Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8899 |
| ensemblid | ENSG00000112739.17 |
| hgncid | 17346 |
| symbol | PRPF4B |
| name | pre-mRNA processing factor 4B |
| refseq_nuc | NM_003913.5 |
| refseq_prot | NP_003904.3 |
| ensembl_nuc | ENST00000337659.11 |
| ensembl_prot | ENSP00000337194.6 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 4021300 |
| end | 4064983 |
| strand | + |
| ver | v1.2 |
| region | chr6:4021300-4064983 |
| region5000 | chr6:4016300-4069983 |
| regionname0 | PRPF4B_chr6_4021300_4064983 |
| regionname5000 | PRPF4B_chr6_4016300_4069983 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1007 | 259 | 60 | 49 | 104 | 13 | 32 | 79 | PRPF4B_chr6_4016300_4069983 | PRPF4B | MAAAE others(1002): Show |
chr6 | 4016300 | 4069983 |
| a0002 | 1/0 | 1007 | 106 | 25 | 22 | 45 | 5 | 8 | 32 | PRPF4B_chr6_4016300_4069983 | PRPF4B | MAAAE others(1002): Show |
chr6 | 4016300 | 4069983 |
| a0003 | 0/0 | 1007 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | MAAAE others(1002): Show |
chr6 | 4016300 | 4069983 |
| a0004 | 0/0 | 1007 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | MAAAE others(1002): Show |
chr6 | 4016300 | 4069983 |
| a0005 | 0/0 | 1007 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | MAAAE others(1002): Show |
chr6 | 4016300 | 4069983 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3021 | 239 | 46 | 48 | 104 | 13 | 27 | PRPF4B_chr6_4016300_4069983 | PRPF4B | ATGGC others(3016): Show |
chr6 | 4016300 | 4069983 | ||
| a0001c0004 | 0/0 | 3021 | 6 | 6 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | ATGGC others(3016): Show |
chr6 | 4016300 | 4069983 | ||
| a0001c0005 | 0/0 | 3021 | 5 | 5 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | ATGGC others(3016): Show |
chr6 | 4016300 | 4069983 | ||
| a0001c0006 | 0/0 | 3021 | 3 | 0 | 0 | 0 | 0 | 3 | PRPF4B_chr6_4016300_4069983 | PRPF4B | ATGGC others(3016): Show |
chr6 | 4016300 | 4069983 | ||
| a0001c0007 | 0/0 | 3021 | 3 | 3 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | ATGGC others(3016): Show |
chr6 | 4016300 | 4069983 | ||
| a0001c0011 | 0/0 | 3021 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | ATGGC others(3016): Show |
chr6 | 4016300 | 4069983 | ||
| a0001c0012 | 0/0 | 3021 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | ATGGC others(3016): Show |
chr6 | 4016300 | 4069983 | ||
| a0001c0015 | 0/0 | 3021 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | ATGGC others(3016): Show |
chr6 | 4016300 | 4069983 | ||
| a0002c0002 | 1/0 | 3021 | 91 | 14 | 19 | 45 | 4 | 8 | PRPF4B_chr6_4016300_4069983 | PRPF4B | ATGGC others(3016): Show |
chr6 | 4016300 | 4069983 | ||
| a0002c0003 | 0/0 | 3021 | 13 | 10 | 2 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | ATGGC others(3016): Show |
chr6 | 4016300 | 4069983 | ||
| a0002c0008 | 0/0 | 3021 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | ATGGC others(3016): Show |
chr6 | 4016300 | 4069983 | ||
| a0002c0009 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | ATGGC others(3016): Show |
chr6 | 4016300 | 4069983 | ||
| a0003c0014 | 0/0 | 3021 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | ATGGC others(3016): Show |
chr6 | 4016300 | 4069983 | ||
| a0004c0013 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | ATGGC others(3016): Show |
chr6 | 4016300 | 4069983 | ||
| a0005c0010 | 0/0 | 3021 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | ATGGC others(3016): Show |
chr6 | 4016300 | 4069983 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 7517 | 146 | 17 | 29 | 61 | 12 | 26 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0001c0001t0002 | 0/0 | 7517 | 2 | 1 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0001c0001t0003 | 0/0 | 7518 | 45 | 0 | 13 | 32 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7513): Show |
chr6 | 4016300 | 4069983 |
| a0001c0001t0004 | 0/0 | 7518 | 23 | 20 | 3 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7513): Show |
chr6 | 4016300 | 4069983 |
| a0001c0001t0006 | 0/0 | 7517 | 3 | 2 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0001c0001t0007 | 0/0 | 7517 | 4 | 0 | 0 | 4 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0001c0001t0008 | 0/0 | 7517 | 3 | 0 | 2 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0001c0001t0009 | 0/0 | 7517 | 3 | 3 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0001c0001t0014 | 0/0 | 7517 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0001c0001t0015 | 0/0 | 7517 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0001c0001t0016 | 0/0 | 7518 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7513): Show |
chr6 | 4016300 | 4069983 |
| a0001c0001t0017 | 0/0 | 7517 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0001c0001t0020 | 0/0 | 7517 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0001c0001t0021 | 0/0 | 7517 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0001c0001t0022 | 0/0 | 7517 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0001c0001t0025 | 0/0 | 7505 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7500): Show |
chr6 | 4016300 | 4069983 |
| a0001c0001t0026 | 0/0 | 7517 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0001c0001t0028 | 0/0 | 7518 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7513): Show |
chr6 | 4016300 | 4069983 |
| a0001c0004t0010 | 0/0 | 7517 | 3 | 3 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0001c0004t0011 | 0/0 | 7517 | 3 | 3 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0001c0005t0006 | 0/0 | 7517 | 5 | 5 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0001c0006t0001 | 0/0 | 7517 | 3 | 0 | 0 | 0 | 0 | 3 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0001c0007t0006 | 0/0 | 7517 | 3 | 3 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0001c0011t0001 | 0/0 | 7517 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0001c0012t0001 | 0/0 | 7517 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0001c0015t0003 | 0/0 | 7518 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7513): Show |
chr6 | 4016300 | 4069983 |
| a0002c0002t0001 | 0/0 | 7517 | 2 | 0 | 0 | 1 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0002c0002t0002 | 0/0 | 7517 | 82 | 14 | 15 | 42 | 4 | 7 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0002c0002t0012 | 1/0 | 7517 | 2 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0002c0002t0013 | 0/0 | 7517 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0002c0002t0023 | 0/0 | 7517 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0002c0002t0024 | 0/0 | 7517 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0002c0002t0027 | 0/0 | 7517 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0002c0003t0005 | 0/0 | 7517 | 13 | 10 | 2 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0002c0008t0002 | 0/0 | 7517 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0002c0009t0018 | 0/0 | 7517 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0003c0014t0001 | 0/0 | 7517 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0004c0013t0019 | 0/0 | 7517 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| a0005c0010t0001 | 0/0 | 7517 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | AGAAC others(7512): Show |
chr6 | 4016300 | 4069983 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0276 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0001 | 0/0 | 7 | 0 | 6 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0004g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0004g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0004g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0006g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0006g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0007g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0007g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0008g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0008g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0009g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0009g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0014g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0015g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0016g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0017g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0020g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0021g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0022g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0025g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0026g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0001t0028g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0004t0010g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0004t0010g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0004t0010g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0004t0011g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0004t0011g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0004t0011g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0005t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0005t0006g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0005t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0005t0006g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0005t0006g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0006t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0006t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0006t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0007t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0007t0006g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0007t0006g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0011t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0012t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0001c0015t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0012g0203 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0012g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0013g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0013g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0023g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0024g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0002t0027g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0003t0005g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0003t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0003t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0003t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0003t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0003t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0003t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0003t0005g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0003t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0003t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0003t0005g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0003t0005g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0008t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0002c0009t0018g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0003c0014t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0004c0013t0019g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| a0005c0010t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0249 | EUR | GBR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | GBR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0314 | EUR | GBR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0246 | EUR | GBR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | FIN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0157 | EUR | FIN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | FIN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00323 | hp2 | a0001 | c0001 | t0008 | g0050 | EUR | FIN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | CHS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | CHS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | CHS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0138 | EAS | CHS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | CHS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0137 | EAS | CHS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00621 | hp1 | a0001 | c0001 | t0015 | g0028 | EAS | CHS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0154 | EAS | CHS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00639 | hp1 | a0002 | c0002 | t0024 | g0182 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0017 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0202 | EAS | CHS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | CHS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00735 | hp1 | a0002 | c0003 | t0005 | g0200 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00738 | hp1 | a0002 | c0003 | t0005 | g0129 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0186 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG00741 | hp2 | a0003 | c0014 | t0001 | g0317 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0101 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01070 | hp1 | a0001 | c0015 | t0003 | g0011 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0175 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0116 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01081 | hp2 | a0001 | c0001 | t0006 | g0021 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01099 | hp1 | a0002 | c0002 | t0023 | g0197 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0104 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01106 | hp2 | a0002 | c0002 | t0012 | g0204 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0080 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0181 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0100 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0109 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0075 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0159 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0187 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0076 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01257 | hp2 | a0001 | c0001 | t0008 | g0008 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01258 | hp1 | a0001 | c0001 | t0008 | g0008 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0017 | EUR | IBS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | IBS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0179 | EUR | IBS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0217 | EUR | IBS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0180 | EUR | IBS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01884 | hp1 | a0001 | c0004 | t0011 | g0232 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0198 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0165 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0110 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01975 | hp1 | a0002 | c0002 | t0027 | g0155 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0032 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0311 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0195 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0031 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02004 | hp2 | a0002 | c0008 | t0002 | g0166 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0136 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0158 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02055 | hp1 | a0001 | c0005 | t0006 | g0308 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02055 | hp2 | a0001 | c0001 | t0026 | g0287 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0117 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0151 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0131 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02145 | hp1 | a0002 | c0003 | t0005 | g0122 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CDX | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02155 | hp2 | a0001 | c0001 | t0022 | g0213 | EAS | CDX | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | CDX | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02257 | hp1 | a0001 | c0005 | t0006 | g0211 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0188 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0091 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0167 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0077 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0145 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0185 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0205 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02572 | hp1 | a0002 | c0002 | t0002 | g0189 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0194 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02615 | hp1 | a0002 | c0003 | t0005 | g0121 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0177 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0021 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02630 | hp2 | a0002 | c0003 | t0005 | g0127 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0113 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0178 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02717 | hp1 | a0002 | c0003 | t0005 | g0123 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0070 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0092 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0176 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0140 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02738 | hp2 | a0001 | c0006 | t0001 | g0292 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0111 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0033 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0219 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0220 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02922 | hp1 | a0002 | c0003 | t0005 | g0014 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02922 | hp2 | a0001 | c0007 | t0006 | g0293 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0328 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0183 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02970 | hp2 | a0002 | c0002 | t0002 | g0190 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0073 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02976 | hp2 | a0002 | c0003 | t0005 | g0125 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0208 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03017 | hp2 | a0001 | c0011 | t0001 | g0058 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03041 | hp1 | a0001 | c0001 | t0016 | g0290 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0079 | AFR | MSL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03098 | hp2 | a0001 | c0004 | t0011 | g0233 | AFR | MSL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0192 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03139 | hp1 | a0001 | c0005 | t0006 | g0305 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0074 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03195 | hp1 | a0002 | c0003 | t0005 | g0014 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0193 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03209 | hp1 | a0002 | c0003 | t0005 | g0120 | AFR | MSL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | MSL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03453 | hp2 | a0001 | c0005 | t0006 | g0306 | AFR | MSL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0133 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03516 | hp2 | a0001 | c0005 | t0006 | g0307 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03540 | hp1 | a0001 | c0004 | t0010 | g0295 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0280 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | MSL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03579 | hp2 | a0002 | c0003 | t0005 | g0128 | AFR | MSL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0196 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0324 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0304 | SAS | BEB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | BEB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0313 | SAS | BEB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03927 | hp1 | a0001 | c0006 | t0001 | g0222 | SAS | BEB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03942 | hp1 | a0001 | c0006 | t0001 | g0310 | SAS | BEB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | BEB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0172 | SAS | BEB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG04199 | hp1 | a0001 | c0012 | t0001 | g0323 | SAS | STU | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | STU | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG04204 | hp1 | a0001 | c0001 | t0020 | g0285 | SAS | STU | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0150 | SAS | STU | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | STU | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18522 | hp1 | a0002 | c0009 | t0018 | g0309 | AFR | YRI | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | CHB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0164 | EAS | CHB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0163 | EAS | CHB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | CHB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18906 | hp1 | a0001 | c0004 | t0010 | g0275 | AFR | YRI | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0212 | AFR | YRI | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18942 | hp2 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18951 | hp1 | a0001 | c0001 | t0007 | g0231 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0206 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18956 | hp1 | a0002 | c0002 | t0013 | g0174 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18969 | hp1 | a0001 | c0001 | t0017 | g0271 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0173 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18983 | hp1 | a0001 | c0001 | t0014 | g0027 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0148 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0201 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0207 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18999 | hp1 | a0001 | c0001 | t0021 | g0242 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19006 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0142 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19010 | hp2 | a0001 | c0001 | t0025 | g0259 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19011 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | LWK | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19030 | hp2 | a0001 | c0004 | t0010 | g0283 | AFR | LWK | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19043 | hp2 | a0004 | c0013 | t0019 | g0279 | AFR | LWK | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0141 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19060 | hp1 | a0002 | c0002 | t0013 | g0152 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19060 | hp2 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0160 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0169 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0161 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19067 | hp1 | a0005 | c0010 | t0001 | g0325 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19067 | hp2 | a0002 | c0002 | t0002 | g0162 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0153 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19077 | hp1 | a0002 | c0002 | t0002 | g0170 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0171 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0130 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0146 | AFR | YRI | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0078 | AFR | YRI | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0254 | EUR | TSI | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | TSI | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA20805 | hp1 | a0002 | c0003 | t0005 | g0126 | EUR | TSI | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | TSI | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | GIH | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | GIH | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0139 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0303 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02486 | hp1 | a0001 | c0004 | t0011 | g0234 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0115 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0112 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG02559 | hp2 | a0002 | c0002 | t0002 | g0147 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03471 | hp1 | a0001 | c0007 | t0006 | g0294 | AFR | MSL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG03471 | hp2 | a0002 | c0002 | t0002 | g0191 | AFR | MSL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG06807 | hp1 | a0001 | c0007 | t0006 | g0210 | AFR | USA | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0184 | AFR | USA | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA20300 | hp1 | a0001 | c0001 | t0028 | g0072 | AFR | USA | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | USA | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA21309 | hp1 | a0002 | c0003 | t0005 | g0124 | AFR | LWK | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0209 | AFR | LWK | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0276 | REF | REF | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0012 | g0203 | REF | REF | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:4031764 | A | G | 4 | a0001 a0003 a0004 others(1): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
missense_variant | MODERATE | c.247A>G | p.Ile83Val | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/15 | 373/7517 | 247/3024 | 83/1007 | chr6 | 4031764 | |||
| chr6:4031926 | T | G | 1 | a0005 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.409T>G | p.Leu137Val | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/15 | 535/7517 | 409/3024 | 137/1007 | chr6 | 4031926 | |||
| chr6:4032439 | C | G | 1 | a0003 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.922C>G | p.Arg308Gly | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/15 | 1048/7517 | 922/3024 | 308/1007 | chr6 | 4032439 | |||
| chr6:4037422 | A | G | 1 | a0004 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.1264A>G | p.Ser422Gly | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/15 | 1390/7517 | 1264/3024 | 422/1007 | chr6 | 4037422 | |||
| chr6:4064981 | T | C | 1 | a0001 | 3 | HG00323.hp2 HG01257.hp2 HG01258.hp1 |
splice_region_variant | LOW | c.*4365T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | chr6 | 4064981 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:4031610 | A | T | 1 | a0001c0015 | 1 | HG01070.hp1 | synonymous_variant | LOW | c.93A>T | p.Val31Val | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/15 | 219/7517 | 93/3024 | 31/1007 | chr6 | 4031610 | |||
| chr6:4031721 | A | G | 1 | a0001c0007 | 3 | HG02922.hp2 HG03471.hp1 HG06807.hp1 |
synonymous_variant | LOW | c.204A>G | p.Lys68Lys | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/15 | 330/7517 | 204/3024 | 68/1007 | chr6 | 4031721 | |||
| chr6:4032606 | A | T | 1 | a0002c0009 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.1089A>T | p.Ser363Ser | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/15 | 1215/7517 | 1089/3024 | 363/1007 | chr6 | 4032606 | |||
| chr6:4037550 | A | G | 1 | a0004c0013 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1392A>G | p.Arg464Arg | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/15 | 1518/7517 | 1392/3024 | 464/1007 | chr6 | 4037550 | |||
| chr6:4040823 | C | T | 1 | a0001c0012 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.1464C>T | p.Arg488Arg | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/15 | 1590/7517 | 1464/3024 | 488/1007 | chr6 | 4040823 | |||
| chr6:4043980 | A | G | 1 | a0002c0003 | 13 | HG00735.hp1 HG00738.hp1 HG02145.hp1 others(10): Show |
synonymous_variant | LOW | c.1818A>G | p.Ser606Ser | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/15 | 1944/7517 | 1818/3024 | 606/1007 | chr6 | 4043980 | |||
| chr6:4049087 | C | T | 1 | a0001c0005 | 5 | HG02055.hp1 HG02257.hp1 HG03139.hp1 others(2): Show |
synonymous_variant | LOW | c.2007C>T | p.Thr669Thr | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 8/15 | 2133/7517 | 2007/3024 | 669/1007 | chr6 | 4049087 | |||
| chr6:4051996 | A | G | 1 | a0001c0004 | 6 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(3): Show |
synonymous_variant | LOW | c.2214A>G | p.Lys738Lys | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/15 | 2340/7517 | 2214/3024 | 738/1007 | chr6 | 4051996 | |||
| chr6:4052014 | T | C | 1 | a0002c0008 | 1 | HG02004.hp2 | synonymous_variant | LOW | c.2232T>C | p.Pro744Pro | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/15 | 2358/7517 | 2232/3024 | 744/1007 | chr6 | 4052014 | |||
| chr6:4052083 | C | T | 1 | a0001c0006 | 3 | HG02738.hp2 HG03927.hp1 HG03942.hp1 |
synonymous_variant | LOW | c.2301C>T | p.Phe767Phe | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/15 | 2427/7517 | 2301/3024 | 767/1007 | chr6 | 4052083 | |||
| chr6:4060529 | G | A | 1 | a0001c0011 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.2937G>A | p.Leu979Leu | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 3063/7517 | 2937/3024 | 979/1007 | chr6 | 4060529 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:4021320 | A | G | 38 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(35): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
5_prime_UTR_variant | MODIFIER | c.-106A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/15 | 106 | chr6 | 4021320 | ||||||
| chr6:4021365 | C | A | 1 | a0001c0001t0014 | 1 | NA18983.hp1 | 5_prime_UTR_variant | MODIFIER | c.-61C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/15 | 61 | chr6 | 4021365 | ||||||
| chr6:4021366 | C | A | 1 | a0001c0001t0015 | 1 | HG00621.hp1 | 5_prime_UTR_variant | MODIFIER | c.-60C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/15 | 60 | chr6 | 4021366 | ||||||
| chr6:4021391 | G | T | 1 | a0002c0002t0013 | 2 | NA18956.hp1 NA19060.hp1 |
5_prime_UTR_variant | MODIFIER | c.-35G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/15 | 35 | chr6 | 4021391 | ||||||
| chr6:4061239 | C | T | 1 | a0001c0001t0028 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*623C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 623 | chr6 | 4061239 | ||||||
| chr6:4061296 | G | A | 1 | a0001c0001t0016 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*680G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 680 | chr6 | 4061296 | ||||||
| chr6:4061465 | C | T | 1 | a0002c0002t0027 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*849C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 849 | chr6 | 4061465 | ||||||
| chr6:4061537 | C | A | 5 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0016 others(2): Show |
71 | HG00609.hp1 HG01069.hp1 HG01070.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*921C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 921 | chr6 | 4061537 | ||||||
| chr6:4061613 | C | G | 1 | a0002c0002t0002 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*997C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 997 | chr6 | 4061613 | ||||||
| chr6:4061672 | T | A | 1 | a0001c0001t0017 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1056T>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 1056 | chr6 | 4061672 | ||||||
| chr6:4061699 | C | T | 1 | a0001c0001t0026 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1083C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 1083 | chr6 | 4061699 | ||||||
| chr6:4061864 | T | G | 1 | a0002c0009t0018 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1248T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 1248 | chr6 | 4061864 | ||||||
| chr6:4062142 | A | T | 2 | a0001c0004t0010 a0001c0004t0011 |
6 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1526A>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 1526 | chr6 | 4062142 | ||||||
| chr6:4062431 | A | G | 3 | a0001c0001t0003 a0001c0001t0028 a0001c0015t0003 |
47 | HG00609.hp1 HG01069.hp1 HG01070.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1815A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 1815 | chr6 | 4062431 | ||||||
| chr6:4062781 | GAGTGAAG others(5): Show |
G | 1 | a0001c0001t0025 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2166_*2177delAGTG others(8): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 2166 | chr6 | 4062781 | ||||||
| chr6:4062795 | A | C | 1 | a0001c0001t0025 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2179A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 2179 | chr6 | 4062795 | ||||||
| chr6:4062799 | A | C | 1 | a0001c0001t0025 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2183A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 2183 | chr6 | 4062799 | ||||||
| chr6:4062803 | C | T | 1 | a0001c0001t0025 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2187C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 2187 | chr6 | 4062803 | ||||||
| chr6:4062947 | G | GT | 5 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0016 others(2): Show |
71 | HG00609.hp1 HG01069.hp1 HG01070.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*2334dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 2335 | INFO_REALIGN_3_PRIME | chr6 | 4062947 | |||||
| chr6:4062986 | C | T | 1 | a0002c0002t0024 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2370C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 2370 | chr6 | 4062986 | ||||||
| chr6:4063306 | C | T | 1 | a0002c0003t0005 | 13 | HG00735.hp1 HG00738.hp1 HG02145.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2690C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 2690 | chr6 | 4063306 | ||||||
| chr6:4063447 | G | A | 29 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(26): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
3_prime_UTR_variant | MODIFIER | c.*2831G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 2831 | chr6 | 4063447 | ||||||
| chr6:4063862 | G | A | 1 | a0002c0002t0023 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3246G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 3246 | chr6 | 4063862 | ||||||
| chr6:4064094 | G | A | 1 | a0004c0013t0019 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3478G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 3478 | chr6 | 4064094 | ||||||
| chr6:4064107 | A | G | 1 | a0002c0003t0005 | 13 | HG00735.hp1 HG00738.hp1 HG02145.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3491A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 3491 | chr6 | 4064107 | ||||||
| chr6:4064304 | T | C | 1 | a0001c0001t0020 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3688T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 3688 | chr6 | 4064304 | ||||||
| chr6:4064431 | A | G | 1 | a0001c0001t0022 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3815A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 3815 | chr6 | 4064431 | ||||||
| chr6:4064469 | G | A | 1 | a0001c0001t0021 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3853G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 3853 | chr6 | 4064469 | ||||||
| chr6:4064477 | G | A | 3 | a0001c0001t0006 a0001c0005t0006 a0001c0007t0006 |
11 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3861G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 3861 | chr6 | 4064477 | ||||||
| chr6:4064552 | T | C | 1 | a0001c0001t0007 | 4 | NA18942.hp2 NA18951.hp1 NA19011.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3936T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 3936 | chr6 | 4064552 | ||||||
| chr6:4064712 | A | G | 1 | a0001c0001t0009 | 3 | HG02895.hp1 HG02896.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4096A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 4096 | chr6 | 4064712 | ||||||
| chr6:4064769 | A | G | 1 | a0001c0004t0011 | 3 | HG01884.hp1 HG02486.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4153A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 4153 | chr6 | 4064769 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:4021476 | C | T | 1 | a0001c0001t0001g0030 | 2 | HG02027.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.41+10C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4021476 | |||||||
| chr6:4021653 | T | C | 99 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0034 others(96): Show |
112 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.41+187T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4021653 | |||||||
| chr6:4021781 | C | T | 1 | a0001c0001t0002g0328 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.41+315C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4021781 | |||||||
| chr6:4021865 | C | T | 16 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(13): Show |
16 | HG00140.hp1 HG00408.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.41+399C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4021865 | |||||||
| chr6:4021975 | C | G | 1 | a0002c0002t0002g0311 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.41+509C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4021975 | |||||||
| chr6:4021979 | C | T | 1 | a0001c0006t0001g0310 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.41+513C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4021979 | |||||||
| chr6:4022085 | C | T | 1 | a0002c0009t0018g0309 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.41+619C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022085 | |||||||
| chr6:4022154 | A | AT | 7 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(4): Show |
7 | HG01515.hp2 HG01517.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+710dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4022154 | ||||||
| chr6:4022154 | A | ATT | 115 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(112): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.41+709_41+710dupTT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4022154 | ||||||
| chr6:4022154 | A | ATTT | 76 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0029 others(73): Show |
90 | HG00609.hp1 HG00621.hp1 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.41+708_41+710dupTT others(1): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4022154 | ||||||
| chr6:4022154 | A | ATTTT | 27 | a0001c0001t0001g0108 a0001c0001t0001g0296 a0001c0001t0001g0297 others(24): Show |
27 | HG00544.hp2 HG01081.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.41+707_41+710dupTT others(2): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4022154 | ||||||
| chr6:4022154 | AT | A | 89 | a0001c0001t0001g0199 a0002c0002t0001g0134 a0002c0002t0001g0194 others(86): Show |
96 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.41+710delT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4022154 | ||||||
| chr6:4022226 | G | C | 12 | a0002c0003t0005g0014 a0002c0003t0005g0120 a0002c0003t0005g0121 others(9): Show |
13 | HG00735.hp1 HG00738.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.41+760G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022226 | |||||||
| chr6:4022249 | A | C | 1 | a0004c0013t0019g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.41+783A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022249 | |||||||
| chr6:4022304 | G | GA | 17 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(14): Show |
17 | HG00673.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.41+851dupA | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4022304 | ||||||
| chr6:4022304 | GA | G | 56 | a0001c0001t0001g0199 a0001c0001t0001g0278 a0001c0001t0001g0304 others(53): Show |
58 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.41+851delA | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4022304 | ||||||
| chr6:4022354 | C | A | 1 | a0001c0001t0009g0212 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.41+888C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022354 | |||||||
| chr6:4022360 | G | A | 12 | a0002c0003t0005g0014 a0002c0003t0005g0120 a0002c0003t0005g0121 others(9): Show |
13 | HG00735.hp1 HG00738.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.41+894G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022360 | |||||||
| chr6:4022377 | A | G | 244 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(241): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.41+911A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022377 | |||||||
| chr6:4022381 | C | G | 1 | a0001c0004t0010g0283 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.41+915C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022381 | |||||||
| chr6:4022453 | GTTTT | G | 10 | a0001c0001t0002g0328 a0001c0001t0006g0021 a0001c0005t0006g0211 others(7): Show |
11 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.41+996_41+999delTT others(2): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4022453 | ||||||
| chr6:4022459 | T | C | 1 | a0002c0002t0002g0178 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.41+993T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022459 | |||||||
| chr6:4022461 | T | TG | 218 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(215): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.41+995_41+996insG | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022461 | |||||||
| chr6:4022476 | T | G | 10 | a0001c0001t0002g0328 a0001c0001t0006g0021 a0001c0005t0006g0211 others(7): Show |
11 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.41+1010T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022476 | |||||||
| chr6:4022477 | TG | T | 10 | a0001c0001t0002g0328 a0001c0001t0006g0021 a0001c0005t0006g0211 others(7): Show |
11 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.41+1012delG | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022477 | |||||||
| chr6:4022478 | G | GT | 193 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.41+1021dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4022478 | ||||||
| chr6:4022479 | T | G | 12 | a0002c0002t0002g0031 a0002c0002t0002g0179 a0002c0002t0002g0180 others(9): Show |
12 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.41+1013T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022479 | |||||||
| chr6:4022639 | A | G | 3 | a0001c0006t0001g0222 a0001c0006t0001g0292 a0001c0006t0001g0310 |
3 | HG02738.hp2 HG03927.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.41+1173A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022639 | |||||||
| chr6:4022826 | G | C | 1 | a0001c0001t0001g0223 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.41+1360G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022826 | |||||||
| chr6:4022910 | C | T | 61 | a0001c0001t0003g0001 a0001c0001t0003g0011 a0001c0001t0003g0012 others(58): Show |
71 | HG00609.hp1 HG01069.hp1 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.41+1444C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022910 | |||||||
| chr6:4022913 | ATTCAT | A | 7 | a0002c0002t0001g0194 a0002c0002t0002g0175 a0002c0002t0002g0176 others(4): Show |
7 | HG01074.hp2 HG01099.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.41+1451_41+1455del others(5): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4022913 | ||||||
| chr6:4022975 | C | G | 1 | a0001c0004t0010g0275 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.41+1509C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022975 | |||||||
| chr6:4023134 | A | G | 1 | a0001c0001t0001g0326 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.41+1668A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4023134 | |||||||
| chr6:4023175 | A | G | 1 | a0001c0001t0001g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.41+1709A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4023175 | |||||||
| chr6:4023193 | G | A | 3 | a0001c0001t0009g0212 a0001c0001t0009g0219 a0001c0001t0009g0220 |
3 | HG02895.hp1 HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.41+1727G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4023193 | |||||||
| chr6:4023380 | AAC | A | 3 | a0001c0001t0009g0212 a0001c0001t0009g0219 a0001c0001t0009g0220 |
3 | HG02895.hp1 HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.41+1918_41+1919del others(2): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4023380 | ||||||
| chr6:4023447 | T | C | 1 | a0002c0002t0002g0130 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.41+1981T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4023447 | |||||||
| chr6:4023507 | G | T | 1 | a0001c0001t0001g0274 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.41+2041G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4023507 | |||||||
| chr6:4023618 | C | G | 1 | a0002c0002t0013g0174 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.41+2152C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4023618 | |||||||
| chr6:4023716 | G | A | 231 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(228): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.41+2250G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4023716 | |||||||
| chr6:4023872 | A | AT | 226 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.41+2419dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4023872 | ||||||
| chr6:4023890 | C | T | 7 | a0001c0001t0001g0218 a0001c0001t0001g0272 a0001c0001t0001g0273 others(4): Show |
7 | NA18944.hp2 NA18969.hp1 NA19057.hp1 others(4): Show |
intron_variant | MODIFIER | c.41+2424C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4023890 | |||||||
| chr6:4023891 | G | A | 1 | a0001c0005t0006g0305 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.41+2425G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4023891 | |||||||
| chr6:4024159 | C | G | 1 | a0001c0001t0008g0008 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.41+2693C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4024159 | |||||||
| chr6:4024160 | G | A | 2 | a0001c0001t0004g0070 a0001c0001t0006g0021 |
3 | HG01081.hp2 HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.41+2694G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4024160 | |||||||
| chr6:4024280 | G | A | 231 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(228): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.41+2814G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4024280 | |||||||
| chr6:4024306 | C | G | 1 | a0001c0001t0001g0060 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.41+2840C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4024306 | |||||||
| chr6:4024330 | C | G | 12 | a0002c0003t0005g0014 a0002c0003t0005g0120 a0002c0003t0005g0121 others(9): Show |
13 | HG00735.hp1 HG00738.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.41+2864C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4024330 | |||||||
| chr6:4024538 | CACTAAG | C | 128 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(125): Show |
146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.41+3077_41+3082del others(6): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4024538 | ||||||
| chr6:4024642 | G | C | 1 | a0002c0002t0002g0208 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.41+3176G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4024642 | |||||||
| chr6:4024743 | C | G | 1 | a0001c0001t0001g0218 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.41+3277C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4024743 | |||||||
| chr6:4024763 | G | A | 4 | a0002c0002t0002g0179 a0002c0002t0002g0180 a0002c0002t0002g0181 others(1): Show |
4 | HG01109.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+3297G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4024763 | |||||||
| chr6:4024879 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0299 |
3 | NA18939.hp1 NA18994.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.41+3413C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4024879 | |||||||
| chr6:4024932 | C | T | 1 | a0001c0001t0003g0101 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.41+3466C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4024932 | |||||||
| chr6:4025021 | C | A | 127 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.41+3555C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4025021 | |||||||
| chr6:4025038 | C | G | 10 | a0001c0001t0002g0328 a0001c0001t0006g0021 a0001c0005t0006g0211 others(7): Show |
11 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.41+3572C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4025038 | |||||||
| chr6:4025281 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.41+3815A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4025281 | |||||||
| chr6:4025388 | A | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0299 |
3 | NA18939.hp1 NA18994.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.41+3922A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4025388 | |||||||
| chr6:4025431 | G | C | 1 | a0001c0001t0003g0071 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.41+3965G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4025431 | |||||||
| chr6:4025493 | C | G | 78 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(75): Show |
89 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.41+4027C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4025493 | |||||||
| chr6:4025529 | G | A | 230 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(227): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.41+4063G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4025529 | |||||||
| chr6:4025602 | A | C | 78 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(75): Show |
89 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.41+4136A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4025602 | |||||||
| chr6:4025641 | T | G | 1 | a0001c0001t0001g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.41+4175T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4025641 | |||||||
| chr6:4025674 | C | G | 1 | a0001c0004t0010g0283 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.41+4208C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4025674 | |||||||
| chr6:4025697 | T | C | 230 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(227): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.41+4231T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4025697 | |||||||
| chr6:4025795 | G | C | 3 | a0001c0007t0006g0210 a0001c0007t0006g0293 a0001c0007t0006g0294 |
3 | HG02922.hp2 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.41+4329G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4025795 | |||||||
| chr6:4026057 | A | G | 1 | a0001c0001t0001g0298 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.41+4591A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026057 | |||||||
| chr6:4026088 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.41+4622G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026088 | |||||||
| chr6:4026144 | G | A | 8 | a0001c0001t0001g0028 a0001c0001t0001g0226 a0001c0001t0001g0227 others(5): Show |
8 | HG00621.hp1 HG02080.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.41+4678G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026144 | |||||||
| chr6:4026163 | G | A | 2 | a0001c0001t0004g0073 a0001c0001t0004g0074 |
2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.41+4697G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026163 | |||||||
| chr6:4026302 | C | G | 1 | a0001c0001t0001g0270 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.41+4836C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026302 | |||||||
| chr6:4026303 | CT | C | 219 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(216): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.41+4853delT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4026303 | ||||||
| chr6:4026330 | T | C | 1 | a0001c0001t0007g0231 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.41+4864T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026330 | |||||||
| chr6:4026369 | C | T | 121 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.41+4903C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026369 | |||||||
| chr6:4026462 | C | G | 1 | a0001c0001t0006g0021 | 2 | HG01081.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.41+4996C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026462 | |||||||
| chr6:4026479 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.41+5013T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026479 | |||||||
| chr6:4026482 | T | C | 7 | a0002c0002t0001g0194 a0002c0002t0002g0175 a0002c0002t0002g0176 others(4): Show |
7 | HG01074.hp2 HG01099.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.41+5016T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026482 | |||||||
| chr6:4026720 | A | G | 1 | a0001c0001t0001g0266 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.42-4839A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026720 | |||||||
| chr6:4026901 | G | C | 1 | a0002c0002t0002g0131 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.42-4658G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026901 | |||||||
| chr6:4026954 | A | G | 1 | a0001c0001t0004g0033 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.42-4605A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026954 | |||||||
| chr6:4026964 | C | T | 229 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(226): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.42-4595C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026964 | |||||||
| chr6:4027275 | A | G | 1 | a0001c0001t0008g0008 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.42-4284A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4027275 | |||||||
| chr6:4027335 | C | A | 1 | a0002c0002t0002g0188 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.42-4224C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4027335 | |||||||
| chr6:4027592 | C | CG | 18 | a0001c0001t0001g0224 a0001c0001t0001g0255 a0001c0001t0001g0256 others(15): Show |
18 | HG01952.hp1 HG02055.hp2 HG02273.hp2 others(15): Show |
intron_variant | MODIFIER | c.42-3965dupG | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4027592 | ||||||
| chr6:4027592 | C | CGG | 9 | a0001c0001t0001g0066 a0001c0001t0001g0216 a0001c0001t0001g0218 others(6): Show |
9 | HG01975.hp2 HG02970.hp1 NA18944.hp2 others(6): Show |
intron_variant | MODIFIER | c.42-3966_42-3965dup others(2): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4027592 | ||||||
| chr6:4027592 | CGGA | C | 14 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG00323.hp1 HG00609.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.42-3964_42-3962del others(3): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4027592 | ||||||
| chr6:4027592 | CGGAG | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0044 a0001c0001t0001g0045 |
4 | HG01256.hp1 HG01258.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-3964_42-3961del others(4): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4027592 | ||||||
| chr6:4027593 | GGA | G | 47 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0039 others(44): Show |
50 | HG00621.hp1 HG01069.hp1 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.42-3964_42-3963del others(2): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4027593 | ||||||
| chr6:4027594 | GA | G | 84 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.42-3964delA | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4027594 | |||||||
| chr6:4027595 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
99 | HG00438.hp2 HG00741.hp1 HG01069.hp2 others(96): Show |
intron_variant | MODIFIER | c.42-3964A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4027595 | |||||||
| chr6:4027600 | T | C | 2 | a0001c0001t0001g0039 a0001c0004t0010g0295 |
2 | HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.42-3959T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4027600 | |||||||
| chr6:4027600 | T | G | 226 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.42-3959T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4027600 | |||||||
| chr6:4027600 | T | TG | 13 | a0002c0002t0001g0134 a0002c0002t0001g0194 a0002c0002t0002g0132 others(10): Show |
13 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.42-3952dupG | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4027600 | ||||||
| chr6:4027603 | G | T | 7 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(4): Show |
7 | HG01255.hp1 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.42-3956G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4027603 | |||||||
| chr6:4027608 | T | G | 16 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(13): Show |
17 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(14): Show |
intron_variant | MODIFIER | c.42-3951T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4027608 | |||||||
| chr6:4027613 | T | G | 2 | a0001c0001t0001g0226 a0001c0001t0003g0081 |
2 | HG02040.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.42-3946T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4027613 | |||||||
| chr6:4027712 | G | A | 1 | a0001c0004t0010g0295 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.42-3847G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4027712 | |||||||
| chr6:4027948 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.42-3611C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4027948 | |||||||
| chr6:4028018 | A | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(266): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.42-3541A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028018 | |||||||
| chr6:4028097 | C | G | 1 | a0001c0004t0010g0275 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.42-3462C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028097 | |||||||
| chr6:4028427 | G | A | 1 | a0002c0002t0024g0182 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.42-3132G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028427 | |||||||
| chr6:4028437 | G | C | 1 | a0001c0001t0004g0303 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.42-3122G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028437 | |||||||
| chr6:4028587 | A | G | 79 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(76): Show |
90 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.42-2972A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028587 | |||||||
| chr6:4028826 | C | T | 1 | a0002c0002t0002g0176 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.42-2733C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028826 | |||||||
| chr6:4028830 | A | T | 127 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.42-2729A>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028830 | |||||||
| chr6:4028845 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.42-2714C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028845 | |||||||
| chr6:4028875 | A | G | 231 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(228): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.42-2684A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028875 | |||||||
| chr6:4028894 | C | T | 1 | a0001c0001t0001g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.42-2665C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028894 | |||||||
| chr6:4028963 | T | C | 1 | a0002c0009t0018g0309 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.42-2596T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028963 | |||||||
| chr6:4028968 | C | T | 228 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(225): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.42-2591C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028968 | |||||||
| chr6:4028969 | C | T | 1 | a0001c0001t0001g0278 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.42-2590C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028969 | |||||||
| chr6:4028976 | TATC | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(1): Show |
4 | HG00099.hp2 HG00280.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-2582_42-2580del others(3): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028976 | |||||||
| chr6:4029012 | C | CT | 15 | a0002c0002t0001g0194 a0002c0002t0002g0020 a0002c0002t0002g0140 others(12): Show |
16 | HG01074.hp2 HG01099.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.42-2526dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029012 | ||||||
| chr6:4029012 | C | CTTTTTTT others(5): Show |
2 | a0002c0003t0005g0121 a0002c0003t0005g0122 |
2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.42-2537_42-2526dup others(12): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029012 | ||||||
| chr6:4029012 | C | CTTTTTTT others(6): Show |
7 | a0002c0003t0005g0014 a0002c0003t0005g0120 a0002c0003t0005g0123 others(4): Show |
8 | HG02630.hp2 HG02717.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.42-2538_42-2526dup others(13): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029012 | ||||||
| chr6:4029012 | C | CTTTTTTT others(7): Show |
4 | a0002c0002t0002g0178 a0002c0003t0005g0128 a0002c0003t0005g0129 others(1): Show |
4 | HG00735.hp1 HG00738.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-2539_42-2526dup others(14): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029012 | ||||||
| chr6:4029012 | C | CTTTTTTT others(8): Show |
3 | a0002c0002t0002g0179 a0002c0002t0002g0183 a0002c0002t0002g0184 |
3 | HG01516.hp2 HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.42-2540_42-2526dup others(15): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029012 | ||||||
| chr6:4029012 | C | CTTTTTTT others(9): Show |
5 | a0002c0002t0002g0180 a0002c0002t0002g0185 a0002c0002t0002g0191 others(2): Show |
5 | HG01517.hp2 HG02293.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-2541_42-2526dup others(16): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029012 | ||||||
| chr6:4029012 | C | CTTTTTTT others(10): Show |
6 | a0002c0002t0002g0031 a0002c0002t0002g0181 a0002c0002t0002g0186 others(3): Show |
6 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-2542_42-2526dup others(17): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029012 | ||||||
| chr6:4029012 | C | CTTTTTTT others(11): Show |
2 | a0002c0002t0002g0192 a0002c0002t0002g0193 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.42-2543_42-2526dup others(18): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029012 | ||||||
| chr6:4029012 | CTTTTTTT others(5): Show |
C | 229 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(226): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.42-2537_42-2526del others(12): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029012 | ||||||
| chr6:4029036 | TGA | T | 12 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(9): Show |
12 | HG01891.hp2 HG02145.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.42-2520_42-2519del others(2): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029036 | ||||||
| chr6:4029074 | C | G | 5 | a0001c0001t0001g0027 a0001c0001t0001g0263 a0001c0001t0001g0266 others(2): Show |
5 | NA18955.hp1 NA18956.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-2485C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4029074 | |||||||
| chr6:4029115 | G | A | 20 | a0002c0002t0002g0031 a0002c0002t0002g0178 a0002c0002t0002g0179 others(17): Show |
20 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.42-2444G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4029115 | |||||||
| chr6:4029226 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.42-2333G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4029226 | |||||||
| chr6:4029238 | G | A | 1 | a0001c0001t0009g0212 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.42-2321G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4029238 | |||||||
| chr6:4029339 | AT | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.42-2199delT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029339 | ||||||
| chr6:4029339 | ATT | A | 12 | a0001c0001t0001g0036 a0001c0001t0001g0047 a0001c0001t0001g0048 others(9): Show |
12 | HG00099.hp2 HG01168.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.42-2200_42-2199del others(2): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029339 | ||||||
| chr6:4029343 | T | A | 1 | a0002c0002t0002g0140 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.42-2216T>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4029343 | |||||||
| chr6:4029380 | G | A | 10 | a0001c0001t0002g0328 a0001c0001t0006g0021 a0001c0005t0006g0211 others(7): Show |
11 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.42-2179G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4029380 | |||||||
| chr6:4029403 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.42-2156G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4029403 | |||||||
| chr6:4029496 | A | G | 4 | a0002c0002t0002g0139 a0002c0002t0002g0165 a0002c0002t0002g0167 others(1): Show |
4 | HG01123.hp2 HG01943.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-2063A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4029496 | |||||||
| chr6:4029711 | C | T | 1 | a0004c0013t0019g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.42-1848C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4029711 | |||||||
| chr6:4029768 | G | A | 1 | a0001c0001t0004g0303 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.42-1791G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4029768 | |||||||
| chr6:4029888 | A | G | 231 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(228): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.42-1671A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4029888 | |||||||
| chr6:4029938 | C | CT | 13 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0001c0001t0001g0278 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.42-1605dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029938 | ||||||
| chr6:4029939 | T | C | 9 | a0001c0001t0006g0021 a0001c0005t0006g0211 a0001c0005t0006g0305 others(6): Show |
10 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.42-1620T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4029939 | |||||||
| chr6:4030202 | C | G | 5 | a0001c0004t0010g0275 a0001c0004t0010g0283 a0001c0004t0011g0232 others(2): Show |
5 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-1357C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030202 | |||||||
| chr6:4030260 | G | T | 78 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(75): Show |
89 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.42-1299G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030260 | |||||||
| chr6:4030306 | T | C | 20 | a0002c0002t0002g0031 a0002c0002t0002g0178 a0002c0002t0002g0179 others(17): Show |
20 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.42-1253T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030306 | |||||||
| chr6:4030320 | T | A | 2 | a0001c0001t0007g0003 a0001c0001t0007g0231 |
4 | NA18942.hp2 NA18951.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-1239T>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030320 | |||||||
| chr6:4030415 | C | T | 1 | a0002c0003t0005g0127 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.42-1144C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030415 | |||||||
| chr6:4030474 | T | C | 79 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(76): Show |
90 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.42-1085T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030474 | |||||||
| chr6:4030481 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.42-1078A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030481 | |||||||
| chr6:4030599 | T | G | 1 | a0001c0001t0001g0298 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.42-960T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030599 | |||||||
| chr6:4030679 | A | G | 232 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(229): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.42-880A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030679 | |||||||
| chr6:4030717 | A | G | 79 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(76): Show |
90 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.42-842A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030717 | |||||||
| chr6:4030759 | G | C | 5 | a0002c0002t0002g0132 a0002c0002t0002g0142 a0002c0002t0002g0143 others(2): Show |
5 | NA18954.hp2 NA18971.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-800G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030759 | |||||||
| chr6:4030775 | A | T | 8 | a0002c0002t0002g0018 a0002c0002t0002g0019 a0002c0002t0002g0130 others(5): Show |
10 | HG00408.hp1 HG00544.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.42-784A>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030775 | |||||||
| chr6:4030777 | T | A | 8 | a0002c0002t0002g0018 a0002c0002t0002g0019 a0002c0002t0002g0130 others(5): Show |
10 | HG00408.hp1 HG00544.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.42-782T>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030777 | |||||||
| chr6:4030891 | T | G | 1 | a0001c0001t0004g0115 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.42-668T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030891 | |||||||
| chr6:4030914 | C | T | 79 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(76): Show |
90 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.42-645C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030914 | |||||||
| chr6:4031050 | C | A | 6 | a0001c0001t0004g0009 a0001c0001t0004g0070 a0001c0001t0004g0073 others(3): Show |
7 | HG01167.hp1 HG01169.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-509C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4031050 | |||||||
| chr6:4031138 | G | A | 41 | a0001c0001t0003g0001 a0001c0001t0003g0011 a0001c0001t0003g0012 others(38): Show |
48 | HG00609.hp1 HG01069.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.42-421G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4031138 | |||||||
| chr6:4031225 | T | G | 231 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(228): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.42-334T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4031225 | |||||||
| chr6:4031393 | G | A | 1 | a0002c0003t0005g0127 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.42-166G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4031393 | |||||||
| chr6:4031482 | A | G | 1 | a0002c0002t0002g0031 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.42-77A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4031482 | |||||||
| chr6:4032831 | A | G | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(267): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1238+76A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4032831 | |||||||
| chr6:4032968 | A | G | 1 | a0001c0001t0001g0320 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1238+213A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4032968 | |||||||
| chr6:4033172 | T | G | 1 | a0001c0001t0001g0236 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1238+417T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4033172 | |||||||
| chr6:4033602 | A | G | 1 | a0001c0001t0020g0285 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1238+847A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4033602 | |||||||
| chr6:4033664 | A | G | 1 | a0001c0005t0006g0211 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1238+909A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4033664 | |||||||
| chr6:4033677 | G | A | 1 | a0002c0002t0002g0188 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1238+922G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4033677 | |||||||
| chr6:4033807 | T | A | 1 | a0001c0001t0001g0237 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1238+1052T>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4033807 | |||||||
| chr6:4033825 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1238+1070T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4033825 | |||||||
| chr6:4033847 | G | A | 19 | a0002c0002t0002g0031 a0002c0002t0002g0178 a0002c0002t0002g0179 others(16): Show |
19 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1238+1092G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4033847 | |||||||
| chr6:4033966 | A | G | 1 | a0002c0002t0002g0139 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1238+1211A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4033966 | |||||||
| chr6:4033997 | TA | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0036 others(6): Show |
10 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(7): Show |
intron_variant | MODIFIER | c.1238+1243delA | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4033997 | |||||||
| chr6:4034020 | A | G | 232 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(229): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1238+1265A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4034020 | |||||||
| chr6:4034143 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0059 |
3 | HG01070.hp2 HG01071.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1238+1388A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4034143 | |||||||
| chr6:4034157 | AT | A | 131 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.1238+1413delT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4034157 | ||||||
| chr6:4034315 | A | G | 1 | a0001c0001t0001g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1238+1560A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4034315 | |||||||
| chr6:4034401 | A | G | 1 | a0002c0002t0002g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1238+1646A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4034401 | |||||||
| chr6:4034662 | G | T | 1 | a0001c0001t0001g0302 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1238+1907G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4034662 | |||||||
| chr6:4034698 | T | C | 12 | a0002c0003t0005g0014 a0002c0003t0005g0120 a0002c0003t0005g0121 others(9): Show |
13 | HG00735.hp1 HG00738.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1238+1943T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4034698 | |||||||
| chr6:4034774 | G | A | 2 | a0001c0001t0001g0312 a0001c0001t0001g0321 |
2 | HG01123.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1238+2019G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4034774 | |||||||
| chr6:4034870 | G | T | 128 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(125): Show |
146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.1238+2115G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4034870 | |||||||
| chr6:4034888 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1238+2133T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4034888 | |||||||
| chr6:4034935 | A | C | 1 | a0001c0001t0004g0080 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1238+2180A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4034935 | |||||||
| chr6:4034947 | G | A | 4 | a0002c0002t0002g0145 a0002c0002t0002g0146 a0002c0002t0002g0147 others(1): Show |
4 | HG02280.hp2 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1238+2192G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4034947 | |||||||
| chr6:4035173 | G | C | 2 | a0001c0001t0003g0086 a0001c0001t0003g0093 |
2 | NA18939.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.1239-2224G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4035173 | |||||||
| chr6:4035221 | A | G | 1 | a0001c0001t0001g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1239-2176A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4035221 | |||||||
| chr6:4035284 | A | ATT | 7 | a0002c0002t0002g0150 a0002c0002t0002g0176 a0002c0002t0002g0188 others(4): Show |
7 | HG00735.hp1 HG00738.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239-2081_1239-208 others(6): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | ||||||
| chr6:4035284 | A | ATTTTT | 7 | a0001c0005t0006g0308 a0001c0007t0006g0293 a0001c0007t0006g0294 others(4): Show |
7 | HG01928.hp1 HG02055.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1239-2084_1239-208 others(9): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | ||||||
| chr6:4035284 | A | ATTTTTTT others(3): Show |
1 | a0002c0002t0002g0147 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1239-2089_1239-208 others(14): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | ||||||
| chr6:4035284 | A | ATTTTTTT others(4): Show |
6 | a0002c0002t0002g0018 a0002c0002t0002g0130 a0002c0002t0002g0131 others(3): Show |
7 | HG00408.hp1 HG01943.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.1239-2090_1239-208 others(15): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | ||||||
| chr6:4035284 | A | ATTTTTTT others(5): Show |
17 | a0002c0002t0001g0134 a0002c0002t0002g0016 a0002c0002t0002g0020 others(14): Show |
19 | HG00280.hp2 HG00438.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.1239-2091_1239-208 others(16): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | ||||||
| chr6:4035284 | A | ATTTTTTT others(6): Show |
8 | a0002c0002t0002g0019 a0002c0002t0002g0136 a0002c0002t0002g0159 others(5): Show |
9 | HG01192.hp1 HG02027.hp2 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.1239-2092_1239-208 others(17): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | ||||||
| chr6:4035284 | A | ATTTTTTT others(7): Show |
3 | a0002c0002t0002g0162 a0002c0002t0002g0164 a0002c0002t0002g0171 |
3 | NA18612.hp2 NA19067.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1239-2093_1239-208 others(18): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | ||||||
| chr6:4035284 | A | ATTTTTTT others(8): Show |
2 | a0002c0002t0002g0167 a0002c0002t0002g0172 |
2 | HG02273.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1239-2094_1239-208 others(19): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | ||||||
| chr6:4035284 | A | ATTTTTTT others(9): Show |
3 | a0002c0002t0002g0017 a0002c0002t0002g0205 a0002c0002t0002g0311 |
4 | HG00642.hp2 HG01515.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1239-2095_1239-208 others(20): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | ||||||
| chr6:4035284 | A | ATTTTTTT others(10): Show |
1 | a0002c0002t0002g0138 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1239-2096_1239-208 others(21): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | ||||||
| chr6:4035284 | A | ATTTTTTT others(11): Show |
1 | a0002c0002t0002g0163 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1239-2097_1239-208 others(22): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | ||||||
| chr6:4035284 | A | ATTTTTTT others(12): Show |
1 | a0002c0002t0002g0206 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1239-2098_1239-208 others(23): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | ||||||
| chr6:4035284 | A | ATTTTTTT others(18): Show |
1 | a0002c0002t0002g0137 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1239-2104_1239-208 others(29): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | ||||||
| chr6:4035284 | AT | A | 14 | a0001c0001t0001g0065 a0001c0001t0001g0298 a0002c0002t0002g0178 others(11): Show |
14 | HG02145.hp2 HG02293.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1239-2080delT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | ||||||
| chr6:4035284 | ATT | A | 13 | a0001c0001t0001g0057 a0001c0001t0001g0061 a0001c0001t0001g0063 others(10): Show |
13 | HG00642.hp1 HG00738.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1239-2081_1239-208 others(6): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | ||||||
| chr6:4035284 | ATTT | A | 31 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0055 others(28): Show |
31 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.1239-2082_1239-208 others(7): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | ||||||
| chr6:4035284 | ATTTT | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
107 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.1239-2083_1239-208 others(8): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | ||||||
| chr6:4035284 | ATTTTT | A | 8 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0216 others(5): Show |
8 | HG00323.hp2 HG01169.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1239-2084_1239-208 others(9): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | ||||||
| chr6:4035284 | ATTTTTT | A | 12 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0068 others(9): Show |
12 | HG00735.hp2 HG01243.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1239-2085_1239-208 others(10): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | ||||||
| chr6:4035284 | ATTTTTTT | A | 30 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(27): Show |
33 | HG00099.hp2 HG00280.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.1239-2086_1239-208 others(11): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | ||||||
| chr6:4035284 | ATTTTTTT others(1): Show |
A | 37 | a0001c0001t0001g0034 a0001c0001t0003g0001 a0001c0001t0003g0011 others(34): Show |
45 | HG00323.hp1 HG00609.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.1239-2087_1239-208 others(12): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | ||||||
| chr6:4035284 | ATTTTTTT others(21): Show |
A | 2 | a0002c0002t0002g0015 a0002c0002t0002g0141 |
3 | NA18951.hp2 NA19006.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1239-2107_1239-208 others(32): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | ||||||
| chr6:4035319 | A | G | 1 | a0002c0002t0002g0158 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1239-2078A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4035319 | |||||||
| chr6:4035340 | T | C | 11 | a0001c0001t0002g0328 a0001c0001t0006g0021 a0001c0001t0006g0280 others(8): Show |
12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1239-2057T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4035340 | |||||||
| chr6:4035371 | T | G | 1 | a0001c0001t0001g0238 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1239-2026T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4035371 | |||||||
| chr6:4035417 | G | A | 2 | a0002c0003t0005g0121 a0002c0003t0005g0122 |
2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1239-1980G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4035417 | |||||||
| chr6:4035600 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1239-1797G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4035600 | |||||||
| chr6:4035838 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1239-1559A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4035838 | |||||||
| chr6:4035927 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1239-1470T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4035927 | |||||||
| chr6:4036022 | GACAA | G | 230 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(227): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.1239-1372_1239-136 others(8): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4036022 | ||||||
| chr6:4036038 | A | G | 1 | a0001c0001t0001g0228 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1239-1359A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036038 | |||||||
| chr6:4036105 | T | C | 1 | a0001c0001t0001g0304 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1239-1292T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036105 | |||||||
| chr6:4036170 | C | A | 1 | a0002c0002t0002g0195 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1239-1227C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036170 | |||||||
| chr6:4036200 | T | C | 2 | a0001c0005t0006g0306 a0001c0005t0006g0307 |
2 | HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1239-1197T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036200 | |||||||
| chr6:4036236 | A | G | 231 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(228): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1239-1161A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036236 | |||||||
| chr6:4036307 | T | C | 5 | a0001c0001t0006g0280 a0001c0004t0011g0232 a0001c0004t0011g0233 others(2): Show |
5 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1239-1090T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036307 | |||||||
| chr6:4036344 | C | T | 3 | a0001c0005t0006g0305 a0001c0005t0006g0306 a0001c0005t0006g0307 |
3 | HG03139.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1239-1053C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036344 | |||||||
| chr6:4036410 | T | G | 3 | a0001c0005t0006g0305 a0001c0005t0006g0306 a0001c0005t0006g0307 |
3 | HG03139.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1239-987T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036410 | |||||||
| chr6:4036419 | G | A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | HG03654.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1239-978G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036419 | |||||||
| chr6:4036511 | C | G | 14 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(11): Show |
15 | HG01081.hp2 HG01891.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1239-886C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036511 | |||||||
| chr6:4036549 | C | G | 227 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(224): Show |
257 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.1239-848C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036549 | |||||||
| chr6:4036735 | A | G | 2 | a0001c0001t0001g0315 a0005c0010t0001g0325 |
2 | HG02165.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1239-662A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036735 | |||||||
| chr6:4036811 | A | AC | 21 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0036 others(18): Show |
23 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.1239-581dupC | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4036811 | ||||||
| chr6:4036862 | A | G | 9 | a0001c0001t0004g0010 a0001c0001t0004g0078 a0001c0001t0004g0111 others(6): Show |
10 | HG01884.hp2 HG02486.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1239-535A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036862 | |||||||
| chr6:4036985 | C | CA | 10 | a0002c0002t0002g0140 a0002c0002t0002g0142 a0002c0002t0002g0149 others(7): Show |
10 | HG01074.hp2 HG01099.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.1239-390dupA | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4036985 | ||||||
| chr6:4036985 | CAAA | C | 12 | a0002c0002t0002g0183 a0002c0003t0005g0014 a0002c0003t0005g0120 others(9): Show |
13 | HG00735.hp1 HG00738.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1239-392_1239-390d others(5): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4036985 | ||||||
| chr6:4036985 | CAAAA | C | 21 | a0001c0001t0001g0043 a0001c0004t0011g0232 a0001c0004t0011g0234 others(18): Show |
21 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1239-393_1239-390d others(6): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4036985 | ||||||
| chr6:4036985 | CAAAAA | C | 223 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(220): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1239-394_1239-390d others(7): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4036985 | ||||||
| chr6:4037158 | A | G | 2 | a0002c0002t0002g0183 a0002c0002t0024g0182 |
2 | HG00639.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1239-239A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4037158 | |||||||
| chr6:4037224 | A | G | 225 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(222): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1239-173A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4037224 | |||||||
| chr6:4037322 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1239-75G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4037322 | |||||||
| chr6:4037348 | C | A | 232 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(229): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1239-49C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4037348 | |||||||
| chr6:4037360 | T | C | 6 | a0001c0004t0010g0275 a0001c0004t0010g0283 a0001c0004t0010g0295 others(3): Show |
6 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1239-37T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4037360 | |||||||
| chr6:4037857 | A | AT | 10 | a0001c0001t0001g0247 a0001c0001t0001g0282 a0001c0001t0003g0119 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1412+302dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr6 | 4037857 | ||||||
| chr6:4037857 | AT | A | 7 | a0001c0001t0001g0216 a0001c0001t0021g0242 a0001c0004t0010g0275 others(4): Show |
7 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1412+302delT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr6 | 4037857 | ||||||
| chr6:4037896 | T | C | 2 | a0001c0001t0001g0313 a0001c0001t0001g0327 |
2 | HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1412+326T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4037896 | |||||||
| chr6:4037911 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1412+341C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4037911 | |||||||
| chr6:4038034 | A | C | 1 | a0001c0001t0001g0269 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1412+464A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038034 | |||||||
| chr6:4038045 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1412+475A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038045 | |||||||
| chr6:4038121 | T | C | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(267): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1412+551T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038121 | |||||||
| chr6:4038122 | G | A | 1 | a0004c0013t0019g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1412+552G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038122 | |||||||
| chr6:4038264 | C | T | 4 | a0001c0001t0001g0047 a0001c0001t0001g0051 a0001c0001t0001g0060 others(1): Show |
4 | HG03017.hp2 HG03491.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1412+694C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038264 | |||||||
| chr6:4038282 | G | GTTTTA | 4 | a0001c0001t0001g0282 a0001c0005t0006g0306 a0001c0005t0006g0307 others(1): Show |
4 | HG02717.hp1 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1412+737_1412+741d others(7): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr6 | 4038282 | ||||||
| chr6:4038336 | C | G | 232 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(229): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1412+766C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038336 | |||||||
| chr6:4038367 | A | C | 35 | a0001c0001t0003g0001 a0001c0001t0003g0011 a0001c0001t0003g0012 others(32): Show |
42 | HG00609.hp1 HG01069.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1412+797A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038367 | |||||||
| chr6:4038393 | T | C | 6 | a0002c0002t0002g0175 a0002c0002t0002g0176 a0002c0002t0002g0195 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1412+823T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038393 | |||||||
| chr6:4038410 | A | C | 1 | a0002c0002t0002g0185 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1412+840A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038410 | |||||||
| chr6:4038462 | G | T | 2 | a0002c0003t0005g0126 a0002c0003t0005g0129 |
2 | HG00738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1412+892G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038462 | |||||||
| chr6:4038540 | G | A | 1 | a0004c0013t0019g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1412+970G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038540 | |||||||
| chr6:4038587 | G | A | 1 | a0001c0001t0006g0021 | 2 | HG01081.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1412+1017G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038587 | |||||||
| chr6:4038718 | C | T | 232 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(229): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1412+1148C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038718 | |||||||
| chr6:4038919 | C | CTT | 230 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(227): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.1412+1358_1412+135 others(6): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr6 | 4038919 | ||||||
| chr6:4039087 | A | G | 1 | a0002c0009t0018g0309 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1412+1517A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4039087 | |||||||
| chr6:4039241 | G | A | 252 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.1413-1531G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4039241 | |||||||
| chr6:4039393 | A | G | 1 | a0001c0001t0001g0320 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1413-1379A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4039393 | |||||||
| chr6:4039602 | C | G | 1 | a0001c0001t0004g0033 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1413-1170C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4039602 | |||||||
| chr6:4039659 | G | A | 6 | a0002c0002t0002g0175 a0002c0002t0002g0176 a0002c0002t0002g0195 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1413-1113G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4039659 | |||||||
| chr6:4039747 | C | T | 1 | a0001c0004t0010g0275 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1413-1025C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4039747 | |||||||
| chr6:4039883 | C | G | 20 | a0001c0001t0001g0282 a0002c0002t0002g0031 a0002c0002t0002g0178 others(17): Show |
20 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1413-889C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4039883 | |||||||
| chr6:4039915 | T | C | 232 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(229): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1413-857T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4039915 | |||||||
| chr6:4040009 | C | T | 1 | a0004c0013t0019g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1413-763C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040009 | |||||||
| chr6:4040113 | C | T | 1 | a0001c0001t0003g0095 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1413-659C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040113 | |||||||
| chr6:4040114 | G | C | 4 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(1): Show |
4 | HG00099.hp2 HG00280.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1413-658G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040114 | |||||||
| chr6:4040121 | C | T | 1 | a0004c0013t0019g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1413-651C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040121 | |||||||
| chr6:4040171 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1413-601C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040171 | |||||||
| chr6:4040187 | T | G | 3 | a0001c0005t0006g0305 a0001c0005t0006g0306 a0001c0005t0006g0307 |
3 | HG03139.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1413-585T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040187 | |||||||
| chr6:4040217 | T | C | 2 | a0002c0002t0002g0179 a0002c0002t0002g0180 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1413-555T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040217 | |||||||
| chr6:4040328 | A | G | 1 | a0002c0009t0018g0309 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1413-444A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040328 | |||||||
| chr6:4040394 | C | T | 1 | a0001c0001t0002g0328 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1413-378C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040394 | |||||||
| chr6:4040399 | G | C | 2 | a0001c0001t0004g0079 a0001c0001t0004g0303 |
2 | HG02109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1413-373G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040399 | |||||||
| chr6:4040401 | G | T | 1 | a0001c0001t0001g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1413-371G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040401 | |||||||
| chr6:4040523 | T | C | 6 | a0001c0004t0010g0275 a0001c0004t0010g0283 a0001c0004t0010g0295 others(3): Show |
6 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1413-249T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040523 | |||||||
| chr6:4040612 | G | A | 1 | a0001c0004t0010g0283 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1413-160G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040612 | |||||||
| chr6:4040688 | A | G | 18 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(15): Show |
19 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.1413-84A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040688 | |||||||
| chr6:4040690 | A | G | 19 | a0002c0002t0002g0031 a0002c0002t0002g0178 a0002c0002t0002g0179 others(16): Show |
19 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1413-82A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040690 | |||||||
| chr6:4040699 | G | C | 1 | a0001c0001t0001g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1413-73G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040699 | |||||||
| chr6:4040978 | T | C | 2 | a0001c0001t0004g0079 a0001c0001t0004g0303 |
2 | HG02109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1568+51T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4040978 | |||||||
| chr6:4040988 | G | A | 11 | a0001c0001t0001g0282 a0001c0001t0006g0021 a0001c0001t0006g0280 others(8): Show |
12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1568+61G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4040988 | |||||||
| chr6:4041187 | A | G | 221 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(218): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1568+260A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4041187 | |||||||
| chr6:4041353 | T | G | 1 | a0001c0005t0006g0306 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1568+426T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4041353 | |||||||
| chr6:4041445 | C | T | 1 | a0002c0002t0002g0196 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1568+518C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4041445 | |||||||
| chr6:4041650 | T | C | 12 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(9): Show |
12 | HG01891.hp2 HG02145.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1568+723T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4041650 | |||||||
| chr6:4041683 | C | CTTG | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(267): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1568+758_1568+760d others(5): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr6 | 4041683 | ||||||
| chr6:4041744 | A | C | 19 | a0001c0001t0001g0282 a0001c0001t0002g0328 a0001c0001t0006g0021 others(16): Show |
20 | HG01074.hp2 HG01081.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1569-743A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4041744 | |||||||
| chr6:4041754 | A | G | 200 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(197): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1569-733A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4041754 | |||||||
| chr6:4041987 | A | C | 1 | a0002c0002t0002g0156 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1569-500A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4041987 | |||||||
| chr6:4042006 | C | T | 3 | a0001c0001t0001g0028 a0001c0001t0015g0028 a0002c0009t0018g0309 |
3 | HG00621.hp1 NA18522.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1569-481C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4042006 | |||||||
| chr6:4042068 | G | A | 1 | a0002c0002t0002g0177 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1569-419G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4042068 | |||||||
| chr6:4042103 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1569-384G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4042103 | |||||||
| chr6:4042163 | G | A | 3 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0026g0287 |
3 | HG01168.hp2 HG01169.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1569-324G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4042163 | |||||||
| chr6:4042712 | A | G | 1 | a0002c0002t0002g0189 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1650+144A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4042712 | |||||||
| chr6:4042775 | T | G | 6 | a0002c0002t0001g0134 a0002c0002t0002g0151 a0002c0002t0002g0157 others(3): Show |
6 | HG00280.hp2 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.1650+207T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4042775 | |||||||
| chr6:4043025 | G | A | 1 | a0001c0001t0001g0302 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1650+457G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4043025 | |||||||
| chr6:4043086 | A | G | 1 | a0002c0002t0002g0171 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1650+518A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4043086 | |||||||
| chr6:4043181 | A | G | 233 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(230): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1650+613A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4043181 | |||||||
| chr6:4043219 | C | T | 1 | a0001c0001t0004g0113 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1651-594C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4043219 | |||||||
| chr6:4043248 | G | A | 1 | a0002c0002t0002g0150 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1651-565G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4043248 | |||||||
| chr6:4043577 | G | T | 1 | a0001c0001t0001g0240 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1651-236G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4043577 | |||||||
| chr6:4043613 | A | C | 201 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1651-200A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4043613 | |||||||
| chr6:4043653 | A | G | 1 | a0001c0001t0001g0273 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1651-160A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4043653 | |||||||
| chr6:4043662 | T | A | 12 | a0001c0001t0001g0282 a0001c0001t0002g0328 a0001c0001t0006g0021 others(9): Show |
13 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1651-151T>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4043662 | |||||||
| chr6:4043664 | C | T | 9 | a0001c0001t0006g0280 a0001c0005t0006g0211 a0001c0005t0006g0305 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1651-149C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4043664 | |||||||
| chr6:4043665 | A | G | 233 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(230): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1651-148A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4043665 | |||||||
| chr6:4043738 | G | A | 3 | a0002c0002t0002g0016 a0002c0002t0002g0135 a0002c0002t0002g0149 |
4 | NA18966.hp2 NA18980.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1651-75G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4043738 | |||||||
| chr6:4044039 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1861+16C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044039 | |||||||
| chr6:4044063 | G | T | 234 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(231): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1861+40G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044063 | |||||||
| chr6:4044092 | G | C | 11 | a0001c0001t0002g0328 a0001c0001t0006g0021 a0001c0001t0006g0280 others(8): Show |
12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1861+69G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044092 | |||||||
| chr6:4044110 | A | G | 245 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(242): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.1861+87A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044110 | |||||||
| chr6:4044252 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1861+229G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044252 | |||||||
| chr6:4044384 | T | C | 1 | a0002c0009t0018g0309 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1861+361T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044384 | |||||||
| chr6:4044393 | C | G | 11 | a0001c0001t0002g0328 a0001c0001t0006g0021 a0001c0001t0006g0280 others(8): Show |
12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1861+370C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044393 | |||||||
| chr6:4044510 | T | C | 1 | a0001c0004t0010g0275 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1861+487T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044510 | |||||||
| chr6:4044682 | T | C | 1 | a0001c0012t0001g0323 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1861+659T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044682 | |||||||
| chr6:4044708 | A | G | 5 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(2): Show |
5 | HG01074.hp1 HG01106.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861+685A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044708 | |||||||
| chr6:4044800 | A | G | 1 | a0002c0002t0002g0157 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1861+777A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044800 | |||||||
| chr6:4044814 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1861+791G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044814 | |||||||
| chr6:4044845 | G | GTTA | 66 | a0001c0001t0001g0022 a0001c0001t0001g0053 a0001c0001t0001g0226 others(63): Show |
77 | HG00544.hp2 HG00609.hp1 HG01069.hp1 others(74): Show |
intron_variant | MODIFIER | c.1861+840_1861+842d others(5): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr6 | 4044845 | ||||||
| chr6:4044860 | A | ATTT | 13 | a0001c0001t0001g0007 a0001c0001t0001g0047 a0001c0001t0001g0052 others(10): Show |
14 | HG00140.hp2 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1861+839_1861+840i others(5): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr6 | 4044860 | ||||||
| chr6:4044860 | A | T | 7 | a0002c0002t0002g0178 a0002c0003t0005g0121 a0002c0003t0005g0122 others(4): Show |
7 | HG00735.hp1 HG00738.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1861+837A>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044860 | |||||||
| chr6:4044862 | TA | T | 5 | a0001c0005t0006g0305 a0001c0005t0006g0306 a0001c0005t0006g0307 others(2): Show |
5 | HG02922.hp2 HG03139.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861+840delA | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044862 | |||||||
| chr6:4044863 | A | ATT | 17 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0036 others(14): Show |
18 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(15): Show |
intron_variant | MODIFIER | c.1861+854_1861+855d others(4): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr6 | 4044863 | ||||||
| chr6:4044863 | A | ATTT | 103 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
117 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.1861+853_1861+855d others(5): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr6 | 4044863 | ||||||
| chr6:4044863 | A | ATTTT | 9 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0065 others(6): Show |
9 | HG01884.hp1 HG02145.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1861+852_1861+855d others(6): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr6 | 4044863 | ||||||
| chr6:4044863 | A | T | 41 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0047 others(38): Show |
43 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.1861+840A>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044863 | |||||||
| chr6:4044863 | AT | A | 7 | a0001c0001t0002g0328 a0001c0001t0006g0021 a0001c0001t0006g0280 others(4): Show |
8 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1861+855delT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr6 | 4044863 | ||||||
| chr6:4044864 | T | TTA | 6 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0044 others(3): Show |
6 | HG01169.hp2 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1861+842_1861+843i others(4): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr6 | 4044864 | ||||||
| chr6:4044866 | T | A | 3 | a0001c0001t0022g0213 a0002c0002t0002g0165 a0002c0002t0002g0185 |
3 | HG01943.hp2 HG02155.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1861+843T>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044866 | |||||||
| chr6:4044904 | C | T | 6 | a0002c0003t0005g0014 a0002c0003t0005g0120 a0002c0003t0005g0123 others(3): Show |
7 | HG02717.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1861+881C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044904 | |||||||
| chr6:4045008 | G | A | 1 | a0002c0009t0018g0309 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1861+985G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4045008 | |||||||
| chr6:4045097 | G | A | 1 | a0001c0001t0001g0023 | 2 | HG01516.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1861+1074G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4045097 | |||||||
| chr6:4045168 | C | T | 11 | a0001c0001t0002g0328 a0001c0001t0006g0021 a0001c0001t0006g0280 others(8): Show |
12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1861+1145C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4045168 | |||||||
| chr6:4045280 | A | G | 221 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(218): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1861+1257A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4045280 | |||||||
| chr6:4045358 | G | A | 12 | a0002c0003t0005g0014 a0002c0003t0005g0120 a0002c0003t0005g0121 others(9): Show |
13 | HG00735.hp1 HG00738.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1861+1335G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4045358 | |||||||
| chr6:4045469 | C | T | 1 | a0002c0003t0005g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1861+1446C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4045469 | |||||||
| chr6:4045599 | A | C | 11 | a0001c0001t0002g0328 a0001c0001t0006g0021 a0001c0001t0006g0280 others(8): Show |
12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1861+1576A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4045599 | |||||||
| chr6:4045684 | T | C | 1 | a0002c0002t0002g0138 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1862-1491T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4045684 | |||||||
| chr6:4045724 | C | G | 1 | a0001c0001t0002g0328 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1862-1451C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4045724 | |||||||
| chr6:4045745 | A | G | 1 | a0001c0004t0011g0233 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1862-1430A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4045745 | |||||||
| chr6:4045746 | G | A | 11 | a0001c0001t0002g0328 a0001c0001t0006g0021 a0001c0001t0006g0280 others(8): Show |
12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1862-1429G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4045746 | |||||||
| chr6:4046010 | A | T | 11 | a0001c0001t0002g0328 a0001c0001t0006g0021 a0001c0001t0006g0280 others(8): Show |
12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1862-1165A>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4046010 | |||||||
| chr6:4046082 | G | A | 1 | a0002c0002t0002g0157 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1862-1093G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4046082 | |||||||
| chr6:4046316 | A | G | 1 | a0001c0001t0003g0093 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1862-859A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4046316 | |||||||
| chr6:4046322 | T | C | 12 | a0002c0003t0005g0014 a0002c0003t0005g0120 a0002c0003t0005g0121 others(9): Show |
13 | HG00735.hp1 HG00738.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1862-853T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4046322 | |||||||
| chr6:4046364 | G | T | 1 | a0001c0007t0006g0293 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1862-811G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4046364 | |||||||
| chr6:4046568 | G | T | 219 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(216): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1862-607G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4046568 | |||||||
| chr6:4046594 | C | G | 200 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(197): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1862-581C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4046594 | |||||||
| chr6:4046660 | C | CT | 16 | a0001c0001t0001g0282 a0001c0001t0002g0328 a0001c0001t0003g0095 others(13): Show |
17 | HG01081.hp2 HG02055.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.1862-499dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr6 | 4046660 | ||||||
| chr6:4046663 | T | C | 1 | a0001c0001t0001g0320 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1862-512T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4046663 | |||||||
| chr6:4046686 | T | C | 3 | a0001c0001t0001g0313 a0001c0001t0001g0324 a0001c0001t0001g0327 |
3 | HG03710.hp2 HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1862-489T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4046686 | |||||||
| chr6:4046697 | C | T | 200 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(197): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1862-478C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4046697 | |||||||
| chr6:4046711 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1862-464G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4046711 | |||||||
| chr6:4046815 | G | C | 1 | a0001c0001t0004g0080 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1862-360G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4046815 | |||||||
| chr6:4047005 | C | T | 1 | a0001c0001t0001g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1862-170C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4047005 | |||||||
| chr6:4047075 | G | A | 11 | a0001c0001t0002g0328 a0001c0001t0006g0021 a0001c0001t0006g0280 others(8): Show |
12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1862-100G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4047075 | |||||||
| chr6:4047363 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1935+115G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4047363 | |||||||
| chr6:4047382 | ACT | A | 6 | a0001c0001t0004g0009 a0001c0001t0004g0070 a0001c0001t0004g0073 others(3): Show |
7 | HG01167.hp1 HG01169.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1935+137_1935+138d others(4): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4047382 | ||||||
| chr6:4047414 | A | G | 1 | a0001c0001t0001g0245 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1935+166A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4047414 | |||||||
| chr6:4047462 | T | G | 1 | a0001c0001t0001g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1935+214T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4047462 | |||||||
| chr6:4047584 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1935+336A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4047584 | |||||||
| chr6:4047639 | C | T | 1 | a0001c0001t0022g0213 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1935+391C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4047639 | |||||||
| chr6:4047791 | A | G | 1 | a0002c0003t0005g0127 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1935+543A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4047791 | |||||||
| chr6:4047901 | T | TAC | 27 | a0001c0001t0001g0006 a0001c0001t0001g0037 a0001c0001t0001g0046 others(24): Show |
30 | HG00735.hp2 HG01099.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.1935+697_1935+698d others(4): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4047901 | ||||||
| chr6:4047901 | T | TACAC | 8 | a0001c0004t0010g0283 a0002c0002t0002g0145 a0002c0002t0002g0158 others(5): Show |
8 | HG00738.hp2 HG02040.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1935+695_1935+698d others(6): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4047901 | ||||||
| chr6:4047901 | TAC | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0024 others(42): Show |
50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.1935+697_1935+698d others(4): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4047901 | ||||||
| chr6:4047901 | TACAC | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0023 others(103): Show |
122 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1935+695_1935+698d others(6): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4047901 | ||||||
| chr6:4047901 | TACACAC | T | 14 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0041 others(11): Show |
17 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1935+693_1935+698d others(8): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4047901 | ||||||
| chr6:4047901 | TACACACA others(1): Show |
T | 29 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0061 others(26): Show |
31 | HG00099.hp1 HG00741.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1935+691_1935+698d others(10): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4047901 | ||||||
| chr6:4047901 | TACACACA others(3): Show |
T | 21 | a0001c0001t0001g0028 a0001c0001t0001g0226 a0001c0001t0001g0227 others(18): Show |
22 | HG00621.hp1 HG00735.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.1935+689_1935+698d others(12): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4047901 | ||||||
| chr6:4047901 | TACACACA others(7): Show |
T | 8 | a0001c0001t0002g0328 a0001c0001t0006g0280 a0001c0005t0006g0305 others(5): Show |
8 | HG02922.hp2 HG02965.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1935+685_1935+698d others(16): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4047901 | ||||||
| chr6:4047901 | TACACACA others(9): Show |
T | 2 | a0001c0005t0006g0211 a0001c0005t0006g0308 |
2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1935+683_1935+698d others(18): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4047901 | ||||||
| chr6:4047901 | TACACACA others(15): Show |
T | 1 | a0004c0013t0019g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1935+677_1935+698d others(24): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4047901 | ||||||
| chr6:4047976 | A | G | 1 | a0001c0001t0004g0033 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1935+728A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4047976 | |||||||
| chr6:4048006 | A | G | 1 | a0001c0001t0001g0244 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1935+758A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048006 | |||||||
| chr6:4048046 | G | T | 2 | a0002c0002t0002g0137 a0002c0002t0002g0206 |
2 | HG00609.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.1935+798G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048046 | |||||||
| chr6:4048058 | T | A | 4 | a0001c0001t0001g0215 a0001c0001t0001g0217 a0001c0001t0001g0246 others(1): Show |
4 | HG00140.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1935+810T>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048058 | |||||||
| chr6:4048150 | G | A | 1 | a0001c0001t0001g0269 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1936-866G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048150 | |||||||
| chr6:4048194 | C | T | 1 | a0002c0009t0018g0309 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1936-822C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048194 | |||||||
| chr6:4048222 | C | CA | 11 | a0001c0001t0002g0328 a0001c0001t0006g0021 a0001c0001t0006g0280 others(8): Show |
12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1936-787dupA | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4048222 | ||||||
| chr6:4048236 | G | A | 4 | a0002c0002t0001g0134 a0002c0002t0002g0151 a0002c0002t0002g0161 others(1): Show |
4 | HG00438.hp1 HG02080.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.1936-780G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048236 | |||||||
| chr6:4048310 | C | T | 6 | a0001c0001t0004g0009 a0001c0001t0004g0070 a0001c0001t0004g0073 others(3): Show |
7 | HG01167.hp1 HG01169.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1936-706C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048310 | |||||||
| chr6:4048357 | C | T | 6 | a0001c0004t0010g0275 a0001c0004t0010g0283 a0001c0004t0010g0295 others(3): Show |
6 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1936-659C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048357 | |||||||
| chr6:4048378 | C | CA | 25 | a0001c0001t0002g0328 a0001c0001t0003g0067 a0001c0001t0003g0085 others(22): Show |
25 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1936-619dupA | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4048378 | ||||||
| chr6:4048378 | CA | C | 148 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.1936-619delA | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4048378 | ||||||
| chr6:4048378 | CAA | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0047 a0001c0001t0001g0062 others(2): Show |
6 | HG01069.hp2 HG01993.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1936-620_1936-619d others(4): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4048378 | ||||||
| chr6:4048464 | G | T | 1 | a0001c0004t0011g0233 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1936-552G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048464 | |||||||
| chr6:4048483 | G | T | 1 | a0004c0013t0019g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1936-533G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048483 | |||||||
| chr6:4048496 | GAATGGTA others(5): Show |
G | 6 | a0002c0002t0002g0175 a0002c0002t0002g0176 a0002c0002t0002g0195 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1936-507_1936-496d others(14): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4048496 | ||||||
| chr6:4048618 | C | T | 219 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(216): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1936-398C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048618 | |||||||
| chr6:4048662 | A | G | 11 | a0001c0001t0002g0328 a0001c0001t0006g0021 a0001c0001t0006g0280 others(8): Show |
12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1936-354A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048662 | |||||||
| chr6:4048733 | C | CT | 19 | a0002c0002t0002g0031 a0002c0002t0002g0178 a0002c0002t0002g0179 others(16): Show |
19 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1936-274dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4048733 | ||||||
| chr6:4048803 | TG | T | 10 | a0001c0001t0002g0328 a0001c0001t0006g0280 a0001c0005t0006g0211 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1936-212delG | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048803 | |||||||
| chr6:4048804 | G | T | 1 | a0002c0003t0005g0014 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1936-212G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048804 | |||||||
| chr6:4048805 | T | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(117): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1936-211T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048805 | |||||||
| chr6:4048806 | T | G | 1 | a0001c0001t0001g0051 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1936-210T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048806 | |||||||
| chr6:4049188 | TG | T | 19 | a0002c0002t0002g0031 a0002c0002t0002g0178 a0002c0002t0002g0179 others(16): Show |
19 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.2026+84delG | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr6 | 4049188 | ||||||
| chr6:4049196 | T | G | 1 | a0001c0001t0001g0256 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2026+90T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 8/14 | chr6 | 4049196 | |||||||
| chr6:4049245 | A | G | 1 | a0002c0009t0018g0309 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2026+139A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 8/14 | chr6 | 4049245 | |||||||
| chr6:4049260 | C | T | 11 | a0001c0001t0002g0328 a0001c0001t0006g0021 a0001c0001t0006g0280 others(8): Show |
12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2026+154C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 8/14 | chr6 | 4049260 | |||||||
| chr6:4049366 | T | C | 11 | a0001c0001t0002g0328 a0001c0001t0006g0021 a0001c0001t0006g0280 others(8): Show |
12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2026+260T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 8/14 | chr6 | 4049366 | |||||||
| chr6:4049726 | T | C | 1 | a0001c0007t0006g0294 | 1 | HG03471.hp1 | splice_region_variant&intron_variant | LOW | c.2027-6T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 8/14 | chr6 | 4049726 | |||||||
| chr6:4050007 | TGGAAACA others(312): Show |
T | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(267): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.2174+145_2174+463d others(2): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr6 | 4050007 | ||||||
| chr6:4050018 | G | GT | 14 | a0002c0002t0002g0015 a0002c0002t0002g0019 a0002c0002t0002g0130 others(11): Show |
14 | HG00621.hp2 HG01106.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.2174+165dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr6 | 4050018 | ||||||
| chr6:4050443 | A | G | 1 | a0004c0013t0019g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2174+564A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4050443 | |||||||
| chr6:4050460 | C | T | 11 | a0001c0001t0002g0328 a0001c0001t0006g0021 a0001c0001t0006g0280 others(8): Show |
12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2174+581C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4050460 | |||||||
| chr6:4050469 | T | C | 12 | a0001c0001t0001g0282 a0001c0001t0002g0328 a0001c0001t0006g0021 others(9): Show |
13 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.2174+590T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4050469 | |||||||
| chr6:4050503 | C | T | 6 | a0001c0004t0010g0275 a0001c0004t0010g0283 a0001c0004t0010g0295 others(3): Show |
6 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2174+624C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4050503 | |||||||
| chr6:4050707 | G | A | 1 | a0002c0002t0002g0178 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2174+828G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4050707 | |||||||
| chr6:4050817 | A | G | 61 | a0001c0001t0003g0001 a0001c0001t0003g0011 a0001c0001t0003g0012 others(58): Show |
71 | HG00609.hp1 HG01069.hp1 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.2174+938A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4050817 | |||||||
| chr6:4050896 | G | GTTGT | 15 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0218 others(12): Show |
16 | HG02129.hp2 NA18944.hp2 NA18954.hp1 others(13): Show |
intron_variant | MODIFIER | c.2174+1036_2174+103 others(8): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr6 | 4050896 | ||||||
| chr6:4051029 | C | A | 1 | a0002c0002t0002g0153 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2175-928C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051029 | |||||||
| chr6:4051066 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2175-891C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051066 | |||||||
| chr6:4051151 | C | G | 19 | a0002c0002t0002g0031 a0002c0002t0002g0178 a0002c0002t0002g0179 others(16): Show |
19 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.2175-806C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051151 | |||||||
| chr6:4051161 | C | T | 19 | a0002c0002t0002g0031 a0002c0002t0002g0178 a0002c0002t0002g0179 others(16): Show |
19 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.2175-796C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051161 | |||||||
| chr6:4051365 | G | T | 12 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(9): Show |
12 | HG01891.hp2 HG02145.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.2175-592G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051365 | |||||||
| chr6:4051369 | G | A | 11 | a0001c0001t0002g0328 a0001c0001t0006g0021 a0001c0001t0006g0280 others(8): Show |
12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2175-588G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051369 | |||||||
| chr6:4051438 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2175-519T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051438 | |||||||
| chr6:4051468 | C | T | 1 | a0001c0001t0004g0033 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2175-489C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051468 | |||||||
| chr6:4051674 | A | T | 1 | a0001c0001t0022g0213 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2175-283A>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051674 | |||||||
| chr6:4051773 | T | C | 1 | a0001c0001t0001g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2175-184T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051773 | |||||||
| chr6:4051827 | A | G | 1 | a0002c0002t0001g0194 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2175-130A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051827 | |||||||
| chr6:4051933 | C | A | 232 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(229): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.2175-24C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051933 | |||||||
| chr6:4051937 | A | G | 19 | a0002c0002t0002g0031 a0002c0002t0002g0178 a0002c0002t0002g0179 others(16): Show |
19 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.2175-20A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051937 | |||||||
| chr6:4051938 | A | AT | 13 | a0001c0001t0001g0025 a0002c0003t0005g0014 a0002c0003t0005g0120 others(10): Show |
15 | HG00735.hp1 HG00738.hp1 HG02145.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.2175-8dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr6 | 4051938 | ||||||
| chr6:4052110 | G | A | 2 | a0001c0001t0001g0315 a0005c0010t0001g0325 |
2 | HG02165.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.2312+16G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | chr6 | 4052110 | |||||||
| chr6:4052149 | G | A | 213 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(210): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.2312+55G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | chr6 | 4052149 | |||||||
| chr6:4052160 | G | A | 1 | a0002c0002t0002g0162 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2312+66G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | chr6 | 4052160 | |||||||
| chr6:4052224 | G | GT | 233 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(230): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.2312+135dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr6 | 4052224 | ||||||
| chr6:4052252 | T | TTTG | 18 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(15): Show |
18 | HG01074.hp2 HG01099.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.2312+183_2312+185d others(5): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr6 | 4052252 | ||||||
| chr6:4052252 | TTTG | T | 23 | a0001c0001t0003g0001 a0001c0001t0003g0011 a0001c0001t0003g0032 others(20): Show |
29 | HG01069.hp1 HG01070.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.2312+183_2312+185d others(5): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr6 | 4052252 | ||||||
| chr6:4052252 | TTTGTTGT others(2): Show |
T | 19 | a0002c0002t0002g0031 a0002c0002t0002g0178 a0002c0002t0002g0179 others(16): Show |
19 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.2312+177_2312+185d others(11): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr6 | 4052252 | ||||||
| chr6:4052318 | G | A | 219 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(216): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.2312+224G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | chr6 | 4052318 | |||||||
| chr6:4052340 | C | T | 1 | a0002c0002t0002g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2312+246C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | chr6 | 4052340 | |||||||
| chr6:4052476 | T | G | 1 | a0001c0001t0001g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2313-244T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | chr6 | 4052476 | |||||||
| chr6:4052573 | T | C | 1 | a0002c0002t0002g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2313-147T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | chr6 | 4052573 | |||||||
| chr6:4052592 | G | T | 1 | a0001c0001t0001g0228 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2313-128G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | chr6 | 4052592 | |||||||
| chr6:4052618 | G | A | 1 | a0004c0013t0019g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2313-102G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | chr6 | 4052618 | |||||||
| chr6:4053082 | A | G | 1 | a0001c0001t0022g0213 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2466+209A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053082 | |||||||
| chr6:4053122 | G | A | 258 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(255): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.2466+249G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053122 | |||||||
| chr6:4053130 | A | G | 1 | a0004c0013t0019g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2466+257A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053130 | |||||||
| chr6:4053192 | T | C | 1 | a0002c0002t0002g0163 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2466+319T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053192 | |||||||
| chr6:4053225 | CT | C | 5 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(2): Show |
5 | HG01074.hp1 HG01106.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.2466+354delT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr6 | 4053225 | ||||||
| chr6:4053367 | G | T | 1 | a0001c0005t0006g0305 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2466+494G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053367 | |||||||
| chr6:4053537 | G | A | 2 | a0002c0002t0002g0137 a0002c0002t0002g0206 |
2 | HG00609.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.2466+664G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053537 | |||||||
| chr6:4053560 | A | AT | 231 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(228): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.2466+687_2466+688i others(3): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053560 | |||||||
| chr6:4053573 | A | G | 1 | a0004c0013t0019g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2466+700A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053573 | |||||||
| chr6:4053655 | T | C | 231 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(228): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.2466+782T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053655 | |||||||
| chr6:4053656 | G | A | 1 | a0001c0004t0010g0295 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2466+783G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053656 | |||||||
| chr6:4053738 | A | C | 1 | a0002c0002t0002g0177 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2466+865A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053738 | |||||||
| chr6:4053899 | G | GCTTTTTT others(2): Show |
6 | a0001c0004t0010g0275 a0001c0004t0010g0283 a0001c0004t0010g0295 others(3): Show |
6 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2466+1026_2466+102 others(13): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053899 | |||||||
| chr6:4053903 | T | G | 6 | a0001c0004t0010g0275 a0001c0004t0010g0283 a0001c0004t0010g0295 others(3): Show |
6 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2466+1030T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053903 | |||||||
| chr6:4053903 | T | TTTTTG | 22 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0036 others(19): Show |
23 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.2466+1051_2466+105 others(9): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr6 | 4053903 | ||||||
| chr6:4053903 | T | TTTTTGTT others(3): Show |
180 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(177): Show |
208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.2466+1046_2466+105 others(14): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr6 | 4053903 | ||||||
| chr6:4053903 | T | TTTTTGTT others(8): Show |
19 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(16): Show |
20 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.2466+1041_2466+105 others(19): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr6 | 4053903 | ||||||
| chr6:4053903 | T | TTTTTGTT others(13): Show |
4 | a0001c0001t0009g0212 a0001c0001t0009g0219 a0001c0001t0009g0220 others(1): Show |
4 | HG02257.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2466+1036_2466+105 others(24): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr6 | 4053903 | ||||||
| chr6:4054000 | C | T | 219 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(216): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.2466+1127C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054000 | |||||||
| chr6:4054085 | A | C | 6 | a0001c0001t0004g0009 a0001c0001t0004g0070 a0001c0001t0004g0073 others(3): Show |
7 | HG01167.hp1 HG01169.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2466+1212A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054085 | |||||||
| chr6:4054460 | A | AT | 201 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.2466+1589dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr6 | 4054460 | ||||||
| chr6:4054487 | G | C | 2 | a0001c0001t0003g0082 a0001c0001t0003g0096 |
2 | NA18998.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2466+1614G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054487 | |||||||
| chr6:4054515 | G | A | 252 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.2466+1642G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054515 | |||||||
| chr6:4054517 | T | A | 2 | a0001c0007t0006g0293 a0001c0007t0006g0294 |
2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2466+1644T>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054517 | |||||||
| chr6:4054611 | T | G | 230 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(227): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.2467-1710T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054611 | |||||||
| chr6:4054665 | C | A | 1 | a0001c0001t0003g0098 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2467-1656C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054665 | |||||||
| chr6:4054694 | C | T | 12 | a0002c0003t0005g0014 a0002c0003t0005g0120 a0002c0003t0005g0121 others(9): Show |
13 | HG00735.hp1 HG00738.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.2467-1627C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054694 | |||||||
| chr6:4054721 | G | A | 12 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(9): Show |
12 | HG01891.hp2 HG02145.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.2467-1600G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054721 | |||||||
| chr6:4054740 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2467-1581G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054740 | |||||||
| chr6:4054894 | G | C | 12 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(9): Show |
12 | HG01891.hp2 HG02145.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.2467-1427G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054894 | |||||||
| chr6:4054961 | T | C | 1 | a0001c0001t0025g0259 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2467-1360T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054961 | |||||||
| chr6:4054964 | A | G | 3 | a0002c0002t0002g0189 a0002c0002t0002g0192 a0002c0002t0002g0193 |
3 | HG02572.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2467-1357A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054964 | |||||||
| chr6:4055004 | C | G | 6 | a0001c0004t0010g0275 a0001c0004t0010g0283 a0001c0004t0010g0295 others(3): Show |
6 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2467-1317C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4055004 | |||||||
| chr6:4055004 | C | T | 1 | a0002c0003t0005g0127 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2467-1317C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4055004 | |||||||
| chr6:4055041 | G | A | 1 | a0002c0009t0018g0309 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2467-1280G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4055041 | |||||||
| chr6:4055182 | A | G | 2 | a0001c0001t0006g0280 a0001c0007t0006g0210 |
2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2467-1139A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4055182 | |||||||
| chr6:4055473 | T | A | 233 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(230): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.2467-848T>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4055473 | |||||||
| chr6:4055553 | G | C | 1 | a0002c0002t0002g0171 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2467-768G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4055553 | |||||||
| chr6:4055737 | A | G | 2 | a0001c0001t0002g0328 a0001c0001t0006g0021 |
3 | HG01081.hp2 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2467-584A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4055737 | |||||||
| chr6:4055770 | G | C | 1 | a0002c0009t0018g0309 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2467-551G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4055770 | |||||||
| chr6:4055901 | T | A | 1 | a0002c0002t0002g0205 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2467-420T>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4055901 | |||||||
| chr6:4055902 | C | T | 6 | a0001c0001t0004g0009 a0001c0001t0004g0070 a0001c0001t0004g0073 others(3): Show |
7 | HG01167.hp1 HG01169.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2467-419C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4055902 | |||||||
| chr6:4056091 | T | C | 220 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(217): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.2467-230T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4056091 | |||||||
| chr6:4056147 | T | TAACTTTT others(82): Show |
1 | a0001c0004t0010g0295 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2467-164_2467-76du others(90): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr6 | 4056147 | ||||||
| chr6:4056494 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2581+59A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 12/14 | chr6 | 4056494 | |||||||
| chr6:4056831 | T | C | 232 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(229): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.2582-205T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 12/14 | chr6 | 4056831 | |||||||
| chr6:4056926 | T | G | 232 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(229): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.2582-110T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 12/14 | chr6 | 4056926 | |||||||
| chr6:4056939 | C | T | 61 | a0001c0001t0003g0001 a0001c0001t0003g0011 a0001c0001t0003g0012 others(58): Show |
71 | HG00609.hp1 HG01069.hp1 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.2582-97C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 12/14 | chr6 | 4056939 | |||||||
| chr6:4056966 | A | G | 232 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(229): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.2582-70A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 12/14 | chr6 | 4056966 | |||||||
| chr6:4056999 | C | T | 233 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(230): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.2582-37C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 12/14 | chr6 | 4056999 | |||||||
| chr6:4057195 | A | G | 232 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(229): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
splice_region_variant&intron_variant | LOW | c.2733+8A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4057195 | |||||||
| chr6:4057308 | T | G | 17 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0036 others(14): Show |
18 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(15): Show |
intron_variant | MODIFIER | c.2733+121T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4057308 | |||||||
| chr6:4057380 | G | A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0199 a0001c0001t0001g0281 |
3 | HG02809.hp1 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2733+193G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4057380 | |||||||
| chr6:4057393 | G | T | 232 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(229): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.2733+206G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4057393 | |||||||
| chr6:4057538 | A | G | 6 | a0002c0003t0005g0014 a0002c0003t0005g0120 a0002c0003t0005g0123 others(3): Show |
7 | HG02717.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.2733+351A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4057538 | |||||||
| chr6:4057751 | C | CT | 6 | a0001c0001t0002g0328 a0002c0002t0002g0020 a0002c0002t0002g0130 others(3): Show |
7 | HG02040.hp1 HG02132.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2733+585dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr6 | 4057751 | ||||||
| chr6:4057751 | CT | C | 140 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
160 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.2733+585delT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr6 | 4057751 | ||||||
| chr6:4057751 | CTT | C | 105 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0036 others(102): Show |
116 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.2733+584_2733+585d others(4): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr6 | 4057751 | ||||||
| chr6:4057751 | CTTT | C | 10 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(7): Show |
10 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2733+583_2733+585d others(5): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr6 | 4057751 | ||||||
| chr6:4057777 | C | T | 214 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(211): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.2733+590C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4057777 | |||||||
| chr6:4057804 | C | G | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(267): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.2733+617C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4057804 | |||||||
| chr6:4057841 | G | T | 4 | a0001c0001t0001g0224 a0001c0001t0001g0241 a0001c0001t0001g0243 others(1): Show |
4 | HG01167.hp2 HG01255.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.2733+654G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4057841 | |||||||
| chr6:4057903 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2733+716C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4057903 | |||||||
| chr6:4057911 | G | T | 1 | a0001c0001t0001g0315 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2733+724G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4057911 | |||||||
| chr6:4057923 | C | T | 1 | a0002c0002t0002g0198 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2733+736C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4057923 | |||||||
| chr6:4058096 | G | A | 1 | a0002c0002t0002g0183 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2734-632G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4058096 | |||||||
| chr6:4058305 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2734-423G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4058305 | |||||||
| chr6:4058548 | C | T | 123 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(120): Show |
141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.2734-180C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4058548 | |||||||
| chr6:4058600 | G | T | 5 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(2): Show |
5 | HG01891.hp2 HG02145.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2734-128G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4058600 | |||||||
| chr6:4058834 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2820+20C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4058834 | |||||||
| chr6:4058879 | G | A | 1 | a0001c0001t0003g0099 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2820+65G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4058879 | |||||||
| chr6:4058909 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2820+95A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4058909 | |||||||
| chr6:4059002 | G | C | 1 | a0001c0001t0001g0256 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2820+188G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4059002 | |||||||
| chr6:4059045 | G | A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | HG03654.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2820+231G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4059045 | |||||||
| chr6:4059145 | A | G | 232 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(229): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.2820+331A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4059145 | |||||||
| chr6:4059187 | A | G | 10 | a0001c0001t0006g0021 a0001c0001t0006g0280 a0001c0005t0006g0211 others(7): Show |
11 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2820+373A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4059187 | |||||||
| chr6:4059295 | G | T | 1 | a0002c0003t0005g0128 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2820+481G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4059295 | |||||||
| chr6:4059298 | C | T | 19 | a0002c0002t0002g0031 a0002c0002t0002g0178 a0002c0002t0002g0179 others(16): Show |
19 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.2820+484C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4059298 | |||||||
| chr6:4059308 | C | G | 11 | a0001c0001t0002g0328 a0001c0001t0006g0021 a0001c0001t0006g0280 others(8): Show |
12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2820+494C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4059308 | |||||||
| chr6:4059382 | A | G | 201 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.2820+568A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4059382 | |||||||
| chr6:4059567 | A | G | 1 | a0001c0001t0002g0328 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2820+753A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4059567 | |||||||
| chr6:4059590 | A | G | 4 | a0001c0001t0006g0280 a0001c0007t0006g0210 a0001c0007t0006g0293 others(1): Show |
4 | HG02922.hp2 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2820+776A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4059590 | |||||||
| chr6:4059640 | C | CT | 264 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(261): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.2821-764dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr6 | 4059640 | ||||||
| chr6:4059802 | C | A | 1 | a0001c0001t0001g0241 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2821-611C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4059802 | |||||||
| chr6:4059907 | A | G | 12 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(9): Show |
12 | HG01891.hp2 HG02145.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.2821-506A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4059907 | |||||||
| chr6:4060143 | G | A | 4 | a0001c0001t0003g0103 a0001c0001t0003g0105 a0001c0001t0003g0106 others(1): Show |
4 | NA18944.hp1 NA18948.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.2821-270G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4060143 | |||||||
| chr6:4060181 | T | C | 1 | a0001c0011t0001g0058 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2821-232T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4060181 | |||||||
| chr6:4060380 | T | C | 1 | a0001c0001t0002g0328 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2821-33T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4060380 |