Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5635 |
| ensemblid | ENSG00000161542.17 |
| hgncid | 9466 |
| symbol | PRPSAP1 |
| name | phosphoribosyl pyrophosphate synthetase associated protein 1 |
| refseq_nuc | NM_002766.3 |
| refseq_prot | NP_002757.2 |
| ensembl_nuc | ENST00000446526.8 |
| ensembl_prot | ENSP00000414624.2 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 76309478 |
| end | 76353916 |
| strand | - |
| ver | v1.2 |
| region | chr17:76309478-76353916 |
| region5000 | chr17:76304478-76358916 |
| regionname0 | PRPSAP1_chr17_76309478_76353916 |
| regionname5000 | PRPSAP1_chr17_76304478_76358916 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 385 | 365 | 91 | 66 | 146 | 16 | 44 | 108 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | MPKKL others(380): Show |
chr17 | 76304478 | 76358916 |
| a0002 | 0/0 | 176 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | MPKKL others(171): Show |
chr17 | 76304478 | 76358916 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1155 | 249 | 68 | 49 | 78 | 13 | 39 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | ATGCC others(1150): Show |
chr17 | 76304478 | 76358916 | ||
| a0001c0002 | 0/0 | 1155 | 116 | 23 | 17 | 68 | 3 | 5 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | ATGCC others(1150): Show |
chr17 | 76304478 | 76358916 | ||
| a0002c0003 | 0/0 | 1144 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | ATGCC others(1139): Show |
chr17 | 76304478 | 76358916 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3435 | 103 | 10 | 27 | 38 | 10 | 16 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3430): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0002 | 0/0 | 3435 | 2 | 0 | 0 | 1 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3430): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0003 | 0/0 | 3436 | 37 | 7 | 4 | 17 | 0 | 9 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3431): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0004 | 0/0 | 3436 | 34 | 2 | 9 | 11 | 3 | 9 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3431): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0005 | 0/0 | 3435 | 19 | 17 | 1 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3430): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0008 | 0/0 | 3434 | 6 | 1 | 0 | 4 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3429): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0009 | 0/0 | 3434 | 5 | 5 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3429): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0010 | 0/0 | 3435 | 5 | 5 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3430): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0012 | 0/0 | 3434 | 4 | 4 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3429): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0014 | 0/0 | 3435 | 3 | 2 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3430): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0016 | 0/0 | 3434 | 3 | 3 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3429): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0017 | 0/0 | 3436 | 3 | 2 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3431): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0019 | 0/0 | 3435 | 2 | 2 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3430): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0020 | 0/0 | 3437 | 2 | 0 | 0 | 1 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3432): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0021 | 0/0 | 3436 | 2 | 2 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3431): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0022 | 0/0 | 3434 | 2 | 1 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3429): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0023 | 0/0 | 3436 | 2 | 1 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3431): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0024 | 0/0 | 3435 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3430): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0025 | 0/0 | 3435 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3430): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0027 | 0/0 | 3435 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3430): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0028 | 0/0 | 3436 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3431): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0029 | 0/0 | 3435 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3430): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0030 | 0/0 | 3436 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3431): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0031 | 0/0 | 3435 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3430): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0032 | 0/0 | 3434 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3429): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0033 | 0/0 | 3435 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3430): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0034 | 0/0 | 3435 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3430): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0035 | 0/0 | 3435 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3430): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0037 | 0/0 | 3436 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3431): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0038 | 0/0 | 3435 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3430): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0040 | 0/0 | 3434 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3429): Show |
chr17 | 76304478 | 76358916 |
| a0001c0001t0041 | 0/0 | 3435 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3430): Show |
chr17 | 76304478 | 76358916 |
| a0001c0002t0001 | 0/0 | 3435 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3430): Show |
chr17 | 76304478 | 76358916 |
| a0001c0002t0002 | 0/0 | 3435 | 68 | 4 | 12 | 45 | 3 | 4 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3430): Show |
chr17 | 76304478 | 76358916 |
| a0001c0002t0003 | 0/0 | 3436 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3431): Show |
chr17 | 76304478 | 76358916 |
| a0001c0002t0006 | 0/0 | 3264 | 16 | 5 | 1 | 10 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3259): Show |
chr17 | 76304478 | 76358916 |
| a0001c0002t0007 | 0/0 | 3265 | 13 | 10 | 3 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3260): Show |
chr17 | 76304478 | 76358916 |
| a0001c0002t0011 | 0/0 | 3264 | 4 | 0 | 0 | 4 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3259): Show |
chr17 | 76304478 | 76358916 |
| a0001c0002t0013 | 0/0 | 3265 | 4 | 0 | 0 | 4 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3260): Show |
chr17 | 76304478 | 76358916 |
| a0001c0002t0015 | 0/0 | 3437 | 3 | 3 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3432): Show |
chr17 | 76304478 | 76358916 |
| a0001c0002t0018 | 0/0 | 3434 | 3 | 0 | 0 | 3 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3429): Show |
chr17 | 76304478 | 76358916 |
| a0001c0002t0026 | 0/0 | 3434 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3429): Show |
chr17 | 76304478 | 76358916 |
| a0001c0002t0036 | 0/0 | 3435 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3430): Show |
chr17 | 76304478 | 76358916 |
| a0001c0002t0039 | 0/0 | 3435 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3430): Show |
chr17 | 76304478 | 76358916 |
| a0002c0003t0003 | 0/0 | 3425 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | GCCTC others(3420): Show |
chr17 | 76304478 | 76358916 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0142 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0004g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0005g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0005g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0008g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0008g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0008g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0008g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0008g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0008g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0009g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0009g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0009g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0009g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0009g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0010g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0010g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0010g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0010g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0010g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0012g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0012g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0012g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0012g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0014g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0014g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0014g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0016g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0016g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0016g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0017g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0017g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0017g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0019g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0019g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0020g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0020g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0021g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0021g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0022g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0022g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0023g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0023g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0024g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0025g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0027g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0028g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0029g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0030g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0031g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0032g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0033g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0034g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0035g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0037g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0038g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0040g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0001t0041g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0006g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0006g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0006g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0006g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0006g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0006g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0006g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0006g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0006g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0006g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0006g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0006g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0006g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0006g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0007g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0007g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0007g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0007g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0007g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0007g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0007g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0007g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0007g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0007g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0011g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0011g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0011g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0011g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0013g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0013g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0013g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0013g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0015g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0015g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0015g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0018g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0018g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0018g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0026g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0036g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0001c0002t0039g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| a0002c0003t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0321 | EUR | GBR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | GBR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0232 | EUR | GBR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0180 | EUR | GBR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0264 | EUR | FIN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | FIN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0050 | EUR | FIN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0250 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0277 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00438 | hp1 | a0001 | c0001 | t0008 | g0271 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0274 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0239 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0205 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0150 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0099 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0289 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0296 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0340 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00738 | hp2 | a0001 | c0002 | t0007 | g0333 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0064 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0095 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01069 | hp1 | a0001 | c0002 | t0007 | g0325 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01069 | hp2 | a0001 | c0001 | t0022 | g0279 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0090 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01071 | hp1 | a0001 | c0002 | t0007 | g0326 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0091 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0149 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0138 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01099 | hp1 | a0001 | c0002 | t0006 | g0056 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01106 | hp1 | a0001 | c0001 | t0014 | g0013 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0342 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0139 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01167 | hp1 | a0001 | c0001 | t0040 | g0355 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01167 | hp2 | a0001 | c0001 | t0034 | g0334 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01169 | hp2 | a0001 | c0001 | t0038 | g0354 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0343 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0301 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0184 | AMR | CLM | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0081 | AMR | CLM | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0067 | AMR | CLM | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01361 | hp2 | a0001 | c0001 | t0017 | g0318 | AMR | CLM | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0234 | AMR | CLM | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0284 | AMR | CLM | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | IBS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0216 | EUR | IBS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | IBS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | IBS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0267 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0311 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01891 | hp2 | a0001 | c0001 | t0016 | g0054 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01928 | hp1 | a0001 | c0002 | t0003 | g0198 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0209 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0135 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0194 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0093 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0137 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02055 | hp1 | a0001 | c0001 | t0023 | g0359 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0305 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0172 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02080 | hp1 | a0001 | c0002 | t0013 | g0353 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0249 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02129 | hp2 | a0001 | c0002 | t0006 | g0259 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0103 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0341 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02145 | hp2 | a0001 | c0001 | t0019 | g0009 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02148 | hp2 | a0001 | c0001 | t0030 | g0122 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CDX | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02165 | hp2 | a0001 | c0002 | t0018 | g0104 | EAS | CDX | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02257 | hp1 | a0001 | c0002 | t0006 | g0345 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02258 | hp1 | a0001 | c0002 | t0007 | g0003 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0238 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02280 | hp1 | a0001 | c0001 | t0017 | g0323 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0233 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0060 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02300 | hp2 | a0001 | c0001 | t0029 | g0083 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02451 | hp2 | a0001 | c0001 | t0008 | g0309 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02572 | hp1 | a0001 | c0002 | t0007 | g0330 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02572 | hp2 | a0001 | c0002 | t0007 | g0324 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0166 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02615 | hp2 | a0001 | c0001 | t0010 | g0331 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02622 | hp1 | a0002 | c0003 | t0003 | g0307 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02622 | hp2 | a0001 | c0001 | t0025 | g0012 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02630 | hp1 | a0001 | c0002 | t0007 | g0327 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0328 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0231 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0196 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02809 | hp1 | a0001 | c0001 | t0012 | g0031 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02809 | hp2 | a0001 | c0001 | t0032 | g0059 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02818 | hp1 | a0001 | c0002 | t0006 | g0313 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0034 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0314 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02886 | hp2 | a0001 | c0001 | t0010 | g0040 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02895 | hp1 | a0001 | c0002 | t0026 | g0317 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0057 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0058 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02896 | hp2 | a0001 | c0001 | t0010 | g0039 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02922 | hp1 | a0001 | c0001 | t0016 | g0048 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02922 | hp2 | a0001 | c0001 | t0010 | g0043 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0245 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0236 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02970 | hp1 | a0001 | c0001 | t0017 | g0329 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02970 | hp2 | a0001 | c0001 | t0009 | g0304 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02976 | hp1 | a0001 | c0002 | t0007 | g0027 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0266 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03017 | hp1 | a0001 | c0001 | t0020 | g0140 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03041 | hp1 | a0001 | c0001 | t0035 | g0316 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0051 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0167 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03098 | hp2 | a0001 | c0002 | t0006 | g0310 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03130 | hp2 | a0001 | c0001 | t0016 | g0191 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03139 | hp1 | a0001 | c0002 | t0007 | g0308 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0237 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03195 | hp1 | a0001 | c0002 | t0007 | g0292 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0038 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03209 | hp1 | a0001 | c0001 | t0014 | g0010 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03209 | hp2 | a0001 | c0002 | t0015 | g0055 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03225 | hp1 | a0001 | c0002 | t0015 | g0029 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0244 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0223 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0036 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0243 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03486 | hp1 | a0001 | c0002 | t0006 | g0241 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03486 | hp2 | a0001 | c0001 | t0014 | g0011 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0069 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0208 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0263 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0207 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0044 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0286 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0283 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0052 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0319 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03579 | hp2 | a0001 | c0001 | t0009 | g0303 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0146 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0082 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0147 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03704 | hp1 | a0001 | c0001 | t0008 | g0153 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0299 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0068 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0181 | SAS | BEB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03927 | hp2 | a0001 | c0001 | t0005 | g0320 | SAS | BEB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0197 | SAS | BEB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0295 | SAS | BEB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0291 | SAS | STU | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0070 | SAS | STU | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0294 | SAS | BEB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | STU | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0281 | SAS | STU | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0145 | SAS | STU | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0224 | SAS | STU | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0252 | SAS | STU | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0297 | SAS | STU | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18522 | hp1 | a0001 | c0001 | t0021 | g0041 | AFR | YRI | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18522 | hp2 | a0001 | c0002 | t0007 | g0003 | AFR | YRI | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0204 | EAS | CHB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0096 | EAS | CHB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0053 | AFR | YRI | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0246 | AFR | YRI | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18939 | hp2 | a0001 | c0002 | t0013 | g0350 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18941 | hp2 | a0001 | c0002 | t0011 | g0336 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0287 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0143 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18946 | hp2 | a0001 | c0002 | t0006 | g0335 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18949 | hp2 | a0001 | c0001 | t0008 | g0116 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18950 | hp2 | a0001 | c0002 | t0006 | g0007 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18954 | hp2 | a0001 | c0001 | t0008 | g0254 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18956 | hp1 | a0001 | c0001 | t0027 | g0148 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18960 | hp1 | a0001 | c0002 | t0006 | g0195 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18964 | hp2 | a0001 | c0002 | t0011 | g0337 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0302 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0115 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18966 | hp1 | a0001 | c0001 | t0031 | g0269 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0288 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18968 | hp1 | a0001 | c0002 | t0006 | g0348 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18977 | hp2 | a0001 | c0001 | t0023 | g0358 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0285 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18979 | hp2 | a0001 | c0001 | t0020 | g0211 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18980 | hp1 | a0001 | c0002 | t0006 | g0203 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18980 | hp2 | a0001 | c0002 | t0011 | g0344 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18982 | hp2 | a0001 | c0002 | t0018 | g0113 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18984 | hp1 | a0001 | c0002 | t0036 | g0092 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18984 | hp2 | a0001 | c0002 | t0013 | g0351 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0101 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18985 | hp2 | a0001 | c0001 | t0028 | g0183 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18986 | hp2 | a0001 | c0002 | t0006 | g0339 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18992 | hp1 | a0001 | c0002 | t0011 | g0338 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0265 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19003 | hp2 | a0001 | c0001 | t0037 | g0349 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19004 | hp1 | a0001 | c0002 | t0018 | g0098 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19004 | hp2 | a0001 | c0002 | t0006 | g0007 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19010 | hp1 | a0001 | c0001 | t0008 | g0298 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19043 | hp1 | a0001 | c0001 | t0009 | g0315 | AFR | LWK | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19043 | hp2 | a0001 | c0002 | t0015 | g0030 | AFR | LWK | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19054 | hp1 | a0001 | c0002 | t0013 | g0352 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0206 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0293 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19072 | hp1 | a0001 | c0002 | t0006 | g0346 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19081 | hp1 | a0001 | c0002 | t0039 | g0356 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0114 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19086 | hp2 | a0001 | c0001 | t0033 | g0199 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19087 | hp2 | a0001 | c0002 | t0006 | g0347 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19240 | hp1 | a0001 | c0001 | t0021 | g0033 | AFR | YRI | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA19240 | hp2 | a0001 | c0001 | t0022 | g0037 | AFR | YRI | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ASW | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA20129 | hp2 | a0001 | c0002 | t0007 | g0332 | AFR | ASW | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0108 | EUR | TSI | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0005 | EUR | TSI | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0105 | EUR | TSI | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA20905 | hp1 | a0001 | c0001 | t0041 | g0357 | SAS | GIH | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0109 | SAS | GIH | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0280 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02109 | hp2 | a0001 | c0001 | t0019 | g0008 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02486 | hp2 | a0001 | c0001 | t0012 | g0235 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02559 | hp1 | a0001 | c0002 | t0007 | g0155 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03471 | hp1 | a0001 | c0001 | t0010 | g0042 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG03471 | hp2 | a0001 | c0001 | t0024 | g0014 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG06807 | hp1 | a0001 | c0002 | t0006 | g0312 | AFR | USA | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | USA | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | USA | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0035 | AFR | USA | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA21309 | hp1 | a0001 | c0001 | t0012 | g0032 | AFR | LWK | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| NA21309 | hp2 | a0001 | c0001 | t0012 | g0072 | AFR | LWK | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0142 | REF | REF | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0079 | REF | REF | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:76344683 | TGTATAAT others(4): Show |
T | 1 | a0002 | 1 | HG02622.hp1 | frameshift_variant | HIGH | c.267_277delTTTCATTA others(3): Show |
p.Phe90fs | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/10 | 490/3435 | 267/1158 | 89/385 | chr17 | 76344683 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:76311656 | T | C | 1 | a0001c0002 | 116 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(113): Show |
synonymous_variant | LOW | c.1044A>G | p.Gln348Gln | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1257/3435 | 1044/1158 | 348/385 | chr17 | 76311656 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:76309588 | C | G | 1 | a0001c0002t0011 | 4 | NA18941.hp2 NA18964.hp2 NA18980.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1954G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1954 | chr17 | 76309588 | ||||||
| chr17:76309603 | A | G | 1 | a0001c0001t0031 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1939T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1939 | chr17 | 76309603 | ||||||
| chr17:76309624 | C | T | 1 | a0001c0001t0016 | 3 | HG01891.hp2 HG02922.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1918G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1918 | chr17 | 76309624 | ||||||
| chr17:76309666 | T | C | 4 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0016 others(1): Show |
13 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1876A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1876 | chr17 | 76309666 | ||||||
| chr17:76309990 | C | CT | 9 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0020 others(6): Show |
50 | HG00408.hp1 HG00408.hp2 HG01361.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1551dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1551 | chr17 | 76309990 | ||||||
| chr17:76309990 | C | CTTT | 5 | a0001c0002t0006 a0001c0002t0007 a0001c0002t0011 others(2): Show |
40 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1549_*1551dupAAA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1551 | chr17 | 76309990 | ||||||
| chr17:76310110 | C | T | 1 | a0001c0001t0009 | 5 | HG01891.hp1 HG02055.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1432G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1432 | chr17 | 76310110 | ||||||
| chr17:76310157 | CGGCTAAT others(166): Show |
C | 4 | a0001c0002t0006 a0001c0002t0007 a0001c0002t0011 others(1): Show |
37 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1212_*1384del | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1212 | chr17 | 76310157 | ||||||
| chr17:76310422 | G | A | 4 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0016 others(1): Show |
13 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1120C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1120 | chr17 | 76310422 | ||||||
| chr17:76310445 | C | A | 11 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0020 others(8): Show |
119 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*1097G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1097 | chr17 | 76310445 | ||||||
| chr17:76310471 | G | GT | 5 | a0001c0001t0004 a0001c0001t0020 a0001c0001t0030 others(2): Show |
39 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1070dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1070 | chr17 | 76310471 | ||||||
| chr17:76310471 | GT | G | 9 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0016 others(6): Show |
53 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1070delA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1070 | chr17 | 76310471 | ||||||
| chr17:76310507 | C | G | 1 | a0001c0001t0017 | 3 | HG01361.hp2 HG02280.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1035G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1035 | chr17 | 76310507 | ||||||
| chr17:76310540 | A | T | 1 | a0001c0001t0029 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1002T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1002 | chr17 | 76310540 | ||||||
| chr17:76310749 | T | C | 21 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(18): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*793A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 793 | chr17 | 76310749 | ||||||
| chr17:76310769 | C | CT | 3 | a0001c0001t0028 a0001c0002t0007 a0001c0002t0013 |
18 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*772dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 772 | chr17 | 76310769 | ||||||
| chr17:76310769 | CT | C | 8 | a0001c0001t0008 a0001c0001t0022 a0001c0001t0033 others(5): Show |
16 | HG00438.hp1 HG01069.hp2 HG01167.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*772delA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 772 | chr17 | 76310769 | ||||||
| chr17:76311021 | G | A | 1 | a0001c0001t0009 | 5 | HG01891.hp1 HG02055.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*521C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 521 | chr17 | 76311021 | ||||||
| chr17:76311030 | T | C | 1 | a0001c0002t0036 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*512A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 512 | chr17 | 76311030 | ||||||
| chr17:76311371 | C | G | 1 | a0001c0001t0027 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*171G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 171 | chr17 | 76311371 | ||||||
| chr17:76311391 | T | C | 4 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0016 others(1): Show |
13 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*151A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 151 | chr17 | 76311391 | ||||||
| chr17:76311425 | A | G | 11 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0012 others(8): Show |
59 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*117T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 117 | chr17 | 76311425 | ||||||
| chr17:76353753 | T | G | 5 | a0001c0001t0037 a0001c0001t0038 a0001c0001t0040 others(2): Show |
8 | HG01167.hp1 HG01169.hp2 HG02080.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-50A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/10 | 50 | chr17 | 76353753 | ||||||
| chr17:76353784 | G | A | 1 | a0001c0001t0041 | 1 | NA20905.hp1 | 5_prime_UTR_variant | MODIFIER | c.-81C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/10 | 81 | chr17 | 76353784 | ||||||
| chr17:76353829 | G | T | 3 | a0001c0001t0014 a0001c0001t0024 a0001c0001t0025 |
5 | HG01106.hp1 HG02622.hp2 HG03209.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-126C>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/10 | 126 | chr17 | 76353829 | ||||||
| chr17:76353837 | T | A | 1 | a0001c0001t0023 | 2 | HG02055.hp1 NA18977.hp2 |
5_prime_UTR_variant | MODIFIER | c.-134A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/10 | 134 | chr17 | 76353837 | ||||||
| chr17:76353867 | A | T | 1 | a0001c0001t0019 | 2 | HG02109.hp2 HG02145.hp2 |
5_prime_UTR_variant | MODIFIER | c.-164T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/10 | 164 | chr17 | 76353867 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:76311931 | T | C | 57 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 others(54): Show |
59 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.1000-231A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76311931 | |||||||
| chr17:76312044 | G | A | 60 | a0001c0001t0004g0068 a0001c0001t0004g0069 a0001c0001t0004g0081 others(57): Show |
60 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.1000-344C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312044 | |||||||
| chr17:76312054 | T | C | 3 | a0001c0001t0016g0048 a0001c0001t0016g0054 a0001c0001t0016g0191 |
3 | HG01891.hp2 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1000-354A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312054 | |||||||
| chr17:76312076 | A | G | 1 | a0001c0001t0010g0043 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1000-376T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312076 | |||||||
| chr17:76312123 | A | G | 3 | a0001c0001t0017g0318 a0001c0001t0017g0323 a0001c0001t0017g0329 |
3 | HG01361.hp2 HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1000-423T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312123 | |||||||
| chr17:76312127 | G | A | 38 | a0001c0002t0006g0007 a0001c0002t0006g0056 a0001c0002t0006g0195 others(35): Show |
40 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.1000-427C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312127 | |||||||
| chr17:76312195 | C | A | 1 | a0001c0001t0001g0156 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1000-495G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312195 | |||||||
| chr17:76312277 | A | C | 242 | a0001c0001t0001g0306 a0001c0001t0002g0212 a0001c0001t0003g0004 others(239): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1000-577T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312277 | |||||||
| chr17:76312291 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.999+579T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312291 | |||||||
| chr17:76312352 | G | A | 117 | a0001c0001t0002g0212 a0001c0001t0003g0004 a0001c0001t0003g0107 others(114): Show |
119 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.999+518C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312352 | |||||||
| chr17:76312353 | T | C | 56 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 others(53): Show |
58 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.999+517A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312353 | |||||||
| chr17:76312431 | C | G | 35 | a0001c0002t0006g0007 a0001c0002t0006g0056 a0001c0002t0006g0195 others(32): Show |
37 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.999+439G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312431 | |||||||
| chr17:76312437 | CA | C | 188 | a0001c0001t0002g0212 a0001c0001t0003g0004 a0001c0001t0003g0107 others(185): Show |
192 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.999+432delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312437 | |||||||
| chr17:76312473 | C | G | 2 | a0001c0001t0001g0119 a0001c0001t0001g0124 |
2 | HG01516.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.999+397G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312473 | |||||||
| chr17:76312558 | C | T | 3 | a0001c0001t0017g0318 a0001c0001t0017g0323 a0001c0001t0017g0329 |
3 | HG01361.hp2 HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.999+312G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312558 | |||||||
| chr17:76312653 | T | C | 42 | a0001c0001t0004g0068 a0001c0001t0004g0069 a0001c0001t0004g0081 others(39): Show |
42 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.999+217A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312653 | |||||||
| chr17:76312810 | T | G | 57 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 others(54): Show |
59 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.999+60A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312810 | |||||||
| chr17:76313183 | A | C | 1 | a0001c0001t0003g0328 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.853-167T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 8/9 | chr17 | 76313183 | |||||||
| chr17:76313203 | T | A | 44 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 others(41): Show |
46 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.853-187A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 8/9 | chr17 | 76313203 | |||||||
| chr17:76313344 | T | C | 243 | a0001c0001t0001g0306 a0001c0001t0002g0212 a0001c0001t0003g0004 others(240): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.853-328A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 8/9 | chr17 | 76313344 | |||||||
| chr17:76313393 | A | G | 243 | a0001c0001t0001g0306 a0001c0001t0002g0212 a0001c0001t0003g0004 others(240): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.853-377T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 8/9 | chr17 | 76313393 | |||||||
| chr17:76313461 | A | G | 1 | a0001c0001t0001g0021 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.852+360T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 8/9 | chr17 | 76313461 | |||||||
| chr17:76313471 | C | T | 5 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 others(2): Show |
5 | HG01891.hp1 HG02055.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.852+350G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 8/9 | chr17 | 76313471 | |||||||
| chr17:76313480 | C | G | 57 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 others(54): Show |
59 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.852+341G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 8/9 | chr17 | 76313480 | |||||||
| chr17:76313491 | G | A | 4 | a0001c0002t0006g0310 a0001c0002t0006g0312 a0001c0002t0006g0313 others(1): Show |
4 | HG02818.hp1 HG02895.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.852+330C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 8/9 | chr17 | 76313491 | |||||||
| chr17:76313810 | T | C | 5 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 others(2): Show |
5 | HG01891.hp1 HG02055.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.852+11A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 8/9 | chr17 | 76313810 | |||||||
| chr17:76314003 | A | C | 52 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0042 others(49): Show |
54 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.782-112T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314003 | |||||||
| chr17:76314111 | T | C | 1 | a0001c0002t0002g0149 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.782-220A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314111 | |||||||
| chr17:76314201 | A | AATGT | 7 | a0001c0001t0003g0223 a0001c0001t0003g0314 a0001c0001t0009g0303 others(4): Show |
7 | HG01891.hp1 HG02055.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.782-314_782-311dup others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314201 | |||||||
| chr17:76314201 | A | AATGTATG others(5): Show |
1 | a0001c0002t0015g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.782-322_782-311dup others(12): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314201 | |||||||
| chr17:76314201 | A | AATGTATG others(9): Show |
35 | a0001c0002t0006g0007 a0001c0002t0006g0056 a0001c0002t0006g0195 others(32): Show |
37 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.782-326_782-311dup others(16): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314201 | |||||||
| chr17:76314201 | A | AATGTATG others(13): Show |
3 | a0001c0002t0006g0345 a0001c0002t0015g0029 a0001c0002t0015g0030 |
3 | HG02257.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.782-330_782-311dup others(20): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314201 | |||||||
| chr17:76314211 | T | C | 11 | a0001c0002t0002g0026 a0001c0002t0002g0090 a0001c0002t0002g0091 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.782-320A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314211 | |||||||
| chr17:76314228 | G | GTATGTAT others(10): Show |
10 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0042 others(7): Show |
10 | HG01891.hp2 HG02615.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.782-338_782-337ins others(17): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314228 | |||||||
| chr17:76314228 | G | GTATGTAT others(14): Show |
2 | a0001c0001t0012g0032 a0001c0001t0012g0072 |
2 | NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.782-338_782-337ins others(21): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314228 | |||||||
| chr17:76314228 | G | GTATGTAT others(18): Show |
1 | a0001c0001t0012g0235 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.782-338_782-337ins others(25): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314228 | |||||||
| chr17:76314281 | G | A | 35 | a0001c0001t0004g0068 a0001c0001t0004g0069 a0001c0001t0004g0081 others(32): Show |
35 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.782-390C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314281 | |||||||
| chr17:76314341 | C | T | 13 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0042 others(10): Show |
13 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.782-450G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314341 | |||||||
| chr17:76314399 | T | C | 36 | a0001c0002t0006g0007 a0001c0002t0006g0056 a0001c0002t0006g0195 others(33): Show |
38 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.782-508A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314399 | |||||||
| chr17:76314480 | G | A | 5 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 others(2): Show |
5 | HG01891.hp1 HG02055.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.782-589C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314480 | |||||||
| chr17:76314514 | A | G | 125 | a0001c0001t0004g0068 a0001c0001t0004g0069 a0001c0001t0004g0081 others(122): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.782-623T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314514 | |||||||
| chr17:76314552 | T | C | 1 | a0001c0001t0004g0297 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.782-661A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314552 | |||||||
| chr17:76314577 | T | C | 39 | a0001c0002t0006g0007 a0001c0002t0006g0056 a0001c0002t0006g0195 others(36): Show |
41 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.782-686A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314577 | |||||||
| chr17:76314620 | TCAGCCTC others(5): Show |
T | 1 | a0001c0002t0002g0265 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.782-741_782-730del others(12): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314620 | |||||||
| chr17:76314673 | C | T | 7 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0036 others(4): Show |
7 | HG02818.hp2 HG02965.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.782-782G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314673 | |||||||
| chr17:76314824 | A | T | 1 | a0001c0001t0001g0217 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.782-933T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314824 | |||||||
| chr17:76314826 | A | G | 36 | a0001c0002t0006g0007 a0001c0002t0006g0056 a0001c0002t0006g0195 others(33): Show |
38 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.782-935T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314826 | |||||||
| chr17:76314838 | C | T | 70 | a0001c0002t0001g0070 a0001c0002t0002g0005 a0001c0002t0002g0015 others(67): Show |
71 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.782-947G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314838 | |||||||
| chr17:76314892 | T | C | 57 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 others(54): Show |
59 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.782-1001A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314892 | |||||||
| chr17:76314895 | C | A | 18 | a0001c0002t0006g0007 a0001c0002t0006g0195 a0001c0002t0006g0203 others(15): Show |
19 | HG02080.hp1 HG02129.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.782-1004G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314895 | |||||||
| chr17:76314903 | T | C | 18 | a0001c0002t0006g0007 a0001c0002t0006g0195 a0001c0002t0006g0203 others(15): Show |
19 | HG02080.hp1 HG02129.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.782-1012A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314903 | |||||||
| chr17:76314922 | T | C | 1 | a0001c0001t0003g0187 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.782-1031A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314922 | |||||||
| chr17:76314998 | T | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0132 |
2 | HG01975.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.782-1107A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314998 | |||||||
| chr17:76315170 | T | C | 52 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0042 others(49): Show |
54 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.782-1279A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315170 | |||||||
| chr17:76315262 | C | T | 243 | a0001c0001t0001g0306 a0001c0001t0002g0212 a0001c0001t0003g0004 others(240): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.782-1371G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315262 | |||||||
| chr17:76315483 | C | G | 56 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 others(53): Show |
58 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.782-1592G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315483 | |||||||
| chr17:76315511 | A | G | 15 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0036 others(12): Show |
15 | HG01361.hp2 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.782-1620T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315511 | |||||||
| chr17:76315580 | C | T | 57 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 others(54): Show |
59 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.782-1689G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315580 | |||||||
| chr17:76315700 | C | CT | 17 | a0001c0001t0001g0050 a0001c0001t0001g0071 a0001c0001t0001g0073 others(14): Show |
17 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.782-1810dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315700 | |||||||
| chr17:76315700 | C | CTTT | 10 | a0001c0001t0005g0045 a0001c0001t0005g0052 a0001c0001t0005g0053 others(7): Show |
10 | HG01106.hp1 HG02559.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.782-1812_782-1810d others(5): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315700 | |||||||
| chr17:76315700 | C | CTTTT | 16 | a0001c0001t0005g0167 a0001c0002t0006g0056 a0001c0002t0006g0203 others(13): Show |
16 | HG01099.hp1 HG02080.hp1 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.782-1813_782-1810d others(6): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315700 | |||||||
| chr17:76315700 | C | CTTTTT | 7 | a0001c0001t0005g0320 a0001c0002t0006g0007 a0001c0002t0006g0195 others(4): Show |
9 | HG02258.hp1 HG02976.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.782-1814_782-1810d others(7): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315700 | |||||||
| chr17:76315700 | C | CTTTTTTT others(4): Show |
1 | a0001c0002t0007g0308 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.782-1820_782-1810d others(13): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315700 | |||||||
| chr17:76315700 | CT | C | 104 | a0001c0001t0001g0087 a0001c0001t0001g0216 a0001c0001t0001g0227 others(101): Show |
106 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.782-1810delA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315700 | |||||||
| chr17:76315700 | CTTTTTTT others(2): Show |
C | 41 | a0001c0001t0003g0299 a0001c0001t0004g0068 a0001c0001t0004g0069 others(38): Show |
41 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(38): Show |
intron_variant | MODIFIER | c.782-1818_782-1810d others(11): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315700 | |||||||
| chr17:76315700 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0034g0334 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.782-1819_782-1810d others(12): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315700 | |||||||
| chr17:76315700 | CTTTTTTT others(5): Show |
C | 5 | a0001c0002t0002g0018 a0001c0002t0002g0019 a0001c0002t0002g0020 others(2): Show |
5 | NA18945.hp1 NA18947.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.782-1821_782-1810d others(14): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315700 | |||||||
| chr17:76315700 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.782-1822_782-1810d others(15): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315700 | |||||||
| chr17:76315729 | T | C | 12 | a0001c0001t0010g0039 a0001c0001t0010g0042 a0001c0001t0010g0043 others(9): Show |
12 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.782-1838A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315729 | |||||||
| chr17:76315841 | A | T | 5 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 others(2): Show |
5 | HG01891.hp1 HG02055.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.782-1950T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315841 | |||||||
| chr17:76315861 | C | T | 53 | a0001c0001t0004g0068 a0001c0001t0004g0069 a0001c0001t0004g0081 others(50): Show |
53 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.782-1970G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315861 | |||||||
| chr17:76315862 | G | A | 5 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 others(2): Show |
5 | HG01891.hp1 HG02055.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.782-1971C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315862 | |||||||
| chr17:76315922 | G | T | 1 | a0001c0002t0011g0336 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.782-2031C>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315922 | |||||||
| chr17:76315953 | G | A | 7 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0036 others(4): Show |
7 | HG02818.hp2 HG02965.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.782-2062C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315953 | |||||||
| chr17:76316021 | T | C | 52 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0042 others(49): Show |
54 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.782-2130A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316021 | |||||||
| chr17:76316031 | A | T | 52 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0042 others(49): Show |
54 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.782-2140T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316031 | |||||||
| chr17:76316174 | T | TA | 6 | a0001c0001t0001g0133 a0001c0001t0004g0294 a0001c0001t0005g0052 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.782-2284dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316174 | |||||||
| chr17:76316174 | TA | T | 7 | a0001c0001t0001g0087 a0001c0001t0003g0187 a0001c0001t0003g0299 others(4): Show |
7 | HG02109.hp1 HG02895.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.782-2284delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316174 | |||||||
| chr17:76316190 | A | G | 1 | a0001c0001t0010g0039 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.782-2299T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316190 | |||||||
| chr17:76316191 | A | AAG | 31 | a0001c0002t0006g0007 a0001c0002t0006g0056 a0001c0002t0006g0203 others(28): Show |
33 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.782-2301_782-2300i others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316191 | |||||||
| chr17:76316191 | A | G | 17 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 others(14): Show |
17 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.782-2300T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316191 | |||||||
| chr17:76316192 | G | A | 49 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 others(46): Show |
51 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.782-2301C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316192 | |||||||
| chr17:76316192 | G | GA | 9 | a0001c0001t0001g0128 a0001c0001t0001g0221 a0001c0001t0001g0306 others(6): Show |
9 | HG01934.hp2 HG02145.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.782-2302dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316192 | |||||||
| chr17:76316266 | G | A | 4 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0036 others(1): Show |
4 | HG02818.hp2 HG03453.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.782-2375C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316266 | |||||||
| chr17:76316300 | C | T | 15 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0036 others(12): Show |
15 | HG01361.hp2 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.782-2409G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316300 | |||||||
| chr17:76316524 | C | A | 5 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 others(2): Show |
5 | HG01891.hp1 HG02055.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.782-2633G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316524 | |||||||
| chr17:76316673 | C | T | 35 | a0001c0002t0006g0007 a0001c0002t0006g0056 a0001c0002t0006g0195 others(32): Show |
37 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.782-2782G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316673 | |||||||
| chr17:76316778 | C | T | 56 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 others(53): Show |
58 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.782-2887G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316778 | |||||||
| chr17:76316800 | T | C | 2 | a0001c0001t0021g0033 a0001c0001t0021g0041 |
2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.782-2909A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316800 | |||||||
| chr17:76316958 | CTAAAG | C | 38 | a0001c0001t0002g0212 a0001c0001t0003g0004 a0001c0001t0003g0107 others(35): Show |
39 | HG00408.hp1 HG00408.hp2 HG01952.hp1 others(36): Show |
intron_variant | MODIFIER | c.782-3072_782-3068d others(7): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316958 | |||||||
| chr17:76317005 | C | T | 53 | a0001c0001t0004g0068 a0001c0001t0004g0069 a0001c0001t0004g0081 others(50): Show |
53 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.782-3114G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317005 | |||||||
| chr17:76317022 | A | G | 1 | a0001c0001t0001g0258 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.782-3131T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317022 | |||||||
| chr17:76317166 | AT | A | 51 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0042 others(48): Show |
53 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.782-3276delA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317166 | |||||||
| chr17:76317219 | A | G | 56 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 others(53): Show |
58 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.782-3328T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317219 | |||||||
| chr17:76317220 | C | G | 13 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0042 others(10): Show |
13 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.782-3329G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317220 | |||||||
| chr17:76317233 | T | C | 56 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 others(53): Show |
58 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.782-3342A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317233 | |||||||
| chr17:76317267 | T | G | 5 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 others(2): Show |
5 | HG01891.hp1 HG02055.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.782-3376A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317267 | |||||||
| chr17:76317285 | G | C | 4 | a0001c0002t0002g0096 a0001c0002t0002g0102 a0001c0002t0002g0150 others(1): Show |
4 | HG00609.hp1 HG00621.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.782-3394C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317285 | |||||||
| chr17:76317316 | C | T | 73 | a0001c0002t0002g0005 a0001c0002t0002g0015 a0001c0002t0002g0017 others(70): Show |
74 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.782-3425G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317316 | |||||||
| chr17:76317364 | A | G | 8 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.782-3473T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317364 | |||||||
| chr17:76317448 | C | G | 3 | a0001c0002t0015g0029 a0001c0002t0015g0030 a0001c0002t0015g0055 |
3 | HG03209.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.782-3557G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317448 | |||||||
| chr17:76317449 | G | A | 12 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0042 others(9): Show |
12 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.782-3558C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317449 | |||||||
| chr17:76317461 | A | C | 242 | a0001c0001t0001g0151 a0001c0001t0001g0306 a0001c0001t0002g0212 others(239): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.782-3570T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317461 | |||||||
| chr17:76317470 | G | A | 12 | a0001c0001t0001g0050 a0001c0001t0001g0071 a0001c0001t0001g0126 others(9): Show |
12 | HG00099.hp1 HG00323.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.782-3579C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317470 | |||||||
| chr17:76317510 | G | C | 51 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0042 others(48): Show |
53 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.782-3619C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317510 | |||||||
| chr17:76317620 | A | C | 2 | a0001c0001t0019g0008 a0001c0001t0019g0009 |
2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.782-3729T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317620 | |||||||
| chr17:76317663 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.782-3772A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317663 | |||||||
| chr17:76317704 | G | A | 3 | a0001c0001t0017g0318 a0001c0001t0017g0323 a0001c0001t0017g0329 |
3 | HG01361.hp2 HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.782-3813C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317704 | |||||||
| chr17:76317728 | C | T | 1 | a0001c0001t0008g0153 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.782-3837G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317728 | |||||||
| chr17:76317729 | G | A | 1 | a0001c0002t0006g0345 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.782-3838C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317729 | |||||||
| chr17:76317816 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.782-3925G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317816 | |||||||
| chr17:76317883 | T | A | 1 | a0001c0001t0004g0276 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.782-3992A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317883 | |||||||
| chr17:76317968 | TA | T | 51 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0042 others(48): Show |
53 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.782-4078delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317968 | |||||||
| chr17:76318014 | G | A | 13 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0042 others(10): Show |
13 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.782-4123C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76318014 | |||||||
| chr17:76318099 | A | G | 35 | a0001c0002t0006g0007 a0001c0002t0006g0056 a0001c0002t0006g0195 others(32): Show |
37 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.782-4208T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76318099 | |||||||
| chr17:76318146 | T | C | 5 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 others(2): Show |
5 | HG01891.hp1 HG02055.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.782-4255A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76318146 | |||||||
| chr17:76318220 | T | C | 66 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0003g0141 others(63): Show |
68 | HG00408.hp2 HG00738.hp2 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.782-4329A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76318220 | |||||||
| chr17:76318397 | C | T | 2 | a0001c0001t0003g0207 a0001c0001t0003g0208 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.782-4506G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76318397 | |||||||
| chr17:76318431 | C | T | 50 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0042 others(47): Show |
52 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.782-4540G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76318431 | |||||||
| chr17:76318504 | A | G | 2 | a0001c0002t0015g0029 a0001c0002t0015g0030 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.782-4613T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76318504 | |||||||
| chr17:76318692 | T | C | 56 | a0001c0001t0001g0273 a0001c0001t0003g0263 a0001c0001t0004g0068 others(53): Show |
56 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.782-4801A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76318692 | |||||||
| chr17:76318694 | A | C | 1 | a0001c0001t0001g0273 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.782-4803T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76318694 | |||||||
| chr17:76318748 | T | C | 64 | a0001c0001t0001g0156 a0001c0001t0003g0141 a0001c0001t0003g0154 others(61): Show |
66 | HG00408.hp2 HG00738.hp2 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.782-4857A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76318748 | |||||||
| chr17:76318804 | C | G | 1 | a0001c0002t0002g0265 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.782-4913G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76318804 | |||||||
| chr17:76318805 | G | C | 1 | a0001c0002t0002g0265 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.782-4914C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76318805 | |||||||
| chr17:76319001 | G | A | 2 | a0001c0001t0004g0137 a0001c0002t0002g0064 |
2 | HG00741.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.782-5110C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319001 | |||||||
| chr17:76319038 | C | T | 39 | a0001c0002t0006g0007 a0001c0002t0006g0056 a0001c0002t0006g0195 others(36): Show |
41 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.782-5147G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319038 | |||||||
| chr17:76319088 | T | C | 2 | a0001c0002t0002g0143 a0001c0002t0002g0144 |
2 | NA18944.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.782-5197A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319088 | |||||||
| chr17:76319089 | G | A | 1 | a0001c0001t0005g0320 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.782-5198C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319089 | |||||||
| chr17:76319096 | G | C | 126 | a0001c0001t0003g0286 a0001c0001t0005g0320 a0001c0001t0009g0303 others(123): Show |
129 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(126): Show |
intron_variant | MODIFIER | c.782-5205C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319096 | |||||||
| chr17:76319308 | G | C | 1 | a0001c0001t0030g0122 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.782-5417C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319308 | |||||||
| chr17:76319326 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.782-5435G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319326 | |||||||
| chr17:76319333 | T | C | 12 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0036 others(9): Show |
12 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.782-5442A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319333 | |||||||
| chr17:76319476 | A | AT | 11 | a0001c0001t0001g0178 a0001c0001t0003g0286 a0001c0001t0005g0051 others(8): Show |
11 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.782-5586dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319476 | |||||||
| chr17:76319491 | C | T | 1 | a0001c0001t0005g0238 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.782-5600G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319491 | |||||||
| chr17:76319520 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.782-5629T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319520 | |||||||
| chr17:76319542 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0131 |
2 | HG03239.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.782-5651G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319542 | |||||||
| chr17:76319555 | G | A | 1 | a0001c0002t0002g0146 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.782-5664C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319555 | |||||||
| chr17:76319564 | G | T | 1 | a0001c0002t0002g0265 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.782-5673C>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319564 | |||||||
| chr17:76319600 | T | C | 56 | a0001c0001t0001g0062 a0001c0001t0001g0065 a0001c0001t0001g0077 others(53): Show |
56 | HG00423.hp2 HG00597.hp2 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.782-5709A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319600 | |||||||
| chr17:76319606 | T | C | 19 | a0001c0001t0003g0286 a0001c0001t0005g0051 a0001c0001t0005g0236 others(16): Show |
19 | HG01361.hp2 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.782-5715A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319606 | |||||||
| chr17:76319617 | C | G | 1 | a0001c0002t0002g0265 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.782-5726G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319617 | |||||||
| chr17:76319617 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.782-5726G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319617 | |||||||
| chr17:76319618 | G | A | 36 | a0001c0001t0001g0062 a0001c0001t0001g0065 a0001c0001t0001g0123 others(33): Show |
36 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.782-5727C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319618 | |||||||
| chr17:76319618 | G | C | 1 | a0001c0002t0002g0265 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.782-5727C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319618 | |||||||
| chr17:76319618 | G | GCCACCAT others(522): Show |
1 | a0001c0002t0002g0025 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.782-5728_782-5727i others(531): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319618 | |||||||
| chr17:76319625 | T | C | 2 | a0001c0001t0004g0135 a0001c0001t0005g0036 |
2 | HG01952.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.782-5734A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319625 | |||||||
| chr17:76319628 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.782-5737A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319628 | |||||||
| chr17:76319630 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.782-5739C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319630 | |||||||
| chr17:76319657 | C | T | 1 | a0001c0002t0002g0005 | 2 | HG02148.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.782-5766G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319657 | |||||||
| chr17:76319668 | C | T | 4 | a0001c0001t0001g0088 a0001c0001t0001g0270 a0001c0002t0002g0110 others(1): Show |
4 | HG00597.hp1 HG02129.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.782-5777G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319668 | |||||||
| chr17:76319669 | G | A | 55 | a0001c0001t0001g0050 a0001c0001t0001g0071 a0001c0001t0001g0080 others(52): Show |
56 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.782-5778C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319669 | |||||||
| chr17:76319669 | GTGTTGGC others(959): Show |
G | 1 | a0001c0002t0011g0344 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.782-6744_782-5779d others(2): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319669 | |||||||
| chr17:76319820 | G | T | 4 | a0001c0001t0001g0306 a0001c0001t0004g0147 a0001c0001t0004g0232 others(1): Show |
4 | HG00140.hp1 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.782-5929C>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319820 | |||||||
| chr17:76319848 | A | G | 1 | a0001c0001t0033g0199 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.782-5957T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319848 | |||||||
| chr17:76319952 | C | G | 1 | a0001c0001t0004g0342 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.782-6061G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319952 | |||||||
| chr17:76319978 | A | C | 2 | a0001c0002t0002g0090 a0001c0002t0002g0091 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.782-6087T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319978 | |||||||
| chr17:76320009 | T | C | 1 | a0001c0001t0031g0269 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.782-6118A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320009 | |||||||
| chr17:76320045 | G | A | 1 | a0001c0002t0039g0356 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.782-6154C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320045 | |||||||
| chr17:76320127 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.782-6236C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320127 | |||||||
| chr17:76320132 | T | C | 1 | a0001c0001t0001g0306 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.782-6241A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320132 | |||||||
| chr17:76320178 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.782-6287C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320178 | |||||||
| chr17:76320256 | GAAAGAAA others(2): Show |
G | 6 | a0001c0001t0003g0286 a0001c0001t0010g0039 a0001c0001t0010g0040 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.782-6374_782-6366d others(11): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320256 | |||||||
| chr17:76320264 | G | A | 130 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(127): Show |
132 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.782-6373C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320264 | |||||||
| chr17:76320265 | A | G | 130 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(127): Show |
132 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.782-6374T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320265 | |||||||
| chr17:76320277 | G | GA | 130 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(127): Show |
132 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.782-6387dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320277 | |||||||
| chr17:76320281 | GA | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(93): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.782-6391delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320281 | |||||||
| chr17:76320285 | A | G | 130 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(127): Show |
132 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.782-6394T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320285 | |||||||
| chr17:76320286 | G | A | 131 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(128): Show |
133 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.782-6395C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320286 | |||||||
| chr17:76320287 | A | G | 1 | a0001c0002t0002g0265 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.782-6396T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320287 | |||||||
| chr17:76320290 | G | GA | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(139): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.782-6400dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320290 | |||||||
| chr17:76320290 | GAAAGAAA others(2): Show |
G | 7 | a0001c0001t0003g0286 a0001c0001t0005g0320 a0001c0001t0010g0039 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.782-6408_782-6400d others(11): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320290 | |||||||
| chr17:76320295 | A | G | 130 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(127): Show |
132 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.782-6404T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320295 | |||||||
| chr17:76320298 | GA | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(139): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.782-6408delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320298 | |||||||
| chr17:76320299 | A | G | 130 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(127): Show |
132 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.782-6408T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320299 | |||||||
| chr17:76320300 | A | G | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.782-6409T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320300 | |||||||
| chr17:76320302 | A | G | 131 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(128): Show |
133 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.782-6411T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320302 | |||||||
| chr17:76320304 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(146): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.782-6413T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320304 | |||||||
| chr17:76320305 | A | AGGG | 131 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(128): Show |
133 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.782-6415_782-6414i others(5): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320305 | |||||||
| chr17:76320305 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(146): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.782-6414T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320305 | |||||||
| chr17:76320317 | A | G | 131 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(128): Show |
133 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.782-6426T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320317 | |||||||
| chr17:76320321 | G | A | 4 | a0001c0001t0016g0048 a0001c0001t0016g0054 a0001c0001t0016g0191 others(1): Show |
4 | HG01891.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.782-6430C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320321 | |||||||
| chr17:76320341 | G | GAGGAAGG others(1): Show |
7 | a0001c0001t0001g0306 a0001c0001t0005g0034 a0001c0001t0005g0035 others(4): Show |
7 | HG02145.hp1 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.782-6458_782-6451d others(10): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320341 | |||||||
| chr17:76320345 | A | G | 128 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(125): Show |
130 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.782-6454T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320345 | |||||||
| chr17:76320349 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.782-6458T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320349 | |||||||
| chr17:76320352 | G | GAAGA | 6 | a0001c0001t0004g0147 a0001c0001t0004g0232 a0001c0001t0004g0233 others(3): Show |
6 | HG00140.hp1 HG01106.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.782-6465_782-6462d others(6): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320352 | |||||||
| chr17:76320352 | G | GAAGGAAG others(1): Show |
35 | a0001c0001t0003g0196 a0001c0001t0004g0341 a0001c0001t0005g0238 others(32): Show |
36 | HG01361.hp2 HG01891.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.782-6462_782-6461i others(10): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320352 | |||||||
| chr17:76320353 | A | AAGGAAGG others(9): Show |
129 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(126): Show |
131 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.782-6463_782-6462i others(18): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320353 | |||||||
| chr17:76320362 | G | T | 5 | a0001c0001t0001g0120 a0001c0001t0001g0173 a0001c0001t0001g0185 others(2): Show |
5 | HG01070.hp2 HG01074.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.782-6471C>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320362 | |||||||
| chr17:76320423 | C | CT | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(94): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.782-6533dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320423 | |||||||
| chr17:76320423 | C | CTT | 13 | a0001c0001t0001g0073 a0001c0001t0001g0084 a0001c0001t0001g0118 others(10): Show |
14 | HG00438.hp1 HG00558.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.782-6534_782-6533d others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320423 | |||||||
| chr17:76320423 | C | CTTT | 84 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0156 others(81): Show |
85 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.782-6535_782-6533d others(5): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320423 | |||||||
| chr17:76320423 | C | CTTTT | 39 | a0001c0001t0001g0136 a0001c0001t0001g0175 a0001c0001t0001g0273 others(36): Show |
39 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.782-6536_782-6533d others(6): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320423 | |||||||
| chr17:76320423 | CT | C | 15 | a0001c0001t0005g0320 a0001c0001t0014g0011 a0001c0001t0014g0013 others(12): Show |
15 | HG01106.hp1 HG03225.hp1 HG03471.hp2 others(12): Show |
intron_variant | MODIFIER | c.782-6533delA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320423 | |||||||
| chr17:76320488 | G | A | 5 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.782-6597C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320488 | |||||||
| chr17:76320539 | C | G | 2 | a0001c0001t0010g0042 a0001c0001t0010g0043 |
2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.782-6648G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320539 | |||||||
| chr17:76320546 | T | A | 2 | a0001c0002t0002g0038 a0001c0002t0002g0044 |
2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.782-6655A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320546 | |||||||
| chr17:76320591 | A | AT | 6 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(3): Show |
6 | HG00323.hp1 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.782-6701dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320591 | |||||||
| chr17:76320591 | A | ATT | 125 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(122): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.782-6702_782-6701d others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320591 | |||||||
| chr17:76320591 | A | ATTT | 9 | a0001c0001t0002g0212 a0001c0001t0003g0248 a0001c0001t0003g0299 others(6): Show |
9 | HG00597.hp2 HG00639.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.782-6703_782-6701d others(5): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320591 | |||||||
| chr17:76320786 | C | CT | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(91): Show |
97 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.782-6896dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320786 | |||||||
| chr17:76320788 | T | C | 2 | a0001c0001t0021g0033 a0001c0001t0021g0041 |
2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.782-6897A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320788 | |||||||
| chr17:76320845 | G | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(144): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.782-6954C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320845 | |||||||
| chr17:76320972 | A | G | 136 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(133): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.782-7081T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320972 | |||||||
| chr17:76321010 | T | C | 1 | a0001c0001t0028g0183 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.782-7119A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76321010 | |||||||
| chr17:76321011 | G | T | 1 | a0001c0001t0028g0183 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.782-7120C>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76321011 | |||||||
| chr17:76321178 | C | G | 1 | a0001c0001t0010g0043 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.782-7287G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76321178 | |||||||
| chr17:76321238 | C | A | 2 | a0001c0001t0019g0008 a0001c0001t0019g0009 |
2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.782-7347G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76321238 | |||||||
| chr17:76321322 | C | T | 2 | a0001c0001t0001g0306 a0001c0001t0005g0244 |
2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.781+7395G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76321322 | |||||||
| chr17:76321358 | C | T | 1 | a0001c0001t0005g0320 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.781+7359G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76321358 | |||||||
| chr17:76321387 | G | A | 2 | a0001c0001t0004g0069 a0001c0002t0001g0070 |
2 | HG03490.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.781+7330C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76321387 | |||||||
| chr17:76321487 | G | A | 2 | a0001c0001t0005g0236 a0001c0001t0005g0237 |
2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.781+7230C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76321487 | |||||||
| chr17:76321640 | T | C | 3 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 |
3 | HG02055.hp2 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.781+7077A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76321640 | |||||||
| chr17:76321884 | TAC | T | 131 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(128): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.781+6831_781+6832d others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76321884 | |||||||
| chr17:76321922 | A | C | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(278): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.781+6795T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76321922 | |||||||
| chr17:76322042 | T | C | 131 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(128): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.781+6675A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322042 | |||||||
| chr17:76322065 | G | A | 5 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+6652C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322065 | |||||||
| chr17:76322075 | C | G | 1 | a0001c0001t0001g0162 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781+6642G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322075 | |||||||
| chr17:76322118 | C | T | 12 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 others(9): Show |
12 | HG02055.hp2 HG02970.hp2 HG03579.hp2 others(9): Show |
intron_variant | MODIFIER | c.781+6599G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322118 | |||||||
| chr17:76322206 | G | A | 131 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(128): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.781+6511C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322206 | |||||||
| chr17:76322345 | G | A | 1 | a0001c0001t0031g0269 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.781+6372C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322345 | |||||||
| chr17:76322428 | G | A | 131 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(128): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.781+6289C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322428 | |||||||
| chr17:76322475 | C | T | 1 | a0001c0001t0005g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.781+6242G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322475 | |||||||
| chr17:76322551 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.781+6166T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322551 | |||||||
| chr17:76322695 | T | C | 5 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+6022A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322695 | |||||||
| chr17:76322743 | C | T | 8 | a0001c0001t0003g0107 a0001c0002t0002g0099 a0001c0002t0002g0100 others(5): Show |
8 | HG00408.hp1 HG00609.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.781+5974G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322743 | |||||||
| chr17:76322744 | G | A | 1 | a0001c0001t0005g0320 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.781+5973C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322744 | |||||||
| chr17:76322911 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.781+5806G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322911 | |||||||
| chr17:76322948 | C | T | 1 | a0001c0002t0015g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.781+5769G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322948 | |||||||
| chr17:76322959 | A | G | 131 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(128): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.781+5758T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322959 | |||||||
| chr17:76322976 | G | C | 4 | a0001c0001t0001g0159 a0001c0001t0008g0153 a0001c0001t0008g0309 others(1): Show |
4 | HG01433.hp1 HG02451.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.781+5741C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322976 | |||||||
| chr17:76323001 | C | T | 1 | a0001c0001t0003g0154 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.781+5716G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323001 | |||||||
| chr17:76323008 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.781+5709C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323008 | |||||||
| chr17:76323025 | C | A | 1 | a0001c0001t0033g0199 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.781+5692G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323025 | |||||||
| chr17:76323027 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.781+5690G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323027 | |||||||
| chr17:76323154 | C | T | 2 | a0001c0002t0002g0200 a0001c0002t0002g0206 |
2 | NA18975.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.781+5563G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323154 | |||||||
| chr17:76323171 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.781+5546C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323171 | |||||||
| chr17:76323179 | T | TAAAAATA others(3045): Show |
1 | a0001c0001t0004g0284 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3054): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3052): Show |
1 | a0001c0001t0003g0224 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3061): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3050): Show |
1 | a0001c0001t0001g0273 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3059): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3049): Show |
1 | a0001c0001t0004g0204 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3058): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3045): Show |
1 | a0001c0001t0003g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3054): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3038): Show |
1 | a0001c0001t0004g0287 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3047): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3038): Show |
1 | a0001c0001t0004g0261 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3047): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3051): Show |
1 | a0001c0001t0033g0199 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3060): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(2698): Show |
1 | a0001c0001t0003g0213 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(2707): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3046): Show |
1 | a0001c0001t0004g0089 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3055): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3045): Show |
1 | a0001c0001t0004g0294 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3054): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3050): Show |
1 | a0001c0001t0012g0031 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3059): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3044): Show |
1 | a0001c0001t0004g0139 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3053): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3045): Show |
1 | a0001c0001t0001g0175 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3054): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3044): Show |
2 | a0001c0001t0003g0267 a0001c0001t0004g0283 |
2 | HG01884.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3053): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3043): Show |
1 | a0001c0002t0006g0056 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3052): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3051): Show |
1 | a0001c0001t0016g0054 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3060): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3050): Show |
2 | a0001c0001t0016g0048 a0001c0002t0007g0292 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3059): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3050): Show |
1 | a0001c0001t0016g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3059): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3050): Show |
1 | a0001c0001t0003g0154 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3059): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3044): Show |
4 | a0001c0001t0005g0166 a0001c0001t0005g0243 a0001c0001t0005g0280 others(1): Show |
4 | HG00639.hp1 HG02109.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3053): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3051): Show |
1 | a0001c0001t0001g0159 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3060): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3049): Show |
1 | a0001c0001t0012g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3058): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3049): Show |
1 | a0001c0001t0003g0246 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3058): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3042): Show |
1 | a0001c0002t0002g0285 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3051): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3043): Show |
11 | a0001c0001t0001g0136 a0001c0001t0004g0081 a0001c0001t0004g0135 others(8): Show |
12 | HG00280.hp1 HG00423.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3052): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3044): Show |
1 | a0001c0001t0004g0276 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3053): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3048): Show |
1 | a0001c0001t0003g0328 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3057): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3049): Show |
3 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0003g0314 |
3 | HG01515.hp1 HG01516.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3058): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3050): Show |
5 | a0001c0001t0001g0047 a0001c0001t0001g0182 a0001c0001t0008g0153 others(2): Show |
5 | HG01169.hp1 HG02451.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3059): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3051): Show |
1 | a0001c0002t0002g0319 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3060): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3053): Show |
1 | a0001c0001t0003g0299 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3062): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3051): Show |
1 | a0001c0001t0001g0163 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3060): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3048): Show |
1 | a0001c0001t0003g0193 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3057): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3049): Show |
6 | a0001c0001t0003g0004 a0001c0001t0003g0190 a0001c0001t0003g0207 others(3): Show |
7 | HG01993.hp1 HG02055.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3058): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3050): Show |
4 | a0001c0001t0001g0063 a0001c0001t0003g0214 a0001c0001t0003g0291 others(1): Show |
4 | HG00408.hp2 HG00597.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3059): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3042): Show |
1 | a0001c0001t0005g0051 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3051): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3043): Show |
1 | a0001c0001t0004g0180 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3052): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3049): Show |
1 | a0001c0001t0019g0008 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3058): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3047): Show |
1 | a0001c0001t0003g0222 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3056): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3048): Show |
1 | a0001c0001t0003g0209 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3057): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3040): Show |
1 | a0001c0001t0005g0057 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3049): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3041): Show |
1 | a0001c0001t0034g0334 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3050): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3040): Show |
1 | a0001c0001t0004g0181 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3049): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3048): Show |
1 | a0001c0002t0006g0195 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3057): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3043): Show |
1 | a0001c0001t0022g0279 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3052): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3051): Show |
1 | a0001c0001t0020g0211 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3060): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3047): Show |
1 | a0002c0003t0003g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3056): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3048): Show |
1 | a0001c0001t0003g0245 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3057): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3049): Show |
1 | a0001c0001t0004g0201 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3058): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3042): Show |
4 | a0001c0001t0003g0266 a0001c0001t0004g0293 a0001c0001t0004g0340 others(1): Show |
4 | HG00735.hp2 HG01071.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3051): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3044): Show |
1 | a0001c0002t0007g0308 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3053): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3049): Show |
1 | a0001c0002t0007g0333 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3058): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3050): Show |
1 | a0001c0002t0007g0330 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3059): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3042): Show |
1 | a0001c0001t0003g0248 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3051): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3047): Show |
1 | a0001c0001t0003g0300 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3056): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3048): Show |
4 | a0001c0001t0003g0194 a0001c0001t0003g0208 a0001c0001t0012g0032 others(1): Show |
4 | HG01928.hp1 HG01975.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3057): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3049): Show |
1 | a0001c0001t0023g0358 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3058): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3041): Show |
3 | a0001c0001t0005g0045 a0001c0001t0005g0052 a0001c0001t0005g0053 |
3 | HG02559.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3050): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3047): Show |
1 | a0001c0001t0003g0192 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3056): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3063): Show |
1 | a0001c0001t0001g0179 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3072): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3043): Show |
1 | a0001c0002t0007g0332 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3052): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3047): Show |
1 | a0001c0001t0001g0156 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3056): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3049): Show |
2 | a0001c0002t0007g0027 a0001c0002t0007g0155 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3058): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3042): Show |
1 | a0001c0001t0003g0263 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3051): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3049): Show |
1 | a0001c0001t0001g0178 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3058): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3044): Show |
1 | a0001c0001t0004g0297 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3053): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3039): Show |
1 | a0001c0001t0004g0232 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3048): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3049): Show |
2 | a0001c0001t0004g0147 a0001c0001t0004g0233 |
2 | HG02280.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3058): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3050): Show |
1 | a0001c0001t0003g0187 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3059): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3053): Show |
1 | a0001c0001t0019g0009 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3062): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3046): Show |
1 | a0001c0001t0004g0295 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3055): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3052): Show |
1 | a0001c0001t0001g0164 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3061): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(2698): Show |
1 | a0001c0001t0002g0212 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(2707): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3046): Show |
1 | a0001c0001t0003g0275 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3055): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3052): Show |
1 | a0001c0001t0020g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3061): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3046): Show |
1 | a0001c0001t0004g0281 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3055): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3045): Show |
1 | a0001c0001t0004g0274 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3054): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3044): Show |
2 | a0001c0001t0004g0343 a0001c0002t0007g0325 |
2 | HG01069.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3053): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3051): Show |
1 | a0001c0002t0002g0044 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3060): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3050): Show |
1 | a0001c0001t0003g0189 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3059): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3051): Show |
2 | a0001c0001t0003g0141 a0001c0002t0006g0203 |
2 | NA18964.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3060): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3043): Show |
1 | a0001c0001t0005g0167 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3052): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3044): Show |
1 | a0001c0001t0004g0068 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3053): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3050): Show |
1 | a0001c0001t0003g0188 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3059): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3042): Show |
1 | a0001c0001t0005g0058 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3051): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3042): Show |
1 | a0001c0002t0002g0262 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3051): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3024): Show |
1 | a0001c0001t0032g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3033): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(2776): Show |
1 | a0001c0002t0006g0241 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(2785): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323179 | T | TAAAAATA others(3046): Show |
1 | a0001c0002t0002g0234 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3055): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | |||||||
| chr17:76323277 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.781+5440C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323277 | |||||||
| chr17:76323296 | T | C | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(278): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.781+5421A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323296 | |||||||
| chr17:76323341 | C | CA | 11 | a0001c0001t0003g0224 a0001c0001t0003g0328 a0001c0001t0004g0276 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.781+5375dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323341 | |||||||
| chr17:76323354 | G | A | 129 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(126): Show |
131 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.781+5363C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323354 | |||||||
| chr17:76323387 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.781+5330T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323387 | |||||||
| chr17:76323466 | C | T | 130 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(127): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.781+5251G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323466 | |||||||
| chr17:76323529 | T | C | 2 | a0001c0001t0021g0033 a0001c0001t0021g0041 |
2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.781+5188A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323529 | |||||||
| chr17:76323549 | G | A | 2 | a0001c0001t0001g0306 a0001c0001t0005g0244 |
2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.781+5168C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323549 | |||||||
| chr17:76323716 | G | GT | 21 | a0001c0001t0003g0196 a0001c0001t0004g0341 a0001c0001t0005g0238 others(18): Show |
22 | HG02080.hp1 HG02129.hp2 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.781+5000dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323716 | |||||||
| chr17:76323847 | T | C | 2 | a0001c0001t0023g0358 a0001c0001t0023g0359 |
2 | HG02055.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.781+4870A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323847 | |||||||
| chr17:76323859 | C | A | 1 | a0001c0001t0001g0321 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.781+4858G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323859 | |||||||
| chr17:76323861 | T | G | 1 | a0001c0001t0001g0306 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.781+4856A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323861 | |||||||
| chr17:76323921 | A | G | 135 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(132): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.781+4796T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323921 | |||||||
| chr17:76324140 | C | CA | 128 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0132 others(125): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.781+4576dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324140 | |||||||
| chr17:76324140 | C | CAA | 6 | a0001c0001t0003g0188 a0001c0001t0004g0135 a0001c0001t0004g0295 others(3): Show |
6 | HG01952.hp2 HG02896.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.781+4575_781+4576d others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324140 | |||||||
| chr17:76324217 | G | A | 1 | a0001c0001t0003g0314 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.781+4500C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324217 | |||||||
| chr17:76324235 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.781+4482G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324235 | |||||||
| chr17:76324236 | G | A | 11 | a0001c0001t0001g0177 a0001c0001t0001g0258 a0001c0002t0002g0026 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.781+4481C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324236 | |||||||
| chr17:76324286 | T | C | 1 | a0001c0001t0003g0314 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.781+4431A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324286 | |||||||
| chr17:76324325 | G | A | 2 | a0001c0002t0002g0103 a0001c0002t0018g0104 |
2 | HG02132.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.781+4392C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324325 | |||||||
| chr17:76324520 | A | G | 130 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(127): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.781+4197T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324520 | |||||||
| chr17:76324527 | G | A | 2 | a0001c0001t0005g0236 a0001c0001t0005g0237 |
2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.781+4190C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324527 | |||||||
| chr17:76324571 | A | G | 1 | a0001c0001t0031g0269 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.781+4146T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324571 | |||||||
| chr17:76324602 | CAA | C | 130 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(127): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.781+4113_781+4114d others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324602 | |||||||
| chr17:76324674 | C | T | 5 | a0001c0001t0014g0010 a0001c0001t0014g0011 a0001c0001t0014g0013 others(2): Show |
5 | HG01106.hp1 HG02622.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.781+4043G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324674 | |||||||
| chr17:76324741 | G | A | 3 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 |
3 | HG02055.hp2 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.781+3976C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324741 | |||||||
| chr17:76324777 | G | A | 8 | a0001c0002t0002g0005 a0001c0002t0002g0064 a0001c0002t0002g0067 others(5): Show |
9 | HG00741.hp1 HG01261.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.781+3940C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324777 | |||||||
| chr17:76324905 | C | CA | 6 | a0001c0001t0001g0073 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG01928.hp2 HG02886.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.781+3811dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324905 | |||||||
| chr17:76324954 | G | A | 6 | a0001c0001t0001g0156 a0001c0002t0007g0027 a0001c0002t0007g0155 others(3): Show |
6 | HG00738.hp2 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.781+3763C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324954 | |||||||
| chr17:76324992 | T | C | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(281): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.781+3725A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324992 | |||||||
| chr17:76324996 | G | A | 130 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(127): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.781+3721C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324996 | |||||||
| chr17:76325025 | C | A | 1 | a0001c0002t0002g0017 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.781+3692G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325025 | |||||||
| chr17:76325045 | G | A | 1 | a0001c0002t0015g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.781+3672C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325045 | |||||||
| chr17:76325069 | CA | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(150): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.781+3647delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325069 | |||||||
| chr17:76325136 | A | G | 140 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(137): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.781+3581T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325136 | |||||||
| chr17:76325289 | G | C | 1 | a0001c0001t0005g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.781+3428C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325289 | |||||||
| chr17:76325334 | G | A | 5 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+3383C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325334 | |||||||
| chr17:76325363 | C | T | 5 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+3354G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325363 | |||||||
| chr17:76325392 | G | A | 9 | a0001c0001t0005g0045 a0001c0001t0005g0051 a0001c0001t0005g0052 others(6): Show |
9 | HG01099.hp1 HG02559.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.781+3325C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325392 | |||||||
| chr17:76325411 | C | CA | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(124): Show |
129 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.781+3305dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325411 | |||||||
| chr17:76325411 | C | CAA | 47 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0066 others(44): Show |
48 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.781+3304_781+3305d others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325411 | |||||||
| chr17:76325411 | CA | C | 73 | a0001c0001t0001g0047 a0001c0001t0001g0136 a0001c0001t0001g0156 others(70): Show |
74 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.781+3305delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325411 | |||||||
| chr17:76325411 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0049 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.781+3291_781+3305d others(17): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325411 | |||||||
| chr17:76325535 | C | T | 1 | a0001c0001t0005g0320 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.781+3182G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325535 | |||||||
| chr17:76325598 | A | AT | 137 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0066 others(134): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.781+3118dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325598 | |||||||
| chr17:76325598 | A | ATT | 13 | a0001c0001t0001g0063 a0001c0001t0003g0154 a0001c0001t0003g0189 others(10): Show |
13 | HG00735.hp2 HG01106.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.781+3117_781+3118d others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325598 | |||||||
| chr17:76325598 | AT | A | 33 | a0001c0001t0003g0196 a0001c0001t0003g0286 a0001c0001t0004g0341 others(30): Show |
34 | HG01361.hp2 HG01891.hp1 HG02080.hp1 others(31): Show |
intron_variant | MODIFIER | c.781+3118delA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325598 | |||||||
| chr17:76325643 | G | A | 1 | a0001c0001t0003g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.781+3074C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325643 | |||||||
| chr17:76325733 | T | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0168 |
2 | HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.781+2984A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325733 | |||||||
| chr17:76325762 | G | A | 1 | a0001c0002t0006g0241 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.781+2955C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325762 | |||||||
| chr17:76325766 | G | A | 1 | a0001c0001t0005g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.781+2951C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325766 | |||||||
| chr17:76325860 | C | G | 130 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(127): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.781+2857G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325860 | |||||||
| chr17:76325914 | G | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(95): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.781+2803C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325914 | |||||||
| chr17:76325947 | G | T | 130 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(127): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.781+2770C>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325947 | |||||||
| chr17:76325992 | A | T | 5 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+2725T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325992 | |||||||
| chr17:76326045 | G | A | 130 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(127): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.781+2672C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76326045 | |||||||
| chr17:76326152 | T | C | 5 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+2565A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76326152 | |||||||
| chr17:76326201 | A | G | 5 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+2516T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76326201 | |||||||
| chr17:76326343 | A | C | 1 | a0001c0001t0001g0258 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.781+2374T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76326343 | |||||||
| chr17:76326399 | GA | G | 131 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(128): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.781+2317delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76326399 | |||||||
| chr17:76326640 | G | A | 130 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(127): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.781+2077C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76326640 | |||||||
| chr17:76326644 | C | T | 356 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(353): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.781+2073G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76326644 | |||||||
| chr17:76326784 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.781+1933A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76326784 | |||||||
| chr17:76326930 | G | GA | 9 | a0001c0001t0001g0130 a0001c0001t0001g0177 a0001c0001t0001g0242 others(6): Show |
9 | HG01081.hp1 HG02056.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.781+1786dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76326930 | |||||||
| chr17:76326942 | C | A | 17 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0061 others(14): Show |
17 | HG00323.hp1 HG01346.hp1 HG02129.hp1 others(14): Show |
intron_variant | MODIFIER | c.781+1775G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76326942 | |||||||
| chr17:76327063 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.781+1654A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327063 | |||||||
| chr17:76327116 | G | A | 130 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(127): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.781+1601C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327116 | |||||||
| chr17:76327164 | A | G | 7 | a0001c0001t0003g0286 a0001c0001t0005g0034 a0001c0001t0005g0035 others(4): Show |
7 | HG02818.hp2 HG02965.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.781+1553T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327164 | |||||||
| chr17:76327257 | A | T | 1 | a0001c0001t0001g0160 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.781+1460T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327257 | |||||||
| chr17:76327430 | G | A | 2 | a0001c0002t0015g0029 a0001c0002t0015g0030 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.781+1287C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327430 | |||||||
| chr17:76327449 | T | C | 135 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(132): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.781+1268A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327449 | |||||||
| chr17:76327522 | G | A | 20 | a0001c0001t0003g0196 a0001c0001t0004g0341 a0001c0001t0005g0238 others(17): Show |
21 | HG02080.hp1 HG02129.hp2 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.781+1195C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327522 | |||||||
| chr17:76327592 | G | A | 8 | a0001c0001t0009g0311 a0001c0001t0009g0315 a0001c0001t0017g0318 others(5): Show |
8 | HG01361.hp2 HG01891.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.781+1125C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327592 | |||||||
| chr17:76327642 | A | T | 1 | a0001c0002t0006g0345 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.781+1075T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327642 | |||||||
| chr17:76327652 | AAAAT | A | 4 | a0001c0001t0001g0186 a0001c0001t0001g0228 a0001c0001t0001g0290 others(1): Show |
4 | NA18969.hp1 NA18969.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.781+1061_781+1064d others(6): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327652 | |||||||
| chr17:76327769 | T | TA | 5 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+947dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327769 | |||||||
| chr17:76327806 | G | A | 4 | a0001c0001t0003g0004 a0001c0001t0003g0194 a0001c0001t0003g0209 others(1): Show |
5 | HG01928.hp1 HG01952.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+911C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327806 | |||||||
| chr17:76327917 | T | C | 3 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 |
3 | HG02055.hp2 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.781+800A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327917 | |||||||
| chr17:76328009 | C | G | 3 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 |
3 | HG02055.hp2 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.781+708G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76328009 | |||||||
| chr17:76328186 | C | CA | 12 | a0001c0001t0001g0186 a0001c0001t0001g0253 a0001c0001t0001g0272 others(9): Show |
12 | HG00438.hp1 HG00597.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.781+530dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76328186 | |||||||
| chr17:76328186 | CA | C | 112 | a0001c0001t0001g0063 a0001c0001t0001g0136 a0001c0001t0001g0156 others(109): Show |
114 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.781+530delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76328186 | |||||||
| chr17:76328211 | G | A | 1 | a0001c0001t0005g0320 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.781+506C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76328211 | |||||||
| chr17:76328246 | A | C | 1 | a0001c0002t0013g0350 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.781+471T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76328246 | |||||||
| chr17:76328290 | C | T | 1 | a0001c0001t0003g0154 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.781+427G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76328290 | |||||||
| chr17:76328295 | T | C | 3 | a0001c0002t0002g0110 a0001c0002t0002g0239 a0001c0002t0002g0252 |
3 | HG00597.hp1 HG04228.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.781+422A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76328295 | |||||||
| chr17:76328635 | A | C | 3 | a0001c0001t0001g0073 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG01928.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.781+82T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76328635 | |||||||
| chr17:76328648 | C | A | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(278): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.781+69G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76328648 | |||||||
| chr17:76328661 | C | CA | 5 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+55dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76328661 | |||||||
| chr17:76328670 | A | C | 5 | a0001c0001t0003g0314 a0001c0001t0003g0328 a0001c0002t0002g0038 others(2): Show |
5 | HG02630.hp2 HG02886.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+47T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76328670 | |||||||
| chr17:76329074 | A | AT | 125 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(122): Show |
127 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.636-213dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 6/9 | chr17 | 76329074 | |||||||
| chr17:76329087 | T | C | 5 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.636-225A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 6/9 | chr17 | 76329087 | |||||||
| chr17:76329112 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.636-250G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 6/9 | chr17 | 76329112 | |||||||
| chr17:76329138 | T | C | 1 | a0001c0001t0003g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.636-276A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 6/9 | chr17 | 76329138 | |||||||
| chr17:76329195 | C | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(138): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.636-333G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 6/9 | chr17 | 76329195 | |||||||
| chr17:76329495 | G | A | 1 | a0001c0002t0015g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.635+548C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 6/9 | chr17 | 76329495 | |||||||
| chr17:76329735 | C | CA | 13 | a0001c0001t0003g0286 a0001c0001t0005g0034 a0001c0001t0005g0035 others(10): Show |
13 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.635+307dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 6/9 | chr17 | 76329735 | |||||||
| chr17:76329746 | C | A | 5 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.635+297G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 6/9 | chr17 | 76329746 | |||||||
| chr17:76329787 | T | C | 130 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(127): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.635+256A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 6/9 | chr17 | 76329787 | |||||||
| chr17:76329865 | T | C | 5 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.635+178A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 6/9 | chr17 | 76329865 | |||||||
| chr17:76329933 | AG | A | 5 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.635+109delC | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 6/9 | chr17 | 76329933 | |||||||
| chr17:76330185 | T | C | 4 | a0001c0001t0001g0159 a0001c0001t0008g0153 a0001c0001t0008g0309 others(1): Show |
4 | HG01433.hp1 HG02451.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-87A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 5/9 | chr17 | 76330185 | |||||||
| chr17:76330352 | G | A | 1 | a0001c0001t0001g0322 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.579+199C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 5/9 | chr17 | 76330352 | |||||||
| chr17:76330395 | G | A | 1 | a0001c0001t0001g0240 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.579+156C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 5/9 | chr17 | 76330395 | |||||||
| chr17:76330472 | G | A | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(281): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.579+79C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 5/9 | chr17 | 76330472 | |||||||
| chr17:76330475 | A | T | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(281): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.579+76T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 5/9 | chr17 | 76330475 | |||||||
| chr17:76330706 | C | T | 5 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-40G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76330706 | |||||||
| chr17:76330979 | G | T | 1 | a0001c0001t0005g0320 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.464-313C>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76330979 | |||||||
| chr17:76330983 | G | T | 5 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-317C>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76330983 | |||||||
| chr17:76331040 | C | T | 2 | a0001c0001t0003g0314 a0001c0001t0003g0328 |
2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.464-374G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76331040 | |||||||
| chr17:76331197 | T | C | 9 | a0001c0001t0005g0045 a0001c0001t0005g0051 a0001c0001t0005g0052 others(6): Show |
9 | HG01099.hp1 HG02559.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.464-531A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76331197 | |||||||
| chr17:76331241 | C | T | 4 | a0001c0001t0001g0306 a0001c0001t0009g0303 a0001c0001t0009g0304 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-575G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76331241 | |||||||
| chr17:76331361 | C | T | 37 | a0001c0001t0003g0196 a0001c0001t0003g0286 a0001c0001t0004g0341 others(34): Show |
38 | HG01361.hp2 HG01891.hp1 HG02080.hp1 others(35): Show |
intron_variant | MODIFIER | c.464-695G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76331361 | |||||||
| chr17:76331371 | G | C | 1 | a0001c0002t0026g0317 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.464-705C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76331371 | |||||||
| chr17:76331381 | T | C | 5 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-715A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76331381 | |||||||
| chr17:76331528 | G | A | 4 | a0001c0001t0001g0306 a0001c0001t0009g0303 a0001c0001t0009g0304 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+735C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76331528 | |||||||
| chr17:76331653 | T | A | 5 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+610A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76331653 | |||||||
| chr17:76331854 | G | A | 2 | a0001c0001t0004g0069 a0001c0002t0001g0070 |
2 | HG03490.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.463+409C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76331854 | |||||||
| chr17:76332088 | C | A | 2 | a0001c0001t0021g0033 a0001c0001t0021g0041 |
2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.463+175G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76332088 | |||||||
| chr17:76332102 | A | T | 5 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+161T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76332102 | |||||||
| chr17:76332137 | C | T | 3 | a0001c0001t0012g0031 a0001c0001t0012g0032 a0001c0001t0012g0235 |
3 | HG02486.hp2 HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.463+126G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76332137 | |||||||
| chr17:76332251 | G | A | 1 | a0001c0001t0003g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.463+12C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76332251 | |||||||
| chr17:76332495 | C | G | 133 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(130): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.291-60G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76332495 | |||||||
| chr17:76332550 | C | G | 1 | a0001c0002t0006g0056 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.291-115G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76332550 | |||||||
| chr17:76332605 | T | C | 135 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(132): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.291-170A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76332605 | |||||||
| chr17:76332606 | T | G | 5 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.291-171A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76332606 | |||||||
| chr17:76332623 | T | C | 135 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(132): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.291-188A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76332623 | |||||||
| chr17:76332704 | G | C | 1 | a0001c0001t0005g0320 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.291-269C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76332704 | |||||||
| chr17:76332892 | A | AT | 8 | a0001c0001t0001g0028 a0001c0001t0001g0073 a0001c0001t0001g0086 others(5): Show |
8 | HG01928.hp2 HG02145.hp2 HG03492.hp2 others(5): Show |
intron_variant | MODIFIER | c.291-458dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76332892 | |||||||
| chr17:76332892 | AT | A | 6 | a0001c0001t0001g0132 a0001c0001t0001g0306 a0001c0001t0003g0286 others(3): Show |
6 | HG01975.hp1 HG02145.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.291-458delA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76332892 | |||||||
| chr17:76332916 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0085 |
2 | NA18939.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.291-481C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76332916 | |||||||
| chr17:76332924 | G | A | 38 | a0001c0001t0001g0063 a0001c0001t0002g0212 a0001c0001t0003g0004 others(35): Show |
39 | HG00408.hp2 HG00597.hp2 HG01928.hp1 others(36): Show |
intron_variant | MODIFIER | c.291-489C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76332924 | |||||||
| chr17:76333113 | C | G | 135 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(132): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.291-678G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76333113 | |||||||
| chr17:76333265 | C | T | 35 | a0001c0001t0003g0196 a0001c0001t0003g0286 a0001c0001t0004g0341 others(32): Show |
36 | HG01361.hp2 HG01891.hp1 HG02080.hp1 others(33): Show |
intron_variant | MODIFIER | c.291-830G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76333265 | |||||||
| chr17:76333402 | A | G | 135 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(132): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.291-967T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76333402 | |||||||
| chr17:76333581 | G | A | 5 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.291-1146C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76333581 | |||||||
| chr17:76333594 | G | A | 1 | a0001c0001t0003g0188 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.291-1159C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76333594 | |||||||
| chr17:76333630 | G | C | 5 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.291-1195C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76333630 | |||||||
| chr17:76333670 | C | CA | 130 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(127): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.291-1236dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76333670 | |||||||
| chr17:76333670 | CA | C | 6 | a0001c0001t0005g0320 a0001c0001t0014g0010 a0001c0001t0014g0011 others(3): Show |
6 | HG01106.hp1 HG02622.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.291-1236delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76333670 | |||||||
| chr17:76333850 | G | GCATT | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(101): Show |
107 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.291-1419_291-1416d others(6): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76333850 | |||||||
| chr17:76333876 | T | A | 135 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(132): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.291-1441A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76333876 | |||||||
| chr17:76333900 | A | G | 1 | a0001c0002t0002g0288 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.291-1465T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76333900 | |||||||
| chr17:76333974 | G | A | 134 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(131): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.291-1539C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76333974 | |||||||
| chr17:76334122 | C | T | 1 | a0001c0001t0004g0302 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.291-1687G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334122 | |||||||
| chr17:76334177 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.291-1742C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334177 | |||||||
| chr17:76334368 | T | C | 2 | a0001c0001t0017g0318 a0001c0002t0006g0313 |
2 | HG01361.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.291-1933A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334368 | |||||||
| chr17:76334431 | G | A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0088 others(5): Show |
8 | HG02129.hp1 HG02165.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.291-1996C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334431 | |||||||
| chr17:76334533 | A | G | 2 | a0001c0001t0021g0033 a0001c0001t0021g0041 |
2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.291-2098T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334533 | |||||||
| chr17:76334542 | C | T | 2 | a0001c0001t0003g0314 a0001c0001t0003g0328 |
2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.291-2107G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334542 | |||||||
| chr17:76334557 | T | C | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(279): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.291-2122A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334557 | |||||||
| chr17:76334582 | T | C | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(283): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.291-2147A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334582 | |||||||
| chr17:76334583 | G | A | 127 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(124): Show |
129 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.291-2148C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334583 | |||||||
| chr17:76334623 | T | C | 12 | a0001c0001t0001g0177 a0001c0001t0001g0258 a0001c0002t0002g0026 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.291-2188A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334623 | |||||||
| chr17:76334627 | AAAAAAC | A | 130 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0136 others(127): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.291-2198_291-2193d others(8): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334627 | |||||||
| chr17:76334641 | A | G | 1 | a0001c0002t0002g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.291-2206T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334641 | |||||||
| chr17:76334649 | A | T | 1 | a0001c0002t0015g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.291-2214T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334649 | |||||||
| chr17:76334761 | C | A | 2 | a0001c0001t0003g0245 a0001c0001t0003g0246 |
2 | HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.291-2326G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334761 | |||||||
| chr17:76334811 | A | G | 1 | a0001c0001t0024g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.291-2376T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334811 | |||||||
| chr17:76335147 | C | T | 5 | a0001c0001t0014g0010 a0001c0001t0014g0011 a0001c0001t0014g0013 others(2): Show |
5 | HG01106.hp1 HG02622.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.291-2712G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76335147 | |||||||
| chr17:76335158 | T | C | 5 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.291-2723A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76335158 | |||||||
| chr17:76335167 | T | C | 2 | a0001c0002t0015g0029 a0001c0002t0015g0030 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.291-2732A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76335167 | |||||||
| chr17:76335212 | G | C | 5 | a0001c0001t0014g0010 a0001c0001t0014g0011 a0001c0001t0014g0013 others(2): Show |
5 | HG01106.hp1 HG02622.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.291-2777C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76335212 | |||||||
| chr17:76335234 | C | T | 8 | a0001c0001t0009g0311 a0001c0001t0009g0315 a0001c0001t0017g0318 others(5): Show |
8 | HG01361.hp2 HG01891.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.291-2799G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76335234 | |||||||
| chr17:76335419 | G | A | 1 | a0001c0001t0003g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.291-2984C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76335419 | |||||||
| chr17:76335591 | G | A | 1 | a0001c0001t0010g0040 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.291-3156C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76335591 | |||||||
| chr17:76335599 | A | C | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(281): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.291-3164T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76335599 | |||||||
| chr17:76335720 | T | C | 52 | a0001c0001t0001g0063 a0001c0001t0002g0212 a0001c0001t0003g0004 others(49): Show |
53 | HG00408.hp2 HG00597.hp2 HG01891.hp2 others(50): Show |
intron_variant | MODIFIER | c.291-3285A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76335720 | |||||||
| chr17:76335887 | G | C | 1 | a0001c0002t0006g0241 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.291-3452C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76335887 | |||||||
| chr17:76335897 | G | A | 14 | a0001c0001t0001g0047 a0001c0001t0001g0159 a0001c0001t0001g0162 others(11): Show |
14 | HG01169.hp1 HG01433.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.291-3462C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76335897 | |||||||
| chr17:76335967 | G | T | 1 | a0001c0001t0004g0181 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.291-3532C>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76335967 | |||||||
| chr17:76336254 | A | G | 1 | a0001c0001t0005g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.291-3819T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336254 | |||||||
| chr17:76336255 | T | C | 5 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.291-3820A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336255 | |||||||
| chr17:76336425 | G | A | 1 | a0001c0001t0025g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.291-3990C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336425 | |||||||
| chr17:76336437 | C | CA | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(184): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.291-4003dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336437 | |||||||
| chr17:76336503 | CA | C | 28 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0075 others(25): Show |
30 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.291-4069delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336503 | |||||||
| chr17:76336521 | C | T | 1 | a0001c0002t0002g0017 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.291-4086G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336521 | |||||||
| chr17:76336660 | A | G | 1 | a0001c0001t0003g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.291-4225T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336660 | |||||||
| chr17:76336732 | C | CA | 7 | a0001c0001t0010g0040 a0001c0001t0010g0042 a0001c0001t0010g0043 others(4): Show |
7 | HG02615.hp2 HG02886.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-4298dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336732 | |||||||
| chr17:76336732 | CA | C | 24 | a0001c0001t0001g0242 a0001c0001t0001g0282 a0001c0001t0003g0197 others(21): Show |
24 | HG00140.hp2 HG00735.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.291-4298delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336732 | |||||||
| chr17:76336732 | CAA | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(203): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.291-4299_291-4298d others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336732 | |||||||
| chr17:76336732 | CAAA | C | 9 | a0001c0001t0001g0021 a0001c0001t0001g0078 a0001c0001t0001g0159 others(6): Show |
9 | HG01169.hp2 HG02145.hp1 HG03834.hp2 others(6): Show |
intron_variant | MODIFIER | c.291-4300_291-4298d others(5): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336732 | |||||||
| chr17:76336732 | CAAAAAAA | C | 40 | a0001c0001t0001g0063 a0001c0001t0002g0212 a0001c0001t0003g0004 others(37): Show |
41 | HG00408.hp2 HG00597.hp2 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.291-4304_291-4298d others(9): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336732 | |||||||
| chr17:76336732 | CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0002g0149 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.291-4307_291-4298d others(12): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336732 | |||||||
| chr17:76336772 | G | A | 3 | a0001c0001t0021g0033 a0001c0001t0021g0041 a0001c0002t0015g0055 |
3 | HG03209.hp2 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.291-4337C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336772 | |||||||
| chr17:76336822 | C | T | 1 | a0001c0001t0001g0016 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.291-4387G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336822 | |||||||
| chr17:76336960 | C | T | 5 | a0001c0001t0014g0010 a0001c0001t0014g0011 a0001c0001t0014g0013 others(2): Show |
5 | HG01106.hp1 HG02622.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.291-4525G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336960 | |||||||
| chr17:76337045 | T | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(230): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.291-4610A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337045 | |||||||
| chr17:76337054 | A | T | 2 | a0001c0001t0003g0291 a0001c0001t0003g0299 |
2 | HG03704.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.291-4619T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337054 | |||||||
| chr17:76337080 | T | C | 1 | a0001c0001t0003g0194 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.291-4645A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337080 | |||||||
| chr17:76337216 | A | C | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(281): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.291-4781T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337216 | |||||||
| chr17:76337423 | A | AAACAACA others(2): Show |
3 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 |
3 | HG02615.hp2 HG02886.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.291-4997_291-4989d others(11): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337423 | |||||||
| chr17:76337448 | A | AAAC | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(228): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.291-5016_291-5014d others(5): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337448 | |||||||
| chr17:76337448 | A | AACAAAC | 7 | a0001c0001t0003g0286 a0001c0001t0005g0034 a0001c0001t0005g0035 others(4): Show |
7 | HG02818.hp2 HG02965.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-5014_291-5013i others(8): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337448 | |||||||
| chr17:76337507 | C | T | 1 | a0001c0001t0005g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.291-5072G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337507 | |||||||
| chr17:76337652 | C | T | 1 | a0001c0001t0004g0341 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.291-5217G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337652 | |||||||
| chr17:76337653 | G | A | 2 | a0001c0001t0004g0295 a0001c0001t0005g0244 |
2 | HG03225.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.291-5218C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337653 | |||||||
| chr17:76337658 | T | C | 1 | a0001c0002t0002g0239 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.291-5223A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337658 | |||||||
| chr17:76337749 | G | A | 4 | a0001c0001t0001g0306 a0001c0001t0009g0303 a0001c0001t0009g0304 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-5314C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337749 | |||||||
| chr17:76337809 | G | A | 4 | a0001c0001t0001g0306 a0001c0001t0009g0303 a0001c0001t0009g0304 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-5374C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337809 | |||||||
| chr17:76337853 | C | A | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(223): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.291-5418G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337853 | |||||||
| chr17:76338018 | TC | T | 39 | a0001c0001t0003g0196 a0001c0001t0003g0286 a0001c0001t0004g0147 others(36): Show |
40 | HG00140.hp1 HG01361.hp2 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.291-5584delG | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76338018 | |||||||
| chr17:76338035 | C | T | 2 | a0001c0002t0015g0029 a0001c0002t0015g0030 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.291-5600G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76338035 | |||||||
| chr17:76338091 | G | C | 1 | a0001c0001t0001g0176 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.291-5656C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76338091 | |||||||
| chr17:76338926 | G | A | 1 | a0001c0001t0004g0341 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.290+5745C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76338926 | |||||||
| chr17:76338947 | C | T | 5 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.290+5724G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76338947 | |||||||
| chr17:76338988 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(240): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.290+5683T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76338988 | |||||||
| chr17:76339066 | G | A | 1 | a0001c0001t0029g0083 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.290+5605C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76339066 | |||||||
| chr17:76339153 | TCAGCACT others(1479): Show |
T | 5 | a0001c0001t0014g0010 a0001c0001t0014g0011 a0001c0001t0014g0013 others(2): Show |
5 | HG01106.hp1 HG02622.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+4032_290+5517d others(2): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76339153 | |||||||
| chr17:76339191 | G | A | 4 | a0001c0001t0001g0306 a0001c0001t0009g0303 a0001c0001t0009g0304 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+5480C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76339191 | |||||||
| chr17:76339353 | C | T | 1 | a0001c0001t0010g0043 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.290+5318G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76339353 | |||||||
| chr17:76339606 | G | A | 1 | a0001c0001t0022g0279 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.290+5065C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76339606 | |||||||
| chr17:76339907 | A | G | 1 | a0001c0001t0017g0323 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.290+4764T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76339907 | |||||||
| chr17:76339948 | A | G | 5 | a0001c0001t0001g0306 a0001c0001t0009g0303 a0001c0001t0009g0304 others(2): Show |
5 | HG02055.hp2 HG02145.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.290+4723T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76339948 | |||||||
| chr17:76340051 | C | T | 1 | a0001c0002t0002g0319 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.290+4620G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340051 | |||||||
| chr17:76340094 | C | T | 3 | a0001c0001t0001g0306 a0001c0002t0006g0241 a0001c0002t0015g0055 |
3 | HG02145.hp1 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.290+4577G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340094 | |||||||
| chr17:76340142 | T | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0118 |
2 | HG00639.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.290+4529A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340142 | |||||||
| chr17:76340145 | C | CA | 117 | a0001c0001t0001g0049 a0001c0001t0001g0063 a0001c0001t0001g0066 others(114): Show |
119 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.290+4525dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340145 | |||||||
| chr17:76340312 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.290+4359A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340312 | |||||||
| chr17:76340333 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.290+4338C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340333 | |||||||
| chr17:76340371 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.290+4300A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340371 | |||||||
| chr17:76340391 | T | A | 45 | a0001c0001t0001g0049 a0001c0001t0001g0075 a0001c0001t0001g0125 others(42): Show |
46 | HG00673.hp2 HG00738.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.290+4280A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340391 | |||||||
| chr17:76340400 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0005g0036 |
2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.290+4271G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340400 | |||||||
| chr17:76340419 | T | C | 11 | a0001c0001t0003g0314 a0001c0001t0005g0035 a0001c0001t0005g0058 others(8): Show |
11 | HG00738.hp2 HG01069.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.290+4252A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340419 | |||||||
| chr17:76340464 | T | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0016 others(103): Show |
108 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.290+4207A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340464 | |||||||
| chr17:76340470 | G | C | 2 | a0001c0001t0005g0034 a0001c0001t0012g0031 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.290+4201C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340470 | |||||||
| chr17:76340499 | GT | G | 54 | a0001c0001t0001g0076 a0001c0001t0001g0086 a0001c0001t0001g0087 others(51): Show |
55 | HG00140.hp2 HG00639.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.290+4171delA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340499 | |||||||
| chr17:76340576 | T | G | 1 | a0001c0001t0004g0145 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.290+4095A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340576 | |||||||
| chr17:76340585 | G | A | 1 | a0001c0001t0003g0267 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.290+4086C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340585 | |||||||
| chr17:76340627 | G | A | 2 | a0001c0001t0021g0033 a0001c0001t0021g0041 |
2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.290+4044C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340627 | |||||||
| chr17:76340651 | G | A | 6 | a0001c0001t0001g0306 a0001c0001t0014g0010 a0001c0001t0014g0011 others(3): Show |
6 | HG01106.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.290+4020C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340651 | |||||||
| chr17:76340720 | G | A | 2 | a0001c0001t0004g0283 a0001c0001t0004g0284 |
2 | HG01433.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.290+3951C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340720 | |||||||
| chr17:76340746 | C | T | 1 | a0001c0001t0005g0238 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.290+3925G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340746 | |||||||
| chr17:76340747 | G | A | 2 | a0001c0001t0010g0042 a0001c0001t0010g0043 |
2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.290+3924C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340747 | |||||||
| chr17:76340749 | G | C | 2 | a0001c0001t0010g0042 a0001c0001t0010g0043 |
2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.290+3922C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340749 | |||||||
| chr17:76340804 | T | C | 103 | a0001c0001t0001g0049 a0001c0001t0001g0063 a0001c0001t0001g0077 others(100): Show |
106 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.290+3867A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340804 | |||||||
| chr17:76340838 | T | G | 1 | a0001c0001t0003g0154 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.290+3833A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340838 | |||||||
| chr17:76340842 | C | G | 46 | a0001c0001t0003g0314 a0001c0001t0003g0328 a0001c0001t0004g0341 others(43): Show |
47 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.290+3829G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340842 | |||||||
| chr17:76340896 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.290+3775G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340896 | |||||||
| chr17:76340919 | G | A | 1 | a0001c0002t0007g0292 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.290+3752C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340919 | |||||||
| chr17:76340928 | G | C | 4 | a0001c0001t0001g0050 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG00323.hp2 HG03710.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+3743C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340928 | |||||||
| chr17:76340972 | T | C | 5 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0036 others(2): Show |
5 | HG02818.hp2 HG03453.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+3699A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340972 | |||||||
| chr17:76340991 | C | CT | 38 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0003g0328 others(35): Show |
39 | HG00099.hp1 HG00738.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.290+3679dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340991 | |||||||
| chr17:76341203 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.290+3468G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341203 | |||||||
| chr17:76341234 | G | GT | 8 | a0001c0001t0001g0177 a0001c0001t0003g0187 a0001c0001t0003g0188 others(5): Show |
8 | HG02055.hp1 HG02056.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.290+3436dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341234 | |||||||
| chr17:76341234 | GTT | G | 14 | a0001c0001t0001g0306 a0001c0001t0005g0320 a0001c0001t0009g0303 others(11): Show |
14 | HG01106.hp1 HG01361.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.290+3435_290+3436d others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341234 | |||||||
| chr17:76341234 | GTTT | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0158 a0001c0001t0001g0185 others(73): Show |
78 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.290+3434_290+3436d others(5): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341234 | |||||||
| chr17:76341234 | GTTTT | G | 143 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(140): Show |
146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.290+3433_290+3436d others(6): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341234 | |||||||
| chr17:76341237 | T | G | 6 | a0001c0001t0005g0320 a0001c0001t0017g0318 a0001c0001t0019g0009 others(3): Show |
6 | HG01361.hp2 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.290+3434A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341237 | |||||||
| chr17:76341238 | T | G | 50 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0003g0314 others(47): Show |
51 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.290+3433A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341238 | |||||||
| chr17:76341240 | T | G | 1 | a0001c0002t0006g0195 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.290+3431A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341240 | |||||||
| chr17:76341241 | T | G | 1 | a0001c0002t0006g0241 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.290+3430A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341241 | |||||||
| chr17:76341244 | T | G | 3 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0021g0041 |
3 | HG02886.hp2 HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.290+3427A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341244 | |||||||
| chr17:76341245 | T | G | 2 | a0001c0002t0002g0143 a0001c0002t0002g0144 |
2 | NA18944.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.290+3426A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341245 | |||||||
| chr17:76341246 | T | G | 4 | a0001c0001t0004g0340 a0001c0001t0004g0342 a0001c0001t0004g0343 others(1): Show |
4 | HG00735.hp2 HG01106.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+3425A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341246 | |||||||
| chr17:76341247 | T | G | 1 | a0001c0001t0004g0145 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.290+3424A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341247 | |||||||
| chr17:76341281 | A | C | 2 | a0001c0001t0004g0201 a0001c0002t0002g0205 |
2 | HG00597.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.290+3390T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341281 | |||||||
| chr17:76341313 | C | G | 1 | a0001c0001t0001g0157 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.290+3358G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341313 | |||||||
| chr17:76341323 | G | A | 1 | a0001c0002t0002g0146 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.290+3348C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341323 | |||||||
| chr17:76341394 | C | T | 1 | a0001c0002t0002g0247 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.290+3277G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341394 | |||||||
| chr17:76341535 | C | T | 10 | a0001c0001t0005g0045 a0001c0001t0005g0051 a0001c0001t0005g0052 others(7): Show |
10 | HG01099.hp1 HG01891.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.290+3136G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341535 | |||||||
| chr17:76341553 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.290+3118A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341553 | |||||||
| chr17:76341668 | C | T | 10 | a0001c0001t0005g0045 a0001c0001t0005g0051 a0001c0001t0005g0052 others(7): Show |
10 | HG01099.hp1 HG01891.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.290+3003G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341668 | |||||||
| chr17:76341669 | G | A | 4 | a0001c0001t0012g0031 a0001c0001t0012g0032 a0001c0002t0015g0029 others(1): Show |
4 | HG02809.hp1 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+3002C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341669 | |||||||
| chr17:76341706 | G | A | 10 | a0001c0001t0005g0045 a0001c0001t0005g0051 a0001c0001t0005g0052 others(7): Show |
10 | HG01099.hp1 HG01891.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.290+2965C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341706 | |||||||
| chr17:76341711 | A | G | 9 | a0001c0001t0001g0306 a0001c0001t0009g0303 a0001c0001t0009g0304 others(6): Show |
9 | HG01106.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.290+2960T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341711 | |||||||
| chr17:76341722 | G | A | 5 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0036 others(2): Show |
5 | HG02818.hp2 HG03453.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+2949C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341722 | |||||||
| chr17:76341796 | G | A | 3 | a0001c0001t0004g0069 a0001c0001t0004g0147 a0001c0002t0001g0070 |
3 | HG03490.hp2 HG03669.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.290+2875C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341796 | |||||||
| chr17:76341892 | T | C | 2 | a0001c0001t0004g0232 a0001c0001t0004g0233 |
2 | HG00140.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.290+2779A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341892 | |||||||
| chr17:76341896 | G | A | 2 | a0001c0001t0004g0201 a0001c0002t0002g0205 |
2 | HG00597.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.290+2775C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341896 | |||||||
| chr17:76341896 | G | C | 2 | a0001c0001t0005g0236 a0001c0001t0005g0237 |
2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.290+2775C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341896 | |||||||
| chr17:76342024 | T | C | 139 | a0001c0001t0001g0049 a0001c0001t0001g0063 a0001c0001t0001g0306 others(136): Show |
142 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.290+2647A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76342024 | |||||||
| chr17:76342148 | A | C | 4 | a0001c0001t0012g0031 a0001c0001t0012g0032 a0001c0002t0015g0029 others(1): Show |
4 | HG02809.hp1 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+2523T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76342148 | |||||||
| chr17:76342169 | C | T | 1 | a0001c0002t0002g0005 | 2 | HG02148.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.290+2502G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76342169 | |||||||
| chr17:76342314 | G | A | 1 | a0001c0001t0003g0196 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.290+2357C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76342314 | |||||||
| chr17:76342390 | C | T | 139 | a0001c0001t0001g0049 a0001c0001t0001g0063 a0001c0001t0001g0306 others(136): Show |
142 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.290+2281G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76342390 | |||||||
| chr17:76342795 | C | T | 48 | a0001c0001t0001g0049 a0001c0001t0001g0063 a0001c0001t0002g0212 others(45): Show |
50 | HG00408.hp2 HG00597.hp2 HG01433.hp1 others(47): Show |
intron_variant | MODIFIER | c.290+1876G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76342795 | |||||||
| chr17:76342927 | A | G | 37 | a0001c0001t0003g0328 a0001c0001t0004g0340 a0001c0001t0004g0341 others(34): Show |
38 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.290+1744T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76342927 | |||||||
| chr17:76343100 | G | A | 48 | a0001c0001t0001g0049 a0001c0001t0001g0063 a0001c0001t0002g0212 others(45): Show |
50 | HG00408.hp2 HG00597.hp2 HG01433.hp1 others(47): Show |
intron_variant | MODIFIER | c.290+1571C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76343100 | |||||||
| chr17:76343244 | C | T | 3 | a0001c0001t0016g0048 a0001c0001t0016g0191 a0001c0002t0007g0027 |
3 | HG02922.hp1 HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.290+1427G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76343244 | |||||||
| chr17:76343343 | C | G | 1 | a0001c0001t0012g0235 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.290+1328G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76343343 | |||||||
| chr17:76343645 | G | C | 5 | a0001c0001t0001g0028 a0001c0001t0001g0176 a0001c0001t0001g0240 others(2): Show |
5 | HG02129.hp2 HG02165.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+1026C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76343645 | |||||||
| chr17:76343663 | T | C | 4 | a0001c0001t0012g0031 a0001c0001t0012g0032 a0001c0002t0015g0029 others(1): Show |
4 | HG02809.hp1 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+1008A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76343663 | |||||||
| chr17:76344219 | C | T | 3 | a0001c0001t0003g0266 a0001c0001t0003g0267 a0001c0002t0007g0292 |
3 | HG01884.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.290+452G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76344219 | |||||||
| chr17:76344230 | C | T | 2 | a0001c0001t0004g0340 a0001c0001t0034g0334 |
2 | HG00735.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.290+441G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76344230 | |||||||
| chr17:76344507 | C | T | 2 | a0001c0002t0002g0038 a0001c0002t0002g0044 |
2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.290+164G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76344507 | |||||||
| chr17:76344517 | G | A | 1 | a0001c0001t0025g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.290+154C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76344517 | |||||||
| chr17:76344537 | T | C | 1 | a0001c0001t0024g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.290+134A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76344537 | |||||||
| chr17:76344649 | ATAAAG | A | 4 | a0001c0001t0012g0031 a0001c0001t0012g0032 a0001c0002t0015g0029 others(1): Show |
4 | HG02809.hp1 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+17_290+21delCT others(3): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76344649 | |||||||
| chr17:76344863 | G | A | 1 | a0001c0002t0013g0353 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.224-126C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76344863 | |||||||
| chr17:76344973 | C | T | 1 | a0001c0002t0002g0082 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.224-236G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76344973 | |||||||
| chr17:76345025 | G | C | 3 | a0001c0001t0035g0316 a0001c0002t0007g0308 a0001c0002t0026g0317 |
3 | HG02895.hp1 HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.224-288C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345025 | |||||||
| chr17:76345033 | A | T | 1 | a0001c0001t0004g0081 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.224-296T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345033 | |||||||
| chr17:76345095 | C | T | 7 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0042 others(4): Show |
7 | HG02886.hp2 HG02896.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.224-358G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345095 | |||||||
| chr17:76345107 | T | C | 139 | a0001c0001t0001g0049 a0001c0001t0001g0063 a0001c0001t0001g0306 others(136): Show |
142 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.224-370A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345107 | |||||||
| chr17:76345127 | C | T | 8 | a0001c0001t0003g0263 a0001c0001t0003g0291 a0001c0001t0004g0261 others(5): Show |
8 | HG00280.hp1 HG03491.hp2 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.224-390G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345127 | |||||||
| chr17:76345130 | G | A | 1 | a0001c0001t0005g0166 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.224-393C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345130 | |||||||
| chr17:76345151 | C | T | 5 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0036 others(2): Show |
5 | HG02818.hp2 HG03453.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-414G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345151 | |||||||
| chr17:76345237 | T | TAA | 14 | a0001c0001t0001g0306 a0001c0001t0009g0303 a0001c0001t0009g0304 others(11): Show |
14 | HG01106.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.224-502_224-501dup others(2): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345237 | |||||||
| chr17:76345237 | T | TAAAAA | 11 | a0001c0001t0001g0061 a0001c0001t0001g0074 a0001c0001t0001g0077 others(8): Show |
11 | HG00099.hp2 HG00323.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.224-505_224-501dup others(5): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345237 | |||||||
| chr17:76345237 | T | TAAAAAA | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(193): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.224-506_224-501dup others(6): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345237 | |||||||
| chr17:76345237 | T | TAAAAAAA | 11 | a0001c0001t0001g0062 a0001c0001t0001g0066 a0001c0001t0001g0182 others(8): Show |
11 | HG00609.hp1 HG01074.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.224-507_224-501dup others(7): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345237 | |||||||
| chr17:76345237 | T | TAAAAAAA others(13): Show |
3 | a0001c0001t0010g0042 a0001c0002t0002g0038 a0001c0002t0002g0044 |
3 | HG03195.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.224-501_224-500ins others(20): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345237 | |||||||
| chr17:76345237 | T | TAAAAAAA others(14): Show |
1 | a0001c0001t0010g0043 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.224-501_224-500ins others(21): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345237 | |||||||
| chr17:76345237 | TA | T | 57 | a0001c0001t0003g0314 a0001c0001t0003g0328 a0001c0001t0004g0340 others(54): Show |
58 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.224-501delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345237 | |||||||
| chr17:76345237 | TAA | T | 54 | a0001c0001t0001g0049 a0001c0001t0001g0063 a0001c0001t0002g0212 others(51): Show |
56 | HG00408.hp2 HG00597.hp2 HG01433.hp1 others(53): Show |
intron_variant | MODIFIER | c.224-502_224-501del others(2): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345237 | |||||||
| chr17:76345336 | G | A | 3 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 |
3 | HG02055.hp2 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.224-599C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345336 | |||||||
| chr17:76345544 | G | A | 5 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0036 others(2): Show |
5 | HG02818.hp2 HG03453.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-807C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345544 | |||||||
| chr17:76345555 | G | T | 5 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0036 others(2): Show |
5 | HG02818.hp2 HG03453.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-818C>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345555 | |||||||
| chr17:76345607 | G | C | 2 | a0001c0002t0002g0231 a0001c0002t0002g0301 |
2 | HG01243.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.224-870C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345607 | |||||||
| chr17:76345609 | G | GA | 76 | a0001c0001t0001g0077 a0001c0001t0001g0151 a0001c0001t0001g0152 others(73): Show |
77 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.224-873dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345609 | |||||||
| chr17:76345609 | GA | G | 55 | a0001c0001t0001g0049 a0001c0001t0001g0063 a0001c0001t0002g0212 others(52): Show |
57 | HG00408.hp2 HG00597.hp2 HG01433.hp1 others(54): Show |
intron_variant | MODIFIER | c.224-873delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345609 | |||||||
| chr17:76345789 | C | CA | 4 | a0001c0001t0012g0031 a0001c0001t0012g0032 a0001c0002t0015g0029 others(1): Show |
4 | HG02809.hp1 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.224-1053dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345789 | |||||||
| chr17:76345818 | C | T | 8 | a0001c0001t0005g0045 a0001c0001t0005g0051 a0001c0001t0005g0052 others(5): Show |
8 | HG01891.hp2 HG02559.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.224-1081G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345818 | |||||||
| chr17:76345910 | T | C | 1 | a0001c0002t0011g0344 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.224-1173A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345910 | |||||||
| chr17:76345930 | A | C | 1 | a0001c0001t0001g0078 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.224-1193T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345930 | |||||||
| chr17:76345932 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.224-1195G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345932 | |||||||
| chr17:76345981 | AG | A | 5 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0036 others(2): Show |
5 | HG02818.hp2 HG03453.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-1245delC | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345981 | |||||||
| chr17:76345985 | G | C | 6 | a0001c0001t0014g0010 a0001c0001t0014g0011 a0001c0001t0014g0013 others(3): Show |
6 | HG01106.hp1 HG02622.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.224-1248C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345985 | |||||||
| chr17:76346019 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.224-1282G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346019 | |||||||
| chr17:76346104 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.224-1367G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346104 | |||||||
| chr17:76346238 | T | A | 1 | a0002c0003t0003g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.224-1501A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346238 | |||||||
| chr17:76346271 | T | C | 9 | a0001c0001t0001g0306 a0001c0001t0009g0303 a0001c0001t0009g0304 others(6): Show |
9 | HG01106.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.224-1534A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346271 | |||||||
| chr17:76346295 | G | A | 2 | a0001c0001t0005g0057 a0001c0001t0005g0058 |
2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.224-1558C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346295 | |||||||
| chr17:76346336 | C | T | 2 | a0001c0002t0002g0231 a0001c0002t0002g0301 |
2 | HG01243.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.224-1599G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346336 | |||||||
| chr17:76346445 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.224-1708A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346445 | |||||||
| chr17:76346558 | T | C | 1 | a0001c0001t0003g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.224-1821A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346558 | |||||||
| chr17:76346640 | T | G | 1 | a0001c0001t0004g0287 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.223+1889A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346640 | |||||||
| chr17:76346645 | A | G | 4 | a0001c0002t0007g0324 a0001c0002t0007g0325 a0001c0002t0007g0326 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+1884T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346645 | |||||||
| chr17:76346757 | C | T | 4 | a0001c0001t0012g0031 a0001c0001t0012g0032 a0001c0002t0015g0029 others(1): Show |
4 | HG02809.hp1 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+1772G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346757 | |||||||
| chr17:76346807 | A | G | 1 | a0001c0001t0003g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.223+1722T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346807 | |||||||
| chr17:76346850 | T | C | 215 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0047 others(212): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.223+1679A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346850 | |||||||
| chr17:76346871 | G | A | 5 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0036 others(2): Show |
5 | HG02818.hp2 HG03453.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+1658C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346871 | |||||||
| chr17:76346874 | C | T | 7 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0042 others(4): Show |
7 | HG02886.hp2 HG02896.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.223+1655G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346874 | |||||||
| chr17:76347017 | C | A | 4 | a0001c0001t0012g0031 a0001c0001t0012g0032 a0001c0002t0015g0029 others(1): Show |
4 | HG02809.hp1 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+1512G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347017 | |||||||
| chr17:76347064 | C | A | 2 | a0001c0001t0003g0222 a0001c0001t0003g0300 |
2 | NA18959.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.223+1465G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347064 | |||||||
| chr17:76347109 | G | A | 1 | a0001c0002t0006g0346 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.223+1420C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347109 | |||||||
| chr17:76347317 | G | A | 1 | a0001c0001t0003g0299 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.223+1212C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347317 | |||||||
| chr17:76347428 | A | G | 2 | a0001c0001t0005g0236 a0001c0001t0005g0237 |
2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.223+1101T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347428 | |||||||
| chr17:76347484 | C | CA | 55 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0062 others(52): Show |
56 | HG00140.hp1 HG00140.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.223+1044dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | |||||||
| chr17:76347484 | C | CAA | 19 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0229 others(16): Show |
19 | HG00735.hp2 HG01106.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.223+1043_223+1044d others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | |||||||
| chr17:76347484 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0003g0187 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.223+1035_223+1044d others(12): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | |||||||
| chr17:76347484 | C | CAAAAAAA others(4): Show |
7 | a0001c0001t0003g0188 a0001c0001t0003g0189 a0001c0001t0003g0190 others(4): Show |
7 | HG02132.hp2 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.223+1034_223+1044d others(13): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | |||||||
| chr17:76347484 | C | CAAAAAAA others(5): Show |
12 | a0001c0001t0001g0063 a0001c0001t0003g0004 a0001c0001t0003g0192 others(9): Show |
13 | HG01975.hp2 HG01993.hp1 HG02273.hp2 others(10): Show |
intron_variant | MODIFIER | c.223+1033_223+1044d others(14): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | |||||||
| chr17:76347484 | C | CAAAAAAA others(6): Show |
7 | a0001c0001t0001g0049 a0001c0001t0003g0197 a0001c0001t0003g0222 others(4): Show |
7 | HG01928.hp1 HG02135.hp1 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.223+1032_223+1044d others(15): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | |||||||
| chr17:76347484 | C | CAAAAAAA others(7): Show |
6 | a0001c0001t0003g0202 a0001c0001t0004g0204 a0001c0001t0023g0359 others(3): Show |
6 | HG00597.hp2 HG02055.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.223+1031_223+1044d others(16): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | |||||||
| chr17:76347484 | C | CAAAAAAA others(8): Show |
1 | a0001c0002t0002g0206 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.223+1030_223+1044d others(17): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | |||||||
| chr17:76347484 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0003g0223 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.223+1029_223+1044d others(18): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | |||||||
| chr17:76347484 | C | CAAAAAAA others(10): Show |
4 | a0001c0001t0003g0207 a0001c0001t0003g0208 a0001c0001t0003g0209 others(1): Show |
4 | HG01952.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+1028_223+1044d others(19): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | |||||||
| chr17:76347484 | C | CAAAAAAA others(11): Show |
3 | a0001c0001t0002g0212 a0001c0001t0003g0210 a0001c0001t0020g0211 |
3 | NA18957.hp2 NA18979.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.223+1027_223+1044d others(20): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | |||||||
| chr17:76347484 | C | CAAAAAAA others(12): Show |
2 | a0001c0001t0003g0213 a0001c0001t0003g0214 |
2 | HG00408.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.223+1026_223+1044d others(21): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | |||||||
| chr17:76347484 | CA | C | 16 | a0001c0001t0001g0061 a0001c0001t0001g0074 a0001c0001t0001g0075 others(13): Show |
16 | HG00099.hp2 HG00323.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.223+1044delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | |||||||
| chr17:76347484 | CAA | C | 32 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0003g0314 others(29): Show |
32 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.223+1043_223+1044d others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | |||||||
| chr17:76347529 | A | T | 1 | a0001c0001t0017g0323 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.223+1000T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347529 | |||||||
| chr17:76347532 | G | C | 5 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0005g0320 others(2): Show |
5 | HG00099.hp1 HG01074.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.223+997C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347532 | |||||||
| chr17:76347606 | C | T | 3 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 |
3 | HG02055.hp2 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.223+923G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347606 | |||||||
| chr17:76347660 | A | C | 1 | a0001c0002t0006g0241 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.223+869T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347660 | |||||||
| chr17:76347668 | A | G | 1 | a0002c0003t0003g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.223+861T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347668 | |||||||
| chr17:76347670 | G | A | 1 | a0002c0003t0003g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.223+859C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347670 | |||||||
| chr17:76347759 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.223+770C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347759 | |||||||
| chr17:76347872 | C | T | 4 | a0001c0001t0012g0031 a0001c0001t0012g0032 a0001c0002t0015g0029 others(1): Show |
4 | HG02809.hp1 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+657G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347872 | |||||||
| chr17:76348043 | C | T | 61 | a0001c0001t0001g0306 a0001c0001t0001g0321 a0001c0001t0001g0322 others(58): Show |
62 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.223+486G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348043 | |||||||
| chr17:76348160 | A | AAAAT | 39 | a0001c0001t0001g0073 a0001c0001t0003g0328 a0001c0001t0004g0340 others(36): Show |
40 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.223+365_223+368dup others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348160 | |||||||
| chr17:76348160 | A | AAAATAAA others(1): Show |
21 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0003g0314 others(18): Show |
21 | HG00099.hp1 HG01074.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.223+361_223+368dup others(8): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348160 | |||||||
| chr17:76348160 | A | AAAATAAA others(5): Show |
8 | a0001c0001t0001g0306 a0001c0001t0008g0309 a0001c0001t0009g0303 others(5): Show |
8 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.223+357_223+368dup others(12): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348160 | |||||||
| chr17:76348160 | A | AAAATAAA others(9): Show |
2 | a0001c0001t0024g0014 a0001c0002t0002g0319 |
2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.223+353_223+368dup others(16): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348160 | |||||||
| chr17:76348160 | A | AAAATAAA others(13): Show |
2 | a0001c0001t0014g0010 a0001c0001t0014g0011 |
2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.223+349_223+368dup others(20): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348160 | |||||||
| chr17:76348160 | AAAATAAA others(5): Show |
A | 2 | a0001c0001t0003g0245 a0001c0001t0003g0246 |
2 | HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.223+357_223+368del others(12): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348160 | |||||||
| chr17:76348172 | T | A | 1 | a0002c0003t0003g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.223+357A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348172 | |||||||
| chr17:76348203 | G | C | 6 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0215 others(3): Show |
6 | HG00323.hp1 HG01346.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.223+326C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348203 | |||||||
| chr17:76348310 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.223+219A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348310 | |||||||
| chr17:76348310 | TAAAAATA others(98): Show |
T | 1 | a0001c0001t0001g0046 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.223+114_223+218del | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348310 | |||||||
| chr17:76348316 | T | C | 37 | a0001c0001t0003g0328 a0001c0001t0004g0340 a0001c0001t0004g0341 others(34): Show |
38 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.223+213A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348316 | |||||||
| chr17:76348330 | G | A | 1 | a0001c0001t0024g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.223+199C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348330 | |||||||
| chr17:76348346 | G | A | 52 | a0001c0001t0001g0049 a0001c0001t0001g0063 a0001c0001t0002g0212 others(49): Show |
54 | HG00408.hp2 HG00597.hp2 HG01433.hp1 others(51): Show |
intron_variant | MODIFIER | c.223+183C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348346 | |||||||
| chr17:76348497 | A | C | 6 | a0001c0001t0037g0349 a0001c0002t0013g0350 a0001c0002t0013g0351 others(3): Show |
6 | HG02080.hp1 NA18939.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.223+32T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348497 | |||||||
| chr17:76348502 | T | A | 1 | a0001c0001t0001g0219 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.223+27A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348502 | |||||||
| chr17:76348587 | G | A | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG01109.hp1 HG01934.hp2 |
splice_region_variant&intron_variant | LOW | c.171-6C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76348587 | |||||||
| chr17:76348686 | C | T | 7 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0042 others(4): Show |
7 | HG02886.hp2 HG02896.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.171-105G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76348686 | |||||||
| chr17:76348689 | T | A | 1 | a0002c0003t0003g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.171-108A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76348689 | |||||||
| chr17:76348878 | C | T | 4 | a0001c0001t0003g0245 a0001c0001t0003g0246 a0001c0001t0005g0243 others(1): Show |
4 | HG02965.hp1 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.171-297G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76348878 | |||||||
| chr17:76348910 | T | A | 1 | a0002c0003t0003g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.171-329A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76348910 | |||||||
| chr17:76348936 | G | A | 1 | a0001c0002t0002g0026 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.171-355C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76348936 | |||||||
| chr17:76349061 | A | G | 1 | a0001c0001t0012g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.171-480T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349061 | |||||||
| chr17:76349100 | C | G | 1 | a0001c0001t0005g0320 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.171-519G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349100 | |||||||
| chr17:76349178 | C | A | 1 | a0001c0002t0006g0345 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.171-597G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349178 | |||||||
| chr17:76349274 | C | T | 1 | a0001c0002t0002g0301 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.171-693G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349274 | |||||||
| chr17:76349406 | C | T | 1 | a0001c0002t0002g0319 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.171-825G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349406 | |||||||
| chr17:76349536 | G | A | 3 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0009g0305 |
3 | HG02055.hp2 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.171-955C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349536 | |||||||
| chr17:76349558 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.171-977G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349558 | |||||||
| chr17:76349561 | G | C | 2 | a0001c0001t0003g0222 a0001c0001t0003g0300 |
2 | NA18959.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.171-980C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349561 | |||||||
| chr17:76349629 | C | T | 10 | a0001c0001t0005g0045 a0001c0001t0005g0051 a0001c0001t0005g0052 others(7): Show |
10 | HG01099.hp1 HG01891.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.171-1048G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349629 | |||||||
| chr17:76349633 | C | T | 1 | a0001c0001t0024g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.171-1052G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349633 | |||||||
| chr17:76349702 | C | T | 2 | a0001c0001t0004g0069 a0001c0002t0001g0070 |
2 | HG03490.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.171-1121G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349702 | |||||||
| chr17:76349703 | G | A | 3 | a0001c0001t0003g0223 a0001c0001t0003g0224 a0001c0002t0002g0005 |
4 | HG02148.hp1 HG03239.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.171-1122C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349703 | |||||||
| chr17:76349992 | C | A | 9 | a0001c0001t0001g0306 a0001c0001t0009g0303 a0001c0001t0009g0304 others(6): Show |
9 | HG01106.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.171-1411G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349992 | |||||||
| chr17:76350074 | C | CA | 6 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(3): Show |
6 | HG02027.hp2 HG02145.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.171-1494dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350074 | |||||||
| chr17:76350165 | C | T | 1 | a0001c0001t0004g0068 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.171-1584G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350165 | |||||||
| chr17:76350194 | C | T | 2 | a0001c0002t0002g0064 a0001c0002t0002g0067 |
2 | HG00741.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.171-1613G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350194 | |||||||
| chr17:76350205 | C | T | 1 | a0001c0001t0021g0033 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.171-1624G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350205 | |||||||
| chr17:76350210 | CG | C | 52 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0003g0314 others(49): Show |
53 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.171-1630delC | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350210 | |||||||
| chr17:76350232 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0230 |
2 | HG00323.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.171-1651C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350232 | |||||||
| chr17:76350332 | G | A | 4 | a0001c0001t0012g0031 a0001c0001t0012g0032 a0001c0002t0015g0029 others(1): Show |
4 | HG02809.hp1 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.171-1751C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350332 | |||||||
| chr17:76350355 | C | T | 5 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0036 others(2): Show |
5 | HG02818.hp2 HG03453.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-1774G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350355 | |||||||
| chr17:76350356 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.171-1775C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350356 | |||||||
| chr17:76350396 | G | A | 1 | a0001c0002t0002g0301 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.171-1815C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350396 | |||||||
| chr17:76350438 | C | CA | 7 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0004g0232 others(4): Show |
7 | HG00140.hp1 HG01243.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.171-1858dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350438 | |||||||
| chr17:76350501 | T | G | 1 | a0001c0001t0004g0302 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.171-1920A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350501 | |||||||
| chr17:76350656 | A | G | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG03710.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.171-2075T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350656 | |||||||
| chr17:76350846 | A | C | 1 | a0001c0002t0002g0064 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.171-2265T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350846 | |||||||
| chr17:76351027 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.171-2446G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76351027 | |||||||
| chr17:76351386 | G | A | 1 | a0001c0002t0002g0234 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.170+2148C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76351386 | |||||||
| chr17:76351494 | G | A | 1 | a0001c0001t0012g0235 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.170+2040C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76351494 | |||||||
| chr17:76351507 | C | T | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0242 |
3 | HG00323.hp1 HG02486.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.170+2027G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76351507 | |||||||
| chr17:76351822 | C | T | 1 | a0001c0002t0006g0241 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.170+1712G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76351822 | |||||||
| chr17:76352046 | C | A | 9 | a0001c0001t0001g0306 a0001c0001t0009g0303 a0001c0001t0009g0304 others(6): Show |
9 | HG01106.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.170+1488G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352046 | |||||||
| chr17:76352217 | GAAAATGG others(12): Show |
G | 9 | a0001c0001t0001g0306 a0001c0001t0009g0303 a0001c0001t0009g0304 others(6): Show |
9 | HG01106.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.170+1298_170+1316d others(21): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352217 | |||||||
| chr17:76352367 | C | G | 1 | a0001c0002t0002g0060 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.170+1167G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352367 | |||||||
| chr17:76352374 | G | C | 1 | a0001c0002t0002g0023 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.170+1160C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352374 | |||||||
| chr17:76352391 | A | G | 10 | a0001c0001t0005g0045 a0001c0001t0005g0051 a0001c0001t0005g0052 others(7): Show |
10 | HG01099.hp1 HG01891.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.170+1143T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352391 | |||||||
| chr17:76352495 | A | T | 1 | a0001c0001t0001g0240 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.170+1039T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352495 | |||||||
| chr17:76352505 | T | C | 2 | a0001c0001t0005g0236 a0001c0001t0005g0237 |
2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.170+1029A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352505 | |||||||
| chr17:76352509 | G | C | 1 | a0001c0001t0005g0238 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.170+1025C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352509 | |||||||
| chr17:76352577 | G | A | 1 | a0001c0002t0002g0239 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.170+957C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352577 | |||||||
| chr17:76352644 | C | CA | 71 | a0001c0001t0001g0006 a0001c0001t0001g0240 a0001c0001t0001g0242 others(68): Show |
72 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.170+889dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352644 | |||||||
| chr17:76352644 | C | CG | 6 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0042 others(3): Show |
6 | HG02886.hp2 HG02896.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.170+889_170+890ins others(1): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352644 | |||||||
| chr17:76352644 | CA | C | 11 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0049 others(8): Show |
11 | HG00323.hp2 HG00639.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.170+889delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352644 | |||||||
| chr17:76352644 | CAAA | C | 9 | a0001c0001t0001g0306 a0001c0001t0009g0303 a0001c0001t0009g0304 others(6): Show |
9 | HG01106.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.170+887_170+889del others(3): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352644 | |||||||
| chr17:76352644 | CAAAAA | C | 33 | a0001c0001t0003g0328 a0001c0001t0004g0340 a0001c0001t0004g0341 others(30): Show |
34 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.170+885_170+889del others(5): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352644 | |||||||
| chr17:76352663 | A | G | 7 | a0001c0001t0010g0039 a0001c0001t0010g0040 a0001c0001t0010g0042 others(4): Show |
7 | HG02886.hp2 HG02896.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.170+871T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352663 | |||||||
| chr17:76352680 | AAAAAG | A | 5 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0036 others(2): Show |
5 | HG02818.hp2 HG03453.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.170+849_170+853del others(5): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352680 | |||||||
| chr17:76352735 | T | C | 5 | a0001c0001t0014g0010 a0001c0001t0014g0011 a0001c0001t0014g0013 others(2): Show |
5 | HG01106.hp1 HG02622.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.170+799A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352735 | |||||||
| chr17:76352886 | G | A | 9 | a0001c0001t0001g0306 a0001c0001t0009g0303 a0001c0001t0009g0304 others(6): Show |
9 | HG01106.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.170+648C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352886 | |||||||
| chr17:76353085 | G | C | 1 | a0002c0003t0003g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.170+449C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76353085 | |||||||
| chr17:76353089 | C | T | 9 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0036 others(6): Show |
9 | HG02809.hp1 HG02818.hp2 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.170+445G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76353089 | |||||||
| chr17:76353116 | G | C | 1 | a0001c0001t0024g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.170+418C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76353116 | |||||||
| chr17:76353301 | A | C | 1 | a0001c0001t0001g0028 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.170+233T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76353301 | |||||||
| chr17:76353434 | G | A | 52 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0003g0314 others(49): Show |
53 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.170+100C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76353434 | |||||||
| chr17:76353438 | A | T | 1 | a0001c0002t0007g0027 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.170+96T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76353438 | |||||||
| chr17:76353505 | C | A | 35 | a0001c0001t0003g0328 a0001c0001t0004g0340 a0001c0001t0004g0341 others(32): Show |
36 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.170+29G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76353505 | |||||||
| chr17:76353526 | C | T | 12 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0002t0002g0015 others(9): Show |
12 | NA18941.hp1 NA18944.hp1 NA18945.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.170+8G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76353526 |