Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 160760 |
| ensemblid | ENSG00000196850.6 |
| hgncid | 30695 |
| symbol | PPTC7 |
| name | protein phosphatase targeting COQ7 |
| refseq_nuc | NM_139283.2 |
| refseq_prot | NP_644812.1 |
| ensembl_nuc | ENST00000354300.5 |
| ensembl_prot | ENSP00000346255.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 110533245 |
| end | 110583318 |
| strand | - |
| ver | v1.2 |
| region | chr12:110533245-110583318 |
| region5000 | chr12:110528245-110588318 |
| regionname0 | PPTC7_chr12_110533245_110583318 |
| regionname5000 | PPTC7_chr12_110528245_110588318 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 304 | 315 | 83 | 59 | 124 | 13 | 35 | 98 | PPTC7_chr12_110528245_110588318 | PPTC7 | MFSVL others(299): Show |
chr12 | 110528245 | 110588318 |
| a0002 | 0/1 | 303 | 13 | 5 | 5 | 0 | 1 | 1 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | MFSVL others(298): Show |
chr12 | 110528245 | 110588318 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 912 | 213 | 66 | 43 | 76 | 8 | 19 | PPTC7_chr12_110528245_110588318 | PPTC7 | ATGTT others(907): Show |
chr12 | 110528245 | 110588318 | ||
| a0001c0002 | 0/0 | 912 | 101 | 16 | 16 | 48 | 5 | 16 | PPTC7_chr12_110528245_110588318 | PPTC7 | ATGTT others(907): Show |
chr12 | 110528245 | 110588318 | ||
| a0001c0004 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | ATGTT others(907): Show |
chr12 | 110528245 | 110588318 | ||
| a0002c0003 | 0/1 | 909 | 13 | 5 | 5 | 0 | 1 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | ATGTT others(904): Show |
chr12 | 110528245 | 110588318 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4994 | 84 | 38 | 19 | 15 | 3 | 8 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4989): Show |
chr12 | 110528245 | 110588318 |
| a0001c0001t0002 | 0/0 | 4994 | 70 | 1 | 9 | 53 | 1 | 6 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4989): Show |
chr12 | 110528245 | 110588318 |
| a0001c0001t0003 | 0/0 | 4993 | 16 | 8 | 2 | 2 | 1 | 3 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4988): Show |
chr12 | 110528245 | 110588318 |
| a0001c0001t0004 | 0/0 | 4994 | 8 | 7 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4989): Show |
chr12 | 110528245 | 110588318 |
| a0001c0001t0005 | 0/0 | 4994 | 6 | 0 | 4 | 0 | 2 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4989): Show |
chr12 | 110528245 | 110588318 |
| a0001c0001t0006 | 0/0 | 4995 | 5 | 0 | 4 | 0 | 1 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4990): Show |
chr12 | 110528245 | 110588318 |
| a0001c0001t0007 | 0/0 | 4993 | 4 | 4 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4988): Show |
chr12 | 110528245 | 110588318 |
| a0001c0001t0008 | 0/0 | 4988 | 4 | 3 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4983): Show |
chr12 | 110528245 | 110588318 |
| a0001c0001t0009 | 0/0 | 4993 | 2 | 2 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4988): Show |
chr12 | 110528245 | 110588318 |
| a0001c0001t0010 | 0/0 | 4995 | 2 | 0 | 2 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4990): Show |
chr12 | 110528245 | 110588318 |
| a0001c0001t0012 | 0/0 | 4994 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4989): Show |
chr12 | 110528245 | 110588318 |
| a0001c0001t0013 | 0/0 | 4994 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4989): Show |
chr12 | 110528245 | 110588318 |
| a0001c0001t0014 | 0/0 | 4995 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4990): Show |
chr12 | 110528245 | 110588318 |
| a0001c0001t0015 | 0/0 | 4994 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4989): Show |
chr12 | 110528245 | 110588318 |
| a0001c0001t0016 | 0/0 | 4994 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4989): Show |
chr12 | 110528245 | 110588318 |
| a0001c0001t0019 | 0/0 | 4996 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4991): Show |
chr12 | 110528245 | 110588318 |
| a0001c0001t0022 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4985): Show |
chr12 | 110528245 | 110588318 |
| a0001c0001t0024 | 0/0 | 4994 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4989): Show |
chr12 | 110528245 | 110588318 |
| a0001c0001t0026 | 0/0 | 4994 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4989): Show |
chr12 | 110528245 | 110588318 |
| a0001c0001t0027 | 0/0 | 4994 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4989): Show |
chr12 | 110528245 | 110588318 |
| a0001c0001t0028 | 0/0 | 4993 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4988): Show |
chr12 | 110528245 | 110588318 |
| a0001c0001t0029 | 0/0 | 4994 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4989): Show |
chr12 | 110528245 | 110588318 |
| a0001c0002t0001 | 0/0 | 4994 | 92 | 12 | 14 | 47 | 5 | 14 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4989): Show |
chr12 | 110528245 | 110588318 |
| a0001c0002t0004 | 0/0 | 4994 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4989): Show |
chr12 | 110528245 | 110588318 |
| a0001c0002t0011 | 0/0 | 4994 | 2 | 2 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4989): Show |
chr12 | 110528245 | 110588318 |
| a0001c0002t0017 | 0/0 | 4994 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4989): Show |
chr12 | 110528245 | 110588318 |
| a0001c0002t0018 | 0/0 | 4994 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4989): Show |
chr12 | 110528245 | 110588318 |
| a0001c0002t0020 | 0/0 | 4994 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4989): Show |
chr12 | 110528245 | 110588318 |
| a0001c0002t0021 | 0/0 | 4993 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4988): Show |
chr12 | 110528245 | 110588318 |
| a0001c0002t0023 | 0/0 | 4994 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4989): Show |
chr12 | 110528245 | 110588318 |
| a0001c0002t0025 | 0/0 | 4994 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4989): Show |
chr12 | 110528245 | 110588318 |
| a0001c0004t0009 | 0/0 | 4993 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4988): Show |
chr12 | 110528245 | 110588318 |
| a0002c0003t0001 | 0/1 | 4991 | 13 | 5 | 5 | 0 | 1 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | GCTAG others(4986): Show |
chr12 | 110528245 | 110588318 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0105 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0009 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0005g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0005g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0006g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0006g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0006g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0006g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0006g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0007g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0007g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0007g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0007g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0008g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0008g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0008g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0008g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0009g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0009g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0010g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0010g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0012g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0013g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0014g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0015g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0016g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0019g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0022g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0024g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0026g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0027g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0028g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0001t0029g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0011g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0011g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0017g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0018g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0020g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0021g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0023g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0002t0025g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0001c0004t0009g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0002c0003t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0002c0003t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0002c0003t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0002c0003t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0002c0003t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0002c0003t0001g0017 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0002c0003t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0002c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0002c0003t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0002c0003t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0002c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0002c0003t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| a0002c0003t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0004 | EUR | GBR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0002 | EUR | GBR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0210 | EUR | GBR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0004 | EUR | GBR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0073 | EUR | FIN | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | FIN | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | FIN | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0304 | EUR | FIN | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | CHS | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | CHS | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | CHS | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | CHS | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | CHS | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | CHS | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0072 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | CHS | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | CHS | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0046 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00735 | hp1 | a0002 | c0003 | t0001 | g0021 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00735 | hp2 | a0001 | c0002 | t0021 | g0260 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00738 | hp1 | a0001 | c0001 | t0010 | g0025 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0168 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG00741 | hp2 | a0002 | c0003 | t0001 | g0023 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01069 | hp1 | a0001 | c0001 | t0010 | g0026 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01069 | hp2 | a0001 | c0001 | t0006 | g0215 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0226 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01074 | hp1 | a0001 | c0002 | t0017 | g0163 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01074 | hp2 | a0002 | c0003 | t0001 | g0016 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01099 | hp1 | a0001 | c0001 | t0008 | g0256 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01099 | hp2 | a0001 | c0001 | t0026 | g0235 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0174 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0176 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0179 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0294 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0181 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0305 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0173 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0074 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0038 | AMR | PUR | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0146 | AMR | CLM | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0155 | AMR | CLM | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0116 | AMR | CLM | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01261 | hp2 | a0002 | c0003 | t0001 | g0020 | AMR | CLM | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01346 | hp1 | a0002 | c0003 | t0001 | g0018 | AMR | CLM | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | CLM | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | CLM | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0307 | AMR | CLM | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0075 | AMR | CLM | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | CLM | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0115 | EUR | IBS | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01884 | hp2 | a0001 | c0001 | t0019 | g0279 | AFR | ACB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01891 | hp2 | a0001 | c0001 | t0028 | g0283 | AFR | ACB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0123 | AMR | PEL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PEL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01943 | hp2 | a0001 | c0001 | t0006 | g0198 | AMR | PEL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0118 | AMR | PEL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0231 | AMR | PEL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | KHV | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | KHV | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02055 | hp1 | a0001 | c0001 | t0009 | g0293 | AFR | ACB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0258 | AFR | ACB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | KHV | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | KHV | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | KHV | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | KHV | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | KHV | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | KHV | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | KHV | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0257 | AFR | ACB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02257 | hp1 | a0001 | c0001 | t0022 | g0277 | AFR | ACB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0151 | AFR | ACB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0295 | AFR | ACB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02293 | hp2 | a0001 | c0001 | t0006 | g0222 | AMR | PEL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0143 | AFR | ACB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02451 | hp2 | a0001 | c0002 | t0004 | g0296 | AFR | ACB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | KHV | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | KHV | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0180 | AFR | GWD | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0299 | AFR | GWD | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0169 | AFR | GWD | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0135 | AFR | GWD | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0297 | AFR | GWD | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0298 | AFR | GWD | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | GWD | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0182 | AFR | GWD | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0145 | SAS | PJL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0124 | SAS | PJL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02717 | hp2 | a0002 | c0003 | t0001 | g0012 | AFR | GWD | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0141 | SAS | PJL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0139 | SAS | PJL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02809 | hp2 | a0001 | c0004 | t0009 | g0292 | AFR | GWD | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0300 | AFR | GWD | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0286 | AFR | GWD | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0284 | AFR | ESN | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02965 | hp2 | a0002 | c0003 | t0001 | g0015 | AFR | ESN | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0289 | AFR | ESN | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ESN | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0311 | AFR | ESN | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | ESN | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | MSL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0301 | AFR | ESN | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03195 | hp1 | a0002 | c0003 | t0001 | g0013 | AFR | ESN | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0285 | AFR | ESN | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0291 | AFR | MSL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0167 | AFR | MSL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | MSL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0140 | AFR | MSL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0157 | AFR | MSL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0287 | SAS | PJL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0306 | SAS | PJL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0161 | SAS | PJL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0162 | SAS | PJL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03516 | hp1 | a0001 | c0002 | t0011 | g0317 | AFR | ESN | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0303 | AFR | ESN | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03540 | hp1 | a0001 | c0002 | t0025 | g0166 | AFR | GWD | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03540 | hp2 | a0001 | c0001 | t0009 | g0290 | AFR | GWD | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0165 | SAS | PJL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0147 | SAS | PJL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03669 | hp2 | a0001 | c0002 | t0023 | g0134 | SAS | PJL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03688 | hp1 | a0001 | c0002 | t0020 | g0117 | SAS | STU | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0136 | SAS | STU | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0138 | SAS | PJL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0201 | SAS | PJL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0265 | SAS | PJL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0312 | SAS | BEB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0027 | SAS | BEB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG04115 | hp1 | a0001 | c0001 | t0024 | g0056 | SAS | STU | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0153 | SAS | STU | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0308 | SAS | BEB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | STU | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG04199 | hp2 | a0001 | c0001 | t0013 | g0011 | SAS | STU | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | STU | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG04204 | hp2 | a0002 | c0003 | t0001 | g0022 | SAS | STU | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0119 | SAS | STU | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0245 | SAS | STU | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18522 | hp1 | a0001 | c0002 | t0011 | g0318 | AFR | YRI | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | YRI | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | CHB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | CHB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18941 | hp1 | a0001 | c0002 | t0018 | g0183 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18945 | hp1 | a0001 | c0001 | t0016 | g0262 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18966 | hp1 | a0001 | c0001 | t0012 | g0010 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18974 | hp1 | a0001 | c0001 | t0014 | g0232 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18989 | hp1 | a0001 | c0001 | t0029 | g0319 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19009 | hp1 | a0001 | c0001 | t0027 | g0261 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19030 | hp1 | a0002 | c0003 | t0001 | g0024 | AFR | LWK | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | LWK | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0282 | AFR | LWK | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0150 | AFR | LWK | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0164 | AFR | YRI | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | YRI | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ASW | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0154 | EUR | TSI | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA20752 | hp2 | a0002 | c0003 | t0001 | g0019 | EUR | TSI | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA20805 | hp1 | a0001 | c0001 | t0006 | g0221 | EUR | TSI | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0144 | EUR | TSI | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | CLM | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0120 | AMR | CLM | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02486 | hp1 | a0001 | c0001 | t0008 | g0259 | AFR | ACB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0302 | AFR | ACB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0156 | AFR | ACB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0288 | AFR | MSL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG03471 | hp2 | a0002 | c0003 | t0001 | g0014 | AFR | MSL | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | USA | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | USA | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA18955 | hp2 | a0001 | c0001 | t0015 | g0230 | EAS | JPT | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | USA | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | USA | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | LWK | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| homoSapiens | chm13v2 | a0002 | c0003 | t0001 | g0017 | REF | REF | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0105 | REF | REF | PPTC7_chr12_110528245_110588318 | PPTC7 | chr12 | 110528245 | 110588318 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110582934 | TCGC | T | 1 | a0002 | 12 | HG00735.hp1 HG00741.hp2 HG01074.hp2 others(9): Show |
disruptive_inframe_deletion | MODERATE | c.95_97delGCG | p.Gly32del | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/6 | 384/4994 | 95/915 | 32/304 | chr12 | 110582934 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110537085 | T | C | 1 | a0001c0002 | 101 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(98): Show |
synonymous_variant | LOW | c.867A>G | p.Pro289Pro | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 1154/4994 | 867/915 | 289/304 | chr12 | 110537085 | |||
| chr12:110546068 | G | T | 1 | a0001c0004 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.414C>A | p.Thr138Thr | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/6 | 701/4994 | 414/915 | 138/304 | chr12 | 110546068 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110533585 | C | CA | 2 | a0001c0001t0004 a0001c0002t0004 |
9 | HG01167.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3451dupT | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 3451 | chr12 | 110533585 | ||||||
| chr12:110533635 | TAC | T | 2 | a0001c0001t0008 a0001c0001t0022 |
5 | HG01099.hp1 HG02055.hp2 HG02145.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3400_*3401delGT | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 3400 | chr12 | 110533635 | ||||||
| chr12:110533637 | C | T | 2 | a0001c0001t0001 a0001c0001t0013 |
8 | HG01081.hp1 HG01943.hp1 HG02647.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3400G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 3400 | chr12 | 110533637 | ||||||
| chr12:110533861 | C | T | 9 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(6): Show |
38 | HG00323.hp2 HG01099.hp1 HG01167.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*3176G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 3176 | chr12 | 110533861 | ||||||
| chr12:110534003 | T | C | 1 | a0001c0001t0010 | 2 | HG00738.hp1 HG01069.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3034A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 3034 | chr12 | 110534003 | ||||||
| chr12:110534097 | G | T | 1 | a0001c0001t0015 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2940C>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 2940 | chr12 | 110534097 | ||||||
| chr12:110534123 | A | AT | 2 | a0001c0001t0006 a0001c0001t0014 |
6 | HG01069.hp2 HG01071.hp1 HG01943.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2913dupA | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 2913 | chr12 | 110534123 | ||||||
| chr12:110534123 | AT | A | 11 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(8): Show |
41 | HG00323.hp2 HG00735.hp2 HG00738.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2913delA | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 2913 | chr12 | 110534123 | ||||||
| chr12:110534143 | C | T | 1 | a0001c0002t0020 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2894G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 2894 | chr12 | 110534143 | ||||||
| chr12:110534160 | T | C | 3 | a0001c0001t0007 a0001c0001t0009 a0001c0004t0009 |
7 | HG02055.hp1 HG02809.hp2 HG02886.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2877A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 2877 | chr12 | 110534160 | ||||||
| chr12:110534397 | C | CGT | 3 | a0001c0001t0010 a0001c0001t0019 a0001c0001t0022 |
4 | HG00738.hp1 HG01069.hp1 HG01884.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2638_*2639dupAC | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 2639 | chr12 | 110534397 | ||||||
| chr12:110534723 | CACT | C | 2 | a0001c0001t0008 a0001c0001t0022 |
5 | HG01099.hp1 HG02055.hp2 HG02145.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2311_*2313delAGT | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 2311 | chr12 | 110534723 | ||||||
| chr12:110534724 | A | G | 1 | a0001c0001t0001 | 2 | HG02886.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2313T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 2313 | chr12 | 110534724 | ||||||
| chr12:110535331 | A | G | 1 | a0001c0002t0018 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1706T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 1706 | chr12 | 110535331 | ||||||
| chr12:110535488 | T | C | 1 | a0001c0001t0016 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1549A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 1549 | chr12 | 110535488 | ||||||
| chr12:110535576 | A | G | 2 | a0001c0001t0009 a0001c0004t0009 |
3 | HG02055.hp1 HG02809.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1461T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 1461 | chr12 | 110535576 | ||||||
| chr12:110535583 | C | T | 1 | a0001c0002t0017 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1454G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 1454 | chr12 | 110535583 | ||||||
| chr12:110536002 | T | C | 1 | a0001c0002t0023 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1035A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 1035 | chr12 | 110536002 | ||||||
| chr12:110536041 | A | C | 8 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0012 others(5): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*996T>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 996 | chr12 | 110536041 | ||||||
| chr12:110536068 | G | C | 1 | a0001c0001t0024 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*969C>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 969 | chr12 | 110536068 | ||||||
| chr12:110536359 | T | C | 1 | a0001c0002t0025 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*678A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 678 | chr12 | 110536359 | ||||||
| chr12:110536382 | T | C | 1 | a0001c0001t0010 | 2 | HG00738.hp1 HG01069.hp1 |
3_prime_UTR_variant | MODIFIER | c.*655A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 655 | chr12 | 110536382 | ||||||
| chr12:110536761 | G | A | 1 | a0001c0001t0026 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*276C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 276 | chr12 | 110536761 | ||||||
| chr12:110536811 | C | A | 1 | a0001c0001t0027 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*226G>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 226 | chr12 | 110536811 | ||||||
| chr12:110536842 | G | A | 1 | a0001c0001t0028 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*195C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 195 | chr12 | 110536842 | ||||||
| chr12:110536853 | G | A | 1 | a0001c0001t0010 | 2 | HG00738.hp1 HG01069.hp1 |
3_prime_UTR_variant | MODIFIER | c.*184C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 184 | chr12 | 110536853 | ||||||
| chr12:110536939 | G | C | 1 | a0001c0001t0005 | 6 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*98C>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 6/6 | 98 | chr12 | 110536939 | ||||||
| chr12:110583047 | C | T | 1 | a0001c0001t0013 | 1 | HG04199.hp2 | 5_prime_UTR_variant | MODIFIER | c.-16G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/6 | 16 | chr12 | 110583047 | ||||||
| chr12:110583165 | G | A | 1 | a0001c0002t0011 | 2 | HG03516.hp1 NA18522.hp1 |
5_prime_UTR_variant | MODIFIER | c.-134C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/6 | 134 | chr12 | 110583165 | ||||||
| chr12:110583262 | A | G | 1 | a0001c0001t0012 | 1 | NA18966.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-231T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/6 | chr12 | 110583262 | |||||||
| chr12:110583268 | G | C | 1 | a0001c0001t0029 | 1 | NA18989.hp1 | 5_prime_UTR_variant | MODIFIER | c.-237C>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/6 | 237 | chr12 | 110583268 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110537314 | C | G | 6 | a0001c0002t0001g0138 a0001c0002t0001g0143 a0001c0002t0001g0144 others(3): Show |
6 | HG00738.hp2 HG01175.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.857-219G>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 5/5 | chr12 | 110537314 | |||||||
| chr12:110537394 | G | A | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.857-299C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 5/5 | chr12 | 110537394 | |||||||
| chr12:110537447 | A | G | 1 | a0001c0001t0015g0230 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.857-352T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 5/5 | chr12 | 110537447 | |||||||
| chr12:110537870 | T | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0028 others(274): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.856+274A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 5/5 | chr12 | 110537870 | |||||||
| chr12:110538075 | C | G | 2 | a0001c0001t0008g0258 a0001c0001t0008g0259 |
2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.856+69G>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 5/5 | chr12 | 110538075 | |||||||
| chr12:110538137 | T | C | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
splice_region_variant&intron_variant | LOW | c.856+7A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 5/5 | chr12 | 110538137 | |||||||
| chr12:110538604 | A | C | 75 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(72): Show |
75 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.727-331T>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 4/5 | chr12 | 110538604 | |||||||
| chr12:110538668 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.727-395G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 4/5 | chr12 | 110538668 | |||||||
| chr12:110538703 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.727-430C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 4/5 | chr12 | 110538703 | |||||||
| chr12:110538900 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.727-627G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 4/5 | chr12 | 110538900 | |||||||
| chr12:110539071 | G | A | 3 | a0001c0001t0008g0256 a0001c0001t0008g0257 a0001c0001t0022g0277 |
3 | HG01099.hp1 HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.726+751C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 4/5 | chr12 | 110539071 | |||||||
| chr12:110539981 | G | T | 9 | a0001c0001t0004g0294 a0001c0001t0004g0295 a0001c0001t0004g0297 others(6): Show |
9 | HG01167.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.603-36C>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110539981 | |||||||
| chr12:110540125 | C | A | 1 | a0001c0001t0002g0195 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.603-180G>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110540125 | |||||||
| chr12:110540227 | C | T | 82 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(79): Show |
82 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.603-282G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110540227 | |||||||
| chr12:110540318 | CG | C | 6 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(3): Show |
6 | HG00738.hp1 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.603-374delC | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110540318 | |||||||
| chr12:110540319 | G | C | 32 | a0001c0001t0003g0284 a0001c0001t0003g0285 a0001c0001t0003g0287 others(29): Show |
32 | HG00323.hp2 HG01069.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.603-374C>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110540319 | |||||||
| chr12:110540321 | C | CT | 193 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0028 others(190): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.603-377dupA | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110540321 | |||||||
| chr12:110540322 | T | C | 15 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(12): Show |
15 | HG00738.hp1 HG01099.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.603-377A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110540322 | |||||||
| chr12:110540323 | T | C | 1 | a0001c0001t0010g0025 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.603-378A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110540323 | |||||||
| chr12:110540554 | G | A | 1 | a0001c0002t0001g0251 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.603-609C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110540554 | |||||||
| chr12:110540702 | C | T | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.603-757G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110540702 | |||||||
| chr12:110540779 | C | CT | 31 | a0001c0001t0002g0197 a0001c0001t0003g0282 a0001c0001t0003g0284 others(28): Show |
31 | HG00738.hp1 HG01167.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.603-835dupA | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110540779 | |||||||
| chr12:110540814 | C | T | 1 | a0001c0001t0002g0196 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.603-869G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110540814 | |||||||
| chr12:110540847 | C | T | 1 | a0001c0001t0003g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.603-902G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110540847 | |||||||
| chr12:110540877 | G | A | 16 | a0001c0001t0003g0287 a0001c0001t0003g0288 a0001c0001t0003g0304 others(13): Show |
16 | HG00323.hp2 HG01175.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.603-932C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110540877 | |||||||
| chr12:110541211 | G | A | 4 | a0001c0001t0002g0009 a0001c0001t0002g0231 a0001c0001t0002g0234 others(1): Show |
5 | HG01934.hp1 HG02004.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.603-1266C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110541211 | |||||||
| chr12:110541242 | C | T | 2 | a0001c0002t0001g0149 a0001c0002t0001g0263 |
2 | NA19011.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.603-1297G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110541242 | |||||||
| chr12:110541254 | C | G | 1 | a0001c0002t0001g0153 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.603-1309G>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110541254 | |||||||
| chr12:110541272 | T | C | 1 | a0001c0001t0002g0224 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.603-1327A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110541272 | |||||||
| chr12:110541413 | T | G | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.603-1468A>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110541413 | |||||||
| chr12:110541473 | C | T | 1 | a0001c0002t0011g0317 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.603-1528G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110541473 | |||||||
| chr12:110541559 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0098 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.603-1614C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110541559 | |||||||
| chr12:110541619 | G | A | 4 | a0001c0001t0002g0229 a0001c0001t0002g0238 a0001c0001t0014g0232 others(1): Show |
4 | HG00673.hp1 HG02135.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.603-1674C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110541619 | |||||||
| chr12:110541700 | C | CA | 15 | a0001c0001t0001g0095 a0001c0001t0001g0098 a0001c0001t0001g0106 others(12): Show |
15 | HG01433.hp2 HG02145.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.603-1756dupT | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110541700 | |||||||
| chr12:110541700 | CA | C | 65 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(62): Show |
65 | HG00323.hp2 HG00558.hp1 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.603-1756delT | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110541700 | |||||||
| chr12:110541700 | CAA | C | 6 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(3): Show |
6 | HG01099.hp1 HG02145.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.603-1757_603-1756d others(4): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110541700 | |||||||
| chr12:110541734 | C | T | 289 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0028 others(286): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.603-1789G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110541734 | |||||||
| chr12:110541790 | A | C | 1 | a0001c0001t0001g0280 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.603-1845T>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110541790 | |||||||
| chr12:110541853 | C | G | 1 | a0001c0002t0011g0317 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.603-1908G>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110541853 | |||||||
| chr12:110541945 | A | G | 1 | a0001c0001t0002g0234 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.603-2000T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110541945 | |||||||
| chr12:110542131 | C | T | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.603-2186G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110542131 | |||||||
| chr12:110542364 | G | A | 5 | a0001c0001t0001g0188 a0001c0002t0001g0150 a0001c0002t0001g0182 others(2): Show |
5 | HG02647.hp1 HG03516.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.603-2419C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110542364 | |||||||
| chr12:110542412 | C | T | 1 | a0001c0002t0011g0317 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.603-2467G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110542412 | |||||||
| chr12:110542482 | C | A | 1 | a0001c0002t0001g0151 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.603-2537G>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110542482 | |||||||
| chr12:110542524 | G | C | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.603-2579C>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110542524 | |||||||
| chr12:110542563 | C | T | 1 | a0001c0002t0001g0120 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.603-2618G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110542563 | |||||||
| chr12:110542574 | A | G | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.603-2629T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110542574 | |||||||
| chr12:110542584 | T | C | 1 | a0001c0002t0001g0116 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.603-2639A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110542584 | |||||||
| chr12:110542673 | C | CA | 44 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(41): Show |
44 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.603-2729dupT | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110542673 | |||||||
| chr12:110542673 | CA | C | 8 | a0001c0001t0001g0029 a0001c0001t0001g0112 a0001c0001t0001g0266 others(5): Show |
8 | HG01081.hp1 HG01099.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.603-2729delT | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110542673 | |||||||
| chr12:110542688 | A | G | 1 | a0001c0001t0003g0287 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.603-2743T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110542688 | |||||||
| chr12:110542689 | A | G | 1 | a0001c0001t0001g0006 | 2 | HG01891.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.603-2744T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110542689 | |||||||
| chr12:110542694 | A | AG | 7 | a0001c0001t0003g0305 a0001c0001t0004g0294 a0001c0001t0004g0295 others(4): Show |
7 | HG01167.hp2 HG01175.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.603-2750_603-2749i others(3): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110542694 | |||||||
| chr12:110542694 | A | G | 31 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(28): Show |
31 | HG00323.hp2 HG01099.hp1 HG01361.hp1 others(28): Show |
intron_variant | MODIFIER | c.603-2749T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110542694 | |||||||
| chr12:110542711 | TA | T | 3 | a0001c0001t0003g0284 a0001c0001t0003g0285 a0001c0001t0028g0283 |
3 | HG01891.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.603-2767delT | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110542711 | |||||||
| chr12:110542715 | G | T | 3 | a0001c0001t0003g0284 a0001c0001t0003g0285 a0001c0001t0028g0283 |
3 | HG01891.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.603-2770C>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110542715 | |||||||
| chr12:110542726 | T | A | 1 | a0001c0001t0002g0190 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.603-2781A>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110542726 | |||||||
| chr12:110542727 | A | T | 1 | a0001c0001t0002g0190 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.603-2782T>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110542727 | |||||||
| chr12:110542880 | G | A | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.603-2935C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110542880 | |||||||
| chr12:110542905 | T | A | 1 | a0001c0001t0001g0036 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.603-2960A>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110542905 | |||||||
| chr12:110542908 | T | A | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.603-2963A>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110542908 | |||||||
| chr12:110543065 | C | T | 1 | a0001c0001t0003g0311 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.602+2815G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110543065 | |||||||
| chr12:110543069 | C | A | 1 | a0001c0002t0001g0208 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.602+2811G>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110543069 | |||||||
| chr12:110543070 | C | A | 1 | a0001c0002t0001g0208 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.602+2810G>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110543070 | |||||||
| chr12:110543110 | G | A | 19 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0051 others(16): Show |
19 | HG00423.hp2 HG00558.hp1 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.602+2770C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110543110 | |||||||
| chr12:110543117 | C | A | 1 | a0001c0001t0001g0059 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.602+2763G>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110543117 | |||||||
| chr12:110543435 | G | GA | 6 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(3): Show |
6 | HG01071.hp2 HG01081.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.602+2444dupT | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110543435 | |||||||
| chr12:110543439 | A | G | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.602+2441T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110543439 | |||||||
| chr12:110543777 | C | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0037 others(5): Show |
9 | HG01168.hp2 HG01169.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.602+2103G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110543777 | |||||||
| chr12:110543813 | G | T | 1 | a0001c0002t0011g0317 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.602+2067C>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110543813 | |||||||
| chr12:110543826 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.602+2054A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110543826 | |||||||
| chr12:110543861 | G | A | 7 | a0001c0002t0001g0084 a0001c0002t0001g0087 a0001c0002t0001g0089 others(4): Show |
7 | HG00621.hp2 HG02135.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.602+2019C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110543861 | |||||||
| chr12:110543933 | G | A | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.602+1947C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110543933 | |||||||
| chr12:110543954 | A | G | 1 | a0001c0001t0001g0313 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.602+1926T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110543954 | |||||||
| chr12:110544082 | T | C | 1 | a0001c0001t0002g0216 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.602+1798A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110544082 | |||||||
| chr12:110544169 | A | G | 1 | a0001c0002t0001g0153 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.602+1711T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110544169 | |||||||
| chr12:110544335 | G | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0069 |
2 | NA18947.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.602+1545C>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110544335 | |||||||
| chr12:110544520 | A | T | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.602+1360T>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110544520 | |||||||
| chr12:110544561 | C | T | 2 | a0002c0003t0001g0018 a0002c0003t0001g0022 |
2 | HG01346.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.602+1319G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110544561 | |||||||
| chr12:110544703 | G | A | 1 | a0001c0001t0022g0277 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.602+1177C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110544703 | |||||||
| chr12:110544879 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.602+1001G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110544879 | |||||||
| chr12:110544933 | T | C | 2 | a0001c0001t0008g0258 a0001c0001t0008g0259 |
2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.602+947A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110544933 | |||||||
| chr12:110545088 | G | A | 2 | a0001c0001t0003g0311 a0001c0002t0001g0144 |
2 | HG02976.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.602+792C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110545088 | |||||||
| chr12:110545382 | C | T | 1 | a0001c0002t0001g0175 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.602+498G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110545382 | |||||||
| chr12:110545413 | C | A | 1 | a0001c0001t0002g0190 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.602+467G>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110545413 | |||||||
| chr12:110545660 | C | A | 1 | a0001c0001t0003g0287 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.602+220G>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110545660 | |||||||
| chr12:110545689 | T | C | 1 | a0001c0001t0002g0209 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.602+191A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110545689 | |||||||
| chr12:110545722 | G | T | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.602+158C>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110545722 | |||||||
| chr12:110545755 | G | T | 1 | a0001c0001t0001g0110 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.602+125C>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110545755 | |||||||
| chr12:110545843 | G | A | 2 | a0001c0001t0008g0256 a0001c0001t0008g0257 |
2 | HG01099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.602+37C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 3/5 | chr12 | 110545843 | |||||||
| chr12:110546243 | T | C | 1 | a0001c0001t0002g0027 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.404-165A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110546243 | |||||||
| chr12:110546263 | G | A | 2 | a0001c0002t0001g0141 a0001c0002t0001g0146 |
2 | HG01255.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.404-185C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110546263 | |||||||
| chr12:110546876 | T | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0113 |
3 | HG01516.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.404-798A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110546876 | |||||||
| chr12:110546927 | G | A | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.404-849C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110546927 | |||||||
| chr12:110547027 | T | C | 5 | a0001c0001t0008g0256 a0001c0001t0008g0257 a0001c0001t0008g0258 others(2): Show |
5 | HG01099.hp1 HG02055.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.404-949A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110547027 | |||||||
| chr12:110547095 | T | TAAAAAAA others(8): Show |
1 | a0001c0001t0002g0190 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.404-1018_404-1017i others(17): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110547095 | |||||||
| chr12:110547118 | G | A | 1 | a0001c0002t0001g0174 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.404-1040C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110547118 | |||||||
| chr12:110547265 | C | T | 1 | a0001c0002t0023g0134 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.404-1187G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110547265 | |||||||
| chr12:110547637 | C | A | 41 | a0001c0001t0001g0313 a0001c0001t0003g0043 a0001c0001t0003g0044 others(38): Show |
41 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.404-1559G>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110547637 | |||||||
| chr12:110547668 | T | C | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.404-1590A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110547668 | |||||||
| chr12:110547692 | A | G | 2 | a0002c0003t0001g0020 a0002c0003t0001g0023 |
2 | HG00741.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.404-1614T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110547692 | |||||||
| chr12:110547819 | A | C | 3 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 |
3 | HG02630.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.404-1741T>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110547819 | |||||||
| chr12:110547843 | G | A | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.404-1765C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110547843 | |||||||
| chr12:110548019 | A | G | 1 | a0001c0001t0002g0233 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.404-1941T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110548019 | |||||||
| chr12:110548106 | C | CA | 8 | a0001c0001t0001g0114 a0001c0001t0001g0177 a0001c0001t0001g0267 others(5): Show |
8 | HG01243.hp1 HG01433.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.404-2029dupT | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110548106 | |||||||
| chr12:110548388 | G | A | 5 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0014 others(2): Show |
5 | HG02717.hp2 HG02965.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.404-2310C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110548388 | |||||||
| chr12:110548428 | C | T | 1 | a0001c0002t0001g0115 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.404-2350G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110548428 | |||||||
| chr12:110548460 | C | T | 1 | a0001c0002t0025g0166 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.404-2382G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110548460 | |||||||
| chr12:110548514 | G | A | 1 | a0001c0001t0022g0277 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.404-2436C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110548514 | |||||||
| chr12:110548702 | T | G | 2 | a0001c0001t0002g0071 a0001c0001t0002g0076 |
2 | HG00741.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.404-2624A>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110548702 | |||||||
| chr12:110548724 | G | A | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.404-2646C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110548724 | |||||||
| chr12:110548745 | G | A | 2 | a0001c0001t0008g0258 a0001c0001t0008g0259 |
2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.404-2667C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110548745 | |||||||
| chr12:110549099 | G | C | 1 | a0001c0001t0001g0188 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.403+2690C>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110549099 | |||||||
| chr12:110549387 | T | A | 2 | a0001c0001t0008g0256 a0001c0001t0008g0257 |
2 | HG01099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.403+2402A>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110549387 | |||||||
| chr12:110549394 | A | C | 2 | a0001c0001t0008g0256 a0001c0001t0008g0257 |
2 | HG01099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.403+2395T>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110549394 | |||||||
| chr12:110549420 | G | T | 1 | a0001c0001t0001g0266 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.403+2369C>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110549420 | |||||||
| chr12:110549481 | T | C | 1 | a0001c0001t0001g0313 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.403+2308A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110549481 | |||||||
| chr12:110549621 | A | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0061 |
2 | HG00423.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.403+2168T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110549621 | |||||||
| chr12:110549711 | G | A | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.403+2078C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110549711 | |||||||
| chr12:110549765 | G | A | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.403+2024C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110549765 | |||||||
| chr12:110549877 | G | T | 2 | a0001c0001t0008g0256 a0001c0001t0008g0257 |
2 | HG01099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.403+1912C>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110549877 | |||||||
| chr12:110550223 | A | AT | 43 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(40): Show |
43 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.403+1565dupA | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110550223 | |||||||
| chr12:110550223 | AT | A | 11 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0110 others(8): Show |
11 | HG00323.hp1 HG01167.hp1 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.403+1565delA | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110550223 | |||||||
| chr12:110550223 | ATTTTTTT others(4): Show |
A | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.403+1555_403+1565d others(13): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110550223 | |||||||
| chr12:110550265 | C | G | 5 | a0001c0001t0002g0008 a0001c0001t0002g0209 a0001c0001t0002g0236 others(2): Show |
6 | NA18945.hp2 NA18946.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.403+1524G>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110550265 | |||||||
| chr12:110550269 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.403+1520G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110550269 | |||||||
| chr12:110550292 | G | A | 2 | a0001c0001t0003g0309 a0001c0001t0003g0310 |
2 | NA18952.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.403+1497C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110550292 | |||||||
| chr12:110550834 | G | T | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.403+955C>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110550834 | |||||||
| chr12:110550889 | C | T | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.403+900G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110550889 | |||||||
| chr12:110551074 | G | C | 1 | a0001c0001t0002g0255 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.403+715C>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110551074 | |||||||
| chr12:110551081 | C | A | 47 | a0001c0001t0001g0029 a0001c0001t0001g0127 a0001c0001t0001g0128 others(44): Show |
47 | HG00323.hp2 HG01081.hp1 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.403+708G>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110551081 | |||||||
| chr12:110551186 | C | T | 1 | a0001c0001t0003g0311 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.403+603G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110551186 | |||||||
| chr12:110551259 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.403+530T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110551259 | |||||||
| chr12:110551574 | C | T | 2 | a0002c0003t0001g0018 a0002c0003t0001g0022 |
2 | HG01346.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.403+215G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 2/5 | chr12 | 110551574 | |||||||
| chr12:110552074 | T | C | 3 | a0001c0001t0003g0284 a0001c0001t0003g0285 a0001c0001t0028g0283 |
3 | HG01891.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.224-106A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110552074 | |||||||
| chr12:110552213 | T | C | 3 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 |
3 | HG02630.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.224-245A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110552213 | |||||||
| chr12:110552248 | T | G | 2 | a0001c0002t0001g0140 a0001c0002t0001g0169 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.224-280A>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110552248 | |||||||
| chr12:110552483 | G | A | 1 | a0001c0002t0001g0081 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.224-515C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110552483 | |||||||
| chr12:110552515 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.224-547A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110552515 | |||||||
| chr12:110552530 | C | T | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.224-562G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110552530 | |||||||
| chr12:110552536 | G | C | 1 | a0002c0003t0001g0024 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.224-568C>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110552536 | |||||||
| chr12:110552598 | C | T | 1 | a0001c0002t0001g0119 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.224-630G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110552598 | |||||||
| chr12:110552646 | C | T | 4 | a0001c0002t0001g0151 a0001c0002t0001g0157 a0001c0002t0001g0164 others(1): Show |
4 | HG02258.hp2 HG02572.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-678G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110552646 | |||||||
| chr12:110552714 | A | T | 3 | a0001c0001t0003g0284 a0001c0001t0003g0285 a0001c0001t0028g0283 |
3 | HG01891.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.224-746T>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110552714 | |||||||
| chr12:110552736 | C | T | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.224-768G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110552736 | |||||||
| chr12:110552776 | T | C | 1 | a0001c0001t0003g0288 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.224-808A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110552776 | |||||||
| chr12:110552840 | G | A | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.224-872C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110552840 | |||||||
| chr12:110552845 | T | C | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.224-877A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110552845 | |||||||
| chr12:110552867 | A | C | 1 | a0001c0001t0001g0281 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.224-899T>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110552867 | |||||||
| chr12:110552867 | AAAAC | A | 5 | a0001c0001t0003g0310 a0002c0003t0001g0012 a0002c0003t0001g0013 others(2): Show |
5 | HG02717.hp2 HG02965.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-903_224-900del others(4): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110552867 | |||||||
| chr12:110552995 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.224-1027T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110552995 | |||||||
| chr12:110553014 | T | C | 8 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(5): Show |
8 | HG01099.hp1 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.224-1046A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110553014 | |||||||
| chr12:110553039 | T | A | 1 | a0001c0001t0007g0286 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.224-1071A>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110553039 | |||||||
| chr12:110553124 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.224-1156C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110553124 | |||||||
| chr12:110553137 | C | T | 1 | a0001c0001t0003g0288 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.224-1169G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110553137 | |||||||
| chr12:110553182 | G | A | 2 | a0001c0002t0001g0077 a0001c0002t0001g0090 |
2 | NA18962.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.224-1214C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110553182 | |||||||
| chr12:110553183 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.224-1215G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110553183 | |||||||
| chr12:110553275 | G | A | 8 | a0001c0001t0001g0029 a0001c0001t0001g0127 a0001c0001t0001g0128 others(5): Show |
8 | HG01081.hp1 HG01943.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.224-1307C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110553275 | |||||||
| chr12:110553296 | C | T | 77 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(74): Show |
81 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.224-1328G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110553296 | |||||||
| chr12:110553307 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.224-1339C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110553307 | |||||||
| chr12:110553707 | T | C | 2 | a0002c0003t0001g0018 a0002c0003t0001g0022 |
2 | HG01346.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.224-1739A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110553707 | |||||||
| chr12:110553844 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.224-1876C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110553844 | |||||||
| chr12:110554115 | G | A | 1 | a0001c0001t0002g0228 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.224-2147C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110554115 | |||||||
| chr12:110554127 | A | G | 6 | a0001c0002t0001g0138 a0001c0002t0001g0143 a0001c0002t0001g0144 others(3): Show |
6 | HG00738.hp2 HG01175.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.224-2159T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110554127 | |||||||
| chr12:110554174 | T | G | 1 | a0002c0003t0001g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.224-2206A>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110554174 | |||||||
| chr12:110554450 | A | T | 1 | a0001c0001t0022g0277 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.224-2482T>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110554450 | |||||||
| chr12:110554699 | T | C | 1 | a0001c0001t0002g0189 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.224-2731A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110554699 | |||||||
| chr12:110554731 | A | G | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.224-2763T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110554731 | |||||||
| chr12:110554756 | C | T | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.224-2788G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110554756 | |||||||
| chr12:110554911 | A | T | 1 | a0001c0002t0001g0136 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.224-2943T>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110554911 | |||||||
| chr12:110554950 | T | C | 38 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(35): Show |
38 | HG00323.hp2 HG01099.hp1 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.224-2982A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110554950 | |||||||
| chr12:110555338 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.224-3370G>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110555338 | |||||||
| chr12:110555377 | G | A | 3 | a0001c0001t0003g0284 a0001c0001t0003g0285 a0001c0001t0028g0283 |
3 | HG01891.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.224-3409C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110555377 | |||||||
| chr12:110555863 | T | C | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.224-3895A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110555863 | |||||||
| chr12:110555986 | G | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0028 others(189): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.224-4018C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110555986 | |||||||
| chr12:110556263 | T | C | 2 | a0001c0001t0003g0304 a0001c0001t0003g0305 |
2 | HG00323.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.224-4295A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110556263 | |||||||
| chr12:110556265 | G | A | 1 | a0001c0002t0001g0156 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.224-4297C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110556265 | |||||||
| chr12:110556422 | T | C | 5 | a0001c0001t0008g0256 a0001c0001t0008g0257 a0001c0001t0008g0258 others(2): Show |
5 | HG01099.hp1 HG02055.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.224-4454A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110556422 | |||||||
| chr12:110556572 | A | G | 3 | a0001c0001t0008g0256 a0001c0001t0008g0257 a0001c0001t0022g0277 |
3 | HG01099.hp1 HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.224-4604T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110556572 | |||||||
| chr12:110556737 | A | G | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.224-4769T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110556737 | |||||||
| chr12:110556744 | G | C | 1 | a0001c0001t0002g0047 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.224-4776C>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110556744 | |||||||
| chr12:110556850 | A | C | 1 | a0001c0001t0007g0286 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.224-4882T>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110556850 | |||||||
| chr12:110556908 | C | G | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.224-4940G>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110556908 | |||||||
| chr12:110557022 | G | T | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.224-5054C>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110557022 | |||||||
| chr12:110557252 | A | G | 2 | a0001c0001t0008g0256 a0001c0001t0008g0257 |
2 | HG01099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.224-5284T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110557252 | |||||||
| chr12:110557437 | G | A | 5 | a0001c0001t0008g0256 a0001c0001t0008g0257 a0001c0001t0008g0258 others(2): Show |
5 | HG01099.hp1 HG02055.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.224-5469C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110557437 | |||||||
| chr12:110557451 | T | A | 2 | a0001c0001t0001g0278 a0001c0001t0019g0279 |
2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.224-5483A>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110557451 | |||||||
| chr12:110557526 | C | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-5558G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110557526 | |||||||
| chr12:110557626 | A | G | 1 | a0001c0002t0001g0079 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.224-5658T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110557626 | |||||||
| chr12:110557641 | T | C | 3 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 |
3 | HG02630.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.224-5673A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110557641 | |||||||
| chr12:110557876 | G | A | 1 | a0001c0001t0002g0233 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.224-5908C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110557876 | |||||||
| chr12:110557878 | G | A | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.224-5910C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110557878 | |||||||
| chr12:110558235 | T | C | 4 | a0001c0001t0002g0213 a0001c0001t0002g0314 a0001c0001t0002g0315 others(1): Show |
4 | HG00558.hp2 HG00673.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-6267A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110558235 | |||||||
| chr12:110558404 | A | G | 2 | a0001c0001t0008g0258 a0001c0001t0008g0259 |
2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.224-6436T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110558404 | |||||||
| chr12:110558458 | T | G | 8 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0076 others(5): Show |
9 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.224-6490A>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110558458 | |||||||
| chr12:110558601 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.224-6633C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110558601 | |||||||
| chr12:110558680 | C | T | 32 | a0001c0001t0003g0282 a0001c0001t0003g0284 a0001c0001t0003g0285 others(29): Show |
32 | HG00323.hp2 HG01099.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.224-6712G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110558680 | |||||||
| chr12:110558807 | C | T | 1 | a0001c0002t0001g0147 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.224-6839G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110558807 | |||||||
| chr12:110558896 | G | A | 8 | a0001c0001t0001g0029 a0001c0001t0001g0127 a0001c0001t0001g0128 others(5): Show |
8 | HG01081.hp1 HG01943.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.224-6928C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110558896 | |||||||
| chr12:110558992 | G | C | 1 | a0001c0001t0003g0044 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.224-7024C>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110558992 | |||||||
| chr12:110559003 | A | G | 1 | a0001c0002t0020g0117 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.224-7035T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110559003 | |||||||
| chr12:110559083 | G | A | 3 | a0001c0001t0008g0256 a0001c0001t0008g0257 a0001c0001t0022g0277 |
3 | HG01099.hp1 HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.224-7115C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110559083 | |||||||
| chr12:110559156 | T | C | 1 | a0001c0002t0001g0094 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.224-7188A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110559156 | |||||||
| chr12:110559164 | C | T | 1 | a0001c0001t0003g0288 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.224-7196G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110559164 | |||||||
| chr12:110559263 | C | G | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.224-7295G>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110559263 | |||||||
| chr12:110559412 | A | AT | 28 | a0001c0001t0003g0284 a0001c0001t0003g0285 a0001c0001t0003g0287 others(25): Show |
28 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.224-7445dupA | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110559412 | |||||||
| chr12:110559412 | AT | A | 6 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(3): Show |
6 | HG01167.hp1 HG03041.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.224-7445delA | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110559412 | |||||||
| chr12:110559413 | T | A | 2 | a0001c0001t0008g0258 a0001c0001t0008g0259 |
2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.224-7445A>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110559413 | |||||||
| chr12:110559414 | T | A | 2 | a0001c0001t0008g0258 a0001c0001t0008g0259 |
2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.224-7446A>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110559414 | |||||||
| chr12:110559443 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.224-7475C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110559443 | |||||||
| chr12:110559551 | C | A | 12 | a0001c0001t0002g0008 a0001c0001t0002g0209 a0001c0001t0002g0228 others(9): Show |
13 | HG00673.hp1 HG02135.hp2 NA18945.hp2 others(10): Show |
intron_variant | MODIFIER | c.224-7583G>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110559551 | |||||||
| chr12:110559552 | C | T | 1 | a0001c0002t0001g0135 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.224-7584G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110559552 | |||||||
| chr12:110559554 | C | T | 2 | a0001c0001t0007g0289 a0001c0001t0007g0303 |
2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.224-7586G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110559554 | |||||||
| chr12:110559625 | C | T | 1 | a0001c0002t0001g0175 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.224-7657G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110559625 | |||||||
| chr12:110559642 | C | T | 1 | a0001c0002t0001g0155 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.224-7674G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110559642 | |||||||
| chr12:110559688 | T | C | 30 | a0001c0001t0003g0282 a0001c0001t0003g0284 a0001c0001t0003g0285 others(27): Show |
30 | HG00323.hp2 HG01167.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.224-7720A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110559688 | |||||||
| chr12:110559704 | C | T | 3 | a0001c0001t0009g0290 a0001c0001t0009g0293 a0001c0004t0009g0292 |
3 | HG02055.hp1 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.224-7736G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110559704 | |||||||
| chr12:110559713 | A | T | 1 | a0001c0001t0001g0188 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.224-7745T>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110559713 | |||||||
| chr12:110559730 | G | GA | 21 | a0001c0001t0001g0101 a0001c0001t0001g0131 a0001c0001t0001g0186 others(18): Show |
21 | HG00735.hp1 HG00738.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.224-7763dupT | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110559730 | |||||||
| chr12:110559730 | GA | G | 7 | a0001c0001t0001g0103 a0001c0001t0003g0043 a0001c0001t0003g0044 others(4): Show |
7 | HG00323.hp1 HG00738.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.224-7763delT | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110559730 | |||||||
| chr12:110559732 | A | G | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.224-7764T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110559732 | |||||||
| chr12:110560046 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0107 |
2 | HG00280.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.224-8078G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110560046 | |||||||
| chr12:110560055 | T | C | 3 | a0001c0002t0001g0126 a0001c0002t0001g0148 a0001c0002t0001g0152 |
3 | HG02129.hp2 HG02523.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.224-8087A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110560055 | |||||||
| chr12:110560181 | T | C | 1 | a0001c0001t0002g0247 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224-8213A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110560181 | |||||||
| chr12:110560274 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.224-8306G>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110560274 | |||||||
| chr12:110560341 | C | A | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.224-8373G>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110560341 | |||||||
| chr12:110560381 | G | A | 5 | a0001c0001t0002g0009 a0001c0001t0002g0231 a0001c0001t0002g0234 others(2): Show |
6 | HG01934.hp1 HG02004.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.224-8413C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110560381 | |||||||
| chr12:110560392 | A | G | 2 | a0001c0001t0003g0285 a0001c0001t0028g0283 |
2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.224-8424T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110560392 | |||||||
| chr12:110560401 | C | CA | 40 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(37): Show |
40 | HG00423.hp2 HG00558.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.224-8434dupT | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110560401 | |||||||
| chr12:110560408 | T | A | 272 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0028 others(269): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.224-8440A>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110560408 | |||||||
| chr12:110560409 | A | T | 1 | a0001c0001t0022g0277 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.224-8441T>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110560409 | |||||||
| chr12:110560422 | A | C | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.224-8454T>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110560422 | |||||||
| chr12:110560609 | C | T | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.224-8641G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110560609 | |||||||
| chr12:110560778 | A | C | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.224-8810T>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110560778 | |||||||
| chr12:110560877 | A | C | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.224-8909T>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110560877 | |||||||
| chr12:110561227 | G | A | 40 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(37): Show |
40 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.224-9259C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110561227 | |||||||
| chr12:110561232 | T | C | 1 | a0001c0002t0001g0084 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.224-9264A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110561232 | |||||||
| chr12:110561399 | C | T | 1 | a0001c0002t0001g0176 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.224-9431G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110561399 | |||||||
| chr12:110561547 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.224-9579G>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110561547 | |||||||
| chr12:110561668 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.224-9700G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110561668 | |||||||
| chr12:110561674 | C | T | 1 | a0001c0002t0001g0142 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.224-9706G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110561674 | |||||||
| chr12:110562199 | C | T | 1 | a0001c0002t0001g0123 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.224-10231G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110562199 | |||||||
| chr12:110562222 | T | C | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.224-10254A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110562222 | |||||||
| chr12:110562224 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.224-10256C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110562224 | |||||||
| chr12:110562252 | A | T | 28 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(25): Show |
28 | HG00423.hp2 HG00558.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.224-10284T>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110562252 | |||||||
| chr12:110562258 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.224-10290C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110562258 | |||||||
| chr12:110562286 | C | CA | 33 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(30): Show |
33 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.224-10319dupT | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110562286 | |||||||
| chr12:110562286 | C | CAA | 12 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(9): Show |
12 | HG01891.hp2 HG02145.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.224-10320_224-1031 others(6): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110562286 | |||||||
| chr12:110562286 | CA | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0028 others(142): Show |
151 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.224-10319delT | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110562286 | |||||||
| chr12:110562286 | CAA | C | 35 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0049 others(32): Show |
35 | HG00423.hp2 HG00558.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.224-10320_224-1031 others(6): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110562286 | |||||||
| chr12:110562286 | CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 |
3 | HG02630.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.224-10329_224-1031 others(15): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110562286 | |||||||
| chr12:110562286 | CAAAAAAA others(5): Show |
C | 1 | a0001c0002t0001g0174 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.224-10330_224-1031 others(16): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110562286 | |||||||
| chr12:110562593 | G | A | 1 | a0001c0001t0003g0282 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.224-10625C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110562593 | |||||||
| chr12:110562623 | T | C | 3 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 |
3 | HG02630.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.224-10655A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110562623 | |||||||
| chr12:110562661 | C | T | 1 | a0001c0002t0001g0142 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.224-10693G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110562661 | |||||||
| chr12:110562774 | C | T | 1 | a0001c0001t0002g0246 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.224-10806G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110562774 | |||||||
| chr12:110562780 | G | A | 1 | a0001c0002t0001g0167 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.224-10812C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110562780 | |||||||
| chr12:110562941 | G | A | 1 | a0001c0002t0001g0085 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.224-10973C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110562941 | |||||||
| chr12:110562942 | C | G | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-10974G>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110562942 | |||||||
| chr12:110563057 | T | G | 1 | a0001c0001t0005g0072 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.224-11089A>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110563057 | |||||||
| chr12:110563122 | C | CA | 34 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0065 others(31): Show |
34 | HG00140.hp1 HG00673.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.224-11155dupT | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110563122 | |||||||
| chr12:110563122 | C | CAA | 8 | a0001c0001t0001g0029 a0001c0001t0001g0281 a0001c0001t0002g0242 others(5): Show |
8 | HG01081.hp1 HG02630.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.224-11156_224-1115 others(6): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110563122 | |||||||
| chr12:110563122 | CA | C | 51 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(48): Show |
52 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.224-11155delT | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110563122 | |||||||
| chr12:110563122 | CAA | C | 30 | a0001c0001t0003g0282 a0001c0001t0003g0287 a0001c0001t0003g0304 others(27): Show |
30 | HG00323.hp2 HG01167.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.224-11156_224-1115 others(6): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110563122 | |||||||
| chr12:110563122 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0003g0284 a0001c0001t0003g0285 a0001c0001t0028g0283 |
3 | HG01891.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.224-11164_224-1115 others(14): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110563122 | |||||||
| chr12:110563146 | A | G | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.224-11178T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110563146 | |||||||
| chr12:110563153 | A | G | 1 | a0001c0001t0002g0229 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.224-11185T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110563153 | |||||||
| chr12:110563355 | G | A | 1 | a0001c0001t0003g0284 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.224-11387C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110563355 | |||||||
| chr12:110563398 | C | A | 3 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 |
3 | HG02630.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.224-11430G>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110563398 | |||||||
| chr12:110563480 | T | C | 2 | a0001c0001t0008g0258 a0001c0001t0008g0259 |
2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.224-11512A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110563480 | |||||||
| chr12:110563491 | T | C | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.224-11523A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110563491 | |||||||
| chr12:110563544 | G | A | 1 | a0001c0002t0001g0276 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.224-11576C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110563544 | |||||||
| chr12:110563564 | G | A | 3 | a0001c0001t0001g0280 a0001c0001t0008g0256 a0001c0001t0008g0257 |
3 | HG01099.hp1 HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.224-11596C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110563564 | |||||||
| chr12:110563592 | G | T | 1 | a0001c0002t0001g0150 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.224-11624C>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110563592 | |||||||
| chr12:110563615 | C | CA | 14 | a0001c0001t0001g0029 a0001c0001t0001g0127 a0001c0001t0001g0128 others(11): Show |
14 | HG01081.hp1 HG01943.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.224-11648dupT | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110563615 | |||||||
| chr12:110563615 | CA | C | 31 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(28): Show |
31 | HG00423.hp2 HG00558.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.224-11648delT | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110563615 | |||||||
| chr12:110563651 | G | A | 4 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0015 others(1): Show |
4 | HG02717.hp2 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-11683C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110563651 | |||||||
| chr12:110563679 | G | T | 1 | a0001c0002t0001g0119 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.224-11711C>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110563679 | |||||||
| chr12:110563802 | C | T | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.224-11834G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110563802 | |||||||
| chr12:110563810 | T | C | 1 | a0001c0001t0003g0282 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.224-11842A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110563810 | |||||||
| chr12:110564506 | A | G | 83 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(80): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.224-12538T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110564506 | |||||||
| chr12:110564578 | C | T | 2 | a0001c0001t0003g0306 a0001c0001t0003g0308 |
2 | HG03491.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.224-12610G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110564578 | |||||||
| chr12:110564660 | G | C | 1 | a0001c0002t0001g0155 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.224-12692C>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110564660 | |||||||
| chr12:110564713 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.224-12745T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110564713 | |||||||
| chr12:110564718 | A | G | 1 | a0001c0001t0002g0223 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.224-12750T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110564718 | |||||||
| chr12:110564732 | A | C | 1 | a0002c0003t0001g0018 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.224-12764T>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110564732 | |||||||
| chr12:110564757 | CATATATA others(52): Show |
C | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.224-12848_224-1279 others(63): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110564757 | |||||||
| chr12:110564769 | C | CATATATA others(40): Show |
1 | a0001c0001t0001g0053 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.224-12802_224-1280 others(51): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110564769 | |||||||
| chr12:110564770 | G | A | 7 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0055 others(4): Show |
7 | HG00558.hp1 NA18947.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.224-12802C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110564770 | |||||||
| chr12:110564772 | A | ATATATAT others(40): Show |
27 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(24): Show |
27 | HG00423.hp2 HG00558.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.224-12851_224-1280 others(51): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110564772 | |||||||
| chr12:110564772 | A | ATATATAT others(66): Show |
1 | a0001c0001t0001g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.224-12805_224-1280 others(77): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110564772 | |||||||
| chr12:110564772 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.224-12804T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110564772 | |||||||
| chr12:110564772 | ATATATAT others(40): Show |
A | 30 | a0001c0001t0003g0282 a0001c0001t0003g0284 a0001c0001t0003g0285 others(27): Show |
30 | HG00323.hp2 HG01167.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.224-12851_224-1280 others(51): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110564772 | |||||||
| chr12:110564793 | A | ATATATAT others(19): Show |
7 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0039 others(4): Show |
8 | HG01168.hp2 HG01169.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.224-12851_224-1282 others(30): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110564793 | |||||||
| chr12:110564800 | T | C | 9 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(6): Show |
9 | HG00280.hp1 HG01099.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.224-12832A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110564800 | |||||||
| chr12:110564805 | G | A | 2 | a0001c0001t0005g0002 a0001c0001t0005g0075 |
2 | HG00099.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.224-12837C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110564805 | |||||||
| chr12:110564819 | G | A | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.224-12851C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110564819 | |||||||
| chr12:110564835 | G | GTT | 80 | a0001c0001t0001g0177 a0001c0001t0002g0088 a0001c0001t0002g0172 others(77): Show |
82 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.224-12869_224-1286 others(6): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110564835 | |||||||
| chr12:110564847 | T | C | 30 | a0001c0001t0003g0282 a0001c0001t0003g0284 a0001c0001t0003g0285 others(27): Show |
30 | HG00323.hp2 HG01167.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.224-12879A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110564847 | |||||||
| chr12:110564858 | G | A | 2 | a0001c0002t0001g0157 a0001c0002t0001g0180 |
2 | HG02572.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.224-12890C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110564858 | |||||||
| chr12:110565031 | T | C | 1 | a0001c0001t0022g0277 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.224-13063A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110565031 | |||||||
| chr12:110565064 | C | T | 3 | a0001c0001t0001g0049 a0001c0001t0001g0066 a0001c0001t0002g0204 |
3 | NA18953.hp1 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.224-13096G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110565064 | |||||||
| chr12:110565153 | C | A | 33 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(30): Show |
33 | HG00423.hp2 HG00558.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.224-13185G>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110565153 | |||||||
| chr12:110565343 | G | A | 22 | a0001c0001t0002g0190 a0001c0001t0002g0191 a0001c0001t0002g0193 others(19): Show |
22 | HG00558.hp2 HG00673.hp2 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.224-13375C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110565343 | |||||||
| chr12:110565437 | G | C | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-13469C>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110565437 | |||||||
| chr12:110565626 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.224-13658T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110565626 | |||||||
| chr12:110565652 | C | T | 40 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(37): Show |
40 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.224-13684G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110565652 | |||||||
| chr12:110565658 | T | A | 1 | a0001c0001t0003g0305 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.224-13690A>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110565658 | |||||||
| chr12:110565732 | G | C | 1 | a0001c0001t0001g0280 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.224-13764C>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110565732 | |||||||
| chr12:110566089 | C | G | 13 | a0001c0001t0003g0284 a0001c0001t0003g0285 a0001c0001t0003g0311 others(10): Show |
13 | HG01167.hp2 HG01891.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.224-14121G>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110566089 | |||||||
| chr12:110566091 | A | G | 1 | a0001c0001t0002g0203 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.224-14123T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110566091 | |||||||
| chr12:110566129 | G | A | 3 | a0001c0001t0002g0254 a0001c0002t0001g0251 a0001c0002t0001g0252 |
3 | NA18955.hp1 NA18957.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.224-14161C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110566129 | |||||||
| chr12:110566164 | A | AG | 316 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(313): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.224-14197dupC | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110566164 | |||||||
| chr12:110566564 | C | G | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.224-14596G>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110566564 | |||||||
| chr12:110566604 | T | C | 7 | a0001c0001t0002g0214 a0001c0001t0002g0225 a0001c0001t0002g0227 others(4): Show |
7 | HG02074.hp2 HG02080.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.224-14636A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110566604 | |||||||
| chr12:110566830 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.224-14862G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110566830 | |||||||
| chr12:110567092 | T | C | 3 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 |
3 | HG02630.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.224-15124A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110567092 | |||||||
| chr12:110567481 | A | G | 3 | a0001c0001t0006g0198 a0001c0001t0006g0215 a0001c0001t0006g0226 |
3 | HG01069.hp2 HG01071.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.223+15328T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110567481 | |||||||
| chr12:110567806 | C | A | 60 | a0001c0001t0002g0088 a0001c0001t0002g0172 a0001c0001t0002g0254 others(57): Show |
62 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.223+15003G>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110567806 | |||||||
| chr12:110567956 | C | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0100 |
2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.223+14853G>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110567956 | |||||||
| chr12:110568125 | T | C | 1 | a0001c0001t0003g0288 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.223+14684A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110568125 | |||||||
| chr12:110568252 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0098 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.223+14557G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110568252 | |||||||
| chr12:110568253 | G | GT | 37 | a0001c0001t0001g0033 a0001c0001t0001g0048 a0001c0001t0001g0055 others(34): Show |
37 | HG00558.hp1 HG00733.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.223+14555dupA | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110568253 | |||||||
| chr12:110568253 | GT | G | 14 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(11): Show |
14 | HG01167.hp2 HG01943.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.223+14555delA | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110568253 | |||||||
| chr12:110568355 | T | C | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.223+14454A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110568355 | |||||||
| chr12:110568377 | T | C | 82 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(79): Show |
82 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.223+14432A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110568377 | |||||||
| chr12:110568495 | G | C | 1 | a0001c0002t0001g0079 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.223+14314C>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110568495 | |||||||
| chr12:110568570 | C | T | 2 | a0001c0001t0008g0256 a0001c0001t0008g0257 |
2 | HG01099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.223+14239G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110568570 | |||||||
| chr12:110568826 | C | T | 4 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0015 others(1): Show |
4 | HG02717.hp2 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+13983G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110568826 | |||||||
| chr12:110568892 | G | A | 1 | a0001c0001t0002g0196 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.223+13917C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110568892 | |||||||
| chr12:110569031 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0110 |
2 | HG02258.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.223+13778G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110569031 | |||||||
| chr12:110569032 | G | GC | 72 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0029 others(69): Show |
73 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.223+13776dupG | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110569032 | |||||||
| chr12:110569032 | GC | G | 100 | a0001c0001t0002g0008 a0001c0001t0002g0047 a0001c0001t0002g0070 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.223+13776delG | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110569032 | |||||||
| chr12:110569036 | C | T | 1 | a0001c0002t0001g0141 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.223+13773G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110569036 | |||||||
| chr12:110569061 | A | G | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.223+13748T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110569061 | |||||||
| chr12:110569114 | C | T | 1 | a0001c0002t0001g0137 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.223+13695G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110569114 | |||||||
| chr12:110569281 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0098 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.223+13528C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110569281 | |||||||
| chr12:110569443 | T | C | 1 | a0001c0002t0001g0081 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.223+13366A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110569443 | |||||||
| chr12:110569474 | G | A | 289 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0028 others(286): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.223+13335C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110569474 | |||||||
| chr12:110569965 | A | G | 2 | a0001c0002t0001g0140 a0001c0002t0001g0169 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.223+12844T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110569965 | |||||||
| chr12:110570098 | G | A | 49 | a0001c0001t0001g0029 a0001c0001t0001g0127 a0001c0001t0001g0128 others(46): Show |
49 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.223+12711C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110570098 | |||||||
| chr12:110570101 | A | G | 1 | a0001c0001t0022g0277 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.223+12708T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110570101 | |||||||
| chr12:110570364 | T | C | 289 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0028 others(286): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.223+12445A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110570364 | |||||||
| chr12:110570447 | C | T | 1 | a0001c0002t0001g0081 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.223+12362G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110570447 | |||||||
| chr12:110570574 | A | G | 4 | a0001c0001t0001g0278 a0001c0001t0001g0280 a0001c0001t0001g0281 others(1): Show |
4 | HG01884.hp2 HG02572.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+12235T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110570574 | |||||||
| chr12:110570614 | G | A | 2 | a0001c0002t0001g0158 a0001c0002t0001g0159 |
2 | NA19074.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.223+12195C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110570614 | |||||||
| chr12:110570680 | T | A | 1 | a0001c0001t0001g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.223+12129A>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110570680 | |||||||
| chr12:110570712 | C | T | 1 | a0001c0002t0001g0139 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.223+12097G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110570712 | |||||||
| chr12:110570859 | C | A | 1 | a0001c0001t0001g0059 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.223+11950G>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110570859 | |||||||
| chr12:110570871 | T | C | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.223+11938A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110570871 | |||||||
| chr12:110570891 | C | A | 1 | a0001c0002t0001g0312 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.223+11918G>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110570891 | |||||||
| chr12:110570931 | A | C | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.223+11878T>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110570931 | |||||||
| chr12:110571111 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.223+11698G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110571111 | |||||||
| chr12:110571112 | G | A | 1 | a0001c0001t0004g0300 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.223+11697C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110571112 | |||||||
| chr12:110571129 | G | A | 2 | a0001c0001t0008g0256 a0001c0001t0008g0257 |
2 | HG01099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.223+11680C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110571129 | |||||||
| chr12:110571324 | T | C | 1 | a0001c0001t0022g0277 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.223+11485A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110571324 | |||||||
| chr12:110571329 | A | G | 1 | a0001c0002t0001g0252 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.223+11480T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110571329 | |||||||
| chr12:110571449 | G | C | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.223+11360C>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110571449 | |||||||
| chr12:110571498 | C | A | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.223+11311G>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110571498 | |||||||
| chr12:110571591 | T | C | 1 | a0001c0001t0002g0227 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.223+11218A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110571591 | |||||||
| chr12:110571762 | T | C | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.223+11047A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110571762 | |||||||
| chr12:110571935 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0098 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.223+10874G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110571935 | |||||||
| chr12:110572237 | A | G | 1 | a0001c0001t0002g0070 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.223+10572T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110572237 | |||||||
| chr12:110572554 | G | A | 2 | a0001c0001t0001g0278 a0001c0001t0019g0279 |
2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.223+10255C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110572554 | |||||||
| chr12:110572836 | T | G | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.223+9973A>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110572836 | |||||||
| chr12:110572837 | T | G | 2 | a0001c0002t0001g0004 a0001c0002t0001g0046 |
3 | HG00099.hp1 HG00140.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.223+9972A>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110572837 | |||||||
| chr12:110572864 | T | A | 1 | a0001c0002t0023g0134 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.223+9945A>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110572864 | |||||||
| chr12:110572869 | TTTTATTT others(1): Show |
T | 16 | a0001c0001t0003g0287 a0001c0001t0003g0288 a0001c0001t0003g0304 others(13): Show |
16 | HG00323.hp2 HG01175.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.223+9932_223+9939d others(10): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110572869 | |||||||
| chr12:110573155 | T | C | 1 | a0001c0001t0002g0196 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.223+9654A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110573155 | |||||||
| chr12:110573176 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.223+9633C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110573176 | |||||||
| chr12:110573415 | A | T | 1 | a0001c0001t0002g0201 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.223+9394T>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110573415 | |||||||
| chr12:110573454 | A | C | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.223+9355T>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110573454 | |||||||
| chr12:110573662 | T | C | 1 | a0001c0001t0001g0313 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.223+9147A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110573662 | |||||||
| chr12:110573664 | A | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.223+9145T>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110573664 | |||||||
| chr12:110573753 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.223+9056C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110573753 | |||||||
| chr12:110573831 | A | C | 6 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(3): Show |
6 | HG01071.hp2 HG01081.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.223+8978T>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110573831 | |||||||
| chr12:110573837 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.223+8972G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110573837 | |||||||
| chr12:110573906 | G | A | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.223+8903C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110573906 | |||||||
| chr12:110573922 | G | A | 1 | a0001c0002t0001g0168 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.223+8887C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110573922 | |||||||
| chr12:110574001 | A | G | 1 | a0001c0002t0001g0160 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.223+8808T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110574001 | |||||||
| chr12:110574085 | C | A | 1 | a0001c0001t0001g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.223+8724G>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110574085 | |||||||
| chr12:110574141 | T | TA | 23 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(20): Show |
23 | HG00323.hp2 HG00733.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.223+8667dupT | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110574141 | |||||||
| chr12:110574141 | T | TAA | 6 | a0001c0001t0001g0099 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.223+8666_223+8667d others(4): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110574141 | |||||||
| chr12:110574141 | TA | T | 128 | a0001c0001t0001g0006 a0001c0001t0001g0039 a0001c0001t0001g0069 others(125): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.223+8667delT | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110574141 | |||||||
| chr12:110574141 | TAA | T | 15 | a0001c0001t0001g0028 a0001c0001t0002g0189 a0001c0001t0002g0190 others(12): Show |
15 | HG00558.hp2 HG01167.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.223+8666_223+8667d others(4): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110574141 | |||||||
| chr12:110574141 | TAAAAAA | T | 6 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0067 others(3): Show |
6 | HG00423.hp2 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.223+8662_223+8667d others(8): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110574141 | |||||||
| chr12:110574141 | TAAAAAAA | T | 24 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(21): Show |
24 | HG00558.hp1 HG02071.hp2 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.223+8661_223+8667d others(9): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110574141 | |||||||
| chr12:110574141 | TAAAAAAA others(5): Show |
T | 4 | a0001c0001t0007g0286 a0001c0001t0008g0256 a0001c0001t0008g0257 others(1): Show |
4 | HG01099.hp1 HG02145.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+8656_223+8667d others(14): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110574141 | |||||||
| chr12:110574942 | C | CT | 46 | a0001c0001t0001g0125 a0001c0001t0002g0200 a0001c0001t0003g0043 others(43): Show |
46 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.223+7866dupA | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110574942 | |||||||
| chr12:110574942 | CT | C | 8 | a0001c0001t0001g0029 a0001c0001t0001g0062 a0001c0001t0001g0063 others(5): Show |
8 | HG01081.hp1 HG02572.hp1 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.223+7866delA | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110574942 | |||||||
| chr12:110574962 | A | T | 97 | a0001c0001t0001g0177 a0001c0001t0002g0088 a0001c0001t0002g0172 others(94): Show |
99 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.223+7847T>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110574962 | |||||||
| chr12:110575127 | C | G | 3 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 |
3 | HG02630.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.223+7682G>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110575127 | |||||||
| chr12:110575140 | T | C | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.223+7669A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110575140 | |||||||
| chr12:110575607 | C | CA | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0064 others(113): Show |
120 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.223+7201dupT | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110575607 | |||||||
| chr12:110575607 | C | CAA | 11 | a0001c0001t0001g0274 a0001c0001t0002g0027 a0001c0001t0002g0244 others(8): Show |
11 | HG00735.hp2 HG01261.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.223+7200_223+7201d others(4): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110575607 | |||||||
| chr12:110575607 | CA | C | 16 | a0001c0001t0001g0029 a0001c0001t0001g0127 a0001c0001t0001g0128 others(13): Show |
16 | HG01081.hp1 HG01943.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.223+7201delT | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110575607 | |||||||
| chr12:110575607 | CAA | C | 17 | a0001c0001t0003g0287 a0001c0001t0003g0288 a0001c0001t0003g0304 others(14): Show |
17 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.223+7200_223+7201d others(4): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110575607 | |||||||
| chr12:110575607 | CAAAAAAA others(8): Show |
C | 2 | a0001c0001t0008g0256 a0001c0001t0008g0257 |
2 | HG01099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.223+7187_223+7201d others(17): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110575607 | |||||||
| chr12:110575836 | G | A | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.223+6973C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110575836 | |||||||
| chr12:110575985 | C | G | 2 | a0001c0002t0001g0004 a0001c0002t0001g0046 |
3 | HG00099.hp1 HG00140.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.223+6824G>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110575985 | |||||||
| chr12:110576001 | T | C | 2 | a0001c0001t0003g0309 a0001c0001t0003g0310 |
2 | NA18952.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.223+6808A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110576001 | |||||||
| chr12:110576010 | C | G | 3 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 |
3 | HG02630.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.223+6799G>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110576010 | |||||||
| chr12:110576280 | T | C | 1 | a0001c0002t0001g0178 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.223+6529A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110576280 | |||||||
| chr12:110576677 | A | G | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.223+6132T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110576677 | |||||||
| chr12:110576838 | C | T | 2 | a0001c0001t0002g0195 a0001c0001t0002g0196 |
2 | HG03239.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.223+5971G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110576838 | |||||||
| chr12:110576996 | G | A | 8 | a0001c0001t0001g0029 a0001c0001t0001g0127 a0001c0001t0001g0128 others(5): Show |
8 | HG01081.hp1 HG01943.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.223+5813C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110576996 | |||||||
| chr12:110577072 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.223+5737G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110577072 | |||||||
| chr12:110577123 | C | T | 1 | a0001c0001t0002g0194 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.223+5686G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110577123 | |||||||
| chr12:110577166 | C | CA | 189 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0041 others(186): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.223+5642dupT | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110577166 | |||||||
| chr12:110577166 | C | CAA | 27 | a0001c0001t0002g0249 a0001c0001t0002g0250 a0001c0001t0003g0043 others(24): Show |
27 | HG00323.hp2 HG00621.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.223+5641_223+5642d others(4): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110577166 | |||||||
| chr12:110577195 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.223+5614G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110577195 | |||||||
| chr12:110577316 | A | G | 289 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0028 others(286): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.223+5493T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110577316 | |||||||
| chr12:110577318 | A | G | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.223+5491T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110577318 | |||||||
| chr12:110577335 | TGA | T | 12 | a0001c0002t0001g0115 a0001c0002t0001g0116 a0001c0002t0001g0118 others(9): Show |
12 | HG00597.hp1 HG01123.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.223+5472_223+5473d others(4): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110577335 | |||||||
| chr12:110577340 | G | C | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.223+5469C>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110577340 | |||||||
| chr12:110577430 | T | C | 1 | a0001c0002t0001g0094 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.223+5379A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110577430 | |||||||
| chr12:110577595 | C | T | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.223+5214G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110577595 | |||||||
| chr12:110577718 | T | TTAAC | 277 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0028 others(274): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.223+5090_223+5091i others(6): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110577718 | |||||||
| chr12:110577908 | A | AAC | 19 | a0001c0001t0002g0088 a0001c0002t0001g0077 a0001c0002t0001g0078 others(16): Show |
19 | HG00621.hp2 HG02074.hp1 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.223+4899_223+4900d others(4): Show |
PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110577908 | |||||||
| chr12:110578171 | A | G | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.223+4638T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110578171 | |||||||
| chr12:110578333 | G | C | 2 | a0001c0001t0003g0309 a0001c0001t0003g0310 |
2 | NA18952.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.223+4476C>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110578333 | |||||||
| chr12:110578358 | C | A | 2 | a0001c0002t0001g0187 a0001c0002t0001g0276 |
2 | HG00597.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.223+4451G>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110578358 | |||||||
| chr12:110578482 | C | T | 16 | a0001c0001t0003g0287 a0001c0001t0003g0288 a0001c0001t0003g0304 others(13): Show |
16 | HG00323.hp2 HG01175.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.223+4327G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110578482 | |||||||
| chr12:110578647 | T | C | 3 | a0001c0001t0003g0284 a0001c0001t0003g0285 a0001c0001t0028g0283 |
3 | HG01891.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.223+4162A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110578647 | |||||||
| chr12:110578752 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.223+4057A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110578752 | |||||||
| chr12:110578761 | C | A | 1 | a0002c0003t0001g0024 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.223+4048G>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110578761 | |||||||
| chr12:110578825 | T | G | 85 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0002g0007 others(82): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.223+3984A>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110578825 | |||||||
| chr12:110578893 | C | T | 8 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0076 others(5): Show |
9 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.223+3916G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110578893 | |||||||
| chr12:110578993 | C | T | 5 | a0001c0001t0008g0256 a0001c0001t0008g0257 a0001c0001t0008g0258 others(2): Show |
5 | HG01099.hp1 HG02055.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.223+3816G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110578993 | |||||||
| chr12:110579148 | C | CA | 9 | a0001c0001t0002g0254 a0001c0001t0003g0282 a0001c0001t0007g0303 others(6): Show |
9 | HG00738.hp1 HG01069.hp1 HG03516.hp2 others(6): Show |
intron_variant | MODIFIER | c.223+3660dupT | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110579148 | |||||||
| chr12:110579252 | G | C | 1 | a0001c0001t0001g0281 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.223+3557C>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110579252 | |||||||
| chr12:110579286 | C | T | 24 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(21): Show |
24 | HG00423.hp2 HG00558.hp1 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.223+3523G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110579286 | |||||||
| chr12:110579351 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.223+3458G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110579351 | |||||||
| chr12:110579400 | C | T | 2 | a0001c0001t0003g0304 a0001c0001t0003g0305 |
2 | HG00323.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.223+3409G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110579400 | |||||||
| chr12:110579442 | G | A | 1 | a0001c0001t0002g0255 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.223+3367C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110579442 | |||||||
| chr12:110579738 | C | A | 1 | a0001c0002t0001g0046 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.223+3071G>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110579738 | |||||||
| chr12:110579740 | C | G | 1 | a0001c0002t0001g0046 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.223+3069G>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110579740 | |||||||
| chr12:110579802 | T | C | 44 | a0001c0001t0001g0278 a0001c0001t0001g0280 a0001c0001t0001g0281 others(41): Show |
44 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.223+3007A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110579802 | |||||||
| chr12:110579883 | C | A | 1 | a0001c0002t0021g0260 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.223+2926G>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110579883 | |||||||
| chr12:110579885 | C | T | 3 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 |
3 | HG02630.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.223+2924G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110579885 | |||||||
| chr12:110579909 | T | C | 2 | a0001c0001t0016g0262 a0001c0001t0027g0261 |
2 | NA18945.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.223+2900A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110579909 | |||||||
| chr12:110579998 | A | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0037 others(5): Show |
9 | HG01168.hp2 HG01169.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.223+2811T>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110579998 | |||||||
| chr12:110580018 | C | T | 3 | a0001c0001t0003g0284 a0001c0001t0003g0285 a0001c0001t0028g0283 |
3 | HG01891.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.223+2791G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110580018 | |||||||
| chr12:110580362 | G | A | 7 | a0001c0001t0003g0304 a0001c0001t0003g0305 a0001c0001t0003g0306 others(4): Show |
7 | HG00323.hp2 HG01175.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.223+2447C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110580362 | |||||||
| chr12:110580407 | C | T | 1 | a0001c0001t0003g0282 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.223+2402G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110580407 | |||||||
| chr12:110580511 | G | C | 1 | a0001c0002t0001g0263 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.223+2298C>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110580511 | |||||||
| chr12:110580544 | T | C | 1 | a0001c0002t0001g0264 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.223+2265A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110580544 | |||||||
| chr12:110580640 | T | C | 1 | a0001c0002t0001g0265 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.223+2169A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110580640 | |||||||
| chr12:110580682 | G | A | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.223+2127C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110580682 | |||||||
| chr12:110580913 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.223+1896C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110580913 | |||||||
| chr12:110580923 | T | A | 1 | a0001c0001t0001g0035 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.223+1886A>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110580923 | |||||||
| chr12:110581095 | T | A | 1 | a0001c0001t0003g0311 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.223+1714A>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110581095 | |||||||
| chr12:110581113 | C | A | 6 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(3): Show |
6 | HG01071.hp2 HG01081.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.223+1696G>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110581113 | |||||||
| chr12:110581353 | G | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+1456C>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110581353 | |||||||
| chr12:110581371 | G | A | 1 | a0001c0001t0002g0275 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.223+1438C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110581371 | |||||||
| chr12:110581554 | C | T | 1 | a0001c0002t0001g0030 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.223+1255G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110581554 | |||||||
| chr12:110581817 | T | C | 1 | a0001c0002t0001g0276 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.223+992A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110581817 | |||||||
| chr12:110581851 | T | C | 5 | a0001c0001t0001g0278 a0001c0001t0001g0280 a0001c0001t0001g0281 others(2): Show |
5 | HG01884.hp2 HG02257.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+958A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110581851 | |||||||
| chr12:110581917 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.223+892T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110581917 | |||||||
| chr12:110582048 | C | T | 1 | a0001c0001t0001g0313 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.223+761G>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110582048 | |||||||
| chr12:110582097 | A | G | 1 | a0001c0001t0001g0028 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.223+712T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110582097 | |||||||
| chr12:110582374 | T | C | 30 | a0001c0001t0003g0282 a0001c0001t0003g0284 a0001c0001t0003g0285 others(27): Show |
30 | HG00323.hp2 HG01167.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.223+435A>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110582374 | |||||||
| chr12:110582502 | G | C | 1 | a0001c0002t0001g0312 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.223+307C>G | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110582502 | |||||||
| chr12:110582510 | G | A | 1 | a0001c0001t0001g0313 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.223+299C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110582510 | |||||||
| chr12:110582520 | G | A | 3 | a0001c0001t0002g0314 a0001c0001t0002g0315 a0001c0001t0002g0316 |
3 | HG00558.hp2 HG00673.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.223+289C>T | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110582520 | |||||||
| chr12:110582545 | G | T | 1 | a0001c0001t0002g0027 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.223+264C>A | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110582545 | |||||||
| chr12:110582785 | A | G | 2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.223+24T>C | PPTC7 | ENSG00000196850.6 | transcript | ENST00000354300.5 | protein_coding | 1/5 | chr12 | 110582785 |