||||
| chr5:136268056 | A | T | 1 | a0001c0002t0002g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1129-1620T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136268056 | |||||||
| chr5:136268290 | T | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0171 others(4): Show |
8 | HG01884.hp1 HG02615.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1129-1854A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136268290 | |||||||
| chr5:136268315 | A | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0204 |
3 | HG02280.hp2 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1129-1879T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136268315 | |||||||
| chr5:136268324 | G | GAGC | 27 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(24): Show |
28 | HG01258.hp1 HG01496.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.1129-1889_1129-188 others(7): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136268324 | |||||||
| chr5:136268479 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1129-2043A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136268479 | |||||||
| chr5:136268485 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1129-2049G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136268485 | |||||||
| chr5:136268725 | T | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0204 |
3 | HG02280.hp2 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1129-2289A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136268725 | |||||||
| chr5:136268878 | A | G | 1 | a0001c0002t0002g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1129-2442T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136268878 | |||||||
| chr5:136269030 | A | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0072 a0001c0001t0001g0073 |
3 | HG01099.hp1 HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1129-2594T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136269030 | |||||||
| chr5:136269073 | G | A | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1129-2637C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136269073 | |||||||
| chr5:136269329 | A | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0158 |
3 | HG00323.hp2 HG00639.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1129-2893T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136269329 | |||||||
| chr5:136269374 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1129-2938C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136269374 | |||||||
| chr5:136269485 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1129-3049T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136269485 | |||||||
| chr5:136269662 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
180 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1129-3226A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136269662 | |||||||
| chr5:136269708 | G | A | 1 | a0001c0002t0002g0228 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1129-3272C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136269708 | |||||||
| chr5:136269713 | G | A | 1 | a0001c0002t0002g0191 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1129-3277C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136269713 | |||||||
| chr5:136269943 | TC | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0204 |
3 | HG02280.hp2 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1129-3508delG | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136269943 | |||||||
| chr5:136270096 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1129-3660G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136270096 | |||||||
| chr5:136270154 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1129-3718C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136270154 | |||||||
| chr5:136270427 | A | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0204 |
3 | HG02280.hp2 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1129-3991T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136270427 | |||||||
| chr5:136270508 | A | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0171 others(4): Show |
8 | HG01884.hp1 HG02615.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1129-4072T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136270508 | |||||||
| chr5:136270621 | G | A | 1 | a0001c0002t0002g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1128+4052C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136270621 | |||||||
| chr5:136270752 | G | T | 1 | a0001c0001t0001g0134 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1128+3921C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136270752 | |||||||
| chr5:136271075 | G | A | 1 | a0001c0003t0001g0169 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1128+3598C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136271075 | |||||||
| chr5:136271328 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0204 |
3 | HG02280.hp2 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1128+3345G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136271328 | |||||||
| chr5:136271340 | T | A | 1 | a0001c0001t0001g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1128+3333A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136271340 | |||||||
| chr5:136271400 | C | G | 21 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0072 others(18): Show |
21 | HG00323.hp1 HG00639.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.1128+3273G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136271400 | |||||||
| chr5:136271454 | T | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0002g0204 |
3 | HG02280.hp2 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1128+3219A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136271454 | |||||||
| chr5:136271501 | A | T | 1 | a0002c0004t0001g0175 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1128+3172T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136271501 | |||||||
| chr5:136271504 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1128+3169C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136271504 | |||||||
| chr5:136271583 | A | G | 2 | a0001c0002t0005g0025 a0001c0002t0005g0028 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1128+3090T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136271583 | |||||||
| chr5:136271859 | G | T | 5 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
5 | NA18986.hp2 NA18988.hp1 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.1128+2814C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136271859 | |||||||
| chr5:136271892 | A | C | 1 | a0001c0002t0002g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1128+2781T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136271892 | |||||||
| chr5:136272051 | T | C | 8 | a0001c0002t0001g0027 a0001c0002t0001g0029 a0001c0002t0002g0204 others(5): Show |
8 | HG01496.hp1 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1128+2622A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136272051 | |||||||
| chr5:136272083 | C | T | 7 | a0001c0002t0001g0029 a0001c0002t0002g0204 a0001c0002t0002g0230 others(4): Show |
7 | HG01496.hp1 HG02109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1128+2590G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136272083 | |||||||
| chr5:136272205 | A | G | 8 | a0001c0002t0001g0027 a0001c0002t0001g0029 a0001c0002t0002g0204 others(5): Show |
8 | HG01496.hp1 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1128+2468T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136272205 | |||||||
| chr5:136272464 | C | A | 1 | a0002c0004t0001g0175 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1128+2209G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136272464 | |||||||
| chr5:136272561 | G | C | 11 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(8): Show |
11 | HG01496.hp1 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1128+2112C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136272561 | |||||||
| chr5:136272834 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
119 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1128+1839C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136272834 | |||||||
| chr5:136272837 | A | G | 40 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(37): Show |
40 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.1128+1836T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136272837 | |||||||
| chr5:136273065 | T | G | 1 | a0001c0001t0001g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1128+1608A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136273065 | |||||||
| chr5:136273105 | G | A | 8 | a0001c0002t0001g0027 a0001c0002t0001g0029 a0001c0002t0002g0204 others(5): Show |
8 | HG01496.hp1 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1128+1568C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136273105 | |||||||
| chr5:136273373 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0104 |
2 | NA18950.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1128+1300G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136273373 | |||||||
| chr5:136273398 | G | A | 8 | a0001c0002t0001g0027 a0001c0002t0001g0029 a0001c0002t0002g0204 others(5): Show |
8 | HG01496.hp1 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1128+1275C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136273398 | |||||||
| chr5:136273439 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1128+1234A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136273439 | |||||||
| chr5:136273468 | C | T | 8 | a0001c0002t0001g0027 a0001c0002t0001g0029 a0001c0002t0002g0204 others(5): Show |
8 | HG01496.hp1 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1128+1205G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136273468 | |||||||
| chr5:136273483 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1128+1190G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136273483 | |||||||
| chr5:136273484 | G | A | 8 | a0001c0002t0001g0027 a0001c0002t0001g0029 a0001c0002t0002g0204 others(5): Show |
8 | HG01496.hp1 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1128+1189C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136273484 | |||||||
| chr5:136273495 | T | G | 3 | a0001c0002t0004g0205 a0001c0002t0004g0206 a0001c0002t0004g0207 |
3 | NA18940.hp2 NA19056.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1128+1178A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136273495 | |||||||
| chr5:136273541 | G | T | 1 | a0001c0002t0002g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1128+1132C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136273541 | |||||||
| chr5:136273800 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1128+873A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136273800 | |||||||
| chr5:136273945 | C | G | 8 | a0001c0002t0001g0027 a0001c0002t0001g0029 a0001c0002t0002g0204 others(5): Show |
8 | HG01496.hp1 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1128+728G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136273945 | |||||||
| chr5:136274047 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1128+626A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136274047 | |||||||
| chr5:136274475 | G | GA | 8 | a0001c0002t0001g0027 a0001c0002t0001g0029 a0001c0002t0002g0204 others(5): Show |
8 | HG01496.hp1 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1128+197dupT | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136274475 | |||||||
| chr5:136274620 | T | G | 1 | a0001c0002t0002g0195 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1128+53A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 4/11 | chr5 | 136274620 | |||||||
| chr5:136274847 | C | G | 1 | a0001c0001t0001g0124 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.964-10G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136274847 | |||||||
| chr5:136275110 | T | C | 7 | a0001c0002t0001g0027 a0001c0002t0001g0029 a0001c0002t0002g0230 others(4): Show |
7 | HG01496.hp1 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.964-273A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136275110 | |||||||
| chr5:136275282 | T | C | 7 | a0001c0002t0001g0027 a0001c0002t0001g0029 a0001c0002t0002g0230 others(4): Show |
7 | HG01496.hp1 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.964-445A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136275282 | |||||||
| chr5:136275382 | TA | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(128): Show |
133 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.964-546delT | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136275382 | |||||||
| chr5:136275497 | T | A | 7 | a0001c0002t0001g0027 a0001c0002t0001g0029 a0001c0002t0002g0230 others(4): Show |
7 | HG01496.hp1 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.964-660A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136275497 | |||||||
| chr5:136275563 | GCTTCCTT others(13): Show |
G | 7 | a0001c0002t0001g0027 a0001c0002t0001g0029 a0001c0002t0002g0230 others(4): Show |
7 | HG01496.hp1 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.964-746_964-727del others(20): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136275563 | |||||||
| chr5:136275698 | C | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(115): Show |
121 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.964-861G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136275698 | |||||||
| chr5:136275754 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
136 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.964-917T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136275754 | |||||||
| chr5:136276062 | C | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0095 a0001c0001t0001g0160 |
3 | HG01109.hp2 HG01175.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.964-1225G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136276062 | |||||||
| chr5:136276075 | A | C | 1 | a0001c0002t0002g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.964-1238T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136276075 | |||||||
| chr5:136276186 | T | C | 1 | a0001c0002t0002g0243 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.964-1349A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136276186 | |||||||
| chr5:136276468 | G | A | 12 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(9): Show |
12 | HG00609.hp2 NA18944.hp2 NA18983.hp1 others(9): Show |
intron_variant | MODIFIER | c.964-1631C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136276468 | |||||||
| chr5:136276704 | A | C | 1 | a0001c0001t0001g0150 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.964-1867T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136276704 | |||||||
| chr5:136276888 | G | T | 1 | a0001c0001t0001g0140 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.964-2051C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136276888 | |||||||
| chr5:136276958 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.964-2121G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136276958 | |||||||
| chr5:136276959 | G | A | 7 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(4): Show |
7 | HG02572.hp1 HG03225.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.964-2122C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136276959 | |||||||
| chr5:136276976 | C | T | 1 | a0001c0002t0002g0185 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.964-2139G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136276976 | |||||||
| chr5:136276981 | C | T | 2 | a0001c0001t0001g0030 a0001c0008t0007g0006 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.964-2144G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136276981 | |||||||
| chr5:136277003 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.964-2166C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136277003 | |||||||
| chr5:136277010 | T | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | HG01099.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.964-2173A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136277010 | |||||||
| chr5:136277055 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.964-2218C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136277055 | |||||||
| chr5:136277062 | A | G | 7 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(4): Show |
7 | HG02572.hp1 HG03225.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.964-2225T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136277062 | |||||||
| chr5:136277237 | G | T | 1 | a0001c0001t0001g0147 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.964-2400C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136277237 | |||||||
| chr5:136277304 | G | T | 1 | a0001c0002t0002g0203 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.964-2467C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136277304 | |||||||
| chr5:136277428 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | NA19003.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.964-2591C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136277428 | |||||||
| chr5:136277501 | AT | A | 5 | a0001c0002t0001g0027 a0001c0002t0001g0029 a0001c0002t0005g0025 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.964-2665delA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136277501 | |||||||
| chr5:136277573 | G | A | 1 | a0001c0008t0007g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.964-2736C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136277573 | |||||||
| chr5:136277700 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.964-2863T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136277700 | |||||||
| chr5:136277718 | T | G | 1 | a0001c0001t0001g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.964-2881A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136277718 | |||||||
| chr5:136277738 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(115): Show |
121 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.964-2901A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136277738 | |||||||
| chr5:136277925 | T | G | 7 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0022 others(4): Show |
8 | HG01069.hp2 HG01071.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.964-3088A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136277925 | |||||||
| chr5:136278044 | T | G | 46 | a0001c0001t0001g0004 a0001c0001t0001g0045 a0001c0001t0001g0052 others(43): Show |
47 | HG00099.hp2 HG00558.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-3207A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136278044 | |||||||
| chr5:136278123 | C | A | 1 | a0001c0002t0002g0242 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.964-3286G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136278123 | |||||||
| chr5:136278293 | G | T | 13 | a0001c0001t0001g0005 a0001c0001t0001g0171 a0001c0001t0001g0172 others(10): Show |
14 | HG00673.hp2 HG01884.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.964-3456C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136278293 | |||||||
| chr5:136278415 | C | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(105): Show |
111 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.964-3578G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136278415 | |||||||
| chr5:136278681 | G | A | 1 | a0001c0002t0002g0209 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.964-3844C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136278681 | |||||||
| chr5:136278839 | C | A | 1 | a0001c0001t0001g0174 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.964-4002G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136278839 | |||||||
| chr5:136279012 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.964-4175A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136279012 | |||||||
| chr5:136279129 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.964-4292G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136279129 | |||||||
| chr5:136279223 | AC | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(1): Show |
4 | HG02572.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.964-4387delG | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136279223 | |||||||
| chr5:136279463 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.964-4626C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136279463 | |||||||
| chr5:136279525 | G | A | 49 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0077 others(46): Show |
50 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.964-4688C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136279525 | |||||||
| chr5:136279718 | C | G | 1 | a0001c0002t0002g0212 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.964-4881G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136279718 | |||||||
| chr5:136279911 | G | T | 1 | a0001c0001t0001g0177 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.964-5074C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136279911 | |||||||
| chr5:136279927 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
182 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.964-5090A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136279927 | |||||||
| chr5:136279928 | G | A | 27 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(24): Show |
27 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.964-5091C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136279928 | |||||||
| chr5:136279984 | C | A | 1 | a0001c0002t0002g0193 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.964-5147G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136279984 | |||||||
| chr5:136279991 | G | GA | 6 | a0001c0001t0001g0021 a0001c0002t0001g0027 a0001c0002t0005g0025 others(3): Show |
6 | HG02280.hp1 HG02886.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.964-5155dupT | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136279991 | |||||||
| chr5:136280013 | A | G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | NA19003.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.964-5176T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136280013 | |||||||
| chr5:136280021 | A | G | 70 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(67): Show |
71 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.964-5184T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136280021 | |||||||
| chr5:136280042 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.964-5205G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136280042 | |||||||
| chr5:136280159 | A | AAAAC | 10 | a0001c0001t0001g0021 a0001c0002t0001g0027 a0001c0002t0001g0029 others(7): Show |
10 | HG01496.hp1 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.964-5326_964-5323d others(6): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136280159 | |||||||
| chr5:136280311 | G | C | 1 | a0001c0001t0001g0167 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.964-5474C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136280311 | |||||||
| chr5:136280450 | G | T | 68 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(65): Show |
69 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.964-5613C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136280450 | |||||||
| chr5:136280639 | G | T | 1 | a0001c0002t0002g0197 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.964-5802C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136280639 | |||||||
| chr5:136280782 | A | C | 68 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(65): Show |
69 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.964-5945T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136280782 | |||||||
| chr5:136280978 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.964-6141A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136280978 | |||||||
| chr5:136281012 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.964-6175A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136281012 | |||||||
| chr5:136281193 | G | A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(131): Show |
136 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.964-6356C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136281193 | |||||||
| chr5:136281352 | C | T | 3 | a0001c0002t0002g0190 a0001c0002t0002g0201 a0001c0007t0002g0189 |
3 | HG01069.hp1 HG01175.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.964-6515G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136281352 | |||||||
| chr5:136281379 | C | T | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.964-6542G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136281379 | |||||||
| chr5:136281419 | T | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.964-6582A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136281419 | |||||||
| chr5:136281454 | A | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.964-6617T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136281454 | |||||||
| chr5:136281511 | C | A | 1 | a0001c0002t0002g0202 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.964-6674G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136281511 | |||||||
| chr5:136281577 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.964-6740A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136281577 | |||||||
| chr5:136281709 | G | T | 1 | a0001c0001t0001g0163 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.964-6872C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136281709 | |||||||
| chr5:136281910 | T | G | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.964-7073A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136281910 | |||||||
| chr5:136282079 | A | G | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.964-7242T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136282079 | |||||||
| chr5:136282258 | A | G | 35 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(32): Show |
37 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.964-7421T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136282258 | |||||||
| chr5:136282382 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.964-7545C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136282382 | |||||||
| chr5:136282412 | C | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.964-7575G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136282412 | |||||||
| chr5:136282469 | A | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.964-7632T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136282469 | |||||||
| chr5:136282516 | G | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.964-7679C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136282516 | |||||||
| chr5:136282567 | T | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.964-7730A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136282567 | |||||||
| chr5:136282662 | G | T | 35 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(32): Show |
37 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.964-7825C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136282662 | |||||||
| chr5:136282739 | A | G | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.964-7902T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136282739 | |||||||
| chr5:136282745 | G | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(32): Show |
37 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.964-7908C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136282745 | |||||||
| chr5:136282964 | CAG | C | 3 | a0001c0002t0002g0190 a0001c0002t0002g0201 a0001c0007t0002g0189 |
3 | HG01069.hp1 HG01175.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.964-8129_964-8128d others(4): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136282964 | |||||||
| chr5:136283031 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.964-8194C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136283031 | |||||||
| chr5:136283405 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.964-8568C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136283405 | |||||||
| chr5:136283515 | C | T | 66 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0021 others(63): Show |
67 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.964-8678G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136283515 | |||||||
| chr5:136283658 | G | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(32): Show |
37 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.964-8821C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136283658 | |||||||
| chr5:136283784 | A | T | 35 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(32): Show |
37 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.964-8947T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136283784 | |||||||
| chr5:136283841 | G | A | 1 | a0001c0002t0002g0216 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.964-9004C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136283841 | |||||||
| chr5:136283929 | G | T | 35 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(32): Show |
37 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.964-9092C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136283929 | |||||||
| chr5:136284219 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.964-9382G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136284219 | |||||||
| chr5:136284357 | G | A | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.964-9520C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136284357 | |||||||
| chr5:136284646 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.964-9809G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136284646 | |||||||
| chr5:136284757 | G | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0038 |
3 | NA19081.hp1 NA19082.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.964-9920C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136284757 | |||||||
| chr5:136284883 | G | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.964-10046C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136284883 | |||||||
| chr5:136284891 | C | G | 1 | a0001c0002t0002g0221 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.964-10054G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136284891 | |||||||
| chr5:136285160 | C | T | 68 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(65): Show |
69 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.964-10323G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136285160 | |||||||
| chr5:136285162 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.964-10325A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136285162 | |||||||
| chr5:136285351 | T | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0181 |
2 | HG02622.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.964-10514A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136285351 | |||||||
| chr5:136285798 | A | G | 1 | a0001c0002t0002g0203 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.964-10961T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136285798 | |||||||
| chr5:136285819 | G | A | 38 | a0001c0002t0001g0114 a0001c0002t0002g0185 a0001c0002t0002g0186 others(35): Show |
38 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.964-10982C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136285819 | |||||||
| chr5:136286034 | G | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(32): Show |
37 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.964-11197C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136286034 | |||||||
| chr5:136286123 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.964-11286C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136286123 | |||||||
| chr5:136286209 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.964-11372C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136286209 | |||||||
| chr5:136286410 | C | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.964-11573G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136286410 | |||||||
| chr5:136286505 | G | C | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.964-11668C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136286505 | |||||||
| chr5:136286566 | A | G | 1 | a0001c0002t0002g0202 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.964-11729T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136286566 | |||||||
| chr5:136286726 | C | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.964-11889G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136286726 | |||||||
| chr5:136287164 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0181 |
2 | HG02622.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.964-12327C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287164 | |||||||
| chr5:136287264 | G | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.964-12427C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287264 | |||||||
| chr5:136287330 | T | C | 134 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(131): Show |
136 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.964-12493A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287330 | |||||||
| chr5:136287356 | G | GGA | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.964-12521_964-1252 others(6): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287356 | |||||||
| chr5:136287661 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.964-12824T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287661 | |||||||
| chr5:136287681 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0093 |
2 | HG03239.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.964-12844C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287681 | |||||||
| chr5:136287687 | C | A | 1 | a0001c0001t0001g0122 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.964-12850G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287687 | |||||||
| chr5:136287687 | C | CA | 14 | a0001c0001t0001g0117 a0001c0001t0001g0123 a0001c0001t0001g0125 others(11): Show |
14 | HG00408.hp1 HG00609.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.964-12851dupT | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287687 | |||||||
| chr5:136287687 | C | CAA | 5 | a0001c0001t0001g0069 a0001c0001t0001g0146 a0001c0001t0001g0155 others(2): Show |
5 | HG02074.hp1 HG02809.hp2 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.964-12852_964-1285 others(6): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287687 | |||||||
| chr5:136287687 | C | CAAA | 8 | a0001c0001t0001g0070 a0001c0001t0001g0115 a0001c0001t0001g0121 others(5): Show |
8 | HG00735.hp1 HG00741.hp1 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.964-12853_964-1285 others(7): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287687 | |||||||
| chr5:136287687 | CA | C | 12 | a0001c0001t0001g0105 a0001c0001t0001g0133 a0001c0001t0001g0134 others(9): Show |
12 | HG01069.hp1 HG01175.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.964-12851delT | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287687 | |||||||
| chr5:136287687 | CAAAAA | C | 11 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(8): Show |
11 | HG00423.hp2 HG01258.hp1 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.964-12855_964-1285 others(9): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287687 | |||||||
| chr5:136287687 | CAAAAAA | C | 26 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(23): Show |
28 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.964-12856_964-1285 others(10): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287687 | |||||||
| chr5:136287687 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.964-12861_964-1285 others(15): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287687 | |||||||
| chr5:136287687 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0077 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.964-12863_964-1285 others(17): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287687 | |||||||
| chr5:136287687 | CAAAAAAA others(7): Show |
C | 1 | a0001c0002t0002g0208 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.964-12864_964-1285 others(18): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287687 | |||||||
| chr5:136287687 | CAAAAAAA others(8): Show |
C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0081 others(3): Show |
7 | HG02280.hp2 HG02622.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.964-12865_964-1285 others(19): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287687 | |||||||
| chr5:136287687 | CAAAAAAA others(9): Show |
C | 17 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0075 others(14): Show |
17 | HG01175.hp2 HG01496.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.964-12866_964-1285 others(20): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287687 | |||||||
| chr5:136287687 | CAAAAAAA others(10): Show |
C | 64 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(61): Show |
65 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.964-12867_964-1285 others(21): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287687 | |||||||
| chr5:136287687 | CAAAAAAA others(11): Show |
C | 39 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(36): Show |
39 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.964-12868_964-1285 others(22): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287687 | |||||||
| chr5:136287687 | CAAAAAAA others(12): Show |
C | 1 | a0003c0006t0001g0026 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.964-12869_964-1285 others(23): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287687 | |||||||
| chr5:136287687 | CAAAAAAA others(13): Show |
C | 7 | a0001c0001t0001g0021 a0001c0001t0001g0147 a0001c0002t0001g0027 others(4): Show |
7 | HG01071.hp1 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.964-12870_964-1285 others(24): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287687 | |||||||
| chr5:136287722 | A | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.964-12885T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287722 | |||||||
| chr5:136287723 | A | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.964-12886T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287723 | |||||||
| chr5:136287725 | A | C | 4 | a0001c0001t0001g0030 a0001c0002t0002g0235 a0001c0002t0002g0236 others(1): Show |
4 | HG01258.hp1 HG03209.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.964-12888T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287725 | |||||||
| chr5:136287999 | A | G | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.964-13162T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136287999 | |||||||
| chr5:136288026 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.964-13189A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136288026 | |||||||
| chr5:136288030 | A | G | 1 | a0001c0002t0002g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.964-13193T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136288030 | |||||||
| chr5:136288037 | G | C | 1 | a0001c0002t0002g0219 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.964-13200C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136288037 | |||||||
| chr5:136288198 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.964-13361A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136288198 | |||||||
| chr5:136288248 | C | T | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.964-13411G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136288248 | |||||||
| chr5:136288311 | A | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0105 |
2 | NA18942.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.964-13474T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136288311 | |||||||
| chr5:136288407 | A | AT | 16 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(13): Show |
18 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.964-13571dupA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136288407 | |||||||
| chr5:136288407 | A | ATT | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.964-13572_964-1357 others(6): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136288407 | |||||||
| chr5:136288407 | AT | A | 69 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(66): Show |
70 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.964-13571delA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136288407 | |||||||
| chr5:136288573 | C | A | 7 | a0001c0002t0002g0233 a0001c0002t0002g0234 a0001c0002t0002g0235 others(4): Show |
7 | HG01258.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.964-13736G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136288573 | |||||||
| chr5:136288682 | T | G | 2 | a0001c0002t0002g0190 a0001c0007t0002g0189 |
2 | HG01069.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.964-13845A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136288682 | |||||||
| chr5:136289239 | A | G | 4 | a0001c0001t0001g0079 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
4 | HG02698.hp2 HG02735.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.964-14402T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136289239 | |||||||
| chr5:136289250 | C | T | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.964-14413G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136289250 | |||||||
| chr5:136289323 | C | T | 1 | a0004c0005t0001g0091 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.964-14486G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136289323 | |||||||
| chr5:136289331 | G | A | 2 | a0001c0002t0002g0244 a0001c0008t0007g0006 |
2 | HG02273.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.964-14494C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136289331 | |||||||
| chr5:136289353 | C | T | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.964-14516G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136289353 | |||||||
| chr5:136289364 | T | G | 1 | a0001c0001t0001g0108 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.964-14527A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136289364 | |||||||
| chr5:136289464 | C | T | 3 | a0001c0001t0001g0157 a0001c0002t0002g0192 a0001c0002t0002g0193 |
3 | HG00639.hp2 HG00735.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.964-14627G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136289464 | |||||||
| chr5:136289483 | A | G | 65 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0076 others(62): Show |
66 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.964-14646T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136289483 | |||||||
| chr5:136289517 | G | T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0182 |
2 | HG00673.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.964-14680C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136289517 | |||||||
| chr5:136289638 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.964-14801G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136289638 | |||||||
| chr5:136289640 | G | T | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.964-14803C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136289640 | |||||||
| chr5:136289887 | C | T | 2 | a0001c0002t0002g0192 a0001c0002t0002g0193 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.964-15050G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136289887 | |||||||
| chr5:136290106 | A | G | 1 | a0001c0002t0002g0235 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.964-15269T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136290106 | |||||||
| chr5:136290116 | G | A | 1 | a0001c0002t0005g0028 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.964-15279C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136290116 | |||||||
| chr5:136290141 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.964-15304A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136290141 | |||||||
| chr5:136290201 | G | A | 1 | a0001c0002t0002g0200 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.964-15364C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136290201 | |||||||
| chr5:136290255 | G | A | 1 | a0001c0002t0002g0210 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.964-15418C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136290255 | |||||||
| chr5:136290343 | C | T | 1 | a0001c0002t0002g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.964-15506G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136290343 | |||||||
| chr5:136290539 | C | T | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.964-15702G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136290539 | |||||||
| chr5:136290669 | T | G | 1 | a0001c0001t0001g0105 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.964-15832A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136290669 | |||||||
| chr5:136290755 | G | A | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.964-15918C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136290755 | |||||||
| chr5:136290969 | A | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.964-16132T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136290969 | |||||||
| chr5:136291082 | A | G | 1 | a0001c0001t0002g0241 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.964-16245T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136291082 | |||||||
| chr5:136291143 | T | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.964-16306A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136291143 | |||||||
| chr5:136291284 | C | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(54): Show |
58 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.964-16447G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136291284 | |||||||
| chr5:136291374 | A | G | 68 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(65): Show |
69 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.964-16537T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136291374 | |||||||
| chr5:136291400 | T | G | 1 | a0001c0002t0002g0231 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.964-16563A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136291400 | |||||||
| chr5:136291406 | G | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0060 |
2 | NA18998.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.964-16569C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136291406 | |||||||
| chr5:136291468 | C | G | 1 | a0001c0002t0002g0251 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.964-16631G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136291468 | |||||||
| chr5:136291470 | A | T | 1 | a0001c0001t0001g0080 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.964-16633T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136291470 | |||||||
| chr5:136291555 | G | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.964-16718C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136291555 | |||||||
| chr5:136291631 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.964-16794C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136291631 | |||||||
| chr5:136291733 | C | T | 1 | a0001c0002t0002g0212 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.964-16896G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136291733 | |||||||
| chr5:136291862 | C | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.964-17025G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136291862 | |||||||
| chr5:136291905 | C | T | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.964-17068G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136291905 | |||||||
| chr5:136291912 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.964-17075A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136291912 | |||||||
| chr5:136292142 | A | C | 68 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(65): Show |
69 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.964-17305T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136292142 | |||||||
| chr5:136292429 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.964-17592A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136292429 | |||||||
| chr5:136292448 | A | C | 1 | a0001c0001t0001g0162 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.964-17611T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136292448 | |||||||
| chr5:136292469 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.964-17632G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136292469 | |||||||
| chr5:136292563 | T | G | 1 | a0001c0001t0001g0176 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.964-17726A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136292563 | |||||||
| chr5:136292639 | G | A | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.964-17802C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136292639 | |||||||
| chr5:136292686 | T | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.964-17849A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136292686 | |||||||
| chr5:136292699 | G | A | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0115 |
3 | NA18988.hp2 NA18990.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.964-17862C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136292699 | |||||||
| chr5:136292720 | G | T | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.964-17883C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136292720 | |||||||
| chr5:136292839 | C | CA | 21 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(18): Show |
22 | HG00323.hp1 HG00733.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.964-18003dupT | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136292839 | |||||||
| chr5:136293155 | G | C | 1 | a0001c0001t0001g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.964-18318C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136293155 | |||||||
| chr5:136293327 | T | C | 66 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0021 others(63): Show |
67 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.964-18490A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136293327 | |||||||
| chr5:136293356 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.964-18519G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136293356 | |||||||
| chr5:136293395 | C | T | 38 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(35): Show |
40 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.964-18558G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136293395 | |||||||
| chr5:136293441 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.964-18604C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136293441 | |||||||
| chr5:136293529 | T | C | 1 | a0001c0002t0002g0242 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.964-18692A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136293529 | |||||||
| chr5:136293564 | T | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.964-18727A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136293564 | |||||||
| chr5:136293629 | T | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.964-18792A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136293629 | |||||||
| chr5:136293728 | T | C | 8 | a0001c0001t0001g0030 a0001c0002t0002g0233 a0001c0002t0002g0234 others(5): Show |
8 | HG01258.hp1 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-18891A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136293728 | |||||||
| chr5:136293736 | G | A | 8 | a0001c0001t0001g0030 a0001c0002t0002g0233 a0001c0002t0002g0234 others(5): Show |
8 | HG01258.hp1 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-18899C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136293736 | |||||||
| chr5:136293749 | C | A | 8 | a0001c0001t0001g0030 a0001c0002t0002g0233 a0001c0002t0002g0234 others(5): Show |
8 | HG01258.hp1 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-18912G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136293749 | |||||||
| chr5:136293787 | C | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.964-18950G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136293787 | |||||||
| chr5:136293817 | G | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02257.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.964-18980C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136293817 | |||||||
| chr5:136293945 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.964-19108T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136293945 | |||||||
| chr5:136293995 | C | G | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.964-19158G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136293995 | |||||||
| chr5:136294137 | A | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(54): Show |
58 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.964-19300T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136294137 | |||||||
| chr5:136294280 | C | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.964-19443G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136294280 | |||||||
| chr5:136294308 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.964-19471C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136294308 | |||||||
| chr5:136294332 | C | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.964-19495G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136294332 | |||||||
| chr5:136294360 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.964-19523C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136294360 | |||||||
| chr5:136294372 | T | A | 1 | a0001c0001t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.964-19535A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136294372 | |||||||
| chr5:136294375 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.964-19538G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136294375 | |||||||
| chr5:136294377 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.964-19540A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136294377 | |||||||
| chr5:136294385 | A | G | 2 | a0001c0002t0005g0025 a0001c0002t0005g0028 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.964-19548T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136294385 | |||||||
| chr5:136294399 | T | G | 1 | a0001c0001t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.964-19562A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136294399 | |||||||
| chr5:136294402 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.964-19565A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136294402 | |||||||
| chr5:136294473 | G | A | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.964-19636C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136294473 | |||||||
| chr5:136294476 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.964-19639C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136294476 | |||||||
| chr5:136294544 | C | T | 8 | a0001c0001t0001g0030 a0001c0002t0002g0233 a0001c0002t0002g0234 others(5): Show |
8 | HG01258.hp1 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-19707G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136294544 | |||||||
| chr5:136294545 | A | T | 2 | a0001c0002t0002g0242 a0001c0002t0002g0253 |
2 | NA18989.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.964-19708T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136294545 | |||||||
| chr5:136294548 | A | G | 1 | a0001c0002t0002g0235 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.964-19711T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136294548 | |||||||
| chr5:136294551 | C | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.964-19714G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136294551 | |||||||
| chr5:136294617 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.964-19780T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136294617 | |||||||
| chr5:136294635 | A | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.964-19798T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136294635 | |||||||
| chr5:136294676 | A | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.964-19839T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136294676 | |||||||
| chr5:136294852 | C | T | 134 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(131): Show |
136 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.964-20015G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136294852 | |||||||
| chr5:136294899 | G | T | 1 | a0001c0001t0001g0081 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.964-20062C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136294899 | |||||||
| chr5:136294948 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.964-20111T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136294948 | |||||||
| chr5:136295098 | T | C | 58 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(55): Show |
59 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.964-20261A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136295098 | |||||||
| chr5:136295486 | G | A | 1 | a0001c0002t0002g0187 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.963+20111C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136295486 | |||||||
| chr5:136295511 | A | G | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+20086T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136295511 | |||||||
| chr5:136295614 | A | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.963+19983T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136295614 | |||||||
| chr5:136295761 | A | G | 21 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(18): Show |
22 | HG00323.hp1 HG00733.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.963+19836T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136295761 | |||||||
| chr5:136295885 | C | G | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.963+19712G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136295885 | |||||||
| chr5:136295899 | C | T | 2 | a0001c0001t0001g0034 a0001c0002t0002g0225 |
2 | HG03225.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.963+19698G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136295899 | |||||||
| chr5:136295900 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.963+19697T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136295900 | |||||||
| chr5:136295983 | T | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+19614A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136295983 | |||||||
| chr5:136295998 | C | T | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+19599G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136295998 | |||||||
| chr5:136296009 | C | G | 1 | a0001c0001t0001g0058 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.963+19588G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136296009 | |||||||
| chr5:136296083 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.963+19514G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136296083 | |||||||
| chr5:136296108 | G | GTGGTGTG others(8): Show |
1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.963+19474_963+1948 others(19): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136296108 | |||||||
| chr5:136296138 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.963+19459C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136296138 | |||||||
| chr5:136296155 | G | T | 67 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(64): Show |
68 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.963+19442C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136296155 | |||||||
| chr5:136296296 | G | A | 1 | a0001c0002t0001g0029 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.963+19301C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136296296 | |||||||
| chr5:136296306 | C | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.963+19291G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136296306 | |||||||
| chr5:136296528 | A | T | 68 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(65): Show |
69 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.963+19069T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136296528 | |||||||
| chr5:136296622 | T | A | 58 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(55): Show |
59 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.963+18975A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136296622 | |||||||
| chr5:136296783 | T | C | 1 | a0001c0002t0001g0114 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.963+18814A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136296783 | |||||||
| chr5:136297133 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963+18464T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136297133 | |||||||
| chr5:136297148 | C | G | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.963+18449G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136297148 | |||||||
| chr5:136297163 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.963+18434G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136297163 | |||||||
| chr5:136297667 | A | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0044 |
3 | NA18960.hp1 NA18980.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.963+17930T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136297667 | |||||||
| chr5:136297703 | T | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+17894A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136297703 | |||||||
| chr5:136297962 | A | ACATT | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+17631_963+1763 others(8): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136297962 | |||||||
| chr5:136298030 | G | C | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.963+17567C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136298030 | |||||||
| chr5:136298053 | G | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+17544C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136298053 | |||||||
| chr5:136298137 | A | C | 1 | a0001c0001t0001g0170 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.963+17460T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136298137 | |||||||
| chr5:136298189 | C | G | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+17408G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136298189 | |||||||
| chr5:136298289 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.963+17308G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136298289 | |||||||
| chr5:136298803 | C | T | 1 | a0001c0002t0002g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.963+16794G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136298803 | |||||||
| chr5:136299119 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(54): Show |
58 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.963+16478A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299119 | |||||||
| chr5:136299162 | G | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+16435C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299162 | |||||||
| chr5:136299168 | G | A | 67 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0021 others(64): Show |
68 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.963+16429C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299168 | |||||||
| chr5:136299292 | T | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+16305A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299292 | |||||||
| chr5:136299300 | C | CA | 8 | a0001c0001t0001g0055 a0001c0002t0002g0233 a0001c0002t0002g0234 others(5): Show |
8 | HG01258.hp1 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.963+16296dupT | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299300 | |||||||
| chr5:136299300 | C | CAA | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+16295_963+1629 others(6): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299300 | |||||||
| chr5:136299300 | CA | C | 17 | a0001c0001t0001g0097 a0001c0001t0001g0144 a0001c0001t0001g0148 others(14): Show |
17 | HG00621.hp1 HG01169.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.963+16296delT | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299300 | |||||||
| chr5:136299323 | T | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+16274A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299323 | |||||||
| chr5:136299332 | GGT | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+16263_963+1626 others(6): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299332 | |||||||
| chr5:136299332 | GGTGTGTG others(7): Show |
G | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.963+16251_963+1626 others(18): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299332 | |||||||
| chr5:136299334 | TGTGTGC | T | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.963+16257_963+1626 others(10): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299334 | |||||||
| chr5:136299336 | TGTGC | T | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
4 | HG02572.hp1 HG03225.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+16257_963+1626 others(8): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299336 | |||||||
| chr5:136299340 | C | CGT | 15 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(12): Show |
15 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.963+16255_963+1625 others(6): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299340 | |||||||
| chr5:136299340 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.963+16257G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299340 | |||||||
| chr5:136299340 | CGT | C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0071 others(13): Show |
17 | HG01257.hp1 HG01258.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.963+16255_963+1625 others(6): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299340 | |||||||
| chr5:136299340 | CGTGT | C | 46 | a0001c0001t0001g0021 a0001c0001t0001g0065 a0001c0001t0001g0076 others(43): Show |
46 | HG00099.hp1 HG00408.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.963+16253_963+1625 others(8): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299340 | |||||||
| chr5:136299340 | CGTGTGT | C | 18 | a0001c0001t0001g0073 a0001c0001t0001g0078 a0001c0002t0002g0234 others(15): Show |
18 | HG00621.hp1 HG01099.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.963+16251_963+1625 others(10): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299340 | |||||||
| chr5:136299340 | CGTGTGTG others(3): Show |
C | 1 | a0001c0002t0002g0214 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.963+16247_963+1625 others(14): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299340 | |||||||
| chr5:136299340 | CGTGTGTG others(5): Show |
C | 3 | a0001c0002t0002g0190 a0001c0002t0002g0201 a0001c0007t0002g0189 |
3 | HG01069.hp1 HG01175.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.963+16245_963+1625 others(16): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299340 | |||||||
| chr5:136299342 | T | C | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(2): Show |
5 | HG02040.hp2 HG02572.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.963+16255A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299342 | |||||||
| chr5:136299344 | T | C | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.963+16253A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299344 | |||||||
| chr5:136299352 | T | C | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.963+16245A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299352 | |||||||
| chr5:136299403 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.963+16194C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299403 | |||||||
| chr5:136299673 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0112 |
2 | HG02486.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.963+15924C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299673 | |||||||
| chr5:136299922 | A | G | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+15675T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299922 | |||||||
| chr5:136299923 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0172 |
2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.963+15674G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136299923 | |||||||
| chr5:136300119 | A | C | 1 | a0001c0002t0002g0212 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.963+15478T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136300119 | |||||||
| chr5:136300120 | C | A | 1 | a0001c0002t0002g0212 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.963+15477G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136300120 | |||||||
| chr5:136300143 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.963+15454C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136300143 | |||||||
| chr5:136300275 | A | G | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+15322T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136300275 | |||||||
| chr5:136300302 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.963+15295C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136300302 | |||||||
| chr5:136300371 | C | A | 1 | a0001c0002t0003g0238 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.963+15226G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136300371 | |||||||
| chr5:136300523 | T | G | 1 | a0001c0001t0001g0151 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.963+15074A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136300523 | |||||||
| chr5:136300594 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.963+15003T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136300594 | |||||||
| chr5:136300668 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.963+14929C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136300668 | |||||||
| chr5:136300679 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.963+14918C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136300679 | |||||||
| chr5:136300738 | G | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(12): Show |
17 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.963+14859C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136300738 | |||||||
| chr5:136301038 | C | T | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+14559G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301038 | |||||||
| chr5:136301050 | G | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.963+14547C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301050 | |||||||
| chr5:136301092 | T | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+14505A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301092 | |||||||
| chr5:136301152 | G | T | 5 | a0001c0002t0001g0027 a0001c0002t0001g0029 a0001c0002t0005g0025 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+14445C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301152 | |||||||
| chr5:136301217 | G | A | 6 | a0001c0002t0002g0188 a0001c0002t0002g0209 a0001c0002t0002g0211 others(3): Show |
6 | HG00741.hp2 HG02818.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.963+14380C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301217 | |||||||
| chr5:136301258 | G | A | 65 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0076 others(62): Show |
66 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.963+14339C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301258 | |||||||
| chr5:136301271 | C | T | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.963+14326G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301271 | |||||||
| chr5:136301292 | G | T | 1 | a0001c0001t0001g0158 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.963+14305C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301292 | |||||||
| chr5:136301294 | T | C | 5 | a0001c0001t0001g0066 a0001c0001t0001g0144 a0001c0001t0001g0145 others(2): Show |
5 | HG00642.hp2 HG03669.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.963+14303A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301294 | |||||||
| chr5:136301304 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.963+14293T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301304 | |||||||
| chr5:136301308 | T | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+14289A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301308 | |||||||
| chr5:136301326 | C | A | 7 | a0001c0002t0002g0233 a0001c0002t0002g0234 a0001c0002t0002g0235 others(4): Show |
7 | HG01258.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.963+14271G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301326 | |||||||
| chr5:136301332 | A | AT | 35 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(32): Show |
36 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.963+14264dupA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301332 | |||||||
| chr5:136301332 | A | ATT | 42 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0036 others(39): Show |
43 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.963+14263_963+1426 others(6): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301332 | |||||||
| chr5:136301332 | A | ATTT | 23 | a0001c0001t0001g0076 a0001c0002t0002g0186 a0001c0002t0002g0188 others(20): Show |
23 | HG00099.hp1 HG00741.hp2 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.963+14262_963+1426 others(7): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301332 | |||||||
| chr5:136301332 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0068 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.963+14255_963+1426 others(14): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301332 | |||||||
| chr5:136301332 | AT | A | 8 | a0001c0001t0001g0030 a0001c0001t0001g0115 a0001c0001t0001g0117 others(5): Show |
8 | HG00741.hp1 HG03209.hp1 NA18978.hp2 others(5): Show |
intron_variant | MODIFIER | c.963+14264delA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301332 | |||||||
| chr5:136301332 | ATT | A | 5 | a0001c0002t0002g0234 a0001c0002t0002g0235 a0001c0002t0002g0237 others(2): Show |
5 | HG01258.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.963+14263_963+1426 others(6): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301332 | |||||||
| chr5:136301349 | TTTTTTTT others(5): Show |
T | 2 | a0001c0002t0002g0230 a0001c0002t0002g0231 |
2 | HG01496.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.963+14236_963+1424 others(16): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301349 | |||||||
| chr5:136301359 | TTA | T | 58 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(55): Show |
59 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.963+14236_963+1423 others(6): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301359 | |||||||
| chr5:136301360 | TA | T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(14): Show |
18 | HG00639.hp2 HG00735.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.963+14236delT | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301360 | |||||||
| chr5:136301361 | A | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(88): Show |
92 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.963+14236T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301361 | |||||||
| chr5:136301389 | C | CA | 6 | a0001c0001t0001g0139 a0001c0001t0001g0146 a0001c0001t0001g0165 others(3): Show |
6 | HG00741.hp1 HG01109.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.963+14207_963+1420 others(5): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301389 | |||||||
| chr5:136301390 | C | A | 6 | a0001c0001t0001g0139 a0001c0001t0001g0146 a0001c0001t0001g0165 others(3): Show |
6 | HG00741.hp1 HG01109.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.963+14207G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301390 | |||||||
| chr5:136301422 | T | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+14175A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301422 | |||||||
| chr5:136301587 | C | A | 1 | a0001c0001t0001g0049 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.963+14010G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301587 | |||||||
| chr5:136301606 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.963+13991A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301606 | |||||||
| chr5:136301736 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.963+13861G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301736 | |||||||
| chr5:136301744 | G | A | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
4 | HG02572.hp1 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+13853C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301744 | |||||||
| chr5:136301890 | T | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+13707A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301890 | |||||||
| chr5:136301941 | C | G | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+13656G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301941 | |||||||
| chr5:136301987 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02559.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+13610G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301987 | |||||||
| chr5:136301988 | G | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+13609C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136301988 | |||||||
| chr5:136302153 | A | G | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+13444T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136302153 | |||||||
| chr5:136302227 | A | G | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+13370T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136302227 | |||||||
| chr5:136302297 | T | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(12): Show |
17 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.963+13300A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136302297 | |||||||
| chr5:136302321 | C | T | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.963+13276G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136302321 | |||||||
| chr5:136302324 | T | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+13273A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136302324 | |||||||
| chr5:136302393 | T | C | 1 | a0001c0002t0002g0232 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.963+13204A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136302393 | |||||||
| chr5:136302541 | G | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(193): Show |
201 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.963+13056C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136302541 | |||||||
| chr5:136302698 | G | A | 1 | a0001c0002t0005g0028 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.963+12899C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136302698 | |||||||
| chr5:136302771 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02257.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.963+12826C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136302771 | |||||||
| chr5:136302859 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.963+12738G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136302859 | |||||||
| chr5:136302972 | A | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+12625T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136302972 | |||||||
| chr5:136302972 | A | G | 67 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(64): Show |
68 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.963+12625T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136302972 | |||||||
| chr5:136303081 | T | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.963+12516A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136303081 | |||||||
| chr5:136303086 | A | G | 1 | a0001c0002t0002g0218 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.963+12511T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136303086 | |||||||
| chr5:136303096 | C | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.963+12501G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136303096 | |||||||
| chr5:136303117 | G | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+12480C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136303117 | |||||||
| chr5:136303209 | T | G | 1 | a0001c0002t0002g0221 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.963+12388A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136303209 | |||||||
| chr5:136303218 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.963+12379A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136303218 | |||||||
| chr5:136303226 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.963+12371C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136303226 | |||||||
| chr5:136303325 | A | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.963+12272T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136303325 | |||||||
| chr5:136303332 | C | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(1): Show |
4 | NA18959.hp2 NA18969.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+12265G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136303332 | |||||||
| chr5:136303366 | C | T | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.963+12231G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136303366 | |||||||
| chr5:136303608 | G | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0095 a0001c0001t0001g0160 |
3 | HG01109.hp2 HG01175.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.963+11989C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136303608 | |||||||
| chr5:136303809 | C | A | 1 | a0001c0002t0002g0188 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.963+11788G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136303809 | |||||||
| chr5:136303826 | A | G | 8 | a0001c0001t0001g0030 a0001c0002t0002g0233 a0001c0002t0002g0234 others(5): Show |
8 | HG01258.hp1 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.963+11771T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136303826 | |||||||
| chr5:136303880 | T | A | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.963+11717A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136303880 | |||||||
| chr5:136304001 | G | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+11596C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136304001 | |||||||
| chr5:136304030 | A | T | 67 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(64): Show |
68 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.963+11567T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136304030 | |||||||
| chr5:136304070 | AG | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(32): Show |
37 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.963+11526delC | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136304070 | |||||||
| chr5:136304135 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.963+11462A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136304135 | |||||||
| chr5:136304139 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.963+11458A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136304139 | |||||||
| chr5:136304142 | C | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.963+11455G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136304142 | |||||||
| chr5:136304190 | T | C | 35 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(32): Show |
37 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.963+11407A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136304190 | |||||||
| chr5:136304234 | G | C | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.963+11363C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136304234 | |||||||
| chr5:136304235 | GA | G | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.963+11361delT | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136304235 | |||||||
| chr5:136304287 | G | A | 68 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0031 others(65): Show |
69 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.963+11310C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136304287 | |||||||
| chr5:136304345 | C | T | 4 | a0001c0002t0002g0224 a0001c0002t0002g0225 a0001c0002t0002g0226 others(1): Show |
4 | HG02132.hp1 NA18979.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+11252G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136304345 | |||||||
| chr5:136304395 | TC | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
176 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.963+11201delG | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136304395 | |||||||
| chr5:136304419 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.963+11178G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136304419 | |||||||
| chr5:136304462 | A | T | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.963+11135T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136304462 | |||||||
| chr5:136304479 | G | A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(131): Show |
136 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.963+11118C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136304479 | |||||||
| chr5:136304484 | C | A | 1 | a0001c0002t0002g0200 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.963+11113G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136304484 | |||||||
| chr5:136304488 | G | A | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(132): Show |
137 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.963+11109C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136304488 | |||||||
| chr5:136304673 | G | A | 1 | a0001c0001t0001g0003 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.963+10924C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136304673 | |||||||
| chr5:136304696 | A | T | 4 | a0001c0001t0001g0079 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
4 | HG02698.hp2 HG02735.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+10901T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136304696 | |||||||
| chr5:136304742 | CG | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.963+10854delC | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136304742 | |||||||
| chr5:136304743 | G | A | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.963+10854C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136304743 | |||||||
| chr5:136304761 | A | G | 1 | a0001c0002t0003g0238 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.963+10836T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136304761 | |||||||
| chr5:136304889 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.963+10708C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136304889 | |||||||
| chr5:136305051 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.963+10546C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136305051 | |||||||
| chr5:136305071 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.963+10526G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136305071 | |||||||
| chr5:136305092 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.963+10505C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136305092 | |||||||
| chr5:136305150 | C | T | 1 | a0001c0002t0002g0187 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.963+10447G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136305150 | |||||||
| chr5:136305295 | T | C | 27 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(24): Show |
27 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.963+10302A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136305295 | |||||||
| chr5:136305306 | C | G | 7 | a0001c0002t0002g0233 a0001c0002t0002g0234 a0001c0002t0002g0235 others(4): Show |
7 | HG01258.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.963+10291G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136305306 | |||||||
| chr5:136305312 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.963+10285G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136305312 | |||||||
| chr5:136305317 | C | G | 67 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0076 others(64): Show |
68 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.963+10280G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136305317 | |||||||
| chr5:136305319 | C | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.963+10278G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136305319 | |||||||
| chr5:136305324 | C | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.963+10273G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136305324 | |||||||
| chr5:136305473 | G | T | 1 | a0001c0002t0002g0223 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.963+10124C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136305473 | |||||||
| chr5:136305590 | A | C | 67 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(64): Show |
68 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.963+10007T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136305590 | |||||||
| chr5:136305669 | C | T | 1 | a0001c0002t0001g0114 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.963+9928G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136305669 | |||||||
| chr5:136305994 | C | T | 67 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(64): Show |
68 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.963+9603G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136305994 | |||||||
| chr5:136306112 | G | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(54): Show |
58 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.963+9485C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136306112 | |||||||
| chr5:136306187 | G | A | 1 | a0001c0002t0002g0217 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.963+9410C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136306187 | |||||||
| chr5:136306213 | A | C | 1 | a0001c0001t0001g0142 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.963+9384T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136306213 | |||||||
| chr5:136306342 | A | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.963+9255T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136306342 | |||||||
| chr5:136306528 | A | G | 8 | a0001c0001t0001g0030 a0001c0002t0002g0233 a0001c0002t0002g0234 others(5): Show |
8 | HG01258.hp1 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.963+9069T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136306528 | |||||||
| chr5:136306594 | G | A | 1 | a0001c0002t0002g0202 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.963+9003C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136306594 | |||||||
| chr5:136306710 | C | T | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.963+8887G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136306710 | |||||||
| chr5:136306846 | C | A | 1 | a0001c0001t0001g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.963+8751G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136306846 | |||||||
| chr5:136306858 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.963+8739A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136306858 | |||||||
| chr5:136306933 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.963+8664C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136306933 | |||||||
| chr5:136306977 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.963+8620G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136306977 | |||||||
| chr5:136306982 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.963+8615T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136306982 | |||||||
| chr5:136306996 | G | A | 1 | a0001c0002t0002g0191 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.963+8601C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136306996 | |||||||
| chr5:136307015 | A | G | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
190 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.963+8582T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136307015 | |||||||
| chr5:136307018 | C | A | 2 | a0001c0002t0002g0230 a0001c0002t0002g0231 |
2 | HG01496.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.963+8579G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136307018 | |||||||
| chr5:136307327 | T | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(34): Show |
39 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+8270A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136307327 | |||||||
| chr5:136307396 | CTT | C | 5 | a0001c0002t0001g0027 a0001c0002t0001g0029 a0001c0002t0005g0025 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+8199_963+8200d others(4): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136307396 | |||||||
| chr5:136307400 | C | T | 1 | a0001c0002t0002g0253 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.963+8197G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136307400 | |||||||
| chr5:136307586 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.963+8011T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136307586 | |||||||
| chr5:136307625 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 |
4 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+7972G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136307625 | |||||||
| chr5:136307642 | A | G | 72 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0069 others(69): Show |
73 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.963+7955T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136307642 | |||||||
| chr5:136307762 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.963+7835G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136307762 | |||||||
| chr5:136307889 | G | C | 1 | a0001c0002t0002g0217 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.963+7708C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136307889 | |||||||
| chr5:136308036 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.963+7561G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136308036 | |||||||
| chr5:136308040 | C | T | 6 | a0001c0002t0002g0188 a0001c0002t0002g0209 a0001c0002t0002g0211 others(3): Show |
6 | HG00741.hp2 HG02818.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.963+7557G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136308040 | |||||||
| chr5:136308044 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.963+7553G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136308044 | |||||||
| chr5:136308071 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.963+7526G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136308071 | |||||||
| chr5:136308180 | G | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.963+7417C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136308180 | |||||||
| chr5:136308255 | C | T | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(227): Show |
234 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.963+7342G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136308255 | |||||||
| chr5:136308731 | G | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+6866C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136308731 | |||||||
| chr5:136308953 | C | T | 7 | a0001c0001t0001g0021 a0001c0002t0001g0027 a0001c0002t0001g0029 others(4): Show |
7 | HG02109.hp1 HG02280.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.963+6644G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136308953 | |||||||
| chr5:136309078 | T | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 |
3 | NA18959.hp2 NA18969.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.963+6519A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136309078 | |||||||
| chr5:136309327 | C | T | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | HG01952.hp1 HG03834.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+6270G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136309327 | |||||||
| chr5:136309356 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.963+6241C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136309356 | |||||||
| chr5:136309379 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.963+6218G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136309379 | |||||||
| chr5:136309394 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.963+6203T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136309394 | |||||||
| chr5:136309514 | C | T | 69 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0076 others(66): Show |
70 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.963+6083G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136309514 | |||||||
| chr5:136309530 | G | A | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.963+6067C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136309530 | |||||||
| chr5:136309652 | T | G | 1 | a0001c0001t0001g0089 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.963+5945A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136309652 | |||||||
| chr5:136310014 | A | G | 72 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0069 others(69): Show |
73 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.963+5583T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136310014 | |||||||
| chr5:136310168 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.963+5429T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136310168 | |||||||
| chr5:136310278 | T | C | 4 | a0001c0002t0002g0196 a0001c0002t0002g0197 a0001c0002t0002g0198 others(1): Show |
4 | HG01243.hp2 HG01884.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+5319A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136310278 | |||||||
| chr5:136310332 | AT | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
109 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.963+5264delA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136310332 | |||||||
| chr5:136310517 | T | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
109 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.963+5080A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136310517 | |||||||
| chr5:136310574 | AG | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(9): Show |
14 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.963+5022delC | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136310574 | |||||||
| chr5:136310760 | G | T | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.963+4837C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136310760 | |||||||
| chr5:136310820 | T | C | 1 | a0001c0002t0002g0191 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.963+4777A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136310820 | |||||||
| chr5:136310851 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.963+4746C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136310851 | |||||||
| chr5:136310913 | C | T | 1 | a0001c0002t0002g0202 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.963+4684G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136310913 | |||||||
| chr5:136311116 | C | T | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.963+4481G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136311116 | |||||||
| chr5:136311307 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.963+4290C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136311307 | |||||||
| chr5:136311324 | G | C | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0042 |
3 | HG00423.hp2 NA19057.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.963+4273C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136311324 | |||||||
| chr5:136311424 | G | A | 4 | a0001c0001t0001g0079 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
4 | HG02698.hp2 HG02735.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+4173C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136311424 | |||||||
| chr5:136311495 | C | A | 4 | a0001c0001t0001g0079 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
4 | HG02698.hp2 HG02735.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+4102G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136311495 | |||||||
| chr5:136311649 | C | A | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.963+3948G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136311649 | |||||||
| chr5:136311808 | G | A | 69 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0076 others(66): Show |
70 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.963+3789C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136311808 | |||||||
| chr5:136311814 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.963+3783C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136311814 | |||||||
| chr5:136312092 | T | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(114): Show |
120 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.963+3505A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136312092 | |||||||
| chr5:136312248 | C | T | 1 | a0001c0002t0002g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.963+3349G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136312248 | |||||||
| chr5:136312429 | G | C | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.963+3168C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136312429 | |||||||
| chr5:136312526 | T | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(1): Show |
5 | HG01243.hp1 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+3071A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136312526 | |||||||
| chr5:136312536 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
97 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.963+3061G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136312536 | |||||||
| chr5:136312884 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.963+2713G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136312884 | |||||||
| chr5:136312972 | C | CT | 71 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0034 others(68): Show |
72 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.963+2624dupA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136312972 | |||||||
| chr5:136312972 | C | CTT | 8 | a0001c0001t0001g0123 a0001c0001t0001g0139 a0001c0001t0001g0140 others(5): Show |
8 | HG00741.hp1 HG01175.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.963+2623_963+2624d others(4): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136312972 | |||||||
| chr5:136312972 | C | CTTTTT | 7 | a0001c0001t0001g0030 a0001c0002t0002g0233 a0001c0002t0002g0234 others(4): Show |
7 | HG01258.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.963+2620_963+2624d others(7): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136312972 | |||||||
| chr5:136312972 | CT | C | 18 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(15): Show |
18 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(15): Show |
intron_variant | MODIFIER | c.963+2624delA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136312972 | |||||||
| chr5:136312972 | CTT | C | 22 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(19): Show |
22 | HG00673.hp1 HG00733.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.963+2623_963+2624d others(4): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136312972 | |||||||
| chr5:136312972 | CTTT | C | 50 | a0001c0001t0001g0021 a0001c0001t0001g0076 a0001c0001t0001g0077 others(47): Show |
50 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.963+2622_963+2624d others(5): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136312972 | |||||||
| chr5:136312972 | CTTTT | C | 6 | a0001c0001t0001g0003 a0001c0002t0002g0188 a0001c0002t0002g0204 others(3): Show |
7 | HG01496.hp1 HG02280.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.963+2621_963+2624d others(6): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136312972 | |||||||
| chr5:136313004 | A | G | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.963+2593T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136313004 | |||||||
| chr5:136313297 | G | C | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.963+2300C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136313297 | |||||||
| chr5:136313371 | ATGTC | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(101): Show |
107 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.963+2222_963+2225d others(6): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136313371 | |||||||
| chr5:136313373 | G | GTCTA | 37 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0017 others(34): Show |
37 | HG00639.hp1 HG00673.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.963+2223_963+2224i others(6): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136313373 | |||||||
| chr5:136313373 | G | GTCTATCT others(1): Show |
4 | a0001c0001t0001g0016 a0001c0001t0001g0146 a0001c0001t0001g0173 others(1): Show |
4 | HG00323.hp2 HG03139.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+2223_963+2224i others(10): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136313373 | |||||||
| chr5:136313373 | GTCTGTCT others(1): Show |
G | 7 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0075 others(4): Show |
8 | HG01243.hp1 HG02074.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.963+2216_963+2223d others(10): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136313373 | |||||||
| chr5:136313373 | GTCTGTCT others(5): Show |
G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0001g0130 |
3 | HG00408.hp1 HG03209.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.963+2212_963+2223d others(14): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136313373 | |||||||
| chr5:136313373 | GTCTGTCT others(9): Show |
G | 7 | a0001c0002t0002g0233 a0001c0002t0002g0234 a0001c0002t0002g0235 others(4): Show |
7 | HG01258.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.963+2208_963+2223d others(18): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136313373 | |||||||
| chr5:136313377 | G | A | 128 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(125): Show |
129 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.963+2220C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136313377 | |||||||
| chr5:136313421 | G | A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(14): Show |
19 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.963+2176C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136313421 | |||||||
| chr5:136313644 | G | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0057 a0001c0001t0001g0061 |
3 | NA18986.hp2 NA18988.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.963+1953C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136313644 | |||||||
| chr5:136313731 | T | G | 1 | a0001c0001t0001g0112 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963+1866A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136313731 | |||||||
| chr5:136313813 | C | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(2): Show |
6 | HG02559.hp2 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.963+1784G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136313813 | |||||||
| chr5:136314002 | C | A | 27 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(24): Show |
27 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.963+1595G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136314002 | |||||||
| chr5:136314571 | T | A | 1 | a0001c0002t0002g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.963+1026A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136314571 | |||||||
| chr5:136314610 | A | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
187 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.963+987T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136314610 | |||||||
| chr5:136314622 | T | C | 1 | a0001c0001t0001g0066 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.963+975A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136314622 | |||||||
| chr5:136314820 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.963+777T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136314820 | |||||||
| chr5:136315173 | A | T | 1 | a0001c0001t0001g0155 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.963+424T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136315173 | |||||||
| chr5:136315289 | G | A | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.963+308C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136315289 | |||||||
| chr5:136315308 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.963+289C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136315308 | |||||||
| chr5:136315555 | G | A | 69 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0076 others(66): Show |
70 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.963+42C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 3/11 | chr5 | 136315555 | |||||||
| chr5:136315921 | A | C | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
26 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.781-142T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136315921 | |||||||
| chr5:136316252 | G | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
187 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.781-473C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136316252 | |||||||
| chr5:136316526 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 |
3 | NA18959.hp2 NA18969.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.781-747C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136316526 | |||||||
| chr5:136316534 | C | T | 60 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(57): Show |
61 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.781-755G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136316534 | |||||||
| chr5:136316587 | C | T | 1 | a0001c0002t0002g0234 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.781-808G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136316587 | |||||||
| chr5:136316737 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.781-958G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136316737 | |||||||
| chr5:136316854 | A | G | 1 | a0001c0002t0002g0215 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.781-1075T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136316854 | |||||||
| chr5:136316953 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.781-1174G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136316953 | |||||||
| chr5:136317055 | C | T | 1 | a0001c0002t0002g0186 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.781-1276G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136317055 | |||||||
| chr5:136317193 | G | A | 1 | a0001c0002t0001g0114 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.781-1414C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136317193 | |||||||
| chr5:136317354 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.781-1575C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136317354 | |||||||
| chr5:136317782 | G | T | 1 | a0001c0002t0003g0246 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.781-2003C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136317782 | |||||||
| chr5:136317817 | T | G | 1 | a0001c0001t0001g0180 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.781-2038A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136317817 | |||||||
| chr5:136317863 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.781-2084G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136317863 | |||||||
| chr5:136317960 | G | T | 1 | a0001c0001t0001g0176 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.781-2181C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136317960 | |||||||
| chr5:136317978 | A | C | 1 | a0001c0001t0001g0176 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.781-2199T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136317978 | |||||||
| chr5:136317999 | A | G | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.781-2220T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136317999 | |||||||
| chr5:136318049 | C | A | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
26 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.781-2270G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136318049 | |||||||
| chr5:136318050 | G | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
187 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.781-2271C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136318050 | |||||||
| chr5:136318092 | A | G | 3 | a0001c0002t0002g0247 a0001c0002t0003g0246 a0001c0002t0003g0248 |
3 | HG00621.hp1 NA18956.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.781-2313T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136318092 | |||||||
| chr5:136318094 | G | A | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
26 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.781-2315C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136318094 | |||||||
| chr5:136318251 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.781-2472T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136318251 | |||||||
| chr5:136318509 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.781-2730G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136318509 | |||||||
| chr5:136318870 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.781-3091G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136318870 | |||||||
| chr5:136319385 | T | C | 8 | a0001c0001t0001g0030 a0001c0002t0002g0233 a0001c0002t0002g0234 others(5): Show |
8 | HG01258.hp1 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.781-3606A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136319385 | |||||||
| chr5:136319411 | A | AT | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.781-3633dupA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136319411 | |||||||
| chr5:136319413 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
187 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.781-3634G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136319413 | |||||||
| chr5:136319448 | T | C | 47 | a0001c0001t0001g0045 a0001c0001t0001g0052 a0001c0001t0001g0053 others(44): Show |
47 | HG00099.hp2 HG00558.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.781-3669A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136319448 | |||||||
| chr5:136319569 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.781-3790A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136319569 | |||||||
| chr5:136319726 | AG | A | 70 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0069 others(67): Show |
71 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.781-3948delC | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136319726 | |||||||
| chr5:136319729 | G | T | 70 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0069 others(67): Show |
71 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.781-3950C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136319729 | |||||||
| chr5:136319731 | T | C | 70 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0069 others(67): Show |
71 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.781-3952A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136319731 | |||||||
| chr5:136319771 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.781-3992G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136319771 | |||||||
| chr5:136319839 | T | A | 60 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(57): Show |
61 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.781-4060A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136319839 | |||||||
| chr5:136319895 | CTG | C | 69 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0076 others(66): Show |
70 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.781-4118_781-4117d others(4): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136319895 | |||||||
| chr5:136320088 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
187 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.781-4309G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136320088 | |||||||
| chr5:136320120 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.781-4341G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136320120 | |||||||
| chr5:136320158 | C | CA | 70 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0076 others(67): Show |
71 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.781-4380dupT | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136320158 | |||||||
| chr5:136320158 | CA | C | 9 | a0001c0001t0001g0030 a0001c0001t0001g0132 a0001c0002t0002g0233 others(6): Show |
9 | HG01258.hp1 HG02647.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.781-4380delT | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136320158 | |||||||
| chr5:136320490 | G | A | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
26 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.781-4711C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136320490 | |||||||
| chr5:136320681 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.781-4902C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136320681 | |||||||
| chr5:136320689 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.781-4910A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136320689 | |||||||
| chr5:136320706 | G | T | 2 | a0001c0002t0002g0244 a0001c0002t0002g0245 |
2 | HG01952.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.781-4927C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136320706 | |||||||
| chr5:136320755 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.781-4976T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136320755 | |||||||
| chr5:136320896 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.781-5117A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136320896 | |||||||
| chr5:136321210 | G | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.781-5431C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136321210 | |||||||
| chr5:136321290 | G | C | 1 | a0001c0001t0001g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.781-5511C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136321290 | |||||||
| chr5:136321404 | G | A | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.781-5625C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136321404 | |||||||
| chr5:136321526 | C | A | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.781-5747G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136321526 | |||||||
| chr5:136321623 | A | G | 1 | a0001c0002t0002g0194 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.781-5844T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136321623 | |||||||
| chr5:136321820 | G | A | 1 | a0001c0002t0002g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.781-6041C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136321820 | |||||||
| chr5:136322019 | AT | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0002t0001g0027 others(5): Show |
8 | HG02109.hp1 HG02280.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.781-6241delA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136322019 | |||||||
| chr5:136322036 | A | G | 69 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0076 others(66): Show |
70 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.781-6257T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136322036 | |||||||
| chr5:136322038 | G | A | 1 | a0001c0008t0007g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.781-6259C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136322038 | |||||||
| chr5:136322149 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.781-6370C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136322149 | |||||||
| chr5:136322171 | A | G | 2 | a0001c0002t0002g0237 a0001c0002t0002g0239 |
2 | HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.781-6392T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136322171 | |||||||
| chr5:136322375 | T | A | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.781-6596A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136322375 | |||||||
| chr5:136322986 | T | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(85): Show |
91 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.781-7207A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136322986 | |||||||
| chr5:136323005 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.781-7226G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136323005 | |||||||
| chr5:136323006 | C | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.781-7227G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136323006 | |||||||
| chr5:136323030 | G | A | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.781-7251C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136323030 | |||||||
| chr5:136323072 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.781-7293C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136323072 | |||||||
| chr5:136323476 | T | C | 1 | a0001c0002t0002g0212 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.781-7697A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136323476 | |||||||
| chr5:136323497 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.781-7718C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136323497 | |||||||
| chr5:136323529 | G | C | 1 | a0001c0001t0001g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.781-7750C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136323529 | |||||||
| chr5:136323621 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.781-7842G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136323621 | |||||||
| chr5:136323765 | C | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0100 |
2 | HG00099.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.781-7986G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136323765 | |||||||
| chr5:136323824 | G | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
187 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.781-8045C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136323824 | |||||||
| chr5:136324116 | T | A | 1 | a0001c0002t0002g0203 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.781-8337A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136324116 | |||||||
| chr5:136324222 | T | C | 1 | a0001c0002t0002g0214 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.781-8443A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136324222 | |||||||
| chr5:136324267 | T | G | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.781-8488A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136324267 | |||||||
| chr5:136324537 | C | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.781-8758G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136324537 | |||||||
| chr5:136324618 | C | T | 1 | a0001c0002t0002g0251 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.781-8839G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136324618 | |||||||
| chr5:136324729 | T | C | 1 | a0001c0002t0002g0231 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.781-8950A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136324729 | |||||||
| chr5:136325018 | T | C | 3 | a0001c0001t0001g0066 a0001c0001t0001g0170 a0001c0003t0001g0169 |
3 | HG00642.hp2 HG03942.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.781-9239A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136325018 | |||||||
| chr5:136325066 | GT | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(227): Show |
234 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.781-9288delA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136325066 | |||||||
| chr5:136325069 | T | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.781-9290A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136325069 | |||||||
| chr5:136325310 | A | T | 1 | a0001c0001t0001g0152 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.781-9531T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136325310 | |||||||
| chr5:136325390 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.781-9611C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136325390 | |||||||
| chr5:136325494 | A | T | 7 | a0001c0001t0001g0021 a0001c0002t0001g0027 a0001c0002t0001g0029 others(4): Show |
7 | HG02109.hp1 HG02280.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.781-9715T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136325494 | |||||||
| chr5:136325605 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.781-9826A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136325605 | |||||||
| chr5:136325704 | GAGGCCAA others(54): Show |
G | 1 | a0001c0002t0002g0232 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.781-9986_781-9926d others(63): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136325704 | |||||||
| chr5:136325919 | C | A | 1 | a0001c0001t0001g0147 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.781-10140G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136325919 | |||||||
| chr5:136326167 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(111): Show |
117 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.781-10388C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136326167 | |||||||
| chr5:136326213 | A | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
187 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.781-10434T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136326213 | |||||||
| chr5:136326239 | T | G | 69 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0076 others(66): Show |
70 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.781-10460A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136326239 | |||||||
| chr5:136326304 | C | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
187 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.781-10525G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136326304 | |||||||
| chr5:136326306 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.781-10527T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136326306 | |||||||
| chr5:136326451 | C | G | 67 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0069 others(64): Show |
68 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.781-10672G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136326451 | |||||||
| chr5:136326465 | T | C | 7 | a0001c0001t0001g0021 a0001c0002t0001g0027 a0001c0002t0001g0029 others(4): Show |
7 | HG02109.hp1 HG02280.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.781-10686A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136326465 | |||||||
| chr5:136326494 | T | C | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
26 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.781-10715A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136326494 | |||||||
| chr5:136326578 | A | C | 1 | a0001c0001t0001g0086 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.781-10799T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136326578 | |||||||
| chr5:136326664 | C | T | 70 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0069 others(67): Show |
71 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.781-10885G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136326664 | |||||||
| chr5:136326834 | A | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
187 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.781-11055T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136326834 | |||||||
| chr5:136326891 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.781-11112C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136326891 | |||||||
| chr5:136327046 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.781-11267C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136327046 | |||||||
| chr5:136327214 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.781-11435G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136327214 | |||||||
| chr5:136327552 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.781-11773A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136327552 | |||||||
| chr5:136327658 | T | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02559.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-11879A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136327658 | |||||||
| chr5:136327904 | A | C | 70 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0069 others(67): Show |
71 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.781-12125T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136327904 | |||||||
| chr5:136328229 | C | T | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.781-12450G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136328229 | |||||||
| chr5:136328403 | T | C | 4 | a0001c0001t0001g0015 a0001c0001t0001g0031 a0001c0001t0001g0032 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-12624A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136328403 | |||||||
| chr5:136328484 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.781-12705G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136328484 | |||||||
| chr5:136328500 | T | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
187 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.781-12721A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136328500 | |||||||
| chr5:136328571 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.781-12792T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136328571 | |||||||
| chr5:136328588 | A | G | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.781-12809T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136328588 | |||||||
| chr5:136328642 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.781-12863T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136328642 | |||||||
| chr5:136328689 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.781-12910G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136328689 | |||||||
| chr5:136328804 | C | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.781-13025G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136328804 | |||||||
| chr5:136329074 | T | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
187 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.781-13295A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136329074 | |||||||
| chr5:136329087 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG02074.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.781-13308C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136329087 | |||||||
| chr5:136329470 | T | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(85): Show |
91 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.781-13691A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136329470 | |||||||
| chr5:136329661 | T | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
187 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.781-13882A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136329661 | |||||||
| chr5:136329729 | G | A | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(227): Show |
234 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.781-13950C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136329729 | |||||||
| chr5:136329807 | G | T | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.781-14028C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136329807 | |||||||
| chr5:136330188 | C | A | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.781-14409G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136330188 | |||||||
| chr5:136330237 | G | T | 1 | a0001c0001t0001g0010 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.781-14458C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136330237 | |||||||
| chr5:136330331 | C | T | 1 | a0001c0002t0002g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.781-14552G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136330331 | |||||||
| chr5:136330359 | A | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(113): Show |
119 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.781-14580T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136330359 | |||||||
| chr5:136330367 | T | C | 1 | a0001c0002t0002g0225 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.781-14588A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136330367 | |||||||
| chr5:136330552 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.781-14773C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136330552 | |||||||
| chr5:136330707 | C | G | 1 | a0001c0001t0001g0170 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.781-14928G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136330707 | |||||||
| chr5:136330801 | G | C | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
26 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.781-15022C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136330801 | |||||||
| chr5:136330999 | C | T | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.781-15220G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136330999 | |||||||
| chr5:136331079 | T | A | 1 | a0001c0002t0002g0188 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.781-15300A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136331079 | |||||||
| chr5:136331117 | T | C | 1 | a0001c0001t0001g0058 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.781-15338A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136331117 | |||||||
| chr5:136331161 | G | A | 1 | a0001c0002t0002g0214 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.781-15382C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136331161 | |||||||
| chr5:136331174 | G | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.781-15395C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136331174 | |||||||
| chr5:136331363 | G | A | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
26 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.781-15584C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136331363 | |||||||
| chr5:136331456 | C | T | 1 | a0001c0002t0002g0229 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.781-15677G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136331456 | |||||||
| chr5:136331697 | C | A | 7 | a0001c0001t0001g0021 a0001c0002t0001g0027 a0001c0002t0001g0029 others(4): Show |
7 | HG02109.hp1 HG02280.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.781-15918G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136331697 | |||||||
| chr5:136331722 | G | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.781-15943C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136331722 | |||||||
| chr5:136331735 | C | T | 1 | a0001c0002t0002g0201 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.781-15956G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136331735 | |||||||
| chr5:136331791 | G | T | 1 | a0001c0001t0001g0121 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.781-16012C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136331791 | |||||||
| chr5:136331982 | G | A | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.781-16203C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136331982 | |||||||
| chr5:136332095 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(113): Show |
119 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.781-16316A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136332095 | |||||||
| chr5:136332183 | C | CA | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.781-16405_781-1640 others(5): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136332183 | |||||||
| chr5:136332183 | C | CG | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(92): Show |
98 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.781-16405dupC | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136332183 | |||||||
| chr5:136332319 | G | C | 1 | a0001c0001t0001g0147 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.781-16540C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136332319 | |||||||
| chr5:136332365 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.781-16586C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136332365 | |||||||
| chr5:136332447 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.781-16668A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136332447 | |||||||
| chr5:136332610 | G | A | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.781-16831C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136332610 | |||||||
| chr5:136332662 | A | AAAAC | 3 | a0001c0001t0001g0131 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | HG01515.hp1 HG01517.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.781-16887_781-1688 others(8): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136332662 | |||||||
| chr5:136332662 | A | C | 1 | a0001c0001t0001g0176 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.781-16883T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136332662 | |||||||
| chr5:136332836 | G | A | 60 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(57): Show |
61 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.781-17057C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136332836 | |||||||
| chr5:136333069 | A | C | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
26 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.781-17290T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136333069 | |||||||
| chr5:136333301 | GT | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(113): Show |
119 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.781-17523delA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136333301 | |||||||
| chr5:136333394 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.781-17615T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136333394 | |||||||
| chr5:136333416 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.781-17637G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136333416 | |||||||
| chr5:136333510 | G | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.781-17731C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136333510 | |||||||
| chr5:136333535 | C | A | 1 | a0001c0001t0001g0104 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.781-17756G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136333535 | |||||||
| chr5:136333777 | C | G | 1 | a0001c0001t0001g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.781-17998G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136333777 | |||||||
| chr5:136334048 | T | A | 1 | a0001c0002t0002g0213 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.781-18269A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136334048 | |||||||
| chr5:136334329 | A | G | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
26 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.781-18550T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136334329 | |||||||
| chr5:136334578 | T | C | 1 | a0001c0002t0002g0214 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.781-18799A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136334578 | |||||||
| chr5:136334630 | C | A | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(246): Show |
254 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.781-18851G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136334630 | |||||||
| chr5:136334650 | T | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.781-18871A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136334650 | |||||||
| chr5:136334704 | A | C | 1 | a0001c0002t0002g0228 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.781-18925T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136334704 | |||||||
| chr5:136334747 | T | C | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.781-18968A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136334747 | |||||||
| chr5:136334821 | A | G | 1 | a0001c0002t0002g0208 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.781-19042T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136334821 | |||||||
| chr5:136335243 | C | A | 2 | a0001c0002t0002g0230 a0001c0002t0002g0231 |
2 | HG01496.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.781-19464G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136335243 | |||||||
| chr5:136335550 | C | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02257.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.781-19771G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136335550 | |||||||
| chr5:136335641 | C | G | 1 | a0001c0001t0001g0122 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.781-19862G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136335641 | |||||||
| chr5:136335642 | G | A | 4 | a0001c0002t0002g0196 a0001c0002t0002g0197 a0001c0002t0002g0198 others(1): Show |
4 | HG01243.hp2 HG01884.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.781-19863C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136335642 | |||||||
| chr5:136335806 | A | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.781-20027T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136335806 | |||||||
| chr5:136335903 | C | CA | 7 | a0001c0001t0001g0045 a0001c0001t0001g0059 a0001c0001t0001g0060 others(4): Show |
7 | HG04115.hp1 NA18978.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.781-20125dupT | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136335903 | |||||||
| chr5:136335903 | CA | C | 58 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0061 others(55): Show |
59 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.781-20125delT | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136335903 | |||||||
| chr5:136335903 | CAA | C | 75 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0042 others(72): Show |
76 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.781-20126_781-2012 others(6): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136335903 | |||||||
| chr5:136335903 | CAAA | C | 27 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(24): Show |
27 | HG00323.hp2 HG00639.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.781-20127_781-2012 others(7): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136335903 | |||||||
| chr5:136335903 | CAAAA | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(9): Show |
14 | HG01069.hp2 HG01071.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.781-20128_781-2012 others(8): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136335903 | |||||||
| chr5:136335935 | G | T | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.781-20156C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136335935 | |||||||
| chr5:136336321 | T | A | 1 | a0001c0001t0001g0070 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.780+20287A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136336321 | |||||||
| chr5:136336573 | A | T | 70 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0069 others(67): Show |
71 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.780+20035T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136336573 | |||||||
| chr5:136336747 | T | C | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.780+19861A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136336747 | |||||||
| chr5:136336925 | G | A | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.780+19683C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136336925 | |||||||
| chr5:136337153 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.780+19455C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136337153 | |||||||
| chr5:136337483 | C | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.780+19125G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136337483 | |||||||
| chr5:136337569 | G | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0075 |
3 | HG03130.hp2 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.780+19039C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136337569 | |||||||
| chr5:136337663 | C | CA | 6 | a0001c0001t0001g0015 a0001c0001t0001g0077 a0001c0001t0001g0079 others(3): Show |
6 | HG02486.hp2 HG02647.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.780+18944dupT | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136337663 | |||||||
| chr5:136337663 | CA | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(84): Show |
90 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.780+18944delT | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136337663 | |||||||
| chr5:136337680 | A | C | 19 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(16): Show |
19 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.780+18928T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136337680 | |||||||
| chr5:136337694 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.780+18914T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136337694 | |||||||
| chr5:136337723 | T | A | 1 | a0001c0002t0002g0202 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.780+18885A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136337723 | |||||||
| chr5:136337826 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.780+18782G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136337826 | |||||||
| chr5:136338063 | A | C | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.780+18545T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136338063 | |||||||
| chr5:136338164 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.780+18444G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136338164 | |||||||
| chr5:136338248 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.780+18360C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136338248 | |||||||
| chr5:136338518 | C | T | 7 | a0001c0001t0001g0021 a0001c0002t0001g0027 a0001c0002t0001g0029 others(4): Show |
7 | HG02109.hp1 HG02280.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.780+18090G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136338518 | |||||||
| chr5:136338534 | G | A | 1 | a0001c0002t0002g0223 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.780+18074C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136338534 | |||||||
| chr5:136338536 | T | C | 4 | a0001c0002t0002g0224 a0001c0002t0002g0225 a0001c0002t0002g0226 others(1): Show |
4 | HG02132.hp1 NA18979.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+18072A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136338536 | |||||||
| chr5:136338709 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.780+17899T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136338709 | |||||||
| chr5:136338761 | A | C | 3 | a0001c0002t0004g0205 a0001c0002t0004g0206 a0001c0002t0004g0207 |
3 | NA18940.hp2 NA19056.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.780+17847T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136338761 | |||||||
| chr5:136338772 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.780+17836G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136338772 | |||||||
| chr5:136339102 | T | C | 1 | a0001c0002t0002g0253 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.780+17506A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136339102 | |||||||
| chr5:136339135 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.780+17473T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136339135 | |||||||
| chr5:136339181 | C | T | 7 | a0001c0001t0001g0117 a0001c0001t0001g0119 a0001c0001t0001g0126 others(4): Show |
7 | HG00621.hp2 HG02015.hp2 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.780+17427G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136339181 | |||||||
| chr5:136339292 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.780+17316G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136339292 | |||||||
| chr5:136339583 | T | C | 1 | a0001c0002t0002g0229 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.780+17025A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136339583 | |||||||
| chr5:136339839 | G | GCAA | 6 | a0001c0001t0001g0014 a0001c0001t0001g0108 a0001c0002t0002g0230 others(3): Show |
6 | HG00733.hp1 HG01258.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.780+16766_780+1676 others(7): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136339839 | |||||||
| chr5:136339839 | G | GCAACAA | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0030 others(3): Show |
6 | HG01071.hp2 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.780+16763_780+1676 others(10): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136339839 | |||||||
| chr5:136339839 | G | GCAACAAC others(2): Show |
5 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(2): Show |
7 | HG01243.hp1 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.780+16760_780+1676 others(13): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136339839 | |||||||
| chr5:136339839 | GCAA | G | 93 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): Show |
94 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.780+16766_780+1676 others(7): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136339839 | |||||||
| chr5:136339852 | C | CAAA | 70 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0069 others(67): Show |
71 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.780+16755_780+1675 others(7): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136339852 | |||||||
| chr5:136339865 | A | C | 1 | a0001c0001t0001g0121 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.780+16743T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136339865 | |||||||
| chr5:136339887 | G | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.780+16721C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136339887 | |||||||
| chr5:136339927 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.780+16681A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136339927 | |||||||
| chr5:136339965 | T | TA | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(85): Show |
91 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.780+16642dupT | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136339965 | |||||||
| chr5:136340170 | C | A | 1 | a0001c0001t0001g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.780+16438G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136340170 | |||||||
| chr5:136340196 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.780+16412A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136340196 | |||||||
| chr5:136340197 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.780+16411C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136340197 | |||||||
| chr5:136340285 | C | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(112): Show |
118 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.780+16323G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136340285 | |||||||
| chr5:136340423 | A | T | 1 | a0001c0001t0001g0150 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.780+16185T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136340423 | |||||||
| chr5:136340662 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.780+15946C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136340662 | |||||||
| chr5:136340752 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.780+15856A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136340752 | |||||||
| chr5:136340761 | G | T | 1 | a0001c0001t0001g0071 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.780+15847C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136340761 | |||||||
| chr5:136340775 | T | TA | 3 | a0001c0001t0001g0024 a0001c0002t0002g0192 a0001c0002t0002g0193 |
3 | HG00639.hp2 HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.780+15832dupT | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136340775 | |||||||
| chr5:136340780 | T | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
188 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.780+15828A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136340780 | |||||||
| chr5:136340818 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(85): Show |
91 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.780+15790T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136340818 | |||||||
| chr5:136340928 | G | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.780+15680C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136340928 | |||||||
| chr5:136341134 | C | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.780+15474G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136341134 | |||||||
| chr5:136341368 | G | T | 1 | a0001c0001t0001g0022 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.780+15240C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136341368 | |||||||
| chr5:136341474 | T | C | 1 | a0001c0002t0002g0228 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.780+15134A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136341474 | |||||||
| chr5:136341474 | T | TAC | 68 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(65): Show |
69 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.780+15132_780+1513 others(6): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136341474 | |||||||
| chr5:136341474 | TAC | T | 100 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(97): Show |
101 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.780+15132_780+1513 others(6): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136341474 | |||||||
| chr5:136341485 | A | T | 1 | a0001c0001t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.780+15123T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136341485 | |||||||
| chr5:136341667 | A | T | 1 | a0001c0002t0002g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.780+14941T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136341667 | |||||||
| chr5:136341707 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.780+14901A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136341707 | |||||||
| chr5:136341722 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | NA19057.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.780+14886C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136341722 | |||||||
| chr5:136342060 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02257.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.780+14548A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136342060 | |||||||
| chr5:136342114 | T | C | 1 | a0001c0002t0002g0203 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.780+14494A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136342114 | |||||||
| chr5:136342159 | C | A | 50 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0117 others(47): Show |
50 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.780+14449G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136342159 | |||||||
| chr5:136342186 | A | G | 67 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0116 others(64): Show |
68 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.780+14422T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136342186 | |||||||
| chr5:136342675 | C | G | 20 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(17): Show |
20 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.780+13933G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136342675 | |||||||
| chr5:136343269 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
185 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.780+13339G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136343269 | |||||||
| chr5:136343308 | T | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(111): Show |
117 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.780+13300A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136343308 | |||||||
| chr5:136343725 | G | T | 1 | a0001c0001t0001g0125 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.780+12883C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136343725 | |||||||
| chr5:136343734 | G | A | 67 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0116 others(64): Show |
68 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.780+12874C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136343734 | |||||||
| chr5:136343809 | G | T | 67 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0116 others(64): Show |
68 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.780+12799C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136343809 | |||||||
| chr5:136343871 | G | T | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.780+12737C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136343871 | |||||||
| chr5:136344005 | G | A | 27 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(24): Show |
27 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.780+12603C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136344005 | |||||||
| chr5:136344225 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.780+12383G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136344225 | |||||||
| chr5:136344245 | G | A | 3 | a0001c0002t0002g0190 a0001c0002t0002g0201 a0001c0007t0002g0189 |
3 | HG01069.hp1 HG01175.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.780+12363C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136344245 | |||||||
| chr5:136344267 | A | C | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.780+12341T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136344267 | |||||||
| chr5:136344398 | G | A | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.780+12210C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136344398 | |||||||
| chr5:136344551 | A | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(82): Show |
88 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.780+12057T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136344551 | |||||||
| chr5:136344738 | G | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.780+11870C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136344738 | |||||||
| chr5:136344753 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.780+11855A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136344753 | |||||||
| chr5:136344793 | T | C | 69 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0039 others(66): Show |
70 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.780+11815A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136344793 | |||||||
| chr5:136344852 | A | G | 22 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(19): Show |
22 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.780+11756T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136344852 | |||||||
| chr5:136344875 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.780+11733C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136344875 | |||||||
| chr5:136344891 | T | A | 7 | a0001c0002t0002g0233 a0001c0002t0002g0234 a0001c0002t0002g0235 others(4): Show |
7 | HG01258.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.780+11717A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136344891 | |||||||
| chr5:136344913 | C | T | 1 | a0001c0002t0002g0231 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.780+11695G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136344913 | |||||||
| chr5:136345083 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
185 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.780+11525G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136345083 | |||||||
| chr5:136345160 | G | A | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 |
3 | HG01099.hp2 HG01169.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.780+11448C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136345160 | |||||||
| chr5:136345305 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.780+11303A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136345305 | |||||||
| chr5:136345376 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.780+11232G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136345376 | |||||||
| chr5:136345384 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.780+11224G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136345384 | |||||||
| chr5:136345421 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0171 a0001c0001t0001g0172 others(2): Show |
6 | HG01884.hp1 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.780+11187G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136345421 | |||||||
| chr5:136345433 | C | T | 8 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0121 others(5): Show |
8 | HG00558.hp2 HG02273.hp1 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.780+11175G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136345433 | |||||||
| chr5:136345509 | C | T | 1 | a0002c0004t0001g0175 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.780+11099G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136345509 | |||||||
| chr5:136345832 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(111): Show |
117 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.780+10776T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136345832 | |||||||
| chr5:136345937 | C | A | 1 | a0001c0002t0002g0203 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.780+10671G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136345937 | |||||||
| chr5:136346058 | G | A | 1 | a0001c0002t0002g0239 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.780+10550C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136346058 | |||||||
| chr5:136346075 | C | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.780+10533G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136346075 | |||||||
| chr5:136346102 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.780+10506C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136346102 | |||||||
| chr5:136346135 | T | C | 20 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(17): Show |
20 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.780+10473A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136346135 | |||||||
| chr5:136346195 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(176): Show |
182 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.780+10413T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136346195 | |||||||
| chr5:136346261 | A | G | 1 | a0001c0002t0002g0242 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.780+10347T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136346261 | |||||||
| chr5:136346443 | C | A | 1 | a0001c0001t0001g0155 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.780+10165G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136346443 | |||||||
| chr5:136346523 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(175): Show |
181 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.780+10085A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136346523 | |||||||
| chr5:136346527 | CCATGTAC others(14): Show |
C | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.780+10060_780+1008 others(25): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136346527 | |||||||
| chr5:136346675 | T | C | 1 | a0001c0002t0002g0203 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.780+9933A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136346675 | |||||||
| chr5:136346842 | G | A | 2 | a0001c0002t0002g0192 a0001c0002t0002g0193 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.780+9766C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136346842 | |||||||
| chr5:136346842 | G | C | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 |
3 | HG01099.hp1 HG02818.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.780+9766C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136346842 | |||||||
| chr5:136346910 | C | T | 1 | a0001c0002t0002g0202 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.780+9698G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136346910 | |||||||
| chr5:136347175 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.780+9433G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136347175 | |||||||
| chr5:136347176 | C | T | 64 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0116 others(61): Show |
65 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.780+9432G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136347176 | |||||||
| chr5:136347309 | C | T | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
4 | NA18940.hp1 NA19081.hp1 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.780+9299G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136347309 | |||||||
| chr5:136347662 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.780+8946C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136347662 | |||||||
| chr5:136347682 | G | T | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.780+8926C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136347682 | |||||||
| chr5:136347739 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.780+8869G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136347739 | |||||||
| chr5:136347805 | G | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.780+8803C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136347805 | |||||||
| chr5:136347954 | G | A | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.780+8654C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136347954 | |||||||
| chr5:136348047 | T | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(175): Show |
181 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.780+8561A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136348047 | |||||||
| chr5:136348439 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.780+8169G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136348439 | |||||||
| chr5:136348511 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.780+8097T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136348511 | |||||||
| chr5:136348545 | G | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(175): Show |
181 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.780+8063C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136348545 | |||||||
| chr5:136348916 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.780+7692C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136348916 | |||||||
| chr5:136349073 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.780+7535C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136349073 | |||||||
| chr5:136349083 | T | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.780+7525A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136349083 | |||||||
| chr5:136349087 | A | T | 72 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0066 others(69): Show |
73 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.780+7521T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136349087 | |||||||
| chr5:136349124 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.780+7484G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136349124 | |||||||
| chr5:136349132 | T | TC | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(108): Show |
114 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.780+7475dupG | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136349132 | |||||||
| chr5:136349337 | G | A | 63 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0116 others(60): Show |
64 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.780+7271C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136349337 | |||||||
| chr5:136349531 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.780+7077A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136349531 | |||||||
| chr5:136349572 | G | C | 1 | a0001c0002t0002g0200 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.780+7036C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136349572 | |||||||
| chr5:136349634 | C | G | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.780+6974G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136349634 | |||||||
| chr5:136350079 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.780+6529T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136350079 | |||||||
| chr5:136350136 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.780+6472C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136350136 | |||||||
| chr5:136350407 | A | T | 60 | a0001c0002t0001g0114 a0001c0002t0002g0185 a0001c0002t0002g0186 others(57): Show |
60 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.780+6201T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136350407 | |||||||
| chr5:136350465 | C | A | 1 | a0001c0002t0002g0185 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.780+6143G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136350465 | |||||||
| chr5:136350642 | G | T | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 |
3 | HG01099.hp1 HG02818.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.780+5966C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136350642 | |||||||
| chr5:136350695 | C | T | 1 | a0001c0002t0002g0203 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.780+5913G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136350695 | |||||||
| chr5:136350696 | C | A | 27 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(24): Show |
27 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.780+5912G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136350696 | |||||||
| chr5:136350696 | C | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(148): Show |
154 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.780+5912G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136350696 | |||||||
| chr5:136350742 | T | A | 1 | a0001c0001t0001g0157 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.780+5866A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136350742 | |||||||
| chr5:136350898 | G | C | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.780+5710C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136350898 | |||||||
| chr5:136351139 | T | A | 1 | a0001c0001t0001g0112 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.780+5469A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136351139 | |||||||
| chr5:136351307 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.780+5301T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136351307 | |||||||
| chr5:136351417 | T | G | 1 | a0001c0008t0007g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.780+5191A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136351417 | |||||||
| chr5:136351435 | A | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.780+5173T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136351435 | |||||||
| chr5:136351541 | C | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(81): Show |
87 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.780+5067G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136351541 | |||||||
| chr5:136351675 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.780+4933C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136351675 | |||||||
| chr5:136352012 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.780+4596G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136352012 | |||||||
| chr5:136352071 | T | C | 73 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0030 others(70): Show |
74 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.780+4537A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136352071 | |||||||
| chr5:136352075 | T | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.780+4533A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136352075 | |||||||
| chr5:136352111 | G | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.780+4497C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136352111 | |||||||
| chr5:136352263 | T | A | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.780+4345A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136352263 | |||||||
| chr5:136352289 | C | T | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.780+4319G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136352289 | |||||||
| chr5:136352659 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0119 |
2 | NA18978.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.780+3949G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136352659 | |||||||
| chr5:136352906 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.780+3702G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136352906 | |||||||
| chr5:136352943 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.780+3665T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136352943 | |||||||
| chr5:136353040 | T | C | 66 | a0001c0002t0001g0027 a0001c0002t0001g0029 a0001c0002t0001g0114 others(63): Show |
66 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.780+3568A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136353040 | |||||||
| chr5:136353121 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.780+3487C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136353121 | |||||||
| chr5:136353137 | C | T | 1 | a0002c0004t0001g0175 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.780+3471G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136353137 | |||||||
| chr5:136353478 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.780+3130G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136353478 | |||||||
| chr5:136353543 | T | C | 65 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0066 others(62): Show |
66 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.780+3065A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136353543 | |||||||
| chr5:136353748 | C | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(174): Show |
180 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.780+2860G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136353748 | |||||||
| chr5:136353883 | T | A | 1 | a0001c0001t0001g0113 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.780+2725A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136353883 | |||||||
| chr5:136353961 | AT | A | 3 | a0001c0002t0002g0188 a0001c0002t0002g0218 a0001c0002t0002g0219 |
3 | HG02818.hp1 HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.780+2646delA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136353961 | |||||||
| chr5:136354069 | C | G | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.780+2539G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136354069 | |||||||
| chr5:136354097 | T | A | 65 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0066 others(62): Show |
66 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.780+2511A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136354097 | |||||||
| chr5:136354151 | G | A | 27 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(24): Show |
27 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.780+2457C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136354151 | |||||||
| chr5:136354211 | C | T | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0115 |
3 | NA18988.hp2 NA18990.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.780+2397G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136354211 | |||||||
| chr5:136354282 | A | T | 1 | a0001c0001t0001g0117 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.780+2326T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136354282 | |||||||
| chr5:136354286 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.780+2322G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136354286 | |||||||
| chr5:136354316 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.780+2292G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136354316 | |||||||
| chr5:136354479 | G | A | 74 | a0001c0002t0001g0027 a0001c0002t0001g0029 a0001c0002t0001g0114 others(71): Show |
74 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.780+2129C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136354479 | |||||||
| chr5:136354684 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(174): Show |
180 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.780+1924A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136354684 | |||||||
| chr5:136354687 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.780+1921G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136354687 | |||||||
| chr5:136354758 | A | C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(8): Show |
13 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.780+1850T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136354758 | |||||||
| chr5:136354892 | G | A | 10 | a0001c0002t0002g0220 a0001c0002t0002g0221 a0001c0002t0002g0222 others(7): Show |
10 | HG00673.hp1 HG02040.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.780+1716C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136354892 | |||||||
| chr5:136354950 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.780+1658G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136354950 | |||||||
| chr5:136355084 | G | A | 64 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0116 others(61): Show |
65 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.780+1524C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136355084 | |||||||
| chr5:136355141 | G | A | 7 | a0001c0002t0002g0233 a0001c0002t0002g0234 a0001c0002t0002g0235 others(4): Show |
7 | HG01258.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.780+1467C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136355141 | |||||||
| chr5:136355340 | A | T | 1 | a0001c0001t0001g0068 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.780+1268T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136355340 | |||||||
| chr5:136355392 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.780+1216C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136355392 | |||||||
| chr5:136355434 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.780+1174A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136355434 | |||||||
| chr5:136355605 | TG | T | 64 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0116 others(61): Show |
65 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.780+1002delC | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136355605 | |||||||
| chr5:136355893 | T | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(174): Show |
180 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.780+715A>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136355893 | |||||||
| chr5:136355990 | T | G | 101 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(98): Show |
101 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.780+618A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136355990 | |||||||
| chr5:136356023 | G | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.780+585C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136356023 | |||||||
| chr5:136356030 | C | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(174): Show |
180 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.780+578G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136356030 | |||||||
| chr5:136356447 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.780+161G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136356447 | |||||||
| chr5:136356455 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(174): Show |
180 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.780+153T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 2/11 | chr5 | 136356455 | |||||||
| chr5:136357984 | C | T | 3 | a0001c0002t0002g0190 a0001c0002t0002g0201 a0001c0007t0002g0189 |
3 | HG01069.hp1 HG01175.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.3-599G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136357984 | |||||||
| chr5:136358049 | C | T | 69 | a0001c0002t0001g0114 a0001c0002t0002g0185 a0001c0002t0002g0186 others(66): Show |
69 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.3-664G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136358049 | |||||||
| chr5:136358115 | C | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0171 a0001c0001t0001g0172 others(2): Show |
6 | HG01884.hp1 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3-730G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136358115 | |||||||
| chr5:136358155 | C | T | 69 | a0001c0002t0001g0114 a0001c0002t0002g0185 a0001c0002t0002g0186 others(66): Show |
69 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.3-770G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136358155 | |||||||
| chr5:136358159 | T | C | 69 | a0001c0002t0001g0114 a0001c0002t0002g0185 a0001c0002t0002g0186 others(66): Show |
69 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.3-774A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136358159 | |||||||
| chr5:136358484 | G | A | 1 | a0001c0008t0007g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3-1099C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136358484 | |||||||
| chr5:136358572 | T | C | 6 | a0001c0002t0002g0234 a0001c0002t0002g0235 a0001c0002t0002g0236 others(3): Show |
6 | HG01258.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.3-1187A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136358572 | |||||||
| chr5:136358839 | T | C | 1 | a0001c0001t0001g0009 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3-1454A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136358839 | |||||||
| chr5:136358893 | A | G | 70 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0002t0002g0185 others(67): Show |
70 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.3-1508T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136358893 | |||||||
| chr5:136359014 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3-1629T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136359014 | |||||||
| chr5:136359266 | G | C | 1 | a0001c0002t0002g0186 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3-1881C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136359266 | |||||||
| chr5:136359299 | A | C | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3-1914T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136359299 | |||||||
| chr5:136359299 | A | G | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.3-1914T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136359299 | |||||||
| chr5:136359366 | A | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG02572.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3-1981T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136359366 | |||||||
| chr5:136359443 | T | G | 1 | a0001c0002t0002g0229 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3-2058A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136359443 | |||||||
| chr5:136359515 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3-2130C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136359515 | |||||||
| chr5:136359548 | G | A | 11 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(8): Show |
11 | HG00609.hp2 NA18944.hp2 NA18983.hp1 others(8): Show |
intron_variant | MODIFIER | c.3-2163C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136359548 | |||||||
| chr5:136359605 | C | T | 7 | a0001c0002t0002g0194 a0001c0002t0002g0195 a0001c0002t0002g0196 others(4): Show |
7 | HG01243.hp2 HG01884.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.3-2220G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136359605 | |||||||
| chr5:136359630 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3-2245T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136359630 | |||||||
| chr5:136359678 | T | C | 7 | a0001c0002t0002g0233 a0001c0002t0002g0234 a0001c0002t0002g0235 others(4): Show |
7 | HG01258.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.3-2293A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136359678 | |||||||
| chr5:136359687 | G | A | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.3-2302C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136359687 | |||||||
| chr5:136359733 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3-2348G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136359733 | |||||||
| chr5:136359774 | G | GCA | 71 | a0001c0001t0001g0005 a0001c0001t0001g0116 a0001c0001t0001g0117 others(68): Show |
72 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.3-2391_3-2390dupTG | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136359774 | |||||||
| chr5:136359851 | A | C | 1 | a0001c0001t0001g0116 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3-2466T>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136359851 | |||||||
| chr5:136359857 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3-2472A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136359857 | |||||||
| chr5:136360098 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3-2713C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136360098 | |||||||
| chr5:136360284 | T | TACAAA | 10 | a0001c0002t0002g0192 a0001c0002t0002g0193 a0001c0002t0002g0233 others(7): Show |
10 | HG00639.hp2 HG00735.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.3-2904_3-2900dupTT others(3): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136360284 | |||||||
| chr5:136360284 | T | TACAAAAC others(3): Show |
59 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0002t0002g0185 others(56): Show |
59 | HG00408.hp2 HG00621.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.3-2909_3-2900dupTT others(8): Show |
TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136360284 | |||||||
| chr5:136360482 | AT | A | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.3-3098delA | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136360482 | |||||||
| chr5:136360509 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.3-3124G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136360509 | |||||||
| chr5:136360669 | C | T | 2 | a0001c0002t0002g0190 a0001c0007t0002g0189 |
2 | HG01069.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.3-3284G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136360669 | |||||||
| chr5:136360779 | C | G | 70 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0002t0002g0185 others(67): Show |
70 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.3-3394G>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136360779 | |||||||
| chr5:136361000 | C | T | 1 | a0001c0002t0002g0188 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3-3615G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136361000 | |||||||
| chr5:136361001 | G | A | 1 | a0001c0002t0002g0230 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3-3616C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136361001 | |||||||
| chr5:136361362 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(180): Show |
186 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.2+3891G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136361362 | |||||||
| chr5:136361499 | G | C | 1 | a0001c0001t0001g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2+3754C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136361499 | |||||||
| chr5:136361663 | T | G | 2 | a0001c0001t0001g0170 a0001c0003t0001g0169 |
2 | HG00642.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2+3590A>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136361663 | |||||||
| chr5:136361796 | C | A | 70 | a0001c0001t0001g0005 a0001c0001t0001g0116 a0001c0001t0001g0117 others(67): Show |
71 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.2+3457G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136361796 | |||||||
| chr5:136361798 | A | G | 1 | a0001c0002t0002g0187 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2+3455T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136361798 | |||||||
| chr5:136361936 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(109): Show |
114 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.2+3317C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136361936 | |||||||
| chr5:136362572 | G | T | 70 | a0001c0001t0001g0005 a0001c0001t0001g0116 a0001c0001t0001g0117 others(67): Show |
71 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.2+2681C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136362572 | |||||||
| chr5:136362920 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2+2333G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136362920 | |||||||
| chr5:136363287 | T | C | 1 | a0001c0002t0002g0231 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2+1966A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136363287 | |||||||
| chr5:136363396 | A | T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(13): Show |
18 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.2+1857T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136363396 | |||||||
| chr5:136363481 | G | C | 1 | a0001c0002t0002g0232 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2+1772C>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136363481 | |||||||
| chr5:136363488 | A | T | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2+1765T>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136363488 | |||||||
| chr5:136363520 | C | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(1): Show |
5 | HG01243.hp1 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2+1733G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136363520 | |||||||
| chr5:136363529 | A | G | 56 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(53): Show |
56 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.2+1724T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136363529 | |||||||
| chr5:136363608 | A | G | 2 | a0001c0002t0002g0185 a0001c0002t0002g0186 |
2 | NA18942.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.2+1645T>C | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136363608 | |||||||
| chr5:136363771 | G | T | 11 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(8): Show |
11 | HG00609.hp2 NA18944.hp2 NA18983.hp1 others(8): Show |
intron_variant | MODIFIER | c.2+1482C>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136363771 | |||||||
| chr5:136363844 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG00323.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.2+1409G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136363844 | |||||||
| chr5:136364165 | C | T | 70 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0002t0002g0185 others(67): Show |
70 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.2+1088G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136364165 | |||||||
| chr5:136364196 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2+1057C>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136364196 | |||||||
| chr5:136364243 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2+1010G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136364243 | |||||||
| chr5:136364717 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2+536A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136364717 | |||||||
| chr5:136364969 | T | C | 7 | a0001c0002t0002g0233 a0001c0002t0002g0234 a0001c0002t0002g0235 others(4): Show |
7 | HG01258.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2+284A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136364969 | |||||||
| chr5:136365018 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02559.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2+235G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136365018 | |||||||
| chr5:136365072 | GA | G | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(184): Show |
190 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.2+180delT | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136365072 | |||||||
| chr5:136365133 | T | C | 1 | a0001c0001t0001g0010 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2+120A>G | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136365133 | |||||||
| chr5:136365144 | C | A | 14 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0002t0002g0242 others(11): Show |
14 | HG00621.hp1 HG01952.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.2+109G>T | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136365144 | |||||||
| chr5:136365182 | C | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(1): Show |
4 | NA18959.hp2 NA18969.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.2+71G>A | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136365182 | |||||||
| chr5:136365212 | G | GA | 70 | a0001c0001t0001g0005 a0001c0001t0001g0116 a0001c0001t0001g0117 others(67): Show |
71 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.2+40dupT | TRPC7 | ENSG00000069018.19 | transcript | ENST00000513104.6 | protein_coding | 1/11 | chr5 | 136365212 |