Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 151987 |
| ensemblid | ENSG00000163605.16 |
| hgncid | 18296 |
| symbol | PPP4R2 |
| name | protein phosphatase 4 regulatory subunit 2 |
| refseq_nuc | NM_174907.4 |
| refseq_prot | NP_777567.1 |
| ensembl_nuc | ENST00000356692.10 |
| ensembl_prot | ENSP00000349124.5 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 72996811 |
| end | 73069198 |
| strand | + |
| ver | v1.2 |
| region | chr3:72996811-73069198 |
| region5000 | chr3:72991811-73074198 |
| regionname0 | PPP4R2_chr3_72996811_73069198 |
| regionname5000 | PPP4R2_chr3_72991811_73074198 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 417 | 351 | 92 | 48 | 159 | 8 | 42 | 132 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | MDVER others(412): Show |
chr3 | 72991811 | 73074198 |
| a0002 | 0/0 | 413 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | MDVER others(408): Show |
chr3 | 72991811 | 73074198 |
| a0003 | 0/0 | 417 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | MDVER others(412): Show |
chr3 | 72991811 | 73074198 |
| a0004 | 0/0 | 417 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | MDVER others(412): Show |
chr3 | 72991811 | 73074198 |
| a0005 | 0/0 | 417 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | MDVER others(412): Show |
chr3 | 72991811 | 73074198 |
| a0006 | 0/0 | 417 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | MDVER others(412): Show |
chr3 | 72991811 | 73074198 |
| a0007 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | MDVER others(412): Show |
chr3 | 72991811 | 73074198 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1251 | 243 | 71 | 41 | 98 | 6 | 25 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | ATGGA others(1246): Show |
chr3 | 72991811 | 73074198 | ||
| a0001c0002 | 0/0 | 1251 | 97 | 10 | 7 | 61 | 2 | 17 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | ATGGA others(1246): Show |
chr3 | 72991811 | 73074198 | ||
| a0001c0003 | 0/0 | 1251 | 10 | 10 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | ATGGA others(1246): Show |
chr3 | 72991811 | 73074198 | ||
| a0001c0010 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | ATGGA others(1246): Show |
chr3 | 72991811 | 73074198 | ||
| a0002c0007 | 0/0 | 1239 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | ATGGA others(1234): Show |
chr3 | 72991811 | 73074198 | ||
| a0002c0011 | 0/0 | 1239 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | ATGGA others(1234): Show |
chr3 | 72991811 | 73074198 | ||
| a0003c0004 | 0/0 | 1251 | 2 | 2 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | ATGGA others(1246): Show |
chr3 | 72991811 | 73074198 | ||
| a0004c0005 | 0/0 | 1251 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | ATGGA others(1246): Show |
chr3 | 72991811 | 73074198 | ||
| a0005c0006 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | ATGGA others(1246): Show |
chr3 | 72991811 | 73074198 | ||
| a0006c0009 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | ATGGA others(1246): Show |
chr3 | 72991811 | 73074198 | ||
| a0007c0008 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | ATGGA others(1246): Show |
chr3 | 72991811 | 73074198 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4956 | 69 | 15 | 14 | 37 | 1 | 2 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4951): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0002 | 0/0 | 4957 | 37 | 1 | 7 | 22 | 2 | 5 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4952): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0003 | 0/0 | 4963 | 4 | 3 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4958): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0004 | 0/1 | 4963 | 25 | 8 | 7 | 5 | 2 | 2 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4958): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0005 | 0/0 | 4958 | 16 | 2 | 2 | 11 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4953): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0007 | 0/0 | 4965 | 11 | 5 | 0 | 4 | 0 | 2 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4960): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0008 | 0/0 | 4967 | 10 | 0 | 4 | 3 | 1 | 2 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4962): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0009 | 0/0 | 4961 | 8 | 8 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4956): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0014 | 0/0 | 4960 | 6 | 3 | 1 | 2 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4955): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0016 | 0/0 | 4956 | 5 | 5 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4951): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0017 | 0/0 | 4959 | 3 | 0 | 0 | 2 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4954): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0018 | 0/0 | 4961 | 4 | 3 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4956): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0019 | 0/0 | 4961 | 4 | 4 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4956): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0021 | 0/0 | 4956 | 3 | 3 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4951): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0022 | 0/0 | 4957 | 3 | 0 | 0 | 3 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4952): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0024 | 0/0 | 4965 | 3 | 3 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4960): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0025 | 0/0 | 4965 | 3 | 0 | 0 | 0 | 0 | 3 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4960): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0026 | 0/0 | 4965 | 2 | 0 | 1 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4960): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0028 | 0/0 | 4954 | 2 | 0 | 0 | 0 | 0 | 2 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4949): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0029 | 0/0 | 4957 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4952): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0034 | 0/0 | 4961 | 2 | 1 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4956): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0035 | 0/0 | 4967 | 2 | 2 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4962): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0036 | 0/0 | 4969 | 2 | 0 | 1 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4964): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0038 | 0/0 | 4944 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4939): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0039 | 0/0 | 4959 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4954): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0040 | 1/0 | 4957 | 1 | 0 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4952): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0041 | 0/0 | 4956 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4951): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0042 | 0/0 | 4958 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4953): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0044 | 0/0 | 4962 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4957): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0046 | 0/0 | 4964 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4959): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0047 | 0/0 | 4956 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4951): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0051 | 0/0 | 4955 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4950): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0054 | 0/0 | 4967 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4962): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0056 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4964): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0057 | 0/0 | 4971 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4966): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0058 | 0/0 | 4971 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4966): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0065 | 0/0 | 4956 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4951): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0066 | 0/0 | 4960 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4955): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0067 | 0/0 | 4957 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4952): Show |
chr3 | 72991811 | 73074198 |
| a0001c0001t0068 | 0/0 | 4959 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4954): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0003 | 0/0 | 4963 | 27 | 0 | 2 | 21 | 0 | 4 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4958): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0006 | 0/0 | 4969 | 11 | 0 | 1 | 8 | 1 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4964): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0010 | 0/0 | 4965 | 8 | 0 | 0 | 6 | 1 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4960): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0011 | 0/0 | 4967 | 8 | 0 | 0 | 6 | 0 | 2 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4962): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0013 | 0/0 | 4965 | 5 | 5 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4960): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0015 | 0/0 | 4962 | 6 | 0 | 0 | 6 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4957): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0019 | 0/0 | 4961 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4956): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0020 | 0/0 | 4972 | 4 | 0 | 0 | 4 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4967): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0023 | 0/0 | 4971 | 3 | 0 | 0 | 1 | 0 | 2 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4966): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0027 | 0/0 | 4964 | 3 | 0 | 0 | 0 | 0 | 3 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4959): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0030 | 0/0 | 4965 | 2 | 2 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4960): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0031 | 0/0 | 4973 | 2 | 0 | 0 | 1 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4968): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0032 | 0/0 | 4977 | 2 | 0 | 2 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4972): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0033 | 0/0 | 4957 | 2 | 2 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4952): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0037 | 0/0 | 4971 | 2 | 0 | 0 | 1 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4966): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0049 | 0/0 | 4975 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4970): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0050 | 0/0 | 4975 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4970): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0052 | 0/0 | 4963 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4958): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0053 | 0/0 | 4968 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4963): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0055 | 0/0 | 4969 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4964): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0059 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4969): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0060 | 0/0 | 4976 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4971): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0061 | 0/0 | 4978 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4973): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0062 | 0/0 | 4982 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4977): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0063 | 0/0 | 4966 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4961): Show |
chr3 | 72991811 | 73074198 |
| a0001c0002t0064 | 0/0 | 4972 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4967): Show |
chr3 | 72991811 | 73074198 |
| a0001c0003t0012 | 0/0 | 4963 | 7 | 7 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4958): Show |
chr3 | 72991811 | 73074198 |
| a0001c0003t0043 | 0/0 | 4960 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4955): Show |
chr3 | 72991811 | 73074198 |
| a0001c0003t0045 | 0/0 | 4962 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4957): Show |
chr3 | 72991811 | 73074198 |
| a0001c0003t0048 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4964): Show |
chr3 | 72991811 | 73074198 |
| a0001c0010t0001 | 0/0 | 4956 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4951): Show |
chr3 | 72991811 | 73074198 |
| a0002c0007t0003 | 0/0 | 4951 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4946): Show |
chr3 | 72991811 | 73074198 |
| a0002c0011t0001 | 0/0 | 4944 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4939): Show |
chr3 | 72991811 | 73074198 |
| a0003c0004t0013 | 0/0 | 4965 | 2 | 2 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4960): Show |
chr3 | 72991811 | 73074198 |
| a0004c0005t0017 | 0/0 | 4959 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4954): Show |
chr3 | 72991811 | 73074198 |
| a0005c0006t0026 | 0/0 | 4965 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4960): Show |
chr3 | 72991811 | 73074198 |
| a0006c0009t0018 | 0/0 | 4961 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4956): Show |
chr3 | 72991811 | 73074198 |
| a0007c0008t0001 | 0/0 | 4956 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | GGGCG others(4951): Show |
chr3 | 72991811 | 73074198 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0004g0181 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0005g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0007g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0007g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0007g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0007g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0007g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0007g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0007g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0007g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0008g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0008g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0008g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0008g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0008g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0008g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0008g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0008g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0008g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0008g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0009g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0009g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0009g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0009g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0009g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0009g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0009g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0014g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0014g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0014g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0014g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0014g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0014g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0016g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0016g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0016g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0016g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0016g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0017g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0017g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0017g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0018g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0018g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0018g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0018g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0019g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0019g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0019g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0019g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0021g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0021g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0021g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0022g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0022g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0022g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0024g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0024g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0024g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0025g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0025g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0025g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0026g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0026g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0028g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0028g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0029g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0029g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0034g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0034g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0035g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0035g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0036g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0036g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0038g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0039g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0040g0324 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0041g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0042g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0044g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0046g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0047g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0051g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0054g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0056g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0057g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0058g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0065g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0066g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0067g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0001t0068g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0006g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0006g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0006g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0006g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0006g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0006g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0006g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0010g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0010g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0010g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0010g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0010g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0010g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0010g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0010g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0011g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0011g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0011g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0011g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0011g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0011g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0011g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0011g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0013g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0013g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0013g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0013g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0013g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0015g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0015g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0015g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0015g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0015g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0015g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0019g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0020g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0020g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0020g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0020g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0023g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0023g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0023g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0027g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0027g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0027g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0030g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0030g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0031g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0031g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0032g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0032g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0033g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0033g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0037g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0037g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0049g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0050g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0052g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0053g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0055g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0059g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0060g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0061g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0062g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0063g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0002t0064g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0003t0012g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0003t0012g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0003t0012g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0003t0012g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0003t0012g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0003t0012g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0003t0012g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0003t0043g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0003t0045g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0003t0048g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0001c0010t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0002c0007t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0002c0011t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0003c0004t0013g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0003c0004t0013g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0004c0005t0017g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0004c0005t0017g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0005c0006t0026g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0006c0009t0018g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| a0007c0008t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0267 | EUR | GBR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00099 | hp2 | a0001 | c0002 | t0006 | g0104 | EUR | GBR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0139 | EUR | GBR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | GBR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00423 | hp1 | a0001 | c0002 | t0010 | g0050 | EAS | CHS | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00438 | hp1 | a0001 | c0001 | t0029 | g0315 | EAS | CHS | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | CHS | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00597 | hp1 | a0001 | c0002 | t0020 | g0042 | EAS | CHS | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00609 | hp1 | a0002 | c0011 | t0001 | g0313 | EAS | CHS | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | CHS | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00621 | hp1 | a0001 | c0002 | t0010 | g0093 | EAS | CHS | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00621 | hp2 | a0001 | c0001 | t0047 | g0291 | EAS | CHS | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00639 | hp1 | a0001 | c0002 | t0061 | g0041 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0166 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00738 | hp1 | a0001 | c0002 | t0003 | g0014 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0275 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG00741 | hp2 | a0001 | c0001 | t0008 | g0137 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01069 | hp1 | a0001 | c0001 | t0008 | g0158 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01069 | hp2 | a0001 | c0002 | t0032 | g0046 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01071 | hp2 | a0001 | c0001 | t0008 | g0179 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0142 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01099 | hp2 | a0001 | c0001 | t0036 | g0192 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01109 | hp1 | a0001 | c0001 | t0057 | g0135 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01109 | hp2 | a0001 | c0001 | t0014 | g0007 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01192 | hp1 | a0001 | c0002 | t0032 | g0019 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01243 | hp1 | a0001 | c0001 | t0018 | g0193 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01243 | hp2 | a0001 | c0002 | t0003 | g0077 | AMR | PUR | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01255 | hp1 | a0001 | c0001 | t0026 | g0185 | AMR | CLM | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0127 | AMR | CLM | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01346 | hp1 | a0001 | c0002 | t0006 | g0108 | AMR | CLM | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0284 | AMR | CLM | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | CLM | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0323 | AMR | CLM | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0160 | EUR | IBS | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0325 | EUR | IBS | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01884 | hp1 | a0001 | c0002 | t0033 | g0099 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01884 | hp2 | a0001 | c0001 | t0018 | g0198 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01891 | hp1 | a0003 | c0004 | t0013 | g0353 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0232 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0308 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0134 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0130 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0298 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01952 | hp2 | a0001 | c0001 | t0058 | g0182 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0129 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0247 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0131 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01993 | hp2 | a0001 | c0002 | t0053 | g0219 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02015 | hp1 | a0001 | c0001 | t0041 | g0259 | EAS | KHV | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | KHV | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | KHV | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02027 | hp2 | a0001 | c0002 | t0019 | g0087 | EAS | KHV | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0128 | EAS | KHV | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02040 | hp2 | a0001 | c0001 | t0007 | g0183 | EAS | KHV | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02055 | hp2 | a0001 | c0002 | t0030 | g0096 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02080 | hp1 | a0001 | c0001 | t0068 | g0330 | EAS | KHV | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02080 | hp2 | a0001 | c0002 | t0062 | g0039 | EAS | KHV | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02083 | hp1 | a0001 | c0001 | t0014 | g0332 | EAS | KHV | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02083 | hp2 | a0001 | c0001 | t0008 | g0147 | EAS | KHV | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | KHV | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02129 | hp2 | a0001 | c0001 | t0008 | g0106 | EAS | KHV | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0143 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02145 | hp2 | a0001 | c0001 | t0009 | g0110 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CDX | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02155 | hp2 | a0001 | c0002 | t0003 | g0073 | EAS | CDX | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02257 | hp1 | a0001 | c0001 | t0024 | g0140 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02257 | hp2 | a0001 | c0001 | t0009 | g0002 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02258 | hp1 | a0001 | c0001 | t0066 | g0196 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0116 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02280 | hp1 | a0001 | c0003 | t0043 | g0201 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02280 | hp2 | a0001 | c0001 | t0016 | g0208 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02293 | hp1 | a0001 | c0001 | t0008 | g0138 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02451 | hp1 | a0001 | c0001 | t0009 | g0118 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02572 | hp2 | a0001 | c0001 | t0019 | g0112 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02602 | hp1 | a0001 | c0001 | t0036 | g0150 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0305 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02615 | hp1 | a0001 | c0001 | t0018 | g0195 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02615 | hp2 | a0001 | c0001 | t0044 | g0214 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0172 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02622 | hp2 | a0001 | c0001 | t0019 | g0113 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02647 | hp1 | a0001 | c0001 | t0021 | g0204 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02647 | hp2 | a0001 | c0003 | t0012 | g0211 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02683 | hp1 | a0001 | c0002 | t0003 | g0091 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02683 | hp2 | a0001 | c0002 | t0006 | g0049 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0322 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02698 | hp2 | a0001 | c0002 | t0027 | g0075 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02717 | hp2 | a0001 | c0001 | t0016 | g0207 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0169 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02723 | hp2 | a0001 | c0003 | t0012 | g0350 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0221 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02735 | hp2 | a0001 | c0001 | t0025 | g0178 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0318 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02738 | hp2 | a0001 | c0002 | t0027 | g0086 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02809 | hp1 | a0001 | c0002 | t0013 | g0101 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0191 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02818 | hp1 | a0001 | c0001 | t0014 | g0008 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0171 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0165 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02886 | hp2 | a0001 | c0003 | t0012 | g0212 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02895 | hp1 | a0001 | c0001 | t0014 | g0010 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02895 | hp2 | a0001 | c0001 | t0034 | g0145 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02922 | hp1 | a0001 | c0002 | t0013 | g0097 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02922 | hp2 | a0001 | c0001 | t0016 | g0206 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0117 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02965 | hp2 | a0001 | c0003 | t0012 | g0348 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02970 | hp2 | a0001 | c0001 | t0016 | g0205 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02976 | hp1 | a0001 | c0002 | t0030 | g0098 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02976 | hp2 | a0001 | c0002 | t0033 | g0100 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0338 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03017 | hp2 | a0001 | c0002 | t0003 | g0061 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03041 | hp1 | a0001 | c0001 | t0024 | g0154 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03041 | hp2 | a0001 | c0001 | t0021 | g0200 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03098 | hp1 | a0001 | c0001 | t0021 | g0203 | AFR | MSL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | MSL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03130 | hp1 | a0001 | c0001 | t0035 | g0148 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03130 | hp2 | a0005 | c0006 | t0026 | g0173 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03195 | hp1 | a0001 | c0001 | t0009 | g0002 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03209 | hp1 | a0001 | c0001 | t0051 | g0199 | AFR | MSL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0170 | AFR | MSL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03225 | hp1 | a0006 | c0009 | t0018 | g0197 | AFR | MSL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03225 | hp2 | a0001 | c0002 | t0013 | g0094 | AFR | MSL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03239 | hp2 | a0001 | c0002 | t0023 | g0085 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03453 | hp1 | a0003 | c0004 | t0013 | g0352 | AFR | MSL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03453 | hp2 | a0001 | c0002 | t0013 | g0102 | AFR | MSL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03486 | hp1 | a0001 | c0001 | t0018 | g0194 | AFR | MSL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0189 | AFR | MSL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03490 | hp1 | a0001 | c0001 | t0007 | g0184 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0268 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03491 | hp1 | a0001 | c0002 | t0023 | g0103 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0151 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03516 | hp1 | a0001 | c0001 | t0024 | g0153 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03516 | hp2 | a0001 | c0010 | t0001 | g0334 | AFR | ESN | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03540 | hp2 | a0001 | c0003 | t0045 | g0202 | AFR | GWD | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03654 | hp1 | a0001 | c0001 | t0054 | g0175 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03654 | hp2 | a0001 | c0001 | t0034 | g0144 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03688 | hp1 | a0001 | c0001 | t0028 | g0273 | SAS | STU | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0161 | SAS | STU | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03704 | hp1 | a0001 | c0002 | t0037 | g0074 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03704 | hp2 | a0001 | c0002 | t0011 | g0062 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03710 | hp1 | a0001 | c0001 | t0028 | g0346 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03710 | hp2 | a0001 | c0002 | t0003 | g0063 | SAS | PJL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03831 | hp1 | a0001 | c0001 | t0008 | g0162 | SAS | BEB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03831 | hp2 | a0001 | c0001 | t0017 | g0320 | SAS | BEB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03834 | hp1 | a0001 | c0001 | t0067 | g0296 | SAS | BEB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03834 | hp2 | a0001 | c0002 | t0011 | g0022 | SAS | BEB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03942 | hp1 | a0001 | c0002 | t0003 | g0092 | SAS | BEB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0285 | SAS | BEB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG04115 | hp1 | a0001 | c0002 | t0063 | g0107 | SAS | STU | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG04115 | hp2 | a0001 | c0001 | t0025 | g0176 | SAS | STU | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG04184 | hp1 | a0001 | c0001 | t0007 | g0187 | SAS | BEB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG04184 | hp2 | a0001 | c0002 | t0027 | g0053 | SAS | BEB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG04199 | hp1 | a0001 | c0001 | t0008 | g0136 | SAS | STU | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG04199 | hp2 | a0001 | c0001 | t0026 | g0174 | SAS | STU | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG04204 | hp1 | a0001 | c0002 | t0031 | g0018 | SAS | STU | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG04204 | hp2 | a0001 | c0002 | t0055 | g0354 | SAS | STU | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18522 | hp1 | a0001 | c0001 | t0056 | g0186 | AFR | YRI | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | YRI | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | CHB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18612 | hp2 | a0001 | c0002 | t0010 | g0083 | EAS | CHB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | CHB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18906 | hp1 | a0001 | c0001 | t0014 | g0006 | AFR | YRI | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | YRI | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18941 | hp1 | a0001 | c0002 | t0003 | g0088 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18941 | hp2 | a0001 | c0001 | t0005 | g0260 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18942 | hp1 | a0001 | c0002 | t0006 | g0043 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18943 | hp1 | a0001 | c0001 | t0007 | g0141 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18943 | hp2 | a0001 | c0002 | t0059 | g0044 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18944 | hp2 | a0001 | c0002 | t0010 | g0012 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18945 | hp2 | a0001 | c0002 | t0060 | g0040 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18946 | hp1 | a0001 | c0001 | t0022 | g0244 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18946 | hp2 | a0001 | c0001 | t0065 | g0316 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18948 | hp1 | a0001 | c0001 | t0005 | g0258 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18948 | hp2 | a0001 | c0002 | t0011 | g0030 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18950 | hp1 | a0001 | c0001 | t0017 | g0347 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18950 | hp2 | a0001 | c0001 | t0005 | g0242 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18951 | hp1 | a0001 | c0002 | t0006 | g0036 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18951 | hp2 | a0001 | c0001 | t0005 | g0264 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18953 | hp2 | a0001 | c0002 | t0015 | g0090 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18954 | hp2 | a0001 | c0002 | t0003 | g0059 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0234 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18956 | hp2 | a0001 | c0002 | t0023 | g0048 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18959 | hp1 | a0001 | c0002 | t0006 | g0035 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18959 | hp2 | a0001 | c0002 | t0015 | g0033 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18960 | hp2 | a0001 | c0001 | t0007 | g0146 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18961 | hp1 | a0001 | c0001 | t0029 | g0337 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18961 | hp2 | a0001 | c0002 | t0003 | g0025 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18963 | hp2 | a0004 | c0005 | t0017 | g0345 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18964 | hp2 | a0001 | c0002 | t0037 | g0072 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18965 | hp2 | a0001 | c0002 | t0020 | g0047 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18966 | hp2 | a0001 | c0002 | t0050 | g0017 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18969 | hp1 | a0001 | c0001 | t0005 | g0309 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18969 | hp2 | a0001 | c0002 | t0052 | g0076 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18970 | hp1 | a0001 | c0002 | t0011 | g0056 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18970 | hp2 | a0001 | c0001 | t0014 | g0329 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18971 | hp1 | a0004 | c0005 | t0017 | g0344 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18972 | hp2 | a0001 | c0002 | t0011 | g0015 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18973 | hp1 | a0001 | c0002 | t0003 | g0026 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18974 | hp1 | a0001 | c0001 | t0022 | g0245 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18978 | hp2 | a0002 | c0007 | t0003 | g0013 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18979 | hp1 | a0001 | c0002 | t0003 | g0028 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0319 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18981 | hp1 | a0001 | c0002 | t0003 | g0089 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18982 | hp1 | a0001 | c0002 | t0015 | g0068 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18983 | hp1 | a0001 | c0002 | t0006 | g0037 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18984 | hp2 | a0001 | c0002 | t0020 | g0034 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18985 | hp2 | a0001 | c0002 | t0006 | g0021 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18990 | hp1 | a0001 | c0002 | t0031 | g0080 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18994 | hp1 | a0001 | c0001 | t0038 | g0279 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18994 | hp2 | a0001 | c0002 | t0015 | g0023 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18995 | hp2 | a0001 | c0002 | t0011 | g0071 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18998 | hp1 | a0001 | c0002 | t0003 | g0064 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18998 | hp2 | a0007 | c0008 | t0001 | g0283 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA18999 | hp2 | a0001 | c0002 | t0003 | g0067 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19000 | hp1 | a0001 | c0002 | t0003 | g0081 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19002 | hp1 | a0001 | c0002 | t0015 | g0060 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19002 | hp2 | a0001 | c0001 | t0042 | g0269 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19004 | hp1 | a0001 | c0002 | t0003 | g0027 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19005 | hp1 | a0001 | c0002 | t0003 | g0070 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19006 | hp2 | a0001 | c0002 | t0003 | g0055 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19007 | hp2 | a0001 | c0002 | t0003 | g0069 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19012 | hp2 | a0001 | c0002 | t0011 | g0029 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19030 | hp1 | a0001 | c0002 | t0013 | g0095 | AFR | LWK | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19030 | hp2 | a0001 | c0001 | t0009 | g0111 | AFR | LWK | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | LWK | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | LWK | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19055 | hp1 | a0001 | c0002 | t0064 | g0032 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19056 | hp1 | a0001 | c0002 | t0015 | g0057 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19064 | hp1 | a0001 | c0002 | t0006 | g0020 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19065 | hp1 | a0001 | c0002 | t0003 | g0078 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19065 | hp2 | a0001 | c0001 | t0005 | g0227 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19066 | hp1 | a0001 | c0002 | t0003 | g0066 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19067 | hp1 | a0001 | c0001 | t0017 | g0253 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19067 | hp2 | a0001 | c0002 | t0003 | g0084 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19068 | hp1 | a0001 | c0001 | t0007 | g0133 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19070 | hp1 | a0001 | c0002 | t0020 | g0045 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19070 | hp2 | a0001 | c0001 | t0005 | g0307 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19074 | hp2 | a0001 | c0002 | t0006 | g0038 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19076 | hp1 | a0001 | c0002 | t0006 | g0031 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19076 | hp2 | a0001 | c0001 | t0022 | g0343 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19077 | hp1 | a0001 | c0002 | t0010 | g0011 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19077 | hp2 | a0001 | c0001 | t0005 | g0262 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19081 | hp1 | a0001 | c0002 | t0003 | g0051 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19081 | hp2 | a0001 | c0001 | t0039 | g0312 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19082 | hp1 | a0001 | c0002 | t0011 | g0016 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19083 | hp1 | a0001 | c0002 | t0003 | g0082 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19084 | hp2 | a0001 | c0002 | t0010 | g0065 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19085 | hp1 | a0001 | c0002 | t0003 | g0024 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19087 | hp1 | a0001 | c0002 | t0003 | g0058 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19088 | hp1 | a0001 | c0001 | t0005 | g0299 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0159 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19091 | hp2 | a0001 | c0001 | t0008 | g0132 | EAS | JPT | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19240 | hp1 | a0001 | c0002 | t0049 | g0052 | AFR | YRI | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA19240 | hp2 | a0001 | c0003 | t0012 | g0351 | AFR | YRI | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA20129 | hp1 | a0001 | c0003 | t0012 | g0209 | AFR | ASW | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0168 | AFR | ASW | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA20805 | hp1 | a0001 | c0002 | t0010 | g0079 | EUR | TSI | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA20805 | hp2 | a0001 | c0001 | t0008 | g0152 | EUR | TSI | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA20905 | hp1 | a0001 | c0002 | t0010 | g0054 | SAS | GIH | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA20905 | hp2 | a0001 | c0001 | t0025 | g0177 | SAS | GIH | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0156 | AMR | CLM | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | CLM | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02109 | hp1 | a0001 | c0003 | t0048 | g0215 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02109 | hp2 | a0001 | c0001 | t0009 | g0119 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02486 | hp1 | a0001 | c0001 | t0035 | g0149 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0188 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0163 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG02559 | hp2 | a0001 | c0003 | t0012 | g0349 | AFR | ACB | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0164 | AFR | MSL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG03471 | hp2 | a0001 | c0001 | t0019 | g0121 | AFR | MSL | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0190 | AFR | USA | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| HG06807 | hp2 | a0001 | c0001 | t0046 | g0213 | AFR | USA | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0167 | AFR | USA | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA20300 | hp2 | a0001 | c0001 | t0016 | g0109 | AFR | USA | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0326 | AFR | LWK | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| NA21309 | hp2 | a0001 | c0001 | t0019 | g0120 | AFR | LWK | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0181 | REF | REF | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0040 | g0324 | REF | REF | PPP4R2_chr3_72991811_73074198 | PPP4R2 | chr3 | 72991811 | 73074198 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:72998089 | G | A | 1 | a0005 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.47G>A | p.Arg16Lys | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/9 | 274/4957 | 47/1254 | 16/417 | chr3 | 72998089 | |||
| chr3:73064029 | C | T | 1 | a0004 | 2 | NA18963.hp2 NA18971.hp1 |
missense_variant | MODERATE | c.521C>T | p.Pro174Leu | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 7/9 | 748/4957 | 521/1254 | 174/417 | chr3 | 73064029 | |||
| chr3:73065004 | C | A | 1 | a0007 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.791C>A | p.Thr264Asn | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 8/9 | 1018/4957 | 791/1254 | 264/417 | chr3 | 73065004 | |||
| chr3:73065103 | CAGAAGAG others(5): Show |
C | 1 | a0002 | 2 | HG00609.hp1 NA18978.hp2 |
disruptive_inframe_deletion | MODERATE | c.906_917delAGAGGATG others(4): Show |
p.Glu303_Glu306del | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 8/9 | 1133/4957 | 906/1254 | 302/417 | INFO_REALIGN_3_PRIME | chr3 | 73065103 | ||
| chr3:73065399 | T | G | 1 | a0006 | 1 | HG03225.hp1 | missense_variant&splice_region_variant | MODERATE | c.931T>G | p.Ser311Ala | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 1158/4957 | 931/1254 | 311/417 | chr3 | 73065399 | |||
| chr3:73065589 | C | A | 1 | a0003 | 2 | HG01891.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.1121C>A | p.Ser374Tyr | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 1348/4957 | 1121/1254 | 374/417 | chr3 | 73065589 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:73064036 | A | G | 1 | a0001c0003 | 10 | HG02109.hp1 HG02280.hp1 HG02559.hp2 others(7): Show |
synonymous_variant | LOW | c.528A>G | p.Pro176Pro | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 7/9 | 755/4957 | 528/1254 | 176/417 | chr3 | 73064036 | |||
| chr3:73064852 | T | C | 2 | a0001c0002 a0002c0007 |
98 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(95): Show |
splice_region_variant&synonymous_variant | LOW | c.639T>C | p.Ser213Ser | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 8/9 | 866/4957 | 639/1254 | 213/417 | chr3 | 73064852 | |||
| chr3:73065545 | A | G | 1 | a0001c0010 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.1077A>G | p.Leu359Leu | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 1304/4957 | 1077/1254 | 359/417 | chr3 | 73065545 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:72996876 | C | T | 1 | a0001c0001t0068 | 1 | HG02080.hp1 | 5_prime_UTR_variant | MODIFIER | c.-162C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/9 | 162 | chr3 | 72996876 | ||||||
| chr3:72996911 | C | G | 1 | a0001c0001t0067 | 1 | HG03834.hp1 | 5_prime_UTR_variant | MODIFIER | c.-127C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/9 | 127 | chr3 | 72996911 | ||||||
| chr3:72996912 | C | T | 1 | a0001c0001t0066 | 1 | HG02258.hp1 | 5_prime_UTR_variant | MODIFIER | c.-126C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/9 | 126 | chr3 | 72996912 | ||||||
| chr3:73065784 | A | G | 1 | a0001c0001t0065 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*62A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 62 | chr3 | 73065784 | ||||||
| chr3:73065839 | A | G | 1 | a0001c0002t0064 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*117A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 117 | chr3 | 73065839 | ||||||
| chr3:73065859 | C | G | 1 | a0001c0001t0066 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*137C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 137 | chr3 | 73065859 | ||||||
| chr3:73065979 | A | AT | 41 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(38): Show |
175 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*272dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 273 | INFO_REALIGN_3_PRIME | chr3 | 73065979 | |||||
| chr3:73065979 | A | ATT | 9 | a0001c0002t0015 a0001c0002t0020 a0001c0002t0027 others(6): Show |
19 | HG00597.hp1 HG00639.hp1 HG02080.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*271_*272dupTT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 273 | INFO_REALIGN_3_PRIME | chr3 | 73065979 | |||||
| chr3:73066024 | A | G | 49 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(46): Show |
187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*302A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 302 | chr3 | 73066024 | ||||||
| chr3:73066079 | G | T | 1 | a0001c0001t0047 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*357G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 357 | chr3 | 73066079 | ||||||
| chr3:73066231 | T | TATAC | 3 | a0001c0001t0018 a0001c0001t0066 a0006c0009t0018 |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*517_*520dupCATA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 521 | INFO_REALIGN_3_PRIME | chr3 | 73066231 | |||||
| chr3:73066239 | C | CAT | 5 | a0001c0001t0005 a0001c0001t0017 a0001c0001t0042 others(2): Show |
23 | HG00741.hp1 HG01346.hp2 HG01891.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*539_*540dupTA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 541 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | |||||
| chr3:73066239 | C | CATACATA others(1): Show |
3 | a0001c0002t0013 a0001c0002t0030 a0003c0004t0013 |
9 | HG01891.hp1 HG02055.hp2 HG02809.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*520_*521insCATATA others(2): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 521 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | |||||
| chr3:73066239 | C | CATACATA others(5): Show |
1 | a0001c0002t0006 | 11 | HG00099.hp2 HG01346.hp1 HG02683.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*520_*521insCATATA others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 521 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | |||||
| chr3:73066239 | C | CATACATA others(7): Show |
3 | a0001c0002t0020 a0001c0002t0023 a0001c0002t0064 |
8 | HG00597.hp1 HG03239.hp2 HG03491.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*520_*521insCATATA others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 521 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | |||||
| chr3:73066239 | C | CATACATA others(9): Show |
3 | a0001c0002t0031 a0001c0002t0049 a0001c0002t0059 |
4 | HG04204.hp1 NA18943.hp2 NA18990.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*520_*521insCATATA others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 521 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | |||||
| chr3:73066239 | C | CATACATA others(11): Show |
2 | a0001c0002t0050 a0001c0002t0060 |
2 | NA18945.hp2 NA18966.hp2 |
3_prime_UTR_variant | MODIFIER | c.*520_*521insCATATA others(12): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 521 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | |||||
| chr3:73066239 | C | CATACATA others(13): Show |
2 | a0001c0002t0032 a0001c0002t0061 |
3 | HG00639.hp1 HG01069.hp2 HG01192.hp1 |
3_prime_UTR_variant | MODIFIER | c.*520_*521insCATATA others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 521 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | |||||
| chr3:73066239 | C | CATACATA others(17): Show |
1 | a0001c0002t0062 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*520_*521insCATATA others(18): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 521 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | |||||
| chr3:73066239 | C | CATAT | 9 | a0001c0001t0009 a0001c0001t0014 a0001c0001t0019 others(6): Show |
30 | HG01109.hp2 HG02027.hp2 HG02083.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*537_*540dupTATA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 541 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | |||||
| chr3:73066239 | C | CATATAT | 9 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0024 others(6): Show |
71 | HG00140.hp1 HG00735.hp2 HG00738.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*535_*540dupTATATA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 541 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | |||||
| chr3:73066239 | C | CATATATA others(1): Show |
7 | a0001c0001t0007 a0001c0001t0025 a0001c0001t0026 others(4): Show |
28 | HG00423.hp1 HG00621.hp1 HG01255.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*533_*540dupTATATA others(2): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 541 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | |||||
| chr3:73066239 | C | CATATATA others(3): Show |
4 | a0001c0001t0008 a0001c0001t0054 a0001c0002t0011 others(1): Show |
20 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*531_*540dupTATATA others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 541 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | |||||
| chr3:73066239 | C | CATATATA others(5): Show |
4 | a0001c0001t0036 a0001c0001t0056 a0001c0002t0055 others(1): Show |
5 | HG01099.hp2 HG02109.hp1 HG02602.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*529_*540dupTATATA others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 541 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | |||||
| chr3:73066239 | C | CATATATA others(7): Show |
3 | a0001c0001t0057 a0001c0001t0058 a0001c0002t0037 |
4 | HG01109.hp1 HG01952.hp2 HG03704.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*527_*540dupTATATA others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 541 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | |||||
| chr3:73066239 | CAT | C | 2 | a0001c0001t0028 a0001c0001t0051 |
3 | HG03209.hp1 HG03688.hp1 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*539_*540delTA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 539 | INFO_REALIGN_3_PRIME | chr3 | 73066239 | |||||
| chr3:73066635 | T | C | 49 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(46): Show |
187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*913T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 913 | chr3 | 73066635 | ||||||
| chr3:73066693 | C | G | 1 | a0001c0001t0022 | 3 | NA18946.hp1 NA18974.hp1 NA19076.hp2 |
3_prime_UTR_variant | MODIFIER | c.*971C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 971 | chr3 | 73066693 | ||||||
| chr3:73067221 | G | T | 3 | a0001c0001t0018 a0001c0001t0066 a0006c0009t0018 |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1499G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 1499 | chr3 | 73067221 | ||||||
| chr3:73067286 | C | G | 29 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(26): Show |
140 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*1564C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 1564 | chr3 | 73067286 | ||||||
| chr3:73067377 | A | G | 3 | a0001c0001t0016 a0001c0001t0044 a0001c0001t0046 |
7 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1655A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 1655 | chr3 | 73067377 | ||||||
| chr3:73067390 | C | T | 4 | a0001c0001t0016 a0001c0001t0021 a0001c0001t0044 others(1): Show |
10 | HG02280.hp2 HG02615.hp2 HG02647.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1668C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 1668 | chr3 | 73067390 | ||||||
| chr3:73067439 | GACTGTCA others(5): Show |
G | 1 | a0001c0001t0038 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1720_*1731delTGTC others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 1720 | INFO_REALIGN_3_PRIME | chr3 | 73067439 | |||||
| chr3:73067565 | A | T | 53 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(50): Show |
197 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*1843A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 1843 | chr3 | 73067565 | ||||||
| chr3:73067693 | T | G | 3 | a0001c0001t0018 a0001c0001t0066 a0006c0009t0018 |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1971T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 1971 | chr3 | 73067693 | ||||||
| chr3:73068369 | G | GAT | 7 | a0001c0001t0024 a0001c0001t0035 a0001c0001t0039 others(4): Show |
10 | HG02257.hp1 HG02486.hp1 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2662_*2663dupAT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 2664 | INFO_REALIGN_3_PRIME | chr3 | 73068369 | |||||
| chr3:73068371 | T | G | 1 | a0001c0002t0030 | 2 | HG02055.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2649T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 2649 | chr3 | 73068371 | ||||||
| chr3:73068372 | A | G | 1 | a0001c0001t0041 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2650A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 2650 | chr3 | 73068372 | ||||||
| chr3:73068495 | A | G | 1 | a0001c0001t0054 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2773A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 2773 | chr3 | 73068495 | ||||||
| chr3:73068572 | T | C | 1 | a0001c0001t0042 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2850T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 2850 | chr3 | 73068572 | ||||||
| chr3:73068684 | C | T | 14 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(11): Show |
64 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*2962C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 2962 | chr3 | 73068684 | ||||||
| chr3:73068803 | A | G | 1 | a0001c0001t0009 | 8 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3081A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 3081 | chr3 | 73068803 | ||||||
| chr3:73068830 | T | C | 2 | a0001c0001t0025 a0001c0001t0054 |
4 | HG02735.hp2 HG03654.hp1 HG04115.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3108T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 3108 | chr3 | 73068830 | ||||||
| chr3:73068854 | C | A | 1 | a0001c0001t0029 | 2 | HG00438.hp1 NA18961.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3132C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 3132 | chr3 | 73068854 | ||||||
| chr3:73068932 | AG | A | 68 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(65): Show |
307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*3212delG | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 3212 | INFO_REALIGN_3_PRIME | chr3 | 73068932 | |||||
| chr3:73069070 | C | A | 73 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(70): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
3_prime_UTR_variant | MODIFIER | c.*3348C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 9/9 | 3348 | chr3 | 73069070 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:72997155 | C | G | 1 | a0001c0002t0055g0354 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.34+84C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997155 | |||||||
| chr3:72997214 | C | G | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.34+143C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997214 | |||||||
| chr3:72997221 | C | T | 4 | a0001c0003t0012g0348 a0001c0003t0012g0349 a0001c0003t0012g0350 others(1): Show |
4 | HG02559.hp2 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+150C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997221 | |||||||
| chr3:72997275 | C | T | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.34+204C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997275 | |||||||
| chr3:72997340 | C | G | 1 | a0001c0001t0017g0347 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.34+269C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997340 | |||||||
| chr3:72997357 | G | C | 218 | a0001c0001t0001g0003 a0001c0001t0001g0122 a0001c0001t0001g0123 others(215): Show |
220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.34+286G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997357 | |||||||
| chr3:72997376 | C | T | 1 | a0001c0001t0028g0346 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.34+305C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997376 | |||||||
| chr3:72997382 | C | A | 1 | a0001c0001t0001g0216 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.34+311C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997382 | |||||||
| chr3:72997389 | C | T | 2 | a0004c0005t0017g0344 a0004c0005t0017g0345 |
2 | NA18963.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.34+318C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997389 | |||||||
| chr3:72997393 | T | C | 196 | a0001c0001t0001g0003 a0001c0001t0001g0122 a0001c0001t0001g0123 others(193): Show |
198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.34+322T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997393 | |||||||
| chr3:72997410 | C | T | 92 | a0001c0001t0001g0003 a0001c0001t0001g0122 a0001c0001t0001g0123 others(89): Show |
94 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.34+339C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997410 | |||||||
| chr3:72997530 | C | T | 1 | a0001c0003t0048g0215 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.34+459C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997530 | |||||||
| chr3:72997580 | C | T | 1 | a0001c0002t0006g0108 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.35-497C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997580 | |||||||
| chr3:72997656 | T | C | 1 | a0001c0001t0016g0109 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.35-421T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997656 | |||||||
| chr3:72997843 | A | G | 1 | a0001c0001t0051g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.35-234A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997843 | |||||||
| chr3:72997993 | A | G | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.35-84A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72997993 | |||||||
| chr3:72998008 | A | G | 1 | a0001c0001t0036g0192 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.35-69A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 1/8 | chr3 | 72998008 | |||||||
| chr3:72998177 | T | C | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+19T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72998177 | |||||||
| chr3:72998326 | A | G | 11 | a0001c0001t0001g0210 a0001c0003t0012g0209 a0001c0003t0012g0211 others(8): Show |
11 | HG02109.hp1 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.116+168A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72998326 | |||||||
| chr3:72998714 | A | G | 1 | a0001c0001t0022g0343 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.116+556A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72998714 | |||||||
| chr3:72998874 | ACTT | A | 3 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0001c0001t0001g0342 |
3 | HG02451.hp2 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.116+720_116+722del others(3): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 72998874 | ||||||
| chr3:72998886 | A | C | 67 | a0001c0001t0003g0129 a0001c0001t0004g0127 a0001c0001t0004g0128 others(64): Show |
67 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.116+728A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72998886 | |||||||
| chr3:72999022 | A | G | 97 | a0001c0001t0002g0105 a0001c0002t0003g0014 a0001c0002t0003g0024 others(94): Show |
97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.116+864A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72999022 | |||||||
| chr3:72999032 | T | A | 1 | a0001c0001t0002g0217 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.116+874T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72999032 | |||||||
| chr3:72999194 | G | C | 186 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(183): Show |
187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+1036G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72999194 | |||||||
| chr3:72999210 | G | C | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+1052G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72999210 | |||||||
| chr3:72999552 | C | T | 1 | a0001c0001t0019g0121 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.116+1394C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72999552 | |||||||
| chr3:72999697 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.116+1539T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72999697 | |||||||
| chr3:72999709 | T | C | 1 | a0001c0001t0002g0217 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.116+1551T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72999709 | |||||||
| chr3:72999764 | C | A | 1 | a0001c0001t0018g0193 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.116+1606C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72999764 | |||||||
| chr3:72999771 | G | A | 1 | a0001c0001t0021g0200 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.116+1613G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72999771 | |||||||
| chr3:72999791 | G | A | 1 | a0001c0002t0053g0219 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.116+1633G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72999791 | |||||||
| chr3:72999842 | A | G | 15 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(12): Show |
16 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.116+1684A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72999842 | |||||||
| chr3:72999934 | A | G | 1 | a0001c0001t0051g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.116+1776A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 72999934 | |||||||
| chr3:73000029 | A | G | 6 | a0001c0001t0001g0339 a0001c0001t0005g0009 a0001c0001t0014g0006 others(3): Show |
6 | HG01109.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+1871A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73000029 | |||||||
| chr3:73000142 | T | G | 5 | a0001c0001t0005g0009 a0001c0001t0014g0006 a0001c0001t0014g0007 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.116+1984T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73000142 | |||||||
| chr3:73000282 | C | A | 96 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(93): Show |
96 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.116+2124C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73000282 | |||||||
| chr3:73000400 | G | T | 1 | a0001c0001t0007g0190 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.116+2242G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73000400 | |||||||
| chr3:73000593 | T | C | 1 | a0001c0001t0004g0127 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.116+2435T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73000593 | |||||||
| chr3:73000604 | C | G | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+2446C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73000604 | |||||||
| chr3:73000755 | T | C | 2 | a0001c0002t0010g0011 a0001c0002t0010g0012 |
2 | NA18944.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.116+2597T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73000755 | |||||||
| chr3:73000857 | A | G | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+2699A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73000857 | |||||||
| chr3:73000921 | T | A | 7 | a0001c0001t0003g0129 a0001c0001t0004g0128 a0001c0001t0004g0130 others(4): Show |
7 | HG01928.hp2 HG01934.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.116+2763T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73000921 | |||||||
| chr3:73000948 | A | G | 1 | a0001c0001t0001g0338 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.116+2790A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73000948 | |||||||
| chr3:73001183 | A | G | 100 | a0001c0001t0002g0105 a0001c0002t0003g0014 a0001c0002t0003g0024 others(97): Show |
100 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.116+3025A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73001183 | |||||||
| chr3:73001463 | A | C | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.116+3305A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73001463 | |||||||
| chr3:73001483 | AG | A | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.116+3327delG | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73001483 | ||||||
| chr3:73001507 | G | C | 2 | a0001c0003t0043g0201 a0001c0003t0045g0202 |
2 | HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.116+3349G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73001507 | |||||||
| chr3:73001550 | G | A | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+3392G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73001550 | |||||||
| chr3:73001582 | A | G | 2 | a0001c0001t0007g0188 a0001c0001t0007g0189 |
2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.116+3424A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73001582 | |||||||
| chr3:73001604 | G | A | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+3446G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73001604 | |||||||
| chr3:73001713 | A | G | 1 | a0001c0001t0029g0337 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.116+3555A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73001713 | |||||||
| chr3:73001763 | T | C | 186 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(183): Show |
187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+3605T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73001763 | |||||||
| chr3:73001791 | A | G | 1 | a0001c0001t0001g0336 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.116+3633A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73001791 | |||||||
| chr3:73001798 | A | T | 183 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(180): Show |
184 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.116+3640A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73001798 | |||||||
| chr3:73001803 | G | A | 183 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(180): Show |
184 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.116+3645G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73001803 | |||||||
| chr3:73001804 | T | G | 81 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(78): Show |
82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+3646T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73001804 | |||||||
| chr3:73002014 | C | A | 97 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(94): Show |
97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.116+3856C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002014 | |||||||
| chr3:73002027 | AATC | A | 65 | a0001c0001t0003g0129 a0001c0001t0004g0127 a0001c0001t0004g0128 others(62): Show |
65 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.116+3874_116+3876d others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002027 | ||||||
| chr3:73002050 | C | G | 2 | a0001c0001t0044g0214 a0001c0001t0046g0213 |
2 | HG02615.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.116+3892C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002050 | |||||||
| chr3:73002165 | C | G | 1 | a0001c0001t0007g0187 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.116+4007C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002165 | |||||||
| chr3:73002223 | A | G | 2 | a0001c0001t0026g0185 a0001c0001t0056g0186 |
2 | HG01255.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.116+4065A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002223 | |||||||
| chr3:73002274 | G | A | 1 | a0001c0001t0004g0128 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.116+4116G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002274 | |||||||
| chr3:73002360 | C | T | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+4202C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002360 | |||||||
| chr3:73002441 | A | G | 1 | a0001c0001t0001g0338 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.116+4283A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002441 | |||||||
| chr3:73002520 | C | G | 1 | a0001c0001t0007g0184 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.116+4362C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002520 | |||||||
| chr3:73002523 | A | G | 186 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(183): Show |
187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.116+4365A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002523 | |||||||
| chr3:73002526 | A | G | 1 | a0001c0001t0056g0186 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.116+4368A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002526 | |||||||
| chr3:73002552 | A | G | 2 | a0001c0001t0005g0009 a0001c0001t0014g0010 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.116+4394A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002552 | |||||||
| chr3:73002598 | C | A | 14 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(11): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+4440C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002598 | |||||||
| chr3:73002604 | T | TTTTTC | 14 | a0001c0001t0001g0003 a0001c0001t0001g0122 a0001c0001t0001g0123 others(11): Show |
15 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+4476_116+4480d others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002604 | ||||||
| chr3:73002604 | TTTTTC | T | 8 | a0001c0001t0001g0331 a0001c0001t0007g0183 a0001c0001t0014g0329 others(5): Show |
8 | HG01884.hp2 HG01952.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.116+4476_116+4480d others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002604 | ||||||
| chr3:73002604 | TTTTTCTT others(3): Show |
T | 3 | a0001c0001t0001g0335 a0001c0001t0002g0333 a0001c0010t0001g0334 |
3 | HG00609.hp2 HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.116+4471_116+4480d others(12): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002604 | ||||||
| chr3:73002619 | C | T | 5 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(2): Show |
5 | HG01243.hp1 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.116+4461C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002619 | |||||||
| chr3:73002624 | C | T | 1 | a0001c0001t0018g0198 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.116+4466C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002624 | |||||||
| chr3:73002629 | C | CTTTTTT | 8 | a0001c0001t0004g0161 a0001c0001t0007g0184 a0001c0001t0007g0187 others(5): Show |
8 | HG00741.hp2 HG01109.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.116+4475_116+4476i others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002629 | ||||||
| chr3:73002629 | C | CTTTTTTT | 6 | a0001c0001t0004g0156 a0001c0001t0004g0163 a0001c0001t0004g0172 others(3): Show |
6 | HG01123.hp1 HG02145.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+4475_116+4476i others(9): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002629 | ||||||
| chr3:73002629 | C | CTTTTTTT others(1): Show |
17 | a0001c0001t0003g0115 a0001c0001t0004g0127 a0001c0001t0004g0128 others(14): Show |
17 | HG01081.hp2 HG01255.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.116+4475_116+4476i others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002629 | ||||||
| chr3:73002629 | C | CTTTTTTT others(2): Show |
15 | a0001c0001t0004g0134 a0001c0001t0004g0139 a0001c0001t0004g0160 others(12): Show |
15 | HG00140.hp1 HG01517.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+4475_116+4476i others(11): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002629 | ||||||
| chr3:73002629 | C | CTTTTTTT others(3): Show |
5 | a0001c0001t0003g0116 a0001c0001t0004g0166 a0001c0001t0009g0117 others(2): Show |
5 | HG00735.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.116+4475_116+4476i others(12): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002629 | ||||||
| chr3:73002629 | C | CTTTTTTT others(4): Show |
3 | a0001c0001t0004g0165 a0001c0001t0019g0121 a0001c0001t0025g0176 |
3 | HG02886.hp1 HG03471.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.116+4475_116+4476i others(13): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002629 | ||||||
| chr3:73002629 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0007g0133 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.116+4475_116+4476i others(15): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002629 | ||||||
| chr3:73002629 | C | T | 6 | a0001c0001t0004g0159 a0001c0001t0007g0171 a0001c0001t0007g0189 others(3): Show |
6 | HG02572.hp2 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.116+4471C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002629 | |||||||
| chr3:73002629 | CTTTTCTT others(11): Show |
C | 1 | a0001c0002t0003g0092 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.116+4476_116+4493d others(20): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002629 | ||||||
| chr3:73002629 | CTTTTCTT others(12): Show |
C | 95 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(92): Show |
95 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.116+4476_116+4494d others(21): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002629 | ||||||
| chr3:73002630 | TTTTC | T | 9 | a0001c0001t0001g0210 a0001c0001t0004g0168 a0001c0001t0018g0193 others(6): Show |
9 | HG01243.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.116+4476_116+4479d others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002630 | ||||||
| chr3:73002633 | T | C | 1 | a0001c0003t0012g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.116+4475T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002633 | |||||||
| chr3:73002634 | C | CT | 16 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0249 others(13): Show |
16 | HG01934.hp1 HG02027.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.116+4501dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002634 | ||||||
| chr3:73002634 | C | CTTTTCT | 6 | a0001c0001t0001g0281 a0001c0001t0005g0284 a0001c0001t0017g0253 others(3): Show |
6 | HG01346.hp2 HG01361.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.116+4480_116+4481i others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002634 | ||||||
| chr3:73002634 | C | CTTTTCTT others(4): Show |
1 | a0001c0001t0001g0327 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.116+4480_116+4481i others(13): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002634 | ||||||
| chr3:73002634 | C | CTTTTCTT others(5): Show |
1 | a0001c0003t0048g0215 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.116+4480_116+4481i others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002634 | ||||||
| chr3:73002634 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0003g0114 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.116+4492_116+4501d others(12): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002634 | ||||||
| chr3:73002634 | C | T | 71 | a0001c0001t0003g0115 a0001c0001t0003g0116 a0001c0001t0004g0127 others(68): Show |
72 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(69): Show |
intron_variant | MODIFIER | c.116+4476C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002634 | |||||||
| chr3:73002634 | CT | C | 10 | a0001c0001t0001g0237 a0001c0001t0001g0278 a0001c0001t0001g0300 others(7): Show |
10 | HG01517.hp2 HG01891.hp1 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.116+4501delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73002634 | ||||||
| chr3:73002703 | G | A | 1 | a0001c0001t0058g0182 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.116+4545G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002703 | |||||||
| chr3:73002711 | G | A | 1 | a0001c0001t0005g0227 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.116+4553G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002711 | |||||||
| chr3:73002860 | T | C | 1 | a0001c0001t0051g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.116+4702T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002860 | |||||||
| chr3:73002887 | C | T | 1 | a0001c0001t0001g0328 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.116+4729C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002887 | |||||||
| chr3:73002899 | C | T | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+4741C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73002899 | |||||||
| chr3:73003078 | C | T | 7 | a0001c0001t0001g0327 a0001c0001t0018g0193 a0001c0001t0018g0194 others(4): Show |
7 | HG01243.hp1 HG01361.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.116+4920C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003078 | |||||||
| chr3:73003118 | AT | A | 175 | a0001c0001t0002g0228 a0001c0001t0003g0114 a0001c0001t0003g0115 others(172): Show |
176 | HG00140.hp1 HG00423.hp1 HG00597.hp1 others(173): Show |
intron_variant | MODIFIER | c.116+4973delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73003118 | ||||||
| chr3:73003197 | A | G | 96 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(93): Show |
96 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.116+5039A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003197 | |||||||
| chr3:73003199 | T | C | 82 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(79): Show |
83 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(80): Show |
intron_variant | MODIFIER | c.116+5041T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003199 | |||||||
| chr3:73003217 | GT | G | 154 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(151): Show |
155 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.116+5071delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73003217 | ||||||
| chr3:73003248 | G | A | 12 | a0001c0001t0004g0163 a0001c0001t0004g0164 a0001c0001t0004g0165 others(9): Show |
12 | HG00735.hp2 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.116+5090G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003248 | |||||||
| chr3:73003288 | C | T | 183 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(180): Show |
184 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.116+5130C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003288 | |||||||
| chr3:73003363 | C | T | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+5205C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003363 | |||||||
| chr3:73003398 | A | G | 1 | a0001c0001t0008g0162 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.116+5240A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003398 | |||||||
| chr3:73003410 | G | A | 96 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(93): Show |
96 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.116+5252G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003410 | |||||||
| chr3:73003598 | T | C | 87 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(84): Show |
87 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.116+5440T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003598 | |||||||
| chr3:73003614 | C | A | 81 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(78): Show |
82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+5456C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003614 | |||||||
| chr3:73003692 | G | GT | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+5543dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73003692 | ||||||
| chr3:73003697 | T | G | 2 | a0001c0001t0007g0190 a0001c0001t0051g0199 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.116+5539T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003697 | |||||||
| chr3:73003706 | T | C | 1 | a0001c0001t0002g0229 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.116+5548T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003706 | |||||||
| chr3:73003711 | T | TG | 81 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(78): Show |
82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+5553_116+5554i others(3): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003711 | |||||||
| chr3:73003712 | T | G | 3 | a0001c0001t0002g0230 a0001c0001t0002g0231 a0001c0001t0018g0194 |
3 | HG03486.hp1 NA19064.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.116+5554T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003712 | |||||||
| chr3:73003722 | A | G | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+5564A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003722 | |||||||
| chr3:73003729 | T | C | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+5571T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003729 | |||||||
| chr3:73003753 | C | T | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+5595C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003753 | |||||||
| chr3:73003820 | T | G | 5 | a0001c0001t0026g0174 a0001c0001t0026g0185 a0001c0001t0056g0186 others(2): Show |
5 | HG01255.hp1 HG01952.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.116+5662T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003820 | |||||||
| chr3:73003897 | T | A | 184 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(181): Show |
185 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.116+5739T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003897 | |||||||
| chr3:73003903 | A | T | 82 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(79): Show |
83 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(80): Show |
intron_variant | MODIFIER | c.116+5745A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73003903 | |||||||
| chr3:73004001 | A | C | 3 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0002t0010g0093 |
3 | HG00621.hp1 NA18944.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.116+5843A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004001 | |||||||
| chr3:73004007 | T | C | 1 | a0001c0001t0014g0006 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.116+5849T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004007 | |||||||
| chr3:73004087 | C | T | 2 | a0001c0002t0003g0091 a0001c0002t0003g0092 |
2 | HG02683.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.116+5929C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004087 | |||||||
| chr3:73004102 | T | C | 348 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(345): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.116+5944T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004102 | |||||||
| chr3:73004104 | G | T | 14 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(11): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+5946G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004104 | |||||||
| chr3:73004125 | T | C | 184 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(181): Show |
185 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.116+5967T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004125 | |||||||
| chr3:73004127 | C | T | 1 | a0001c0001t0051g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.116+5969C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004127 | |||||||
| chr3:73004182 | CT | C | 177 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(174): Show |
178 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.116+6037delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004182 | ||||||
| chr3:73004217 | T | G | 1 | a0001c0001t0004g0130 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.116+6059T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004217 | |||||||
| chr3:73004280 | A | G | 11 | a0001c0001t0001g0210 a0001c0003t0012g0209 a0001c0003t0012g0211 others(8): Show |
11 | HG02109.hp1 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.116+6122A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004280 | |||||||
| chr3:73004316 | T | C | 8 | a0001c0001t0001g0339 a0001c0001t0005g0009 a0001c0001t0014g0006 others(5): Show |
8 | HG01109.hp2 HG02818.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.116+6158T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004316 | |||||||
| chr3:73004337 | G | A | 81 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(78): Show |
82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.116+6179G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004337 | |||||||
| chr3:73004375 | A | T | 1 | a0001c0002t0003g0088 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.116+6217A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004375 | |||||||
| chr3:73004422 | T | G | 1 | a0001c0001t0005g0232 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.116+6264T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004422 | |||||||
| chr3:73004448 | A | G | 66 | a0001c0001t0003g0129 a0001c0001t0004g0127 a0001c0001t0004g0128 others(63): Show |
66 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.116+6290A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004448 | |||||||
| chr3:73004480 | G | T | 1 | a0001c0001t0051g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.116+6322G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004480 | |||||||
| chr3:73004499 | C | T | 1 | a0001c0001t0004g0161 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.116+6341C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004499 | |||||||
| chr3:73004500 | G | A | 9 | a0001c0001t0016g0205 a0001c0001t0016g0206 a0001c0001t0016g0207 others(6): Show |
9 | HG02280.hp2 HG02615.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.116+6342G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004500 | |||||||
| chr3:73004736 | A | G | 83 | a0001c0001t0002g0322 a0001c0001t0003g0114 a0001c0001t0003g0115 others(80): Show |
84 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(81): Show |
intron_variant | MODIFIER | c.116+6578A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004736 | |||||||
| chr3:73004793 | A | C | 184 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(181): Show |
185 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.116+6635A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004793 | |||||||
| chr3:73004793 | A | G | 1 | a0001c0001t0002g0321 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.116+6635A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004793 | |||||||
| chr3:73004844 | G | GGT | 18 | a0001c0001t0002g0241 a0001c0001t0017g0320 a0001c0002t0003g0051 others(15): Show |
18 | HG00597.hp1 HG02922.hp1 HG03831.hp2 others(15): Show |
intron_variant | MODIFIER | c.116+6711_116+6712d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004844 | ||||||
| chr3:73004844 | G | GT | 3 | a0001c0002t0011g0062 a0001c0002t0033g0100 a0001c0002t0037g0074 |
3 | HG02976.hp2 HG03704.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.116+6686_116+6687i others(3): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004844 | |||||||
| chr3:73004846 | T | G | 3 | a0001c0001t0066g0196 a0003c0004t0013g0352 a0003c0004t0013g0353 |
3 | HG01891.hp1 HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+6688T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004846 | |||||||
| chr3:73004848 | T | G | 4 | a0001c0001t0005g0009 a0001c0001t0014g0006 a0001c0001t0014g0007 others(1): Show |
4 | HG01109.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.116+6690T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004848 | |||||||
| chr3:73004857 | GTGTGTGT others(11): Show |
G | 82 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(79): Show |
83 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(80): Show |
intron_variant | MODIFIER | c.116+6703_116+6720d others(20): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004857 | ||||||
| chr3:73004863 | GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0001g0263 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.116+6709_116+6720d others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004863 | ||||||
| chr3:73004867 | GTGTT | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(104): Show |
110 | HG00140.hp2 HG00423.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.116+6725_116+6728d others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004867 | ||||||
| chr3:73004867 | GTGTTTGT others(1): Show |
G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0246 a0001c0001t0001g0249 others(7): Show |
10 | HG00597.hp2 NA18612.hp1 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.116+6721_116+6728d others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004867 | ||||||
| chr3:73004867 | GTGTTTGT others(5): Show |
G | 2 | a0001c0002t0013g0094 a0001c0002t0013g0095 |
2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116+6717_116+6728d others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004867 | ||||||
| chr3:73004869 | GTT | G | 19 | a0001c0001t0001g0210 a0001c0001t0001g0281 a0001c0001t0001g0294 others(16): Show |
19 | HG00438.hp2 HG01243.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.116+6713_116+6714d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004869 | ||||||
| chr3:73004869 | GTTTGTT | G | 3 | a0001c0001t0001g0248 a0001c0002t0003g0058 a0001c0002t0010g0050 |
3 | HG00423.hp1 NA19063.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.116+6713_116+6718d others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004869 | ||||||
| chr3:73004871 | T | G | 86 | a0001c0001t0021g0200 a0001c0002t0003g0024 a0001c0002t0003g0025 others(83): Show |
86 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.116+6713T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004871 | |||||||
| chr3:73004875 | T | G | 98 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(95): Show |
98 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.116+6717T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004875 | |||||||
| chr3:73004879 | T | G | 2 | a0001c0001t0018g0194 a0001c0002t0003g0014 |
2 | HG00738.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.116+6721T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004879 | |||||||
| chr3:73004905 | G | A | 1 | a0001c0002t0010g0093 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.116+6747G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004905 | |||||||
| chr3:73004910 | CATGTGTG others(47): Show |
C | 1 | a0001c0002t0019g0087 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.116+6753_116+6806d others(56): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004910 | |||||||
| chr3:73004911 | A | G | 182 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(179): Show |
183 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.116+6753A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004911 | |||||||
| chr3:73004923 | T | G | 1 | a0001c0001t0007g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.116+6765T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004923 | |||||||
| chr3:73004923 | T | TTGTGTG | 176 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(173): Show |
177 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.116+6767_116+6772d others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004923 | ||||||
| chr3:73004923 | TTGTGTGT others(19): Show |
T | 2 | a0001c0002t0030g0096 a0001c0002t0030g0098 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.116+6773_116+6798d others(28): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004923 | ||||||
| chr3:73004923 | TTGTGTGT others(21): Show |
T | 2 | a0001c0002t0013g0097 a0001c0002t0033g0100 |
2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.116+6773_116+6800d others(30): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004923 | ||||||
| chr3:73004923 | TTGTGTGT others(23): Show |
T | 2 | a0001c0002t0013g0101 a0001c0002t0033g0099 |
2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.116+6773_116+6802d others(32): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004923 | ||||||
| chr3:73004944 | C | CGT | 7 | a0001c0001t0002g0298 a0001c0001t0002g0305 a0001c0001t0002g0326 others(4): Show |
7 | HG00735.hp2 HG01952.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.116+6831_116+6832d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004944 | ||||||
| chr3:73004944 | CGT | C | 36 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0306 others(33): Show |
37 | HG00741.hp2 HG01123.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.116+6831_116+6832d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004944 | ||||||
| chr3:73004944 | CGTGT | C | 64 | a0001c0001t0001g0239 a0001c0001t0001g0257 a0001c0001t0001g0336 others(61): Show |
64 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.116+6829_116+6832d others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004944 | ||||||
| chr3:73004944 | CGTGTGT | C | 88 | a0001c0001t0001g0210 a0001c0001t0001g0248 a0001c0001t0001g0251 others(85): Show |
88 | HG00140.hp1 HG00597.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.116+6827_116+6832d others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004944 | ||||||
| chr3:73004944 | CGTGTGTG others(1): Show |
C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(92): Show |
98 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.116+6825_116+6832d others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004944 | ||||||
| chr3:73004944 | CGTGTGTG others(3): Show |
C | 17 | a0001c0001t0001g0218 a0001c0001t0005g0227 a0001c0001t0005g0299 others(14): Show |
17 | HG01255.hp1 HG01884.hp2 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.116+6823_116+6832d others(12): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004944 | ||||||
| chr3:73004944 | CGTGTGTG others(5): Show |
C | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG02155.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+6821_116+6832d others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004944 | ||||||
| chr3:73004944 | CGTGTGTG others(9): Show |
C | 3 | a0001c0001t0066g0196 a0003c0004t0013g0352 a0003c0004t0013g0353 |
3 | HG01891.hp1 HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+6817_116+6832d others(18): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004944 | ||||||
| chr3:73004944 | CGTGTGTG others(11): Show |
C | 1 | a0001c0002t0003g0088 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.116+6815_116+6832d others(20): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004944 | ||||||
| chr3:73004944 | CGTGTGTG others(15): Show |
C | 1 | a0001c0001t0017g0253 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.116+6811_116+6832d others(24): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004944 | ||||||
| chr3:73004950 | T | TGTGTGTG others(91): Show |
1 | a0001c0002t0010g0065 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.116+6818_116+6819i others(100): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004950 | ||||||
| chr3:73004951 | G | T | 1 | a0001c0001t0021g0204 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.116+6793G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004951 | |||||||
| chr3:73004953 | G | T | 12 | a0001c0001t0001g0210 a0001c0001t0021g0200 a0001c0001t0021g0203 others(9): Show |
12 | HG02280.hp1 HG02559.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.116+6795G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004953 | |||||||
| chr3:73004957 | G | T | 7 | a0001c0001t0016g0205 a0001c0001t0016g0206 a0001c0001t0016g0207 others(4): Show |
7 | HG02109.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.116+6799G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004957 | |||||||
| chr3:73004977 | G | T | 1 | a0001c0002t0019g0087 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.116+6819G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004977 | |||||||
| chr3:73004985 | GTGTGT | G | 4 | a0001c0001t0001g0005 a0001c0001t0029g0315 a0001c0002t0003g0082 others(1): Show |
4 | HG00438.hp1 NA18971.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+6829_116+6833d others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73004985 | ||||||
| chr3:73004991 | T | G | 1 | a0001c0002t0033g0100 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.116+6833T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004991 | |||||||
| chr3:73004999 | G | A | 1 | a0001c0001t0021g0200 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.116+6841G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73004999 | |||||||
| chr3:73005008 | C | A | 4 | a0001c0001t0008g0136 a0001c0001t0008g0137 a0001c0001t0008g0138 others(1): Show |
4 | HG00741.hp2 HG01109.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.116+6850C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005008 | |||||||
| chr3:73005061 | C | T | 1 | a0001c0001t0004g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.116+6903C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005061 | |||||||
| chr3:73005337 | CT | C | 151 | a0001c0001t0002g0233 a0001c0001t0003g0129 a0001c0001t0004g0127 others(148): Show |
151 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.116+7194delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73005337 | ||||||
| chr3:73005337 | CTT | C | 11 | a0001c0001t0004g0163 a0001c0001t0004g0164 a0001c0001t0004g0165 others(8): Show |
11 | HG00735.hp2 HG02559.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.116+7193_116+7194d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73005337 | ||||||
| chr3:73005370 | C | G | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+7212C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005370 | |||||||
| chr3:73005393 | G | A | 14 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(11): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+7235G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005393 | |||||||
| chr3:73005480 | A | G | 1 | a0001c0001t0017g0320 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.116+7322A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005480 | |||||||
| chr3:73005620 | C | G | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+7462C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005620 | |||||||
| chr3:73005623 | C | T | 94 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(91): Show |
94 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.116+7465C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005623 | |||||||
| chr3:73005711 | G | C | 6 | a0001c0002t0013g0097 a0001c0002t0013g0101 a0001c0002t0030g0096 others(3): Show |
6 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+7553G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005711 | |||||||
| chr3:73005734 | A | G | 7 | a0001c0001t0003g0129 a0001c0001t0004g0128 a0001c0001t0004g0130 others(4): Show |
7 | HG01928.hp2 HG01934.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.116+7576A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005734 | |||||||
| chr3:73005761 | G | A | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.116+7603G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005761 | |||||||
| chr3:73005806 | T | C | 96 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(93): Show |
96 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.116+7648T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005806 | |||||||
| chr3:73005825 | T | A | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+7667T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005825 | |||||||
| chr3:73005833 | C | CA | 8 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 others(5): Show |
8 | HG01891.hp1 HG02155.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.116+7688dupA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73005833 | ||||||
| chr3:73005833 | C | CAAAAAAA others(2): Show |
91 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(88): Show |
92 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.116+7680_116+7688d others(11): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73005833 | ||||||
| chr3:73005833 | C | CAAAAAAA others(3): Show |
21 | a0001c0001t0004g0160 a0001c0001t0009g0110 a0001c0001t0009g0111 others(18): Show |
21 | HG00738.hp1 HG01192.hp1 HG01517.hp1 others(18): Show |
intron_variant | MODIFIER | c.116+7679_116+7688d others(12): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73005833 | ||||||
| chr3:73005833 | C | CAAAAAAA others(4): Show |
45 | a0001c0001t0003g0129 a0001c0001t0004g0127 a0001c0001t0004g0128 others(42): Show |
45 | HG01069.hp1 HG01071.hp2 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.116+7678_116+7688d others(13): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73005833 | ||||||
| chr3:73005833 | C | CAAAAAAA others(5): Show |
20 | a0001c0001t0004g0131 a0001c0001t0004g0139 a0001c0001t0004g0142 others(17): Show |
20 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.116+7677_116+7688d others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73005833 | ||||||
| chr3:73005890 | A | G | 1 | a0001c0002t0023g0085 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.116+7732A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005890 | |||||||
| chr3:73005922 | T | C | 4 | a0001c0002t0011g0015 a0001c0002t0011g0016 a0001c0002t0011g0029 others(1): Show |
4 | NA18948.hp2 NA18972.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+7764T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73005922 | |||||||
| chr3:73006036 | C | T | 2 | a0001c0002t0013g0094 a0001c0002t0013g0095 |
2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116+7878C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006036 | |||||||
| chr3:73006096 | G | A | 1 | a0001c0001t0054g0175 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.116+7938G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006096 | |||||||
| chr3:73006106 | G | A | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+7948G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006106 | |||||||
| chr3:73006190 | A | AT | 29 | a0001c0001t0001g0001 a0001c0001t0001g0216 a0001c0001t0001g0310 others(26): Show |
31 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.116+8059dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73006190 | ||||||
| chr3:73006190 | ATTTTTTT | A | 9 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.116+8053_116+8059d others(9): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73006190 | ||||||
| chr3:73006190 | ATTTTTTT others(1): Show |
A | 60 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(57): Show |
60 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.116+8052_116+8059d others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73006190 | ||||||
| chr3:73006190 | ATTTTTTT others(2): Show |
A | 33 | a0001c0002t0003g0091 a0001c0002t0006g0020 a0001c0002t0006g0021 others(30): Show |
33 | HG00597.hp1 HG00639.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.116+8051_116+8059d others(11): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73006190 | ||||||
| chr3:73006190 | ATTTTTTT others(3): Show |
A | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.116+8050_116+8059d others(12): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73006190 | ||||||
| chr3:73006190 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0007g0146 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.116+8049_116+8059d others(13): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73006190 | ||||||
| chr3:73006225 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.116+8067A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006225 | |||||||
| chr3:73006344 | G | A | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+8186G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006344 | |||||||
| chr3:73006377 | T | G | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+8219T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006377 | |||||||
| chr3:73006387 | C | T | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+8229C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006387 | |||||||
| chr3:73006403 | G | A | 1 | a0001c0002t0055g0354 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.116+8245G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006403 | |||||||
| chr3:73006668 | G | T | 1 | a0001c0001t0004g0159 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.116+8510G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006668 | |||||||
| chr3:73006681 | A | C | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.116+8523A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006681 | |||||||
| chr3:73006773 | C | T | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+8615C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006773 | |||||||
| chr3:73006806 | G | A | 1 | a0001c0001t0004g0161 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.116+8648G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006806 | |||||||
| chr3:73006892 | G | A | 9 | a0001c0001t0001g0239 a0001c0001t0002g0217 a0001c0001t0002g0233 others(6): Show |
9 | HG00609.hp2 HG02015.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.116+8734G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73006892 | |||||||
| chr3:73006945 | T | TG | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+8788dupG | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73006945 | ||||||
| chr3:73007008 | C | T | 1 | a0006c0009t0018g0197 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.116+8850C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007008 | |||||||
| chr3:73007072 | T | C | 183 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(180): Show |
184 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.116+8914T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007072 | |||||||
| chr3:73007187 | A | G | 2 | a0001c0001t0005g0307 a0001c0001t0005g0319 |
2 | NA18979.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.116+9029A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007187 | |||||||
| chr3:73007219 | G | A | 5 | a0001c0001t0002g0004 a0001c0001t0002g0229 a0001c0001t0022g0244 others(2): Show |
6 | NA18946.hp1 NA18974.hp1 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+9061G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007219 | |||||||
| chr3:73007226 | A | G | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+9068A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007226 | |||||||
| chr3:73007227 | A | G | 98 | a0001c0001t0005g0232 a0001c0002t0003g0014 a0001c0002t0003g0024 others(95): Show |
98 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.116+9069A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007227 | |||||||
| chr3:73007238 | T | C | 1 | a0001c0001t0017g0320 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.116+9080T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007238 | |||||||
| chr3:73007312 | A | G | 1 | a0001c0001t0002g0243 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.116+9154A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007312 | |||||||
| chr3:73007332 | A | G | 14 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(11): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+9174A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007332 | |||||||
| chr3:73007347 | G | T | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+9189G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007347 | |||||||
| chr3:73007397 | T | C | 1 | a0001c0001t0008g0147 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.116+9239T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007397 | |||||||
| chr3:73007484 | GT | G | 183 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(180): Show |
184 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.116+9335delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73007484 | ||||||
| chr3:73007568 | GGGTTCAA others(7): Show |
G | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+9420_116+9433d others(16): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73007568 | ||||||
| chr3:73007575 | A | G | 6 | a0001c0001t0001g0339 a0001c0001t0005g0009 a0001c0001t0014g0006 others(3): Show |
6 | HG01109.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+9417A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007575 | |||||||
| chr3:73007734 | C | G | 2 | a0001c0002t0013g0094 a0001c0002t0013g0095 |
2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116+9576C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007734 | |||||||
| chr3:73007780 | C | T | 1 | a0001c0001t0036g0192 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.116+9622C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007780 | |||||||
| chr3:73007785 | G | A | 2 | a0001c0001t0035g0148 a0001c0001t0035g0149 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.116+9627G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007785 | |||||||
| chr3:73007834 | G | A | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.116+9676G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007834 | |||||||
| chr3:73007861 | T | C | 1 | a0001c0001t0001g0246 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.116+9703T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007861 | |||||||
| chr3:73007928 | ATTAC | A | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.116+9773_116+9776d others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73007928 | ||||||
| chr3:73007999 | C | A | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.116+9841C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73007999 | |||||||
| chr3:73008039 | A | AC | 43 | a0001c0001t0001g0220 a0001c0001t0001g0248 a0001c0001t0001g0249 others(40): Show |
43 | HG00423.hp1 HG00423.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.116+9888dupC | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73008039 | ||||||
| chr3:73008055 | C | G | 1 | a0001c0001t0001g0306 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.116+9897C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008055 | |||||||
| chr3:73008114 | G | GCTT | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.116+9957_116+9959d others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73008114 | ||||||
| chr3:73008163 | C | T | 2 | a0001c0002t0006g0049 a0001c0002t0006g0108 |
2 | HG01346.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.116+10005C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008163 | |||||||
| chr3:73008276 | T | G | 1 | a0001c0002t0015g0090 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.116+10118T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008276 | |||||||
| chr3:73008295 | G | A | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.116+10137G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008295 | |||||||
| chr3:73008296 | T | A | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+10138T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008296 | |||||||
| chr3:73008299 | A | G | 2 | a0001c0001t0002g0318 a0001c0001t0002g0326 |
2 | HG02738.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.116+10141A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008299 | |||||||
| chr3:73008499 | T | G | 1 | a0001c0001t0007g0190 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.116+10341T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008499 | |||||||
| chr3:73008535 | G | C | 1 | a0001c0001t0001g0239 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.116+10377G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008535 | |||||||
| chr3:73008543 | C | T | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+10385C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008543 | |||||||
| chr3:73008727 | A | T | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.116+10569A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008727 | |||||||
| chr3:73008747 | A | C | 183 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(180): Show |
184 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.116+10589A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008747 | |||||||
| chr3:73008772 | A | G | 1 | a0001c0001t0002g0305 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.116+10614A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008772 | |||||||
| chr3:73008773 | T | TAGAATGA others(76): Show |
1 | a0001c0001t0068g0330 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.116+10617_116+1069 others(87): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73008773 | ||||||
| chr3:73008796 | C | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0216 a0001c0001t0001g0301 others(7): Show |
12 | HG03516.hp2 NA18747.hp1 NA18946.hp2 others(9): Show |
intron_variant | MODIFIER | c.116+10638C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008796 | |||||||
| chr3:73008838 | A | G | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+10680A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73008838 | |||||||
| chr3:73009090 | T | G | 49 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(46): Show |
50 | HG00140.hp1 HG00741.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.116+10932T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73009090 | |||||||
| chr3:73009095 | T | G | 11 | a0001c0001t0001g0210 a0001c0003t0012g0209 a0001c0003t0012g0211 others(8): Show |
11 | HG02109.hp1 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.116+10937T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73009095 | |||||||
| chr3:73009097 | A | C | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.116+10939A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73009097 | |||||||
| chr3:73009145 | A | T | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.116+10987A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73009145 | |||||||
| chr3:73009430 | CAA | C | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+11274_116+1127 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73009430 | ||||||
| chr3:73009559 | A | G | 1 | a0001c0001t0004g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.116+11401A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73009559 | |||||||
| chr3:73009568 | T | C | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+11410T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73009568 | |||||||
| chr3:73009612 | CTTCAGAT others(13): Show |
C | 14 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(11): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+11455_116+1147 others(24): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73009612 | |||||||
| chr3:73009676 | G | A | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.116+11518G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73009676 | |||||||
| chr3:73009699 | C | T | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.116+11541C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73009699 | |||||||
| chr3:73009750 | C | T | 14 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(11): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+11592C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73009750 | |||||||
| chr3:73009980 | A | G | 2 | a0001c0001t0008g0158 a0001c0001t0008g0179 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.116+11822A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73009980 | |||||||
| chr3:73010009 | C | T | 1 | a0001c0002t0013g0101 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.116+11851C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010009 | |||||||
| chr3:73010183 | G | T | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+12025G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010183 | |||||||
| chr3:73010232 | G | GT | 14 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(11): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+12082dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73010232 | ||||||
| chr3:73010261 | C | T | 1 | a0001c0001t0001g0300 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.116+12103C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010261 | |||||||
| chr3:73010294 | C | T | 2 | a0001c0001t0001g0304 a0001c0001t0001g0317 |
2 | NA19000.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.116+12136C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010294 | |||||||
| chr3:73010299 | T | C | 1 | a0001c0002t0049g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.116+12141T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010299 | |||||||
| chr3:73010342 | C | T | 1 | a0001c0001t0007g0190 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.116+12184C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010342 | |||||||
| chr3:73010516 | G | A | 2 | a0001c0002t0006g0104 a0001c0002t0023g0103 |
2 | HG00099.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.116+12358G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010516 | |||||||
| chr3:73010564 | CT | C | 179 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(176): Show |
180 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.116+12418delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73010564 | ||||||
| chr3:73010618 | G | A | 14 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(11): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+12460G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010618 | |||||||
| chr3:73010702 | G | A | 1 | a0001c0001t0021g0203 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.116+12544G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010702 | |||||||
| chr3:73010717 | A | G | 31 | a0001c0001t0003g0129 a0001c0001t0004g0128 a0001c0001t0004g0130 others(28): Show |
31 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.116+12559A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010717 | |||||||
| chr3:73010747 | C | T | 3 | a0001c0002t0003g0027 a0001c0002t0003g0028 a0001c0002t0003g0081 |
3 | NA18979.hp1 NA19000.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.116+12589C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010747 | |||||||
| chr3:73010801 | G | C | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.116+12643G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010801 | |||||||
| chr3:73010820 | A | G | 184 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(181): Show |
185 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.116+12662A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010820 | |||||||
| chr3:73010953 | G | A | 1 | a0001c0002t0050g0017 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.116+12795G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73010953 | |||||||
| chr3:73011005 | A | G | 2 | a0001c0001t0005g0009 a0001c0001t0014g0010 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.116+12847A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011005 | |||||||
| chr3:73011025 | C | CTGA | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+12868_116+1286 others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73011025 | ||||||
| chr3:73011056 | C | T | 1 | a0001c0001t0051g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.116+12898C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011056 | |||||||
| chr3:73011186 | G | T | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+13028G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011186 | |||||||
| chr3:73011306 | C | A | 4 | a0001c0001t0025g0176 a0001c0001t0025g0177 a0001c0001t0025g0178 others(1): Show |
4 | HG02735.hp2 HG03654.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+13148C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011306 | |||||||
| chr3:73011308 | T | C | 31 | a0001c0001t0003g0129 a0001c0001t0004g0128 a0001c0001t0004g0130 others(28): Show |
31 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.116+13150T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011308 | |||||||
| chr3:73011373 | C | T | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.116+13215C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011373 | |||||||
| chr3:73011482 | GA | G | 98 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(95): Show |
98 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.116+13335delA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73011482 | ||||||
| chr3:73011531 | G | A | 1 | a0001c0001t0051g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.116+13373G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011531 | |||||||
| chr3:73011712 | A | C | 2 | a0001c0001t0005g0307 a0001c0001t0005g0319 |
2 | NA18979.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.116+13554A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011712 | |||||||
| chr3:73011773 | GT | G | 105 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(102): Show |
105 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.116+13616delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011773 | |||||||
| chr3:73011776 | T | C | 105 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(102): Show |
105 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.116+13618T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011776 | |||||||
| chr3:73011818 | A | G | 19 | a0001c0001t0003g0129 a0001c0001t0004g0128 a0001c0001t0004g0130 others(16): Show |
19 | HG00735.hp2 HG01928.hp2 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.116+13660A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011818 | |||||||
| chr3:73011933 | T | C | 5 | a0001c0001t0002g0247 a0001c0001t0002g0254 a0001c0001t0002g0255 others(2): Show |
5 | HG01081.hp1 HG01928.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.116+13775T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011933 | |||||||
| chr3:73011953 | C | A | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.116+13795C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73011953 | |||||||
| chr3:73012023 | T | G | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.116+13865T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012023 | |||||||
| chr3:73012279 | G | T | 1 | a0001c0001t0001g0126 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.116+14121G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012279 | |||||||
| chr3:73012323 | G | A | 65 | a0001c0001t0003g0129 a0001c0001t0004g0127 a0001c0001t0004g0128 others(62): Show |
65 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.116+14165G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012323 | |||||||
| chr3:73012328 | C | T | 99 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(96): Show |
99 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.116+14170C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012328 | |||||||
| chr3:73012387 | G | C | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+14229G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012387 | |||||||
| chr3:73012401 | G | A | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.116+14243G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012401 | |||||||
| chr3:73012424 | C | T | 2 | a0001c0001t0005g0227 a0001c0001t0005g0299 |
2 | NA19065.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.116+14266C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012424 | |||||||
| chr3:73012472 | T | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0310 |
4 | NA18747.hp1 NA18972.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.116+14314T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012472 | |||||||
| chr3:73012549 | C | A | 1 | a0001c0001t0001g0311 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.116+14391C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012549 | |||||||
| chr3:73012621 | C | G | 105 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(102): Show |
105 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.116+14463C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012621 | |||||||
| chr3:73012698 | C | G | 1 | a0001c0001t0002g0256 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.116+14540C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012698 | |||||||
| chr3:73012768 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.116+14610G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012768 | |||||||
| chr3:73012902 | C | CT | 22 | a0001c0001t0001g0311 a0001c0001t0002g0231 a0001c0001t0002g0298 others(19): Show |
23 | HG01243.hp1 HG01884.hp2 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.116+14762dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73012902 | ||||||
| chr3:73012902 | CT | C | 81 | a0001c0001t0001g0331 a0001c0001t0001g0336 a0001c0001t0001g0339 others(78): Show |
81 | HG00423.hp1 HG00621.hp1 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.116+14762delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73012902 | ||||||
| chr3:73012902 | CTT | C | 23 | a0001c0001t0001g0210 a0001c0001t0016g0109 a0001c0001t0016g0205 others(20): Show |
23 | HG02109.hp1 HG02280.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.116+14761_116+1476 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73012902 | ||||||
| chr3:73012953 | A | T | 1 | a0001c0001t0008g0147 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.116+14795A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012953 | |||||||
| chr3:73012991 | AGTCGTGT others(4): Show |
A | 1 | a0001c0001t0029g0337 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.116+14834_116+1484 others(15): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73012991 | |||||||
| chr3:73013027 | C | A | 183 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(180): Show |
184 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.116+14869C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73013027 | |||||||
| chr3:73013041 | C | T | 3 | a0001c0001t0019g0112 a0001c0001t0019g0113 a0001c0001t0019g0120 |
3 | HG02572.hp2 HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.116+14883C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73013041 | |||||||
| chr3:73013142 | A | G | 1 | a0001c0001t0051g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.116+14984A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73013142 | |||||||
| chr3:73013431 | A | C | 1 | a0001c0001t0009g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.116+15273A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73013431 | |||||||
| chr3:73013492 | A | AAAAG | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+15337_116+1533 others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73013492 | ||||||
| chr3:73013589 | A | G | 1 | a0001c0001t0017g0253 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.116+15431A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73013589 | |||||||
| chr3:73013646 | C | CT | 9 | a0001c0001t0001g0339 a0001c0001t0005g0009 a0001c0001t0014g0006 others(6): Show |
9 | HG01109.hp2 HG02615.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.116+15500dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73013646 | ||||||
| chr3:73013646 | CT | C | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+15500delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73013646 | ||||||
| chr3:73013729 | C | T | 183 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(180): Show |
184 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.116+15571C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73013729 | |||||||
| chr3:73013779 | C | T | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+15621C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73013779 | |||||||
| chr3:73013798 | C | T | 2 | a0001c0002t0003g0014 a0001c0002t0010g0079 |
2 | HG00738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.116+15640C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73013798 | |||||||
| chr3:73013825 | G | C | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.116+15667G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73013825 | |||||||
| chr3:73013827 | G | C | 1 | a0001c0001t0051g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.116+15669G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73013827 | |||||||
| chr3:73013926 | CCACCGCG others(470): Show |
C | 65 | a0001c0001t0003g0129 a0001c0001t0004g0127 a0001c0001t0004g0128 others(62): Show |
65 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.116+15769_116+1624 others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73013926 | |||||||
| chr3:73013936 | C | T | 15 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(12): Show |
16 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.116+15778C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73013936 | |||||||
| chr3:73014102 | T | C | 2 | a0001c0002t0006g0049 a0001c0002t0006g0108 |
2 | HG01346.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.116+15944T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73014102 | |||||||
| chr3:73014236 | T | C | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+16078T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73014236 | |||||||
| chr3:73014470 | A | G | 97 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(94): Show |
97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.116+16312A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73014470 | |||||||
| chr3:73014686 | G | GT | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+16537dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73014686 | ||||||
| chr3:73014775 | A | G | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.116+16617A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73014775 | |||||||
| chr3:73014908 | T | C | 2 | a0001c0001t0001g0248 a0001c0001t0001g0263 |
2 | NA18965.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.116+16750T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73014908 | |||||||
| chr3:73014952 | C | T | 1 | a0001c0002t0013g0102 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.116+16794C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73014952 | |||||||
| chr3:73014965 | A | G | 1 | a0001c0001t0002g0325 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.116+16807A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73014965 | |||||||
| chr3:73015165 | A | G | 5 | a0001c0001t0002g0004 a0001c0001t0002g0229 a0001c0001t0022g0244 others(2): Show |
6 | NA18946.hp1 NA18974.hp1 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+17007A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015165 | |||||||
| chr3:73015216 | G | A | 65 | a0001c0001t0003g0129 a0001c0001t0004g0127 a0001c0001t0004g0128 others(62): Show |
65 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.116+17058G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015216 | |||||||
| chr3:73015226 | G | C | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+17068G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015226 | |||||||
| chr3:73015234 | C | T | 2 | a0001c0002t0003g0051 a0001c0002t0003g0078 |
2 | NA19065.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.116+17076C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015234 | |||||||
| chr3:73015259 | C | A | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+17101C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015259 | |||||||
| chr3:73015327 | G | A | 1 | a0001c0001t0008g0147 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.116+17169G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015327 | |||||||
| chr3:73015364 | A | T | 1 | a0001c0001t0002g0256 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.116+17206A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015364 | |||||||
| chr3:73015372 | T | A | 1 | a0001c0001t0007g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.116+17214T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015372 | |||||||
| chr3:73015481 | CT | C | 174 | a0001c0001t0001g0328 a0001c0001t0001g0339 a0001c0001t0002g0217 others(171): Show |
175 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.116+17340delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73015481 | ||||||
| chr3:73015488 | T | C | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+17330T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015488 | |||||||
| chr3:73015506 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
5 | HG00140.hp2 HG00738.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.116+17348C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015506 | |||||||
| chr3:73015594 | G | C | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.116+17436G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015594 | |||||||
| chr3:73015598 | C | G | 1 | a0001c0002t0013g0102 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.116+17440C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015598 | |||||||
| chr3:73015648 | T | G | 1 | a0001c0002t0023g0103 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.116+17490T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015648 | |||||||
| chr3:73015757 | C | T | 1 | a0001c0001t0002g0233 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.116+17599C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015757 | |||||||
| chr3:73015777 | A | G | 1 | a0001c0001t0002g0322 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.116+17619A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015777 | |||||||
| chr3:73015878 | T | C | 1 | a0001c0001t0058g0182 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.116+17720T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015878 | |||||||
| chr3:73015888 | T | G | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+17730T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015888 | |||||||
| chr3:73015965 | A | G | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+17807A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73015965 | |||||||
| chr3:73016019 | G | A | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.116+17861G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016019 | |||||||
| chr3:73016073 | A | G | 2 | a0001c0001t0001g0297 a0001c0001t0001g0306 |
2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.116+17915A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016073 | |||||||
| chr3:73016081 | C | A | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+17923C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016081 | |||||||
| chr3:73016125 | T | C | 65 | a0001c0001t0003g0129 a0001c0001t0004g0127 a0001c0001t0004g0128 others(62): Show |
65 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.116+17967T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016125 | |||||||
| chr3:73016184 | C | G | 97 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(94): Show |
97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.116+18026C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016184 | |||||||
| chr3:73016186 | G | A | 2 | a0001c0001t0004g0139 a0001c0001t0036g0150 |
2 | HG00140.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.116+18028G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016186 | |||||||
| chr3:73016226 | A | G | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+18068A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016226 | |||||||
| chr3:73016272 | CT | C | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+18124delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73016272 | ||||||
| chr3:73016334 | T | C | 2 | a0001c0002t0013g0094 a0001c0002t0013g0095 |
2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116+18176T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016334 | |||||||
| chr3:73016418 | T | C | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+18260T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016418 | |||||||
| chr3:73016427 | C | T | 4 | a0001c0001t0002g0247 a0001c0001t0002g0254 a0001c0001t0002g0255 others(1): Show |
4 | HG01928.hp1 HG01934.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+18269C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016427 | |||||||
| chr3:73016439 | A | G | 1 | a0001c0002t0013g0102 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.116+18281A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016439 | |||||||
| chr3:73016440 | G | T | 10 | a0001c0001t0016g0109 a0001c0001t0016g0205 a0001c0001t0016g0206 others(7): Show |
10 | HG02280.hp2 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.116+18282G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016440 | |||||||
| chr3:73016459 | G | C | 65 | a0001c0001t0003g0129 a0001c0001t0004g0127 a0001c0001t0004g0128 others(62): Show |
65 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.116+18301G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016459 | |||||||
| chr3:73016729 | G | GTTTC | 3 | a0001c0002t0006g0104 a0001c0002t0010g0054 a0001c0002t0055g0354 |
3 | HG00099.hp2 HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.116+18574_116+1857 others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73016729 | ||||||
| chr3:73016729 | G | GTTTCT | 69 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(66): Show |
69 | HG00423.hp1 HG00597.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.116+18574_116+1857 others(9): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73016729 | ||||||
| chr3:73016729 | G | GTTTCTT | 27 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(24): Show |
27 | HG00621.hp1 HG01069.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.116+18574_116+1857 others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73016729 | ||||||
| chr3:73016731 | T | TTC | 4 | a0001c0001t0008g0158 a0001c0001t0008g0179 a0001c0001t0025g0176 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.116+18574_116+1857 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73016731 | ||||||
| chr3:73016732 | T | TC | 25 | a0001c0001t0003g0129 a0001c0001t0004g0130 a0001c0001t0004g0131 others(22): Show |
25 | HG00735.hp2 HG01255.hp1 HG01928.hp2 others(22): Show |
intron_variant | MODIFIER | c.116+18574_116+1857 others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016732 | |||||||
| chr3:73016733 | A | C | 55 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(52): Show |
56 | HG00140.hp1 HG00741.hp2 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.116+18575A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016733 | |||||||
| chr3:73016733 | A | T | 130 | a0001c0001t0003g0129 a0001c0001t0004g0130 a0001c0001t0004g0131 others(127): Show |
130 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(127): Show |
intron_variant | MODIFIER | c.116+18575A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016733 | |||||||
| chr3:73016735 | TTTTATTA others(71): Show |
T | 1 | a0001c0002t0023g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.116+18581_116+1865 others(82): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73016735 | ||||||
| chr3:73016737 | TTA | T | 3 | a0001c0002t0003g0084 a0003c0004t0013g0352 a0003c0004t0013g0353 |
3 | HG01891.hp1 HG03453.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.116+18581_116+1858 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73016737 | ||||||
| chr3:73016739 | A | T | 179 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(176): Show |
180 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.116+18581A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016739 | |||||||
| chr3:73016741 | TA | T | 10 | a0001c0001t0016g0109 a0001c0001t0016g0205 a0001c0001t0016g0206 others(7): Show |
10 | HG02280.hp2 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.116+18584delA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016741 | |||||||
| chr3:73016742 | A | T | 195 | a0001c0001t0001g0210 a0001c0001t0003g0114 a0001c0001t0003g0115 others(192): Show |
196 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.116+18584A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016742 | |||||||
| chr3:73016745 | T | A | 15 | a0001c0001t0001g0288 a0001c0001t0001g0294 a0001c0001t0001g0331 others(12): Show |
15 | HG02572.hp1 HG02630.hp2 HG03139.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+18587T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016745 | |||||||
| chr3:73016775 | C | T | 3 | a0001c0001t0018g0193 a0001c0001t0018g0195 a0001c0001t0018g0198 |
3 | HG01243.hp1 HG01884.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.116+18617C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016775 | |||||||
| chr3:73016776 | A | G | 184 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(181): Show |
185 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.116+18618A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016776 | |||||||
| chr3:73016813 | C | CT | 29 | a0001c0001t0001g0210 a0001c0001t0001g0248 a0001c0001t0001g0310 others(26): Show |
29 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.116+18677dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73016813 | ||||||
| chr3:73016813 | C | CTT | 79 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(76): Show |
79 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.116+18676_116+1867 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73016813 | ||||||
| chr3:73016813 | C | CTTT | 10 | a0001c0002t0003g0077 a0001c0002t0003g0084 a0001c0002t0006g0104 others(7): Show |
10 | HG00099.hp2 HG01243.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.116+18675_116+1867 others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73016813 | ||||||
| chr3:73016813 | CT | C | 7 | a0001c0001t0001g0239 a0001c0001t0001g0265 a0001c0001t0001g0292 others(4): Show |
7 | HG02129.hp1 NA18946.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.116+18677delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73016813 | ||||||
| chr3:73016813 | CTTTTT | C | 75 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(72): Show |
76 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.116+18673_116+1867 others(9): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73016813 | ||||||
| chr3:73016817 | T | C | 1 | a0001c0001t0001g0336 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.116+18659T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016817 | |||||||
| chr3:73016818 | T | C | 1 | a0001c0001t0002g0243 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.116+18660T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73016818 | |||||||
| chr3:73017159 | A | G | 1 | a0001c0001t0005g0242 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.116+19001A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73017159 | |||||||
| chr3:73017345 | A | T | 1 | a0001c0001t0067g0296 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.116+19187A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73017345 | |||||||
| chr3:73017346 | T | C | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+19188T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73017346 | |||||||
| chr3:73017357 | G | GT | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+19200dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73017357 | ||||||
| chr3:73017411 | C | G | 1 | a0001c0002t0055g0354 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.116+19253C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73017411 | |||||||
| chr3:73017715 | C | T | 21 | a0001c0001t0001g0001 a0001c0001t0001g0216 a0001c0001t0001g0225 others(18): Show |
23 | HG00621.hp2 HG00639.hp2 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.116+19557C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73017715 | |||||||
| chr3:73017888 | C | T | 97 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(94): Show |
97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.116+19730C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73017888 | |||||||
| chr3:73017956 | T | G | 1 | a0004c0005t0017g0345 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.116+19798T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73017956 | |||||||
| chr3:73017967 | A | G | 105 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(102): Show |
105 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.116+19809A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73017967 | |||||||
| chr3:73018023 | C | T | 1 | a0001c0001t0004g0163 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.116+19865C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018023 | |||||||
| chr3:73018066 | A | T | 1 | a0001c0001t0036g0192 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.116+19908A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018066 | |||||||
| chr3:73018172 | T | A | 1 | a0001c0002t0010g0093 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.116+20014T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018172 | |||||||
| chr3:73018187 | C | A | 1 | a0001c0001t0004g0168 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.116+20029C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018187 | |||||||
| chr3:73018201 | C | T | 1 | a0001c0001t0007g0190 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.116+20043C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018201 | |||||||
| chr3:73018317 | C | T | 14 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(11): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+20159C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018317 | |||||||
| chr3:73018357 | C | T | 1 | a0001c0001t0068g0330 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.116+20199C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018357 | |||||||
| chr3:73018407 | C | CGTTAT | 54 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0123 others(51): Show |
57 | HG00140.hp2 HG00423.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.116+20290_116+2029 others(9): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73018407 | ||||||
| chr3:73018407 | C | CGTTATGT others(3): Show |
55 | a0001c0001t0001g0001 a0001c0001t0001g0225 a0001c0001t0001g0235 others(52): Show |
57 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.116+20285_116+2029 others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73018407 | ||||||
| chr3:73018407 | C | CGTTATGT others(8): Show |
43 | a0001c0001t0001g0210 a0001c0001t0001g0246 a0001c0001t0001g0263 others(40): Show |
43 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.116+20280_116+2029 others(19): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73018407 | ||||||
| chr3:73018407 | C | CGTTATGT others(13): Show |
7 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0341 others(4): Show |
7 | HG02451.hp2 NA18948.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.116+20275_116+2029 others(24): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73018407 | ||||||
| chr3:73018407 | C | CGTTATGT others(77): Show |
3 | a0001c0001t0004g0166 a0001c0001t0004g0167 a0001c0001t0004g0172 |
3 | HG00735.hp2 HG02622.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.116+20292_116+2029 others(88): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73018407 | ||||||
| chr3:73018407 | CGTTATGT others(3): Show |
C | 1 | a0001c0001t0001g0239 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.116+20285_116+2029 others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73018407 | ||||||
| chr3:73018408 | G | GTTATGTT others(66): Show |
1 | a0001c0001t0051g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.116+20292_116+2029 others(77): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73018408 | ||||||
| chr3:73018408 | G | GTTATGTT others(72): Show |
2 | a0001c0001t0003g0129 a0001c0001t0004g0163 |
2 | HG01975.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.116+20292_116+2029 others(83): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73018408 | ||||||
| chr3:73018448 | GTTAT | G | 9 | a0001c0002t0003g0055 a0001c0002t0003g0059 a0001c0002t0003g0077 others(6): Show |
9 | HG01243.hp2 HG03225.hp2 NA18944.hp2 others(6): Show |
intron_variant | MODIFIER | c.116+20295_116+2029 others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73018448 | ||||||
| chr3:73018452 | T | TG | 25 | a0001c0001t0003g0129 a0001c0001t0004g0163 a0001c0001t0004g0166 others(22): Show |
25 | HG00735.hp2 HG01884.hp2 HG01975.hp1 others(22): Show |
intron_variant | MODIFIER | c.116+20294_116+2029 others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATG | 34 | a0001c0001t0018g0194 a0001c0001t0018g0195 a0001c0002t0003g0026 others(31): Show |
34 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.116+20294_116+2029 others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(4): Show |
24 | a0001c0001t0018g0193 a0001c0002t0003g0014 a0001c0002t0003g0027 others(21): Show |
24 | HG00099.hp2 HG00738.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.116+20294_116+2029 others(15): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(9): Show |
14 | a0001c0002t0003g0025 a0001c0002t0003g0028 a0001c0002t0003g0058 others(11): Show |
14 | HG00423.hp1 HG01069.hp2 HG03710.hp2 others(11): Show |
intron_variant | MODIFIER | c.116+20294_116+2029 others(20): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(14): Show |
4 | a0001c0002t0003g0082 a0001c0002t0020g0034 a0001c0002t0033g0099 others(1): Show |
4 | HG01884.hp1 HG02976.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+20294_116+2029 others(25): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(88): Show |
1 | a0001c0001t0007g0183 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(99): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(83): Show |
1 | a0001c0001t0004g0151 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(94): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(93): Show |
1 | a0001c0001t0004g0157 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(104): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(93): Show |
1 | a0001c0001t0004g0180 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.116+20294_116+2029 others(104): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(113): Show |
1 | a0001c0001t0025g0176 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(124): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(77): Show |
1 | a0001c0001t0009g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(88): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(79): Show |
1 | a0001c0001t0004g0159 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(90): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(78): Show |
2 | a0001c0001t0008g0158 a0001c0001t0008g0179 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(89): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(88): Show |
1 | a0001c0001t0008g0132 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(99): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(73): Show |
1 | a0001c0001t0004g0160 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.116+20294_116+2029 others(84): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(88): Show |
3 | a0001c0001t0004g0155 a0001c0001t0008g0138 a0001c0001t0024g0154 |
3 | HG02293.hp1 HG03041.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(99): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(93): Show |
2 | a0001c0001t0008g0147 a0001c0001t0057g0135 |
2 | HG01109.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(104): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(103): Show |
1 | a0001c0001t0025g0177 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(114): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(78): Show |
1 | a0001c0001t0034g0144 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(89): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(67): Show |
1 | a0001c0001t0009g0191 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(78): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(77): Show |
1 | a0001c0001t0003g0116 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(88): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(83): Show |
1 | a0001c0001t0004g0130 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(94): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(88): Show |
1 | a0001c0001t0004g0128 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.116+20294_116+2029 others(99): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(68): Show |
1 | a0001c0001t0007g0187 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.116+20294_116+2029 others(79): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(78): Show |
2 | a0001c0001t0004g0127 a0001c0001t0036g0192 |
2 | HG01099.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(89): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(83): Show |
8 | a0001c0001t0004g0139 a0001c0001t0004g0161 a0001c0001t0007g0141 others(5): Show |
8 | HG00140.hp1 HG00741.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.116+20294_116+2029 others(94): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(88): Show |
2 | a0001c0001t0007g0143 a0001c0001t0008g0136 |
2 | HG02145.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(99): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(99): Show |
1 | a0001c0001t0054g0175 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.116+20294_116+2029 others(110): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(67): Show |
2 | a0001c0001t0009g0002 a0001c0001t0009g0110 |
3 | HG02145.hp2 HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(78): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(43): Show |
1 | a0001c0001t0024g0153 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.116+20294_116+2029 others(54): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(63): Show |
1 | a0001c0001t0007g0133 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.116+20294_116+2029 others(74): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(68): Show |
1 | a0001c0001t0026g0174 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(79): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(83): Show |
2 | a0001c0001t0004g0131 a0001c0001t0004g0164 |
2 | HG01978.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(94): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(88): Show |
2 | a0001c0001t0026g0185 a0001c0001t0056g0186 |
2 | HG01255.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(99): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(63): Show |
2 | a0001c0001t0004g0142 a0001c0001t0034g0145 |
2 | HG01081.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(74): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(73): Show |
1 | a0001c0001t0025g0178 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(84): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(78): Show |
2 | a0001c0001t0004g0156 a0001c0001t0008g0162 |
2 | HG01123.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(89): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(83): Show |
2 | a0001c0001t0035g0148 a0001c0001t0035g0149 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(94): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(88): Show |
2 | a0001c0001t0008g0106 a0001c0001t0024g0140 |
2 | HG02129.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(99): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(57): Show |
4 | a0001c0001t0009g0117 a0001c0001t0009g0118 a0001c0001t0009g0119 others(1): Show |
4 | HG02109.hp2 HG02451.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.116+20294_116+2029 others(68): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTATGT others(62): Show |
1 | a0001c0001t0019g0112 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(73): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTTGTT others(73): Show |
1 | a0001c0001t0058g0182 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(84): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTTGTT others(78): Show |
5 | a0001c0001t0004g0134 a0001c0001t0004g0165 a0001c0001t0004g0169 others(2): Show |
5 | HG01928.hp2 HG02486.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.116+20294_116+2029 others(89): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTTGTT others(83): Show |
1 | a0001c0001t0004g0168 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(94): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTTGTT others(88): Show |
3 | a0001c0001t0007g0171 a0001c0001t0007g0189 a0005c0006t0026g0173 |
3 | HG02818.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(99): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTTGTT others(73): Show |
1 | a0001c0001t0007g0190 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.116+20294_116+2029 others(84): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTTGTT others(52): Show |
2 | a0001c0001t0003g0114 a0001c0001t0019g0121 |
2 | HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.116+20294_116+2029 others(63): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTTGTT others(57): Show |
1 | a0001c0001t0019g0113 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(68): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018452 | T | TGTTTGTT others(62): Show |
1 | a0001c0001t0003g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.116+20294_116+2029 others(73): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018452 | |||||||
| chr3:73018534 | G | C | 1 | a0001c0002t0031g0018 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.116+20376G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018534 | |||||||
| chr3:73018612 | A | C | 15 | a0001c0001t0001g0239 a0001c0001t0002g0217 a0001c0001t0002g0228 others(12): Show |
15 | HG00438.hp1 HG00609.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+20454A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018612 | |||||||
| chr3:73018647 | C | G | 3 | a0001c0002t0013g0101 a0001c0002t0033g0099 a0001c0002t0033g0100 |
3 | HG01884.hp1 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.116+20489C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018647 | |||||||
| chr3:73018724 | A | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0125 |
3 | HG00738.hp2 HG01071.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.116+20566A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018724 | |||||||
| chr3:73018759 | C | T | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | NA18954.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.116+20601C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018759 | |||||||
| chr3:73018840 | T | G | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+20682T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018840 | |||||||
| chr3:73018934 | A | G | 1 | a0001c0002t0027g0075 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.116+20776A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73018934 | |||||||
| chr3:73019015 | T | TG | 65 | a0001c0001t0003g0129 a0001c0001t0004g0127 a0001c0001t0004g0128 others(62): Show |
65 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.116+20858dupG | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73019015 | ||||||
| chr3:73019054 | C | T | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.116+20896C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73019054 | |||||||
| chr3:73019322 | C | T | 14 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(11): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+21164C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73019322 | |||||||
| chr3:73019580 | G | T | 1 | a0001c0001t0001g0295 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.116+21422G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73019580 | |||||||
| chr3:73019627 | G | A | 3 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 |
3 | HG02055.hp1 HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.116+21469G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73019627 | |||||||
| chr3:73019660 | A | C | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+21502A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73019660 | |||||||
| chr3:73019669 | C | T | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+21511C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73019669 | |||||||
| chr3:73019778 | G | GCT | 31 | a0001c0001t0003g0129 a0001c0001t0004g0128 a0001c0001t0004g0130 others(28): Show |
31 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.116+21629_116+2163 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73019778 | ||||||
| chr3:73019967 | C | T | 1 | a0001c0001t0001g0295 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.116+21809C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73019967 | |||||||
| chr3:73020010 | A | G | 2 | a0001c0001t0001g0314 a0001c0001t0014g0332 |
2 | HG00438.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.116+21852A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020010 | |||||||
| chr3:73020227 | G | T | 1 | a0001c0002t0037g0074 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.116+22069G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020227 | |||||||
| chr3:73020330 | A | G | 2 | a0001c0002t0006g0035 a0001c0002t0006g0043 |
2 | NA18942.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.116+22172A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020330 | |||||||
| chr3:73020400 | G | C | 1 | a0006c0009t0018g0197 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.116+22242G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020400 | |||||||
| chr3:73020514 | C | G | 1 | a0001c0002t0003g0081 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.116+22356C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020514 | |||||||
| chr3:73020543 | G | T | 66 | a0001c0001t0003g0129 a0001c0001t0004g0127 a0001c0001t0004g0128 others(63): Show |
66 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.116+22385G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020543 | |||||||
| chr3:73020545 | C | T | 1 | a0001c0001t0035g0148 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.116+22387C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020545 | |||||||
| chr3:73020588 | T | A | 2 | a0001c0002t0013g0094 a0001c0002t0013g0095 |
2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116+22430T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020588 | |||||||
| chr3:73020672 | T | TAAAAAAA others(3): Show |
2 | a0001c0002t0013g0094 a0001c0002t0013g0095 |
2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116+22524_116+2253 others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73020672 | ||||||
| chr3:73020672 | T | TTAA | 7 | a0001c0001t0004g0168 a0001c0001t0007g0190 a0001c0001t0026g0174 others(4): Show |
7 | HG01255.hp1 HG01952.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.116+22514_116+2251 others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020672 | |||||||
| chr3:73020672 | T | TTAAA | 23 | a0001c0001t0003g0129 a0001c0001t0004g0128 a0001c0001t0004g0130 others(20): Show |
23 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.116+22514_116+2251 others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020672 | |||||||
| chr3:73020672 | T | TTAAAA | 54 | a0001c0001t0003g0115 a0001c0001t0003g0116 a0001c0001t0004g0127 others(51): Show |
55 | HG00140.hp1 HG00741.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.116+22514_116+2251 others(9): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020672 | |||||||
| chr3:73020672 | T | TTAAAAA | 76 | a0001c0001t0003g0114 a0001c0001t0008g0136 a0001c0001t0009g0110 others(73): Show |
76 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.116+22514_116+2251 others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020672 | |||||||
| chr3:73020672 | T | TTAAAAAA | 15 | a0001c0002t0003g0055 a0001c0002t0003g0058 a0001c0002t0010g0011 others(12): Show |
15 | HG00423.hp1 HG01192.hp1 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.116+22514_116+2251 others(11): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020672 | |||||||
| chr3:73020672 | T | TTAAAAAA others(1): Show |
4 | a0001c0002t0003g0091 a0001c0002t0011g0016 a0001c0002t0027g0075 others(1): Show |
4 | HG02683.hp1 HG02698.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+22514_116+2251 others(12): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020672 | |||||||
| chr3:73020672 | TA | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(80): Show |
87 | HG00140.hp2 HG00438.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.116+22533delA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73020672 | ||||||
| chr3:73020691 | A | AAAAAAAA others(3): Show |
2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+22533_116+2253 others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020691 | |||||||
| chr3:73020869 | A | G | 2 | a0001c0002t0013g0094 a0001c0002t0013g0095 |
2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116+22711A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020869 | |||||||
| chr3:73020907 | G | C | 1 | a0001c0001t0001g0265 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.116+22749G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020907 | |||||||
| chr3:73020948 | A | G | 1 | a0001c0001t0025g0176 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.116+22790A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73020948 | |||||||
| chr3:73021093 | A | T | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+22935A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021093 | |||||||
| chr3:73021110 | T | G | 1 | a0001c0001t0008g0106 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.116+22952T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021110 | |||||||
| chr3:73021224 | TA | T | 66 | a0001c0001t0003g0129 a0001c0001t0004g0127 a0001c0001t0004g0128 others(63): Show |
66 | HG00140.hp1 HG00741.hp2 HG01081.hp2 others(63): Show |
intron_variant | MODIFIER | c.116+23075delA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021224 | ||||||
| chr3:73021232 | AAT | A | 16 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(13): Show |
17 | HG01069.hp1 HG01071.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.116+23075_116+2307 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021232 | |||||||
| chr3:73021232 | AATTTTTT others(4): Show |
A | 97 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(94): Show |
97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.116+23075_116+2308 others(15): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021232 | |||||||
| chr3:73021233 | A | AT | 9 | a0001c0001t0001g0124 a0001c0001t0001g0218 a0001c0001t0001g0281 others(6): Show |
9 | HG01361.hp1 HG01361.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.116+23092dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021233 | ||||||
| chr3:73021233 | A | T | 13 | a0001c0001t0002g0318 a0001c0001t0004g0157 a0001c0001t0004g0166 others(10): Show |
13 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.116+23075A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021233 | |||||||
| chr3:73021250 | T | G | 1 | a0001c0001t0007g0187 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.116+23092T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021250 | |||||||
| chr3:73021251 | G | T | 97 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(94): Show |
97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.116+23093G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021251 | |||||||
| chr3:73021314 | G | A | 1 | a0001c0001t0007g0190 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.116+23156G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021314 | |||||||
| chr3:73021346 | G | A | 214 | a0001c0001t0001g0210 a0001c0001t0001g0331 a0001c0001t0001g0336 others(211): Show |
215 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.116+23188G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021346 | |||||||
| chr3:73021527 | C | T | 55 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(52): Show |
56 | HG00140.hp1 HG00741.hp2 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.116+23369C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021527 | |||||||
| chr3:73021605 | G | A | 1 | a0001c0003t0045g0202 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.116+23447G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021605 | |||||||
| chr3:73021678 | C | T | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+23520C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021678 | |||||||
| chr3:73021844 | C | CTGTG | 5 | a0001c0001t0004g0130 a0001c0001t0004g0131 a0001c0001t0004g0134 others(2): Show |
5 | HG01928.hp2 HG01934.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.116+23687_116+2368 others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021844 | ||||||
| chr3:73021844 | CTA | C | 15 | a0001c0001t0004g0163 a0001c0001t0004g0164 a0001c0001t0004g0165 others(12): Show |
15 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+23690_116+2369 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021844 | ||||||
| chr3:73021844 | CTATA | C | 3 | a0001c0001t0026g0174 a0001c0001t0056g0186 a0005c0006t0026g0173 |
3 | HG03130.hp2 HG04199.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.116+23688_116+2369 others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021844 | ||||||
| chr3:73021844 | CTATATG | C | 3 | a0001c0001t0025g0176 a0001c0001t0025g0177 a0001c0001t0025g0178 |
3 | HG02735.hp2 HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.116+23688_116+2369 others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021844 | ||||||
| chr3:73021846 | A | G | 10 | a0001c0001t0003g0129 a0001c0001t0004g0128 a0001c0001t0004g0130 others(7): Show |
10 | HG01255.hp1 HG01928.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.116+23688A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021846 | |||||||
| chr3:73021848 | A | ATG | 41 | a0001c0001t0001g0124 a0001c0001t0001g0223 a0001c0001t0001g0224 others(38): Show |
41 | HG00609.hp1 HG01069.hp2 HG01346.hp2 others(38): Show |
intron_variant | MODIFIER | c.116+23722_116+2372 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021848 | ||||||
| chr3:73021848 | A | ATGTG | 4 | a0001c0001t0001g0220 a0001c0001t0002g0004 a0001c0002t0003g0084 others(1): Show |
5 | HG01433.hp2 HG04115.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.116+23720_116+2372 others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021848 | ||||||
| chr3:73021848 | A | ATGTGTGT others(5): Show |
2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+23712_116+2372 others(16): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021848 | ||||||
| chr3:73021848 | A | G | 28 | a0001c0001t0003g0129 a0001c0001t0004g0128 a0001c0001t0004g0130 others(25): Show |
28 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.116+23690A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021848 | |||||||
| chr3:73021848 | ATG | A | 24 | a0001c0001t0001g0210 a0001c0001t0001g0300 a0001c0001t0001g0331 others(21): Show |
24 | HG02055.hp1 HG02280.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.116+23722_116+2372 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021848 | ||||||
| chr3:73021848 | ATGTG | A | 21 | a0001c0001t0003g0115 a0001c0001t0009g0002 a0001c0001t0009g0110 others(18): Show |
22 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.116+23720_116+2372 others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021848 | ||||||
| chr3:73021850 | G | A | 1 | a0001c0001t0001g0336 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.116+23692G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021850 | |||||||
| chr3:73021880 | G | A | 95 | a0001c0001t0001g0210 a0001c0001t0003g0114 a0001c0001t0003g0115 others(92): Show |
96 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(93): Show |
intron_variant | MODIFIER | c.116+23722G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021880 | |||||||
| chr3:73021880 | G | GTA | 3 | a0001c0001t0004g0157 a0001c0001t0007g0183 a0001c0001t0008g0138 |
3 | HG02040.hp2 HG02293.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.116+23728_116+2372 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021880 | ||||||
| chr3:73021882 | A | G | 14 | a0001c0001t0001g0003 a0001c0001t0001g0124 a0001c0001t0001g0125 others(11): Show |
15 | HG00735.hp1 HG00738.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.116+23724A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021882 | |||||||
| chr3:73021886 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.116+23728A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021886 | |||||||
| chr3:73021887 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.116+23729T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021887 | |||||||
| chr3:73021888 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.116+23730G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021888 | |||||||
| chr3:73021889 | C | CAT | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(137): Show |
144 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.116+23742_116+2374 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021889 | ||||||
| chr3:73021889 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.116+23731C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021889 | |||||||
| chr3:73021900 | A | AT | 45 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0265 others(42): Show |
46 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.116+23758dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021900 | ||||||
| chr3:73021900 | ATT | A | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+23757_116+2375 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73021900 | ||||||
| chr3:73021901 | T | TA | 17 | a0001c0001t0001g0226 a0001c0001t0001g0235 a0001c0001t0001g0239 others(14): Show |
17 | HG00438.hp2 HG00609.hp1 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.116+23743_116+2374 others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021901 | |||||||
| chr3:73021901 | T | TATA | 108 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(105): Show |
109 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.116+23743_116+2374 others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021901 | |||||||
| chr3:73021901 | T | TATATA | 4 | a0001c0001t0019g0112 a0001c0001t0019g0113 a0001c0001t0019g0120 others(1): Show |
4 | HG02027.hp2 HG02572.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+23743_116+2374 others(9): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021901 | |||||||
| chr3:73021902 | T | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0122 others(115): Show |
121 | HG00140.hp1 HG00140.hp2 HG00621.hp2 others(118): Show |
intron_variant | MODIFIER | c.116+23744T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021902 | |||||||
| chr3:73021903 | T | A | 35 | a0001c0001t0001g0226 a0001c0001t0001g0303 a0001c0001t0001g0317 others(32): Show |
36 | HG01975.hp1 HG02027.hp2 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.116+23745T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021903 | |||||||
| chr3:73021904 | T | A | 56 | a0001c0001t0001g0210 a0001c0001t0001g0295 a0001c0001t0001g0338 others(53): Show |
56 | HG00741.hp2 HG01081.hp2 HG01099.hp2 others(53): Show |
intron_variant | MODIFIER | c.116+23746T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021904 | |||||||
| chr3:73021905 | T | A | 10 | a0001c0001t0003g0115 a0001c0001t0003g0116 a0001c0001t0009g0110 others(7): Show |
10 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.116+23747T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021905 | |||||||
| chr3:73021906 | T | A | 4 | a0001c0001t0018g0193 a0001c0001t0018g0195 a0001c0001t0018g0198 others(1): Show |
4 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+23748T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021906 | |||||||
| chr3:73021923 | A | G | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+23765A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73021923 | |||||||
| chr3:73022062 | A | C | 1 | a0001c0001t0034g0145 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.116+23904A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022062 | |||||||
| chr3:73022232 | G | A | 1 | a0001c0001t0002g0270 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.116+24074G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022232 | |||||||
| chr3:73022245 | C | G | 2 | a0001c0001t0001g0314 a0001c0001t0014g0332 |
2 | HG00438.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.116+24087C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022245 | |||||||
| chr3:73022333 | A | AT | 32 | a0001c0001t0004g0127 a0001c0001t0004g0139 a0001c0001t0004g0142 others(29): Show |
32 | HG00140.hp1 HG00741.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.116+24180dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73022333 | ||||||
| chr3:73022400 | T | C | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+24242T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022400 | |||||||
| chr3:73022412 | T | G | 1 | a0001c0001t0004g0157 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.116+24254T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022412 | |||||||
| chr3:73022463 | A | T | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.116+24305A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022463 | |||||||
| chr3:73022477 | G | A | 1 | a0001c0002t0063g0107 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.116+24319G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022477 | |||||||
| chr3:73022498 | G | A | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+24340G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022498 | |||||||
| chr3:73022727 | G | A | 183 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(180): Show |
184 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.117-24459G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022727 | |||||||
| chr3:73022768 | C | CT | 13 | a0001c0001t0001g0210 a0001c0001t0001g0250 a0001c0001t0016g0208 others(10): Show |
13 | HG00423.hp2 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.117-24400dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73022768 | ||||||
| chr3:73022768 | CT | C | 115 | a0001c0001t0001g0235 a0001c0001t0001g0263 a0001c0001t0001g0274 others(112): Show |
115 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.117-24400delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73022768 | ||||||
| chr3:73022771 | T | TC | 14 | a0001c0001t0004g0163 a0001c0001t0004g0164 a0001c0001t0004g0165 others(11): Show |
14 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.117-24415_117-2441 others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022771 | |||||||
| chr3:73022772 | T | C | 72 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(69): Show |
73 | HG00140.hp1 HG00741.hp2 HG01081.hp2 others(70): Show |
intron_variant | MODIFIER | c.117-24414T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022772 | |||||||
| chr3:73022773 | T | C | 95 | a0001c0001t0007g0190 a0001c0001t0034g0145 a0001c0002t0003g0014 others(92): Show |
95 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.117-24413T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022773 | |||||||
| chr3:73022774 | T | C | 2 | a0001c0002t0006g0031 a0001c0002t0020g0047 |
2 | NA18965.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.117-24412T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73022774 | |||||||
| chr3:73022884 | TG | T | 86 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(83): Show |
87 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.117-24300delG | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73022884 | ||||||
| chr3:73023008 | A | G | 86 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(83): Show |
87 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.117-24178A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023008 | |||||||
| chr3:73023091 | A | G | 183 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(180): Show |
184 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.117-24095A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023091 | |||||||
| chr3:73023119 | A | T | 1 | a0001c0001t0002g0238 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.117-24067A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023119 | |||||||
| chr3:73023170 | C | T | 14 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(11): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.117-24016C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023170 | |||||||
| chr3:73023171 | T | G | 86 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(83): Show |
87 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.117-24015T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023171 | |||||||
| chr3:73023181 | CT | C | 182 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(179): Show |
183 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.117-23997delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73023181 | ||||||
| chr3:73023189 | T | G | 1 | a0001c0002t0055g0354 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.117-23997T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023189 | |||||||
| chr3:73023190 | G | T | 1 | a0001c0002t0055g0354 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.117-23996G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023190 | |||||||
| chr3:73023213 | C | G | 6 | a0001c0002t0013g0097 a0001c0002t0013g0101 a0001c0002t0030g0096 others(3): Show |
6 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.117-23973C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023213 | |||||||
| chr3:73023270 | A | C | 1 | a0001c0001t0002g0270 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.117-23916A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023270 | |||||||
| chr3:73023294 | A | G | 1 | a0001c0001t0051g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.117-23892A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023294 | |||||||
| chr3:73023296 | T | TCTC | 183 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(180): Show |
184 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.117-23888_117-2388 others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73023296 | ||||||
| chr3:73023417 | C | G | 1 | a0001c0001t0001g0289 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.117-23769C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023417 | |||||||
| chr3:73023433 | G | A | 1 | a0001c0001t0003g0114 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.117-23753G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023433 | |||||||
| chr3:73023475 | A | G | 2 | a0001c0001t0009g0111 a0001c0001t0009g0117 |
2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.117-23711A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023475 | |||||||
| chr3:73023551 | A | G | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.117-23635A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023551 | |||||||
| chr3:73023912 | C | G | 2 | a0001c0002t0003g0026 a0001c0002t0003g0089 |
2 | NA18973.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.117-23274C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73023912 | |||||||
| chr3:73024076 | A | T | 2 | a0001c0001t0001g0250 a0007c0008t0001g0283 |
2 | HG00423.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.117-23110A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024076 | |||||||
| chr3:73024078 | G | T | 2 | a0001c0001t0001g0250 a0007c0008t0001g0283 |
2 | HG00423.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.117-23108G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024078 | |||||||
| chr3:73024083 | G | T | 2 | a0001c0001t0001g0250 a0007c0008t0001g0283 |
2 | HG00423.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.117-23103G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024083 | |||||||
| chr3:73024188 | A | T | 7 | a0001c0001t0003g0129 a0001c0001t0004g0128 a0001c0001t0004g0130 others(4): Show |
7 | HG01928.hp2 HG01934.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.117-22998A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024188 | |||||||
| chr3:73024219 | A | G | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.117-22967A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024219 | |||||||
| chr3:73024378 | A | G | 19 | a0001c0001t0003g0129 a0001c0001t0004g0128 a0001c0001t0004g0130 others(16): Show |
19 | HG00735.hp2 HG01928.hp2 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.117-22808A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024378 | |||||||
| chr3:73024491 | T | C | 2 | a0001c0001t0002g0240 a0001c0001t0002g0241 |
2 | NA19005.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.117-22695T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024491 | |||||||
| chr3:73024498 | C | T | 1 | a0001c0002t0006g0049 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.117-22688C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024498 | |||||||
| chr3:73024523 | G | C | 1 | a0001c0002t0010g0079 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.117-22663G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024523 | |||||||
| chr3:73024552 | A | C | 86 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(83): Show |
87 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.117-22634A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024552 | |||||||
| chr3:73024646 | C | A | 97 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(94): Show |
97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.117-22540C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024646 | |||||||
| chr3:73024728 | A | G | 99 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(96): Show |
99 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.117-22458A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024728 | |||||||
| chr3:73024923 | C | G | 97 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(94): Show |
97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.117-22263C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024923 | |||||||
| chr3:73024928 | C | T | 5 | a0001c0001t0026g0174 a0001c0001t0026g0185 a0001c0001t0056g0186 others(2): Show |
5 | HG01255.hp1 HG01952.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.117-22258C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024928 | |||||||
| chr3:73024972 | T | C | 87 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(84): Show |
88 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.117-22214T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73024972 | |||||||
| chr3:73025385 | G | C | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.117-21801G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73025385 | |||||||
| chr3:73025508 | G | C | 99 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(96): Show |
99 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.117-21678G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73025508 | |||||||
| chr3:73025591 | A | G | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.117-21595A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73025591 | |||||||
| chr3:73025612 | A | G | 14 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(11): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.117-21574A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73025612 | |||||||
| chr3:73025757 | A | G | 99 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(96): Show |
99 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.117-21429A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73025757 | |||||||
| chr3:73025953 | A | G | 14 | a0001c0001t0001g0218 a0001c0001t0005g0227 a0001c0001t0005g0234 others(11): Show |
14 | HG00741.hp1 NA18941.hp2 NA18948.hp1 others(11): Show |
intron_variant | MODIFIER | c.117-21233A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73025953 | |||||||
| chr3:73026202 | C | G | 1 | a0001c0001t0002g0298 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.117-20984C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026202 | |||||||
| chr3:73026259 | G | A | 65 | a0001c0001t0003g0129 a0001c0001t0004g0127 a0001c0001t0004g0128 others(62): Show |
65 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.117-20927G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026259 | |||||||
| chr3:73026329 | G | A | 1 | a0001c0001t0004g0157 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.117-20857G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026329 | |||||||
| chr3:73026398 | G | C | 1 | a0005c0006t0026g0173 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.117-20788G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026398 | |||||||
| chr3:73026501 | A | ATT | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.117-20685_117-2068 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026501 | |||||||
| chr3:73026661 | A | G | 99 | a0001c0001t0002g0268 a0001c0001t0067g0296 a0001c0002t0003g0014 others(96): Show |
99 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.117-20525A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026661 | |||||||
| chr3:73026674 | T | G | 33 | a0001c0001t0004g0127 a0001c0001t0004g0139 a0001c0001t0004g0142 others(30): Show |
33 | HG00140.hp1 HG00741.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.117-20512T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026674 | |||||||
| chr3:73026682 | A | T | 97 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(94): Show |
97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.117-20504A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026682 | |||||||
| chr3:73026701 | AT | A | 185 | a0001c0001t0001g0263 a0001c0001t0003g0114 a0001c0001t0003g0115 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.117-20476delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73026701 | ||||||
| chr3:73026710 | T | A | 1 | a0001c0001t0025g0177 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.117-20476T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026710 | |||||||
| chr3:73026743 | T | C | 1 | a0001c0001t0001g0265 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.117-20443T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026743 | |||||||
| chr3:73026765 | C | G | 1 | a0001c0001t0067g0296 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.117-20421C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026765 | |||||||
| chr3:73026827 | A | G | 2 | a0001c0001t0002g0261 a0001c0001t0068g0330 |
2 | HG02080.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.117-20359A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026827 | |||||||
| chr3:73026903 | C | T | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.117-20283C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026903 | |||||||
| chr3:73026983 | C | A | 96 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(93): Show |
96 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.117-20203C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73026983 | |||||||
| chr3:73027013 | T | C | 1 | a0001c0001t0051g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.117-20173T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73027013 | |||||||
| chr3:73027133 | G | A | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.117-20053G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73027133 | |||||||
| chr3:73027252 | A | T | 86 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(83): Show |
87 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.117-19934A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73027252 | |||||||
| chr3:73027272 | G | A | 1 | a0001c0001t0001g0303 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.117-19914G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73027272 | |||||||
| chr3:73027365 | A | C | 4 | a0001c0001t0001g0218 a0001c0001t0005g0227 a0001c0001t0005g0299 others(1): Show |
4 | NA18970.hp2 NA19011.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-19821A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73027365 | |||||||
| chr3:73027393 | T | C | 99 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(96): Show |
99 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.117-19793T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73027393 | |||||||
| chr3:73027404 | G | A | 1 | a0001c0001t0051g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.117-19782G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73027404 | |||||||
| chr3:73027659 | G | GGTGT | 4 | a0001c0002t0003g0073 a0001c0002t0013g0094 a0001c0002t0013g0095 others(1): Show |
4 | HG02155.hp2 HG03225.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-19504_117-1950 others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027659 | ||||||
| chr3:73027659 | G | GGTGTGT | 69 | a0001c0002t0003g0024 a0001c0002t0003g0025 a0001c0002t0003g0026 others(66): Show |
69 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.117-19506_117-1950 others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027659 | ||||||
| chr3:73027659 | G | GGTGTGTG others(1): Show |
18 | a0001c0002t0003g0014 a0001c0002t0003g0061 a0001c0002t0003g0077 others(15): Show |
18 | HG00738.hp1 HG01243.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.117-19508_117-1950 others(12): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027659 | ||||||
| chr3:73027659 | G | GGTGTGTG others(3): Show |
5 | a0001c0002t0013g0097 a0001c0002t0013g0101 a0001c0002t0015g0057 others(2): Show |
5 | HG01884.hp1 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.117-19510_117-1950 others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027659 | ||||||
| chr3:73027659 | G | GGTGTGTG others(5): Show |
1 | a0001c0002t0011g0056 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.117-19512_117-1950 others(16): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027659 | ||||||
| chr3:73027659 | GGT | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0210 others(56): Show |
62 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.117-19502_117-1950 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027659 | ||||||
| chr3:73027659 | GGTGT | G | 85 | a0001c0001t0001g0328 a0001c0001t0003g0129 a0001c0001t0004g0127 others(82): Show |
86 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(83): Show |
intron_variant | MODIFIER | c.117-19504_117-1950 others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027659 | ||||||
| chr3:73027659 | GGTGTGTG others(3): Show |
G | 1 | a0001c0001t0002g0256 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.117-19510_117-1950 others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027659 | ||||||
| chr3:73027909 | C | CT | 47 | a0001c0001t0001g0306 a0001c0001t0001g0317 a0001c0001t0003g0114 others(44): Show |
48 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.117-19263dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027909 | ||||||
| chr3:73027944 | A | AT | 14 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0340 others(11): Show |
14 | HG01884.hp1 HG01891.hp1 HG02897.hp2 others(11): Show |
intron_variant | MODIFIER | c.117-19226dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027944 | ||||||
| chr3:73027944 | A | ATT | 91 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(88): Show |
91 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.117-19227_117-1922 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027944 | ||||||
| chr3:73027944 | AT | A | 35 | a0001c0001t0001g0249 a0001c0001t0001g0335 a0001c0001t0003g0129 others(32): Show |
35 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.117-19226delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027944 | ||||||
| chr3:73027944 | ATT | A | 7 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(4): Show |
7 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.117-19227_117-1922 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73027944 | ||||||
| chr3:73027970 | G | A | 1 | a0001c0001t0008g0147 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.117-19216G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73027970 | |||||||
| chr3:73027971 | G | A | 1 | a0001c0001t0004g0161 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.117-19215G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73027971 | |||||||
| chr3:73028014 | T | C | 86 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(83): Show |
87 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.117-19172T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028014 | |||||||
| chr3:73028028 | A | G | 1 | a0001c0001t0017g0320 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.117-19158A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028028 | |||||||
| chr3:73028063 | C | G | 86 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(83): Show |
87 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.117-19123C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028063 | |||||||
| chr3:73028118 | G | A | 1 | a0001c0001t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.117-19068G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028118 | |||||||
| chr3:73028194 | TTGCAGTG others(7): Show |
T | 97 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(94): Show |
97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.117-18991_117-1897 others(18): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028194 | |||||||
| chr3:73028196 | G | T | 14 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(11): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.117-18990G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028196 | |||||||
| chr3:73028256 | CA | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0122 others(84): Show |
89 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.117-18911delA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73028256 | ||||||
| chr3:73028256 | CAA | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0210 a0001c0001t0001g0216 others(62): Show |
67 | HG00140.hp1 HG00741.hp2 HG01081.hp2 others(64): Show |
intron_variant | MODIFIER | c.117-18912_117-1891 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73028256 | ||||||
| chr3:73028256 | CAAA | C | 142 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(139): Show |
143 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(140): Show |
intron_variant | MODIFIER | c.117-18913_117-1891 others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73028256 | ||||||
| chr3:73028381 | T | C | 2 | a0001c0002t0013g0094 a0001c0002t0013g0095 |
2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.117-18805T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028381 | |||||||
| chr3:73028427 | C | T | 1 | a0001c0001t0051g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.117-18759C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028427 | |||||||
| chr3:73028442 | AGAT | A | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.117-18743_117-1874 others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028442 | |||||||
| chr3:73028489 | G | C | 97 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(94): Show |
97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.117-18697G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028489 | |||||||
| chr3:73028602 | A | G | 1 | a0001c0002t0020g0034 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.117-18584A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028602 | |||||||
| chr3:73028648 | C | G | 97 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(94): Show |
97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.117-18538C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028648 | |||||||
| chr3:73028673 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0310 |
4 | NA18747.hp1 NA18972.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.117-18513C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028673 | |||||||
| chr3:73028680 | C | T | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.117-18506C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028680 | |||||||
| chr3:73028685 | G | A | 86 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(83): Show |
87 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.117-18501G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028685 | |||||||
| chr3:73028763 | G | T | 1 | a0001c0001t0001g0331 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.117-18423G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028763 | |||||||
| chr3:73028788 | T | G | 1 | a0001c0001t0025g0178 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.117-18398T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028788 | |||||||
| chr3:73028846 | AAGGAG | A | 10 | a0001c0001t0016g0109 a0001c0001t0016g0205 a0001c0001t0016g0206 others(7): Show |
10 | HG02280.hp2 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.117-18334_117-1833 others(9): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73028846 | ||||||
| chr3:73028876 | A | G | 1 | a0006c0009t0018g0197 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.117-18310A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028876 | |||||||
| chr3:73028881 | T | C | 98 | a0001c0001t0024g0153 a0001c0002t0003g0014 a0001c0002t0003g0024 others(95): Show |
98 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.117-18305T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028881 | |||||||
| chr3:73028893 | A | G | 86 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(83): Show |
87 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.117-18293A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028893 | |||||||
| chr3:73028940 | G | A | 1 | a0001c0001t0051g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.117-18246G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028940 | |||||||
| chr3:73028942 | C | T | 310 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(307): Show |
315 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.117-18244C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73028942 | |||||||
| chr3:73029030 | C | G | 1 | a0001c0002t0013g0102 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.117-18156C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73029030 | |||||||
| chr3:73029527 | TTGTC | T | 3 | a0001c0003t0012g0209 a0001c0003t0012g0211 a0001c0003t0012g0212 |
3 | HG02647.hp2 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.117-17656_117-1765 others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73029527 | ||||||
| chr3:73029574 | A | AAG | 86 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(83): Show |
87 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.117-17611_117-1761 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73029574 | ||||||
| chr3:73029608 | A | G | 1 | a0001c0001t0038g0279 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.117-17578A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73029608 | |||||||
| chr3:73029675 | G | A | 1 | a0001c0002t0003g0026 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.117-17511G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73029675 | |||||||
| chr3:73029741 | T | G | 2 | a0001c0003t0043g0201 a0001c0003t0045g0202 |
2 | HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.117-17445T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73029741 | |||||||
| chr3:73029816 | A | G | 1 | a0001c0001t0021g0204 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.117-17370A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73029816 | |||||||
| chr3:73030292 | A | G | 1 | a0001c0001t0016g0109 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.117-16894A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73030292 | |||||||
| chr3:73030432 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.117-16754A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73030432 | |||||||
| chr3:73030596 | G | C | 7 | a0001c0002t0006g0020 a0001c0002t0006g0021 a0001c0002t0006g0031 others(4): Show |
7 | NA18942.hp1 NA18951.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.117-16590G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73030596 | |||||||
| chr3:73030612 | A | AT | 32 | a0001c0001t0001g0001 a0001c0001t0001g0216 a0001c0001t0001g0301 others(29): Show |
34 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.117-16559dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73030612 | ||||||
| chr3:73030612 | A | ATT | 8 | a0001c0001t0025g0177 a0001c0001t0025g0178 a0001c0001t0026g0174 others(5): Show |
8 | HG01255.hp1 HG01952.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.117-16560_117-1655 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73030612 | ||||||
| chr3:73030612 | AT | A | 115 | a0001c0001t0001g0311 a0001c0001t0003g0114 a0001c0001t0003g0115 others(112): Show |
116 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(113): Show |
intron_variant | MODIFIER | c.117-16559delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73030612 | ||||||
| chr3:73030666 | A | AT | 14 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(11): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.117-16519dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73030666 | ||||||
| chr3:73030922 | G | A | 6 | a0001c0001t0001g0235 a0001c0001t0001g0314 a0001c0001t0014g0332 others(3): Show |
6 | HG00438.hp2 HG00609.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.117-16264G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73030922 | |||||||
| chr3:73031055 | A | G | 1 | a0001c0002t0027g0053 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.117-16131A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73031055 | |||||||
| chr3:73031180 | G | C | 1 | a0001c0002t0011g0062 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.117-16006G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73031180 | |||||||
| chr3:73031297 | T | C | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.117-15889T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73031297 | |||||||
| chr3:73031489 | C | T | 1 | a0001c0001t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.117-15697C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73031489 | |||||||
| chr3:73031553 | GA | G | 184 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(181): Show |
185 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.117-15626delA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73031553 | ||||||
| chr3:73031654 | G | A | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.117-15532G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73031654 | |||||||
| chr3:73031707 | A | G | 1 | a0001c0002t0027g0053 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.117-15479A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73031707 | |||||||
| chr3:73031850 | C | T | 2 | a0001c0001t0001g0251 a0001c0001t0041g0259 |
2 | HG02015.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.117-15336C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73031850 | |||||||
| chr3:73032005 | A | G | 2 | a0001c0001t0008g0158 a0001c0001t0008g0179 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.117-15181A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032005 | |||||||
| chr3:73032027 | G | A | 2 | a0004c0005t0017g0344 a0004c0005t0017g0345 |
2 | NA18963.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.117-15159G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032027 | |||||||
| chr3:73032036 | T | A | 80 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(77): Show |
81 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.117-15150T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032036 | |||||||
| chr3:73032036 | T | G | 127 | a0001c0001t0001g0210 a0001c0001t0001g0274 a0001c0001t0016g0109 others(124): Show |
127 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.117-15150T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032036 | |||||||
| chr3:73032097 | T | A | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.117-15089T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032097 | |||||||
| chr3:73032289 | C | CT | 8 | a0001c0001t0018g0194 a0001c0001t0018g0198 a0001c0001t0034g0144 others(5): Show |
8 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.117-14884dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73032289 | ||||||
| chr3:73032289 | C | CTT | 94 | a0001c0001t0018g0193 a0001c0001t0018g0195 a0001c0002t0003g0014 others(91): Show |
94 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.117-14885_117-1488 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73032289 | ||||||
| chr3:73032304 | A | G | 1 | a0001c0001t0007g0133 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.117-14882A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032304 | |||||||
| chr3:73032315 | C | A | 5 | a0001c0002t0006g0020 a0001c0002t0006g0021 a0001c0002t0006g0031 others(2): Show |
5 | NA18951.hp1 NA18983.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.117-14871C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032315 | |||||||
| chr3:73032316 | G | A | 1 | a0001c0001t0002g0326 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.117-14870G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032316 | |||||||
| chr3:73032395 | TCTCCTGC others(6): Show |
T | 97 | a0001c0001t0001g0210 a0001c0001t0003g0114 a0001c0001t0003g0115 others(94): Show |
98 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(95): Show |
intron_variant | MODIFIER | c.117-14784_117-1477 others(17): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73032395 | ||||||
| chr3:73032447 | C | T | 1 | a0001c0002t0003g0014 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.117-14739C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032447 | |||||||
| chr3:73032477 | C | T | 1 | a0001c0002t0013g0102 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.117-14709C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032477 | |||||||
| chr3:73032685 | A | G | 2 | a0001c0001t0001g0301 a0001c0001t0001g0302 |
2 | NA18947.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.117-14501A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032685 | |||||||
| chr3:73032732 | G | T | 98 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(95): Show |
98 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.117-14454G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032732 | |||||||
| chr3:73032807 | A | G | 1 | a0001c0002t0023g0085 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.117-14379A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032807 | |||||||
| chr3:73032826 | T | C | 3 | a0001c0001t0001g0210 a0001c0001t0021g0203 a0001c0001t0021g0204 |
3 | HG02630.hp1 HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.117-14360T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73032826 | |||||||
| chr3:73033027 | G | A | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.117-14159G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73033027 | |||||||
| chr3:73033101 | T | G | 2 | a0001c0001t0001g0248 a0001c0001t0001g0263 |
2 | NA18965.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.117-14085T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73033101 | |||||||
| chr3:73033178 | T | C | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.117-14008T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73033178 | |||||||
| chr3:73033406 | T | C | 1 | a0001c0001t0008g0106 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.117-13780T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73033406 | |||||||
| chr3:73033562 | C | T | 94 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(91): Show |
94 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.117-13624C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73033562 | |||||||
| chr3:73033647 | A | T | 14 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(11): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.117-13539A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73033647 | |||||||
| chr3:73033948 | C | T | 1 | a0001c0001t0002g0233 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.117-13238C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73033948 | |||||||
| chr3:73034104 | C | T | 186 | a0001c0001t0002g0267 a0001c0001t0003g0114 a0001c0001t0003g0115 others(183): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.117-13082C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73034104 | |||||||
| chr3:73034114 | T | C | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.117-13072T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73034114 | |||||||
| chr3:73034135 | GGTGT | G | 96 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(93): Show |
96 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.117-13046_117-1304 others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73034135 | ||||||
| chr3:73034377 | G | C | 1 | a0001c0002t0023g0085 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.117-12809G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73034377 | |||||||
| chr3:73034402 | G | A | 1 | a0001c0002t0011g0056 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.117-12784G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73034402 | |||||||
| chr3:73034749 | A | T | 207 | a0001c0001t0001g0210 a0001c0001t0002g0267 a0001c0001t0003g0114 others(204): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.117-12437A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73034749 | |||||||
| chr3:73034846 | T | TA | 151 | a0001c0001t0002g0261 a0001c0001t0002g0267 a0001c0001t0003g0129 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.117-12327dupA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73034846 | ||||||
| chr3:73034846 | T | TAA | 23 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(20): Show |
24 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.117-12328_117-1232 others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73034846 | ||||||
| chr3:73034846 | TA | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0246 a0001c0001t0001g0248 others(13): Show |
17 | HG00423.hp2 HG00597.hp2 HG02129.hp1 others(14): Show |
intron_variant | MODIFIER | c.117-12327delA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73034846 | ||||||
| chr3:73035028 | A | C | 5 | a0001c0001t0001g0220 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG01346.hp2 HG01358.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.117-12158A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73035028 | |||||||
| chr3:73035125 | T | A | 14 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(11): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.117-12061T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73035125 | |||||||
| chr3:73035136 | A | G | 14 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(11): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.117-12050A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73035136 | |||||||
| chr3:73035172 | T | C | 3 | a0001c0001t0005g0009 a0001c0001t0014g0007 a0001c0001t0014g0010 |
3 | HG01109.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.117-12014T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73035172 | |||||||
| chr3:73035305 | T | G | 1 | a0001c0001t0009g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.117-11881T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73035305 | |||||||
| chr3:73035420 | T | C | 1 | a0001c0002t0013g0094 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.117-11766T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73035420 | |||||||
| chr3:73035490 | C | G | 3 | a0001c0002t0013g0101 a0001c0002t0033g0099 a0001c0002t0033g0100 |
3 | HG01884.hp1 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.117-11696C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73035490 | |||||||
| chr3:73035559 | A | G | 1 | a0001c0002t0010g0054 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.117-11627A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73035559 | |||||||
| chr3:73035782 | C | T | 1 | a0001c0001t0002g0105 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.117-11404C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73035782 | |||||||
| chr3:73035945 | A | G | 2 | a0001c0001t0016g0109 a0001c0001t0016g0205 |
2 | HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.117-11241A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73035945 | |||||||
| chr3:73036407 | C | T | 3 | a0001c0002t0013g0101 a0001c0002t0033g0099 a0001c0002t0033g0100 |
3 | HG01884.hp1 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.117-10779C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73036407 | |||||||
| chr3:73036471 | A | G | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.117-10715A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73036471 | |||||||
| chr3:73036835 | A | G | 2 | a0001c0002t0013g0094 a0001c0002t0013g0095 |
2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.117-10351A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73036835 | |||||||
| chr3:73036860 | A | G | 1 | a0001c0002t0003g0055 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.117-10326A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73036860 | |||||||
| chr3:73036872 | ATTG | A | 139 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(136): Show |
140 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(137): Show |
intron_variant | MODIFIER | c.117-10311_117-1030 others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73036872 | ||||||
| chr3:73036972 | T | C | 186 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(183): Show |
187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117-10214T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73036972 | |||||||
| chr3:73036996 | C | T | 1 | a0001c0001t0002g0261 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.117-10190C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73036996 | |||||||
| chr3:73037014 | A | G | 11 | a0001c0001t0001g0210 a0001c0001t0016g0109 a0001c0001t0016g0205 others(8): Show |
11 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.117-10172A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73037014 | |||||||
| chr3:73037120 | AT | A | 4 | a0001c0001t0002g0233 a0001c0001t0002g0268 a0001c0002t0013g0094 others(1): Show |
4 | HG02015.hp2 HG03225.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-10058delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73037120 | ||||||
| chr3:73037128 | T | C | 1 | a0001c0001t0002g0233 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.117-10058T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73037128 | |||||||
| chr3:73037240 | A | C | 3 | a0001c0001t0019g0112 a0001c0001t0019g0113 a0001c0001t0019g0120 |
3 | HG02572.hp2 HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.117-9946A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73037240 | |||||||
| chr3:73037327 | A | G | 1 | a0001c0002t0020g0045 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.117-9859A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73037327 | |||||||
| chr3:73037352 | T | C | 2 | a0001c0002t0013g0094 a0001c0002t0013g0095 |
2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.117-9834T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73037352 | |||||||
| chr3:73037442 | T | C | 1 | a0001c0001t0007g0190 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.117-9744T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73037442 | |||||||
| chr3:73037456 | C | G | 40 | a0001c0002t0006g0020 a0001c0002t0006g0021 a0001c0002t0006g0031 others(37): Show |
40 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.117-9730C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73037456 | |||||||
| chr3:73037890 | TTTTG | T | 8 | a0001c0002t0006g0020 a0001c0002t0006g0021 a0001c0002t0006g0031 others(5): Show |
8 | NA18942.hp1 NA18951.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.117-9292_117-9289d others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73037890 | ||||||
| chr3:73037987 | T | C | 2 | a0001c0002t0030g0096 a0001c0002t0030g0098 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.117-9199T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73037987 | |||||||
| chr3:73038238 | A | G | 139 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(136): Show |
140 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(137): Show |
intron_variant | MODIFIER | c.117-8948A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73038238 | |||||||
| chr3:73038285 | A | G | 1 | a0001c0002t0052g0076 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.117-8901A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73038285 | |||||||
| chr3:73038292 | T | C | 6 | a0001c0001t0001g0339 a0001c0001t0005g0009 a0001c0001t0014g0006 others(3): Show |
6 | HG01109.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.117-8894T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73038292 | |||||||
| chr3:73038345 | A | G | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.117-8841A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73038345 | |||||||
| chr3:73038469 | C | T | 1 | a0001c0003t0048g0215 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.117-8717C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73038469 | |||||||
| chr3:73038476 | A | G | 2 | a0001c0001t0002g0266 a0001c0001t0002g0272 |
2 | NA18971.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.117-8710A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73038476 | |||||||
| chr3:73038684 | G | A | 124 | a0001c0001t0003g0129 a0001c0001t0004g0127 a0001c0001t0004g0128 others(121): Show |
124 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(121): Show |
intron_variant | MODIFIER | c.117-8502G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73038684 | |||||||
| chr3:73039021 | C | A | 2 | a0001c0001t0018g0193 a0001c0001t0018g0195 |
2 | HG01243.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.117-8165C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039021 | |||||||
| chr3:73039288 | C | T | 1 | a0001c0001t0001g0331 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.117-7898C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039288 | |||||||
| chr3:73039331 | T | C | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.117-7855T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039331 | |||||||
| chr3:73039337 | G | A | 139 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(136): Show |
140 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(137): Show |
intron_variant | MODIFIER | c.117-7849G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039337 | |||||||
| chr3:73039408 | C | T | 2 | a0001c0002t0013g0094 a0001c0002t0013g0095 |
2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.117-7778C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039408 | |||||||
| chr3:73039481 | G | A | 91 | a0001c0001t0004g0127 a0001c0001t0004g0139 a0001c0001t0004g0142 others(88): Show |
91 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.117-7705G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039481 | |||||||
| chr3:73039539 | G | A | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.117-7647G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039539 | |||||||
| chr3:73039554 | G | C | 3 | a0001c0001t0018g0193 a0001c0001t0018g0195 a0001c0001t0018g0198 |
3 | HG01243.hp1 HG01884.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.117-7632G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039554 | |||||||
| chr3:73039598 | T | G | 1 | a0001c0002t0037g0074 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.117-7588T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039598 | |||||||
| chr3:73039692 | G | A | 4 | a0001c0001t0008g0136 a0001c0001t0008g0137 a0001c0001t0008g0138 others(1): Show |
4 | HG00741.hp2 HG01109.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.117-7494G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039692 | |||||||
| chr3:73039713 | G | A | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.117-7473G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039713 | |||||||
| chr3:73039823 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.117-7363C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039823 | |||||||
| chr3:73039828 | A | G | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.117-7358A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039828 | |||||||
| chr3:73039977 | C | G | 1 | a0001c0001t0001g0331 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.117-7209C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73039977 | |||||||
| chr3:73040032 | A | G | 1 | a0001c0002t0049g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.117-7154A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73040032 | |||||||
| chr3:73040351 | C | T | 40 | a0001c0002t0006g0020 a0001c0002t0006g0021 a0001c0002t0006g0031 others(37): Show |
40 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.117-6835C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73040351 | |||||||
| chr3:73040434 | T | C | 145 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(142): Show |
146 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(143): Show |
intron_variant | MODIFIER | c.117-6752T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73040434 | |||||||
| chr3:73040499 | A | ATTTTTTT | 73 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(70): Show |
73 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.117-6674_117-6668d others(9): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73040499 | ||||||
| chr3:73040499 | A | ATTTTTTT others(1): Show |
17 | a0001c0002t0003g0026 a0001c0002t0003g0058 a0001c0002t0003g0078 others(14): Show |
17 | HG00639.hp1 HG02080.hp2 HG02922.hp1 others(14): Show |
intron_variant | MODIFIER | c.117-6675_117-6668d others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73040499 | ||||||
| chr3:73040499 | AT | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(191): Show |
199 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.117-6668delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73040499 | ||||||
| chr3:73040840 | T | A | 146 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(143): Show |
147 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(144): Show |
intron_variant | MODIFIER | c.117-6346T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73040840 | |||||||
| chr3:73040901 | A | C | 60 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(57): Show |
60 | HG00423.hp1 HG00621.hp1 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.117-6285A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73040901 | |||||||
| chr3:73041017 | A | ATTT | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.117-6168_117-6167i others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73041017 | ||||||
| chr3:73041022 | T | C | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.117-6164T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73041022 | |||||||
| chr3:73041073 | A | G | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.117-6113A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73041073 | |||||||
| chr3:73041124 | A | G | 1 | a0001c0001t0003g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.117-6062A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73041124 | |||||||
| chr3:73041198 | C | T | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.117-5988C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73041198 | |||||||
| chr3:73041255 | A | G | 1 | a0001c0001t0028g0346 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.117-5931A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73041255 | |||||||
| chr3:73041311 | G | T | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.117-5875G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73041311 | |||||||
| chr3:73041449 | A | T | 1 | a0001c0001t0054g0175 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.117-5737A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73041449 | |||||||
| chr3:73041580 | C | A | 5 | a0001c0001t0002g0228 a0001c0001t0029g0315 a0001c0001t0029g0337 others(2): Show |
5 | HG00438.hp1 NA18747.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.117-5606C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73041580 | |||||||
| chr3:73041736 | TTAG | T | 4 | a0001c0001t0025g0176 a0001c0001t0025g0177 a0001c0001t0025g0178 others(1): Show |
4 | HG02735.hp2 HG03654.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-5446_117-5444d others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73041736 | ||||||
| chr3:73041857 | A | C | 147 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(144): Show |
148 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(145): Show |
intron_variant | MODIFIER | c.117-5329A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73041857 | |||||||
| chr3:73041974 | T | C | 1 | a0001c0002t0015g0068 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.117-5212T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73041974 | |||||||
| chr3:73042130 | T | C | 1 | a0001c0002t0019g0087 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.117-5056T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73042130 | |||||||
| chr3:73042176 | T | G | 2 | a0001c0003t0043g0201 a0001c0003t0045g0202 |
2 | HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.117-5010T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73042176 | |||||||
| chr3:73042242 | G | A | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.117-4944G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73042242 | |||||||
| chr3:73042275 | G | A | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.117-4911G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73042275 | |||||||
| chr3:73042281 | A | G | 1 | a0001c0002t0003g0070 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.117-4905A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73042281 | |||||||
| chr3:73042296 | T | G | 97 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(94): Show |
97 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.117-4890T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73042296 | |||||||
| chr3:73042335 | C | T | 1 | a0001c0001t0018g0195 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.117-4851C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73042335 | |||||||
| chr3:73042361 | C | CT | 9 | a0001c0002t0006g0031 a0001c0002t0006g0038 a0001c0002t0013g0095 others(6): Show |
9 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.117-4804dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73042361 | ||||||
| chr3:73042361 | CT | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(225): Show |
234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.117-4804delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73042361 | ||||||
| chr3:73042361 | CTT | C | 56 | a0001c0001t0001g0210 a0001c0001t0001g0263 a0001c0001t0003g0129 others(53): Show |
56 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(53): Show |
intron_variant | MODIFIER | c.117-4805_117-4804d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73042361 | ||||||
| chr3:73042361 | CTTTTTTT others(1): Show |
C | 6 | a0001c0001t0001g0339 a0001c0001t0005g0009 a0001c0001t0014g0006 others(3): Show |
6 | HG01109.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.117-4811_117-4804d others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73042361 | ||||||
| chr3:73042395 | C | T | 2 | a0001c0001t0008g0158 a0001c0001t0008g0179 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.117-4791C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73042395 | |||||||
| chr3:73042426 | G | A | 31 | a0001c0001t0003g0129 a0001c0001t0004g0128 a0001c0001t0004g0130 others(28): Show |
31 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.117-4760G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73042426 | |||||||
| chr3:73042686 | A | C | 145 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(142): Show |
146 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(143): Show |
intron_variant | MODIFIER | c.117-4500A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73042686 | |||||||
| chr3:73042766 | C | T | 4 | a0001c0003t0012g0348 a0001c0003t0012g0349 a0001c0003t0012g0350 others(1): Show |
4 | HG02559.hp2 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-4420C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73042766 | |||||||
| chr3:73042958 | A | G | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.117-4228A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73042958 | |||||||
| chr3:73043102 | T | TAGTG | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.117-4084_117-4083i others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043102 | |||||||
| chr3:73043206 | G | A | 1 | a0001c0001t0051g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.117-3980G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043206 | |||||||
| chr3:73043300 | G | GAAATT | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.117-3882_117-3878d others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73043300 | ||||||
| chr3:73043361 | G | A | 1 | a0001c0001t0004g0128 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.117-3825G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043361 | |||||||
| chr3:73043362 | G | A | 2 | a0001c0001t0021g0203 a0001c0001t0021g0204 |
2 | HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.117-3824G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043362 | |||||||
| chr3:73043498 | C | A | 1 | a0001c0001t0001g0342 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.117-3688C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043498 | |||||||
| chr3:73043587 | A | G | 2 | a0001c0001t0001g0331 a0001c0001t0001g0336 |
2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.117-3599A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043587 | |||||||
| chr3:73043636 | A | T | 1 | a0001c0002t0013g0097 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.117-3550A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043636 | |||||||
| chr3:73043643 | G | T | 1 | a0001c0001t0018g0194 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.117-3543G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043643 | |||||||
| chr3:73043786 | T | C | 1 | a0001c0001t0004g0161 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.117-3400T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043786 | |||||||
| chr3:73043790 | T | G | 208 | a0001c0001t0001g0210 a0001c0001t0002g0318 a0001c0001t0003g0114 others(205): Show |
209 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.117-3396T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043790 | |||||||
| chr3:73043837 | C | G | 5 | a0001c0001t0005g0009 a0001c0001t0014g0006 a0001c0001t0014g0007 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.117-3349C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043837 | |||||||
| chr3:73043845 | A | G | 2 | a0001c0001t0009g0110 a0001c0001t0009g0118 |
2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.117-3341A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043845 | |||||||
| chr3:73043961 | G | C | 2 | a0001c0002t0013g0094 a0001c0002t0013g0095 |
2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.117-3225G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73043961 | |||||||
| chr3:73044220 | T | TTTG | 165 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(162): Show |
166 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.117-2945_117-2943d others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73044220 | ||||||
| chr3:73044220 | T | TTTGTTG | 9 | a0001c0001t0003g0129 a0001c0001t0004g0128 a0001c0001t0004g0130 others(6): Show |
9 | HG01928.hp2 HG01934.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.117-2948_117-2943d others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73044220 | ||||||
| chr3:73044235 | G | T | 10 | a0001c0001t0016g0109 a0001c0001t0016g0205 a0001c0001t0016g0206 others(7): Show |
10 | HG02280.hp2 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.117-2951G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73044235 | |||||||
| chr3:73044337 | C | T | 1 | a0001c0001t0001g0336 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.117-2849C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73044337 | |||||||
| chr3:73044418 | C | T | 6 | a0001c0001t0001g0235 a0001c0001t0001g0314 a0001c0001t0014g0332 others(3): Show |
6 | HG00438.hp2 HG00609.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.117-2768C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73044418 | |||||||
| chr3:73044527 | A | G | 31 | a0001c0001t0003g0129 a0001c0001t0004g0128 a0001c0001t0004g0130 others(28): Show |
31 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.117-2659A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73044527 | |||||||
| chr3:73044568 | G | A | 179 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(176): Show |
180 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.117-2618G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73044568 | |||||||
| chr3:73044570 | A | T | 1 | a0001c0001t0001g0317 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.117-2616A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73044570 | |||||||
| chr3:73044582 | T | G | 14 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(11): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.117-2604T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73044582 | |||||||
| chr3:73044598 | C | G | 1 | a0001c0002t0053g0219 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.117-2588C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73044598 | |||||||
| chr3:73044639 | GT | G | 10 | a0001c0001t0016g0109 a0001c0001t0016g0205 a0001c0001t0016g0206 others(7): Show |
10 | HG02280.hp2 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.117-2541delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73044639 | ||||||
| chr3:73044862 | A | T | 1 | a0001c0002t0013g0097 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.117-2324A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73044862 | |||||||
| chr3:73044871 | T | G | 148 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(145): Show |
149 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(146): Show |
intron_variant | MODIFIER | c.117-2315T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73044871 | |||||||
| chr3:73044896 | G | T | 1 | a0001c0001t0051g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.117-2290G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73044896 | |||||||
| chr3:73044907 | C | T | 186 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(183): Show |
187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117-2279C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73044907 | |||||||
| chr3:73045047 | C | G | 186 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(183): Show |
187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117-2139C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045047 | |||||||
| chr3:73045086 | T | G | 2 | a0001c0001t0008g0158 a0001c0001t0008g0179 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.117-2100T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045086 | |||||||
| chr3:73045111 | G | T | 1 | a0001c0001t0002g0326 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.117-2075G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045111 | |||||||
| chr3:73045193 | G | A | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.117-1993G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045193 | |||||||
| chr3:73045255 | G | A | 1 | a0001c0001t0065g0316 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.117-1931G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045255 | |||||||
| chr3:73045295 | A | G | 1 | a0001c0001t0041g0259 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.117-1891A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045295 | |||||||
| chr3:73045451 | T | C | 5 | a0001c0001t0024g0140 a0001c0001t0024g0153 a0001c0001t0024g0154 others(2): Show |
5 | HG02257.hp1 HG02486.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.117-1735T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045451 | |||||||
| chr3:73045526 | A | AT | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(87): Show |
95 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.117-1644dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73045526 | ||||||
| chr3:73045526 | A | ATT | 140 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(137): Show |
141 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(138): Show |
intron_variant | MODIFIER | c.117-1645_117-1644d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73045526 | ||||||
| chr3:73045526 | A | ATTTTTTT | 27 | a0001c0002t0006g0049 a0001c0002t0006g0104 a0001c0002t0006g0108 others(24): Show |
27 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.117-1650_117-1644d others(9): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73045526 | ||||||
| chr3:73045526 | AT | A | 9 | a0001c0001t0002g0325 a0001c0002t0006g0020 a0001c0002t0006g0021 others(6): Show |
9 | HG01517.hp2 NA18942.hp1 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.117-1644delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr3 | 73045526 | ||||||
| chr3:73045747 | G | A | 1 | a0001c0001t0001g0303 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.117-1439G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045747 | |||||||
| chr3:73045749 | A | T | 38 | a0001c0002t0006g0020 a0001c0002t0006g0021 a0001c0002t0006g0031 others(35): Show |
38 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.117-1437A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045749 | |||||||
| chr3:73045752 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.117-1434C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045752 | |||||||
| chr3:73045774 | G | T | 1 | a0001c0001t0001g0338 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.117-1412G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045774 | |||||||
| chr3:73045778 | G | A | 1 | a0001c0002t0060g0040 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.117-1408G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045778 | |||||||
| chr3:73045804 | C | T | 124 | a0001c0001t0003g0129 a0001c0001t0004g0127 a0001c0001t0004g0128 others(121): Show |
124 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(121): Show |
intron_variant | MODIFIER | c.117-1382C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045804 | |||||||
| chr3:73045848 | C | A | 1 | a0001c0001t0001g0223 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.117-1338C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045848 | |||||||
| chr3:73045893 | G | A | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.117-1293G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045893 | |||||||
| chr3:73045896 | G | A | 1 | a0001c0002t0031g0018 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.117-1290G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045896 | |||||||
| chr3:73045927 | T | C | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.117-1259T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045927 | |||||||
| chr3:73045929 | A | G | 1 | a0001c0001t0028g0346 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.117-1257A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045929 | |||||||
| chr3:73045948 | C | T | 2 | a0001c0002t0003g0091 a0001c0002t0003g0092 |
2 | HG02683.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.117-1238C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73045948 | |||||||
| chr3:73046031 | A | G | 9 | a0001c0001t0001g0235 a0001c0001t0001g0286 a0001c0001t0001g0314 others(6): Show |
9 | HG00438.hp2 HG00609.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.117-1155A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73046031 | |||||||
| chr3:73046109 | A | G | 145 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(142): Show |
146 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(143): Show |
intron_variant | MODIFIER | c.117-1077A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73046109 | |||||||
| chr3:73046143 | A | G | 1 | a0001c0001t0007g0183 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.117-1043A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73046143 | |||||||
| chr3:73046331 | C | T | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.117-855C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73046331 | |||||||
| chr3:73046363 | A | G | 1 | a0001c0001t0051g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.117-823A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73046363 | |||||||
| chr3:73046410 | G | C | 14 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(11): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.117-776G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73046410 | |||||||
| chr3:73046416 | G | A | 14 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(11): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.117-770G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73046416 | |||||||
| chr3:73046441 | C | G | 38 | a0001c0002t0006g0020 a0001c0002t0006g0021 a0001c0002t0006g0031 others(35): Show |
38 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.117-745C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73046441 | |||||||
| chr3:73046583 | A | C | 2 | a0001c0003t0043g0201 a0001c0003t0045g0202 |
2 | HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.117-603A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73046583 | |||||||
| chr3:73046628 | G | T | 1 | a0001c0002t0020g0047 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.117-558G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73046628 | |||||||
| chr3:73046981 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.117-205T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73046981 | |||||||
| chr3:73047047 | A | G | 1 | a0001c0001t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.117-139A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73047047 | |||||||
| chr3:73047052 | G | A | 2 | a0001c0001t0004g0139 a0001c0001t0036g0150 |
2 | HG00140.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.117-134G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 2/8 | chr3 | 73047052 | |||||||
| chr3:73047440 | A | ATAAT | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.287+85_287+86insAA others(2): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73047440 | ||||||
| chr3:73047642 | C | T | 3 | a0001c0001t0001g0286 a0001c0001t0001g0335 a0001c0010t0001g0334 |
3 | HG03098.hp2 HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.287+286C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73047642 | |||||||
| chr3:73047809 | C | T | 15 | a0001c0001t0001g0292 a0001c0001t0003g0114 a0001c0001t0003g0115 others(12): Show |
16 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.287+453C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73047809 | |||||||
| chr3:73047865 | C | T | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.287+509C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73047865 | |||||||
| chr3:73047908 | G | A | 1 | a0001c0001t0004g0155 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.287+552G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73047908 | |||||||
| chr3:73047950 | C | T | 4 | a0001c0002t0013g0094 a0001c0002t0013g0095 a0003c0004t0013g0352 others(1): Show |
4 | HG01891.hp1 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.287+594C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73047950 | |||||||
| chr3:73047978 | G | A | 2 | a0001c0001t0001g0286 a0001c0001t0001g0335 |
2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.287+622G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73047978 | |||||||
| chr3:73048130 | C | T | 1 | a0001c0002t0003g0082 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.287+774C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73048130 | |||||||
| chr3:73048381 | C | A | 3 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 |
3 | HG02055.hp1 HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.287+1025C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73048381 | |||||||
| chr3:73048408 | C | T | 6 | a0001c0001t0001g0339 a0001c0001t0005g0009 a0001c0001t0014g0006 others(3): Show |
6 | HG01109.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.287+1052C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73048408 | |||||||
| chr3:73048661 | C | G | 168 | a0001c0001t0003g0129 a0001c0001t0004g0127 a0001c0001t0004g0128 others(165): Show |
168 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.287+1305C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73048661 | |||||||
| chr3:73048693 | G | A | 6 | a0001c0002t0013g0097 a0001c0002t0013g0101 a0001c0002t0030g0096 others(3): Show |
6 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.287+1337G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73048693 | |||||||
| chr3:73048800 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.287+1444T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73048800 | |||||||
| chr3:73048901 | G | T | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.287+1545G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73048901 | |||||||
| chr3:73048904 | G | A | 1 | a0001c0001t0001g0295 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.287+1548G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73048904 | |||||||
| chr3:73048924 | G | A | 1 | a0001c0001t0016g0206 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.287+1568G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73048924 | |||||||
| chr3:73049096 | G | GA | 13 | a0001c0001t0001g0223 a0001c0001t0002g0105 a0001c0001t0002g0298 others(10): Show |
13 | HG00741.hp2 HG01123.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.287+1748dupA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73049096 | ||||||
| chr3:73049144 | C | T | 5 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0340 others(2): Show |
5 | HG02451.hp2 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.287+1788C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049144 | |||||||
| chr3:73049175 | G | A | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.287+1819G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049175 | |||||||
| chr3:73049237 | G | A | 1 | a0001c0001t0004g0170 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.287+1881G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049237 | |||||||
| chr3:73049240 | T | C | 1 | a0001c0001t0001g0216 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.287+1884T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049240 | |||||||
| chr3:73049368 | G | A | 1 | a0003c0004t0013g0352 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.287+2012G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049368 | |||||||
| chr3:73049422 | C | T | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.287+2066C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049422 | |||||||
| chr3:73049523 | G | A | 2 | a0001c0002t0003g0051 a0001c0002t0003g0078 |
2 | NA19065.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.287+2167G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049523 | |||||||
| chr3:73049572 | G | C | 206 | a0001c0001t0001g0210 a0001c0001t0003g0114 a0001c0001t0003g0115 others(203): Show |
207 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.287+2216G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049572 | |||||||
| chr3:73049674 | T | C | 1 | a0001c0001t0021g0200 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.287+2318T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049674 | |||||||
| chr3:73049724 | G | A | 1 | a0001c0001t0017g0320 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.287+2368G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049724 | |||||||
| chr3:73049780 | T | C | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.287+2424T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049780 | |||||||
| chr3:73049929 | A | G | 1 | a0001c0001t0054g0175 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.287+2573A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049929 | |||||||
| chr3:73049995 | C | T | 1 | a0001c0001t0054g0175 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.287+2639C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73049995 | |||||||
| chr3:73050128 | A | G | 1 | a0001c0002t0013g0102 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.287+2772A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73050128 | |||||||
| chr3:73050256 | C | T | 1 | a0001c0001t0004g0131 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.287+2900C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73050256 | |||||||
| chr3:73050266 | G | A | 1 | a0001c0002t0052g0076 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.287+2910G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73050266 | |||||||
| chr3:73050421 | CAT | C | 35 | a0001c0002t0006g0020 a0001c0002t0006g0021 a0001c0002t0006g0031 others(32): Show |
35 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.287+3066_287+3067d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73050421 | |||||||
| chr3:73050440 | A | G | 39 | a0001c0002t0006g0020 a0001c0002t0006g0021 a0001c0002t0006g0031 others(36): Show |
39 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.287+3084A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73050440 | |||||||
| chr3:73050457 | A | T | 146 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(143): Show |
147 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(144): Show |
intron_variant | MODIFIER | c.287+3101A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73050457 | |||||||
| chr3:73050459 | A | G | 94 | a0001c0001t0004g0127 a0001c0001t0004g0139 a0001c0001t0004g0142 others(91): Show |
94 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.287+3103A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73050459 | |||||||
| chr3:73050569 | C | G | 1 | a0001c0002t0011g0062 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.287+3213C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73050569 | |||||||
| chr3:73050654 | A | G | 1 | a0006c0009t0018g0197 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.287+3298A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73050654 | |||||||
| chr3:73050701 | C | G | 1 | a0001c0001t0002g0298 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.287+3345C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73050701 | |||||||
| chr3:73050843 | T | G | 6 | a0001c0001t0001g0339 a0001c0001t0005g0009 a0001c0001t0014g0006 others(3): Show |
6 | HG01109.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.287+3487T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73050843 | |||||||
| chr3:73050912 | C | T | 3 | a0001c0001t0026g0174 a0001c0001t0056g0186 a0005c0006t0026g0173 |
3 | HG03130.hp2 HG04199.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.287+3556C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73050912 | |||||||
| chr3:73051003 | C | T | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.287+3647C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73051003 | |||||||
| chr3:73051022 | C | A | 1 | a0001c0001t0029g0337 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.287+3666C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73051022 | |||||||
| chr3:73051049 | C | G | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.287+3693C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73051049 | |||||||
| chr3:73051110 | T | C | 1 | a0001c0002t0013g0102 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.287+3754T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73051110 | |||||||
| chr3:73051310 | C | G | 1 | a0001c0001t0004g0142 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.287+3954C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73051310 | |||||||
| chr3:73051354 | T | C | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.287+3998T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73051354 | |||||||
| chr3:73051539 | T | C | 2 | a0001c0002t0003g0027 a0001c0002t0003g0028 |
2 | NA18979.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.287+4183T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73051539 | |||||||
| chr3:73051543 | A | G | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.287+4187A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73051543 | |||||||
| chr3:73051567 | C | T | 1 | a0001c0001t0004g0151 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.287+4211C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73051567 | |||||||
| chr3:73051866 | C | T | 1 | a0001c0002t0030g0096 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.287+4510C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73051866 | |||||||
| chr3:73051992 | T | C | 1 | a0001c0001t0034g0144 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.287+4636T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73051992 | |||||||
| chr3:73051994 | T | C | 81 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(78): Show |
82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.287+4638T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73051994 | |||||||
| chr3:73052020 | G | A | 10 | a0001c0003t0012g0209 a0001c0003t0012g0211 a0001c0003t0012g0212 others(7): Show |
10 | HG02109.hp1 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.287+4664G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052020 | |||||||
| chr3:73052022 | C | A | 1 | a0001c0001t0028g0346 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.287+4666C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052022 | |||||||
| chr3:73052175 | A | C | 14 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(11): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.287+4819A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052175 | |||||||
| chr3:73052241 | C | CT | 35 | a0001c0001t0009g0117 a0001c0001t0034g0144 a0001c0001t0036g0150 others(32): Show |
35 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.287+4889dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73052241 | ||||||
| chr3:73052241 | C | CTT | 116 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(113): Show |
117 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.287+4888_287+4889d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73052241 | ||||||
| chr3:73052241 | C | CTTT | 29 | a0001c0001t0004g0128 a0001c0001t0004g0131 a0001c0001t0004g0134 others(26): Show |
29 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.287+4887_287+4889d others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73052241 | ||||||
| chr3:73052246 | C | T | 184 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(181): Show |
185 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.287+4890C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052246 | |||||||
| chr3:73052287 | T | C | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.287+4931T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052287 | |||||||
| chr3:73052398 | A | G | 1 | a0001c0003t0012g0211 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.287+5042A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052398 | |||||||
| chr3:73052406 | G | A | 7 | a0001c0001t0001g0235 a0001c0001t0001g0286 a0001c0001t0001g0314 others(4): Show |
7 | HG00438.hp2 HG00609.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.287+5050G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052406 | |||||||
| chr3:73052434 | C | G | 39 | a0001c0002t0006g0020 a0001c0002t0006g0021 a0001c0002t0006g0031 others(36): Show |
39 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.287+5078C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052434 | |||||||
| chr3:73052583 | TTTG | T | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.287+5231_287+5233d others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73052583 | ||||||
| chr3:73052699 | T | C | 96 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(93): Show |
96 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.287+5343T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052699 | |||||||
| chr3:73052765 | C | A | 1 | a0001c0001t0009g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.287+5409C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052765 | |||||||
| chr3:73052781 | A | G | 1 | a0001c0001t0001g0331 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.287+5425A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052781 | |||||||
| chr3:73052862 | A | G | 94 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(91): Show |
94 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.287+5506A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052862 | |||||||
| chr3:73052900 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.287+5544G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052900 | |||||||
| chr3:73052990 | C | T | 79 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(76): Show |
80 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.287+5634C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73052990 | |||||||
| chr3:73053061 | T | G | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.287+5705T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73053061 | |||||||
| chr3:73053081 | C | T | 1 | a0001c0002t0027g0086 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.287+5725C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73053081 | |||||||
| chr3:73053091 | T | C | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.287+5735T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73053091 | |||||||
| chr3:73053198 | G | A | 31 | a0001c0001t0003g0129 a0001c0001t0004g0128 a0001c0001t0004g0130 others(28): Show |
31 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.288-5839G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73053198 | |||||||
| chr3:73053282 | C | G | 1 | a0001c0002t0003g0059 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.288-5755C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73053282 | |||||||
| chr3:73053318 | G | A | 1 | a0002c0007t0003g0013 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.288-5719G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73053318 | |||||||
| chr3:73053324 | C | T | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.288-5713C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73053324 | |||||||
| chr3:73053415 | T | G | 2 | a0001c0003t0043g0201 a0001c0003t0045g0202 |
2 | HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.288-5622T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73053415 | |||||||
| chr3:73053574 | A | G | 31 | a0001c0001t0003g0129 a0001c0001t0004g0128 a0001c0001t0004g0130 others(28): Show |
31 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.288-5463A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73053574 | |||||||
| chr3:73053691 | T | C | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.288-5346T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73053691 | |||||||
| chr3:73053787 | T | G | 5 | a0001c0001t0024g0140 a0001c0001t0024g0153 a0001c0001t0024g0154 others(2): Show |
5 | HG02257.hp1 HG02486.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.288-5250T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73053787 | |||||||
| chr3:73053801 | C | T | 7 | a0001c0001t0016g0109 a0001c0001t0016g0205 a0001c0001t0016g0206 others(4): Show |
7 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.288-5236C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73053801 | |||||||
| chr3:73053908 | C | CA | 19 | a0001c0001t0001g0210 a0001c0001t0001g0226 a0001c0001t0001g0252 others(16): Show |
19 | HG01109.hp2 HG02280.hp2 HG02293.hp2 others(16): Show |
intron_variant | MODIFIER | c.288-5113dupA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73053908 | ||||||
| chr3:73053908 | C | CAA | 53 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(50): Show |
54 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.288-5114_288-5113d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73053908 | ||||||
| chr3:73053908 | C | CAAA | 7 | a0001c0001t0007g0190 a0001c0001t0018g0195 a0001c0001t0051g0199 others(4): Show |
7 | HG02055.hp2 HG02615.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.288-5115_288-5113d others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73053908 | ||||||
| chr3:73053908 | C | CAAAA | 104 | a0001c0001t0003g0129 a0001c0001t0004g0128 a0001c0001t0004g0130 others(101): Show |
104 | HG00140.hp1 HG00621.hp1 HG00735.hp2 others(101): Show |
intron_variant | MODIFIER | c.288-5116_288-5113d others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73053908 | ||||||
| chr3:73053908 | C | CAAAAA | 20 | a0001c0001t0004g0127 a0001c0001t0004g0155 a0001c0001t0004g0180 others(17): Show |
20 | HG00423.hp1 HG01255.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.288-5117_288-5113d others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73053908 | ||||||
| chr3:73054018 | A | G | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.288-5019A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054018 | |||||||
| chr3:73054038 | A | G | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.288-4999A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054038 | |||||||
| chr3:73054070 | A | G | 1 | a0001c0001t0051g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.288-4967A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054070 | |||||||
| chr3:73054169 | C | T | 2 | a0001c0002t0003g0027 a0001c0002t0003g0028 |
2 | NA18979.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.288-4868C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054169 | |||||||
| chr3:73054206 | C | T | 1 | a0001c0002t0003g0024 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.288-4831C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054206 | |||||||
| chr3:73054270 | G | C | 1 | a0001c0001t0051g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.288-4767G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054270 | |||||||
| chr3:73054282 | C | G | 1 | a0001c0002t0011g0062 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.288-4755C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054282 | |||||||
| chr3:73054438 | A | G | 5 | a0001c0001t0005g0009 a0001c0001t0014g0006 a0001c0001t0014g0007 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.288-4599A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054438 | |||||||
| chr3:73054540 | TGTG | T | 5 | a0001c0001t0016g0109 a0001c0001t0016g0205 a0001c0001t0016g0206 others(2): Show |
5 | HG02280.hp2 HG02717.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.288-4494_288-4492d others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73054540 | ||||||
| chr3:73054585 | G | A | 4 | a0001c0001t0025g0176 a0001c0001t0025g0177 a0001c0001t0025g0178 others(1): Show |
4 | HG02735.hp2 HG03654.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.288-4452G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054585 | |||||||
| chr3:73054614 | C | CT | 8 | a0001c0001t0009g0002 a0001c0001t0009g0110 a0001c0001t0009g0111 others(5): Show |
9 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.288-4414dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73054614 | ||||||
| chr3:73054759 | T | A | 1 | a0001c0001t0009g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.288-4278T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054759 | |||||||
| chr3:73054875 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.288-4162G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054875 | |||||||
| chr3:73054890 | A | G | 2 | a0001c0001t0018g0193 a0001c0001t0018g0195 |
2 | HG01243.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.288-4147A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054890 | |||||||
| chr3:73054958 | A | G | 1 | a0001c0002t0003g0084 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.288-4079A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73054958 | |||||||
| chr3:73055066 | A | G | 1 | a0001c0002t0003g0059 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.288-3971A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73055066 | |||||||
| chr3:73055135 | C | G | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.288-3902C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73055135 | |||||||
| chr3:73055226 | G | A | 186 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(183): Show |
187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.288-3811G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73055226 | |||||||
| chr3:73055417 | C | CGT | 23 | a0001c0001t0003g0129 a0001c0001t0004g0128 a0001c0001t0004g0130 others(20): Show |
23 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.288-3583_288-3582d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | ||||||
| chr3:73055417 | C | CGTGT | 11 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0286 others(8): Show |
11 | HG01109.hp2 HG01255.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.288-3585_288-3582d others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | ||||||
| chr3:73055417 | C | CGTGTGT | 53 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0123 others(50): Show |
55 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.288-3587_288-3582d others(8): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | ||||||
| chr3:73055417 | C | CGTGTGTG others(1): Show |
29 | a0001c0001t0001g0122 a0001c0001t0001g0126 a0001c0001t0001g0249 others(26): Show |
29 | HG01123.hp1 HG01361.hp2 HG01952.hp2 others(26): Show |
intron_variant | MODIFIER | c.288-3589_288-3582d others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | ||||||
| chr3:73055417 | C | CGTGTGTG others(3): Show |
33 | a0001c0001t0001g0281 a0001c0001t0001g0300 a0001c0001t0001g0339 others(30): Show |
33 | HG00140.hp1 HG00609.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.288-3591_288-3582d others(12): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | ||||||
| chr3:73055417 | C | CGTGTGTG others(5): Show |
11 | a0001c0001t0001g0210 a0001c0001t0001g0235 a0001c0001t0004g0151 others(8): Show |
12 | HG01517.hp1 HG02083.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.288-3593_288-3582d others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | ||||||
| chr3:73055417 | C | CGTGTGTG others(7): Show |
7 | a0001c0001t0001g0246 a0001c0001t0003g0114 a0001c0001t0007g0146 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.288-3595_288-3582d others(16): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | ||||||
| chr3:73055417 | C | CGTGTGTG others(9): Show |
1 | a0001c0001t0008g0137 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.288-3597_288-3582d others(18): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | ||||||
| chr3:73055417 | CGT | C | 17 | a0001c0001t0002g0105 a0001c0001t0002g0243 a0001c0001t0002g0247 others(14): Show |
17 | HG01123.hp2 HG01928.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.288-3583_288-3582d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | ||||||
| chr3:73055417 | CGTGT | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0216 a0001c0001t0001g0218 others(52): Show |
58 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.288-3585_288-3582d others(6): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | ||||||
| chr3:73055417 | CGTGTGTG others(1): Show |
C | 4 | a0001c0001t0007g0143 a0001c0001t0008g0162 a0001c0001t0021g0200 others(1): Show |
4 | HG01099.hp2 HG02145.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.288-3589_288-3582d others(10): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | ||||||
| chr3:73055417 | CGTGTGTG others(5): Show |
C | 11 | a0001c0002t0003g0014 a0001c0002t0003g0063 a0001c0002t0003g0077 others(8): Show |
11 | HG00738.hp1 HG01243.hp2 HG03225.hp2 others(8): Show |
intron_variant | MODIFIER | c.288-3593_288-3582d others(14): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | ||||||
| chr3:73055417 | CGTGTGTG others(7): Show |
C | 88 | a0001c0001t0002g0256 a0001c0002t0003g0024 a0001c0002t0003g0025 others(85): Show |
88 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.288-3595_288-3582d others(16): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055417 | ||||||
| chr3:73055463 | T | A | 1 | a0001c0001t0035g0149 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.288-3574T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73055463 | |||||||
| chr3:73055468 | A | G | 1 | a0001c0001t0008g0106 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.288-3569A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73055468 | |||||||
| chr3:73055575 | A | AT | 11 | a0001c0001t0001g0210 a0001c0003t0012g0209 a0001c0003t0012g0211 others(8): Show |
11 | HG02109.hp1 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.288-3461dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055575 | ||||||
| chr3:73055667 | C | CT | 183 | a0001c0001t0001g0125 a0001c0001t0001g0249 a0001c0001t0002g0231 others(180): Show |
184 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.288-3358dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055667 | ||||||
| chr3:73055667 | C | CTT | 7 | a0001c0001t0008g0136 a0001c0001t0009g0118 a0001c0001t0019g0112 others(4): Show |
7 | HG00738.hp1 HG01891.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.288-3359_288-3358d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055667 | ||||||
| chr3:73055667 | CT | C | 11 | a0001c0001t0001g0235 a0001c0001t0001g0286 a0001c0001t0001g0314 others(8): Show |
11 | HG00438.hp2 HG00609.hp1 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.288-3358delT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73055667 | ||||||
| chr3:73055724 | C | T | 1 | a0001c0001t0035g0148 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.288-3313C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73055724 | |||||||
| chr3:73055725 | A | G | 311 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(308): Show |
316 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.288-3312A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73055725 | |||||||
| chr3:73055730 | C | A | 5 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.288-3307C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73055730 | |||||||
| chr3:73055835 | G | C | 1 | a0001c0001t0001g0288 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.288-3202G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73055835 | |||||||
| chr3:73055848 | C | A | 1 | a0001c0001t0018g0198 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.288-3189C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73055848 | |||||||
| chr3:73055910 | G | A | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.288-3127G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73055910 | |||||||
| chr3:73056016 | T | C | 186 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(183): Show |
187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.288-3021T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73056016 | |||||||
| chr3:73056296 | TAC | T | 34 | a0001c0001t0004g0127 a0001c0001t0004g0139 a0001c0001t0004g0142 others(31): Show |
34 | HG00140.hp1 HG00741.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.288-2739_288-2738d others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73056296 | ||||||
| chr3:73056357 | A | G | 1 | a0001c0001t0008g0136 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.288-2680A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73056357 | |||||||
| chr3:73056447 | C | T | 7 | a0001c0003t0012g0209 a0001c0003t0012g0211 a0001c0003t0012g0212 others(4): Show |
7 | HG02559.hp2 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.288-2590C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73056447 | |||||||
| chr3:73056491 | G | T | 1 | a0001c0002t0037g0072 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.288-2546G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73056491 | |||||||
| chr3:73056543 | GTGT | G | 34 | a0001c0001t0004g0127 a0001c0001t0004g0139 a0001c0001t0004g0142 others(31): Show |
34 | HG00140.hp1 HG00741.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.288-2490_288-2488d others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73056543 | ||||||
| chr3:73056599 | GCTT | G | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.288-2434_288-2432d others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73056599 | ||||||
| chr3:73056862 | A | G | 95 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(92): Show |
95 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.288-2175A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73056862 | |||||||
| chr3:73056902 | T | C | 1 | a0001c0001t0002g0298 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.288-2135T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73056902 | |||||||
| chr3:73057135 | A | G | 1 | a0001c0001t0002g0285 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.288-1902A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73057135 | |||||||
| chr3:73057270 | A | G | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.288-1767A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73057270 | |||||||
| chr3:73057309 | G | A | 1 | a0001c0001t0051g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.288-1728G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73057309 | |||||||
| chr3:73057355 | C | G | 1 | a0001c0001t0002g0105 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.288-1682C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73057355 | |||||||
| chr3:73057449 | A | G | 1 | a0001c0002t0013g0102 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.288-1588A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73057449 | |||||||
| chr3:73057693 | T | G | 1 | a0001c0001t0001g0252 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.288-1344T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73057693 | |||||||
| chr3:73057860 | G | A | 6 | a0001c0001t0001g0339 a0001c0001t0005g0009 a0001c0001t0014g0006 others(3): Show |
6 | HG01109.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.288-1177G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73057860 | |||||||
| chr3:73058101 | CTTAAAAA others(2): Show |
C | 81 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(78): Show |
82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.288-933_288-925del others(9): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73058101 | ||||||
| chr3:73058128 | G | A | 19 | a0001c0001t0003g0129 a0001c0001t0004g0128 a0001c0001t0004g0130 others(16): Show |
19 | HG00735.hp2 HG01928.hp2 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.288-909G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058128 | |||||||
| chr3:73058130 | T | A | 2 | a0001c0001t0008g0158 a0001c0001t0008g0179 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.288-907T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058130 | |||||||
| chr3:73058137 | T | C | 1 | a0001c0001t0007g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.288-900T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058137 | |||||||
| chr3:73058139 | T | C | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.288-898T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058139 | |||||||
| chr3:73058143 | A | C | 2 | a0001c0002t0013g0094 a0001c0002t0013g0095 |
2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.288-894A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058143 | |||||||
| chr3:73058249 | A | G | 96 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(93): Show |
96 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.288-788A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058249 | |||||||
| chr3:73058275 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.288-762A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058275 | |||||||
| chr3:73058486 | A | G | 7 | a0001c0003t0012g0209 a0001c0003t0012g0211 a0001c0003t0012g0212 others(4): Show |
7 | HG02559.hp2 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.288-551A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058486 | |||||||
| chr3:73058492 | G | T | 1 | a0001c0001t0007g0133 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.288-545G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058492 | |||||||
| chr3:73058515 | T | A | 7 | a0001c0001t0001g0220 a0001c0001t0001g0223 a0001c0001t0001g0224 others(4): Show |
7 | HG01346.hp2 HG01358.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.288-522T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058515 | |||||||
| chr3:73058516 | A | T | 102 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(99): Show |
102 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.288-521A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058516 | |||||||
| chr3:73058583 | A | G | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.288-454A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058583 | |||||||
| chr3:73058617 | A | T | 1 | a0001c0002t0062g0039 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.288-420A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058617 | |||||||
| chr3:73058712 | G | T | 7 | a0001c0003t0012g0209 a0001c0003t0012g0211 a0001c0003t0012g0212 others(4): Show |
7 | HG02559.hp2 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.288-325G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058712 | |||||||
| chr3:73058820 | AAAGG | A | 3 | a0001c0001t0001g0286 a0001c0001t0001g0335 a0001c0010t0001g0334 |
3 | HG03098.hp2 HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.288-212_288-209del others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73058820 | ||||||
| chr3:73058836 | G | GT | 8 | a0001c0001t0001g0263 a0001c0001t0001g0304 a0001c0001t0001g0314 others(5): Show |
8 | HG00438.hp2 HG02258.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.288-194dupT | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | 73058836 | ||||||
| chr3:73058941 | G | A | 95 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(92): Show |
95 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.288-96G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058941 | |||||||
| chr3:73058995 | A | G | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.288-42A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 3/8 | chr3 | 73058995 | |||||||
| chr3:73059166 | G | A | 1 | a0001c0001t0001g0288 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.381+36G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73059166 | |||||||
| chr3:73059275 | A | G | 1 | a0001c0001t0051g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.381+145A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73059275 | |||||||
| chr3:73059295 | A | G | 1 | a0001c0001t0017g0320 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.381+165A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73059295 | |||||||
| chr3:73059384 | G | A | 1 | a0001c0010t0001g0334 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.381+254G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73059384 | |||||||
| chr3:73059517 | C | T | 186 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(183): Show |
187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.381+387C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73059517 | |||||||
| chr3:73059528 | C | T | 1 | a0001c0001t0051g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.381+398C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73059528 | |||||||
| chr3:73059826 | C | T | 81 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(78): Show |
82 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.381+696C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73059826 | |||||||
| chr3:73059922 | G | C | 1 | a0001c0001t0005g0284 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.381+792G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73059922 | |||||||
| chr3:73059936 | GA | G | 182 | a0001c0001t0002g0318 a0001c0001t0003g0114 a0001c0001t0003g0115 others(179): Show |
183 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.381+822delA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr3 | 73059936 | ||||||
| chr3:73060044 | G | T | 1 | a0001c0001t0002g0267 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.381+914G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73060044 | |||||||
| chr3:73060089 | G | A | 186 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(183): Show |
187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.382-934G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73060089 | |||||||
| chr3:73060240 | C | A | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.382-783C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73060240 | |||||||
| chr3:73060267 | C | T | 1 | a0001c0002t0049g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.382-756C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73060267 | |||||||
| chr3:73060305 | G | C | 6 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-718G>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73060305 | |||||||
| chr3:73060306 | C | T | 1 | a0001c0001t0004g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.382-717C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73060306 | |||||||
| chr3:73060335 | A | G | 1 | a0001c0001t0051g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.382-688A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73060335 | |||||||
| chr3:73060593 | TGAGTCTC | T | 140 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(137): Show |
141 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(138): Show |
intron_variant | MODIFIER | c.382-429_382-423del others(7): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73060593 | |||||||
| chr3:73060685 | A | T | 2 | a0001c0001t0004g0139 a0001c0001t0036g0150 |
2 | HG00140.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.382-338A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73060685 | |||||||
| chr3:73060740 | G | A | 46 | a0001c0001t0018g0193 a0001c0001t0018g0194 a0001c0001t0018g0195 others(43): Show |
46 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.382-283G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73060740 | |||||||
| chr3:73060799 | GA | G | 6 | a0001c0001t0001g0276 a0001c0001t0002g0323 a0001c0001t0004g0164 others(3): Show |
6 | HG01433.hp1 HG01891.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-214delA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr3 | 73060799 | ||||||
| chr3:73060829 | T | G | 1 | a0001c0001t0007g0171 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.382-194T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73060829 | |||||||
| chr3:73060925 | G | A | 185 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.382-98G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73060925 | |||||||
| chr3:73061015 | T | A | 3 | a0001c0003t0012g0209 a0001c0003t0012g0211 a0001c0003t0012g0212 |
3 | HG02647.hp2 HG02886.hp2 NA20129.hp1 |
splice_region_variant&intron_variant | LOW | c.382-8T>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 4/8 | chr3 | 73061015 | |||||||
| chr3:73061134 | C | T | 1 | a0001c0003t0012g0349 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.419+74C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73061134 | |||||||
| chr3:73061366 | G | A | 29 | a0001c0002t0006g0020 a0001c0002t0006g0021 a0001c0002t0006g0031 others(26): Show |
29 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.419+306G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73061366 | |||||||
| chr3:73061489 | A | G | 1 | a0001c0002t0003g0055 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.419+429A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73061489 | |||||||
| chr3:73061566 | GTT | G | 4 | a0001c0001t0025g0176 a0001c0001t0025g0177 a0001c0001t0025g0178 others(1): Show |
4 | HG02735.hp2 HG03654.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.419+508_419+509del others(2): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 73061566 | ||||||
| chr3:73061634 | A | T | 1 | a0001c0001t0058g0182 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.419+574A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73061634 | |||||||
| chr3:73061746 | C | T | 1 | a0001c0002t0013g0102 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.419+686C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73061746 | |||||||
| chr3:73061750 | C | G | 3 | a0001c0002t0013g0101 a0001c0002t0033g0099 a0001c0002t0033g0100 |
3 | HG01884.hp1 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.419+690C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73061750 | |||||||
| chr3:73061864 | A | G | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.419+804A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73061864 | |||||||
| chr3:73061902 | A | G | 125 | a0001c0001t0003g0129 a0001c0001t0004g0127 a0001c0001t0004g0128 others(122): Show |
125 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(122): Show |
intron_variant | MODIFIER | c.419+842A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73061902 | |||||||
| chr3:73061996 | G | A | 1 | a0001c0002t0013g0102 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.419+936G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73061996 | |||||||
| chr3:73062025 | G | A | 3 | a0001c0002t0003g0027 a0001c0002t0003g0028 a0001c0002t0003g0081 |
3 | NA18979.hp1 NA19000.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.419+965G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062025 | |||||||
| chr3:73062217 | T | C | 186 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(183): Show |
187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.419+1157T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062217 | |||||||
| chr3:73062274 | A | G | 1 | a0001c0001t0001g0331 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.419+1214A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062274 | |||||||
| chr3:73062291 | C | T | 2 | a0003c0004t0013g0352 a0003c0004t0013g0353 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.419+1231C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062291 | |||||||
| chr3:73062330 | C | CA | 96 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0025 others(93): Show |
96 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.419+1271dupA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 73062330 | ||||||
| chr3:73062349 | G | T | 2 | a0001c0002t0003g0084 a0001c0002t0010g0065 |
2 | NA19067.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.419+1289G>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062349 | |||||||
| chr3:73062352 | T | TTGG | 5 | a0001c0002t0003g0014 a0001c0002t0003g0063 a0001c0002t0003g0077 others(2): Show |
5 | HG00738.hp1 HG01243.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.419+1293_419+1295d others(5): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 73062352 | ||||||
| chr3:73062399 | A | C | 1 | a0001c0001t0001g0226 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.420-1274A>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062399 | |||||||
| chr3:73062573 | T | G | 1 | a0001c0002t0023g0085 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.420-1100T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062573 | |||||||
| chr3:73062596 | C | T | 2 | a0001c0001t0002g0268 a0001c0001t0067g0296 |
2 | HG03490.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.420-1077C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062596 | |||||||
| chr3:73062658 | A | G | 186 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(183): Show |
187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.420-1015A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062658 | |||||||
| chr3:73062728 | T | G | 4 | a0001c0001t0002g0247 a0001c0001t0002g0254 a0001c0001t0002g0255 others(1): Show |
4 | HG01928.hp1 HG01934.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.420-945T>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062728 | |||||||
| chr3:73062749 | C | A | 2 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
2 | HG02897.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.420-924C>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062749 | |||||||
| chr3:73062822 | A | G | 224 | a0001c0001t0001g0210 a0001c0001t0001g0235 a0001c0001t0001g0286 others(221): Show |
225 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.420-851A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062822 | |||||||
| chr3:73062847 | C | T | 186 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(183): Show |
187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.420-826C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062847 | |||||||
| chr3:73062977 | C | T | 1 | a0001c0001t0051g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.420-696C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73062977 | |||||||
| chr3:73063034 | A | G | 11 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(8): Show |
12 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.420-639A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73063034 | |||||||
| chr3:73063044 | T | C | 4 | a0001c0001t0001g0210 a0001c0001t0021g0200 a0001c0001t0021g0203 others(1): Show |
4 | HG02630.hp1 HG02647.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.420-629T>C | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73063044 | |||||||
| chr3:73063226 | C | T | 19 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(16): Show |
20 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.420-447C>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73063226 | |||||||
| chr3:73063227 | A | G | 182 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(179): Show |
183 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.420-446A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73063227 | |||||||
| chr3:73063262 | G | A | 2 | a0001c0002t0003g0091 a0001c0002t0003g0092 |
2 | HG02683.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.420-411G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73063262 | |||||||
| chr3:73063293 | C | G | 1 | a0001c0001t0005g0232 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.420-380C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73063293 | |||||||
| chr3:73063318 | T | TA | 17 | a0001c0001t0001g0226 a0001c0001t0001g0328 a0001c0001t0001g0339 others(14): Show |
17 | HG02129.hp1 HG02280.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.420-333dupA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 73063318 | ||||||
| chr3:73063318 | T | TAA | 9 | a0001c0001t0001g0210 a0001c0003t0012g0209 a0001c0003t0012g0211 others(6): Show |
9 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.420-334_420-333dup others(2): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 73063318 | ||||||
| chr3:73063318 | TA | T | 9 | a0001c0001t0001g0237 a0001c0001t0001g0281 a0001c0001t0001g0311 others(6): Show |
9 | HG01361.hp1 HG01975.hp2 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.420-333delA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 73063318 | ||||||
| chr3:73063338 | A | AAAAG | 96 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(93): Show |
96 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.420-333_420-332ins others(4): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 73063338 | ||||||
| chr3:73063338 | A | AAAG | 69 | a0001c0001t0003g0129 a0001c0001t0004g0127 a0001c0001t0004g0128 others(66): Show |
70 | HG00140.hp1 HG00597.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.420-334_420-332dup others(3): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 73063338 | ||||||
| chr3:73063338 | A | AAG | 11 | a0001c0001t0004g0151 a0001c0001t0004g0168 a0001c0001t0008g0132 others(8): Show |
11 | HG01069.hp1 HG01243.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.420-334_420-333ins others(2): Show |
PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 73063338 | ||||||
| chr3:73063338 | A | G | 1 | a0001c0002t0052g0076 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.420-335A>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 5/8 | chr3 | 73063338 | |||||||
| chr3:73063768 | T | TA | 182 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(179): Show |
183 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.494+22dupA | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr3 | 73063768 | ||||||
| chr3:73063805 | A | T | 5 | a0001c0001t0024g0140 a0001c0001t0024g0153 a0001c0001t0024g0154 others(2): Show |
5 | HG02257.hp1 HG02486.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.494+58A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 6/8 | chr3 | 73063805 | |||||||
| chr3:73063823 | A | T | 186 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(183): Show |
187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.494+76A>T | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 6/8 | chr3 | 73063823 | |||||||
| chr3:73064377 | C | G | 182 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(179): Show |
183 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.638+231C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 7/8 | chr3 | 73064377 | |||||||
| chr3:73064577 | G | A | 14 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(11): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.639-275G>A | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 7/8 | chr3 | 73064577 | |||||||
| chr3:73064746 | C | G | 1 | a0001c0001t0068g0330 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.639-106C>G | PPP4R2 | ENSG00000163605.16 | transcript | ENST00000356692.10 | protein_coding | 7/8 | chr3 | 73064746 |