Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10196 |
| ensemblid | ENSG00000185238.13 |
| hgncid | 30163 |
| symbol | PRMT3 |
| name | protein arginine methyltransferase 3 |
| refseq_nuc | NM_005788.4 |
| refseq_prot | NP_005779.1 |
| ensembl_nuc | ENST00000331079.11 |
| ensembl_prot | ENSP00000331879.6 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 20387716 |
| end | 20509338 |
| strand | + |
| ver | v1.2 |
| region | chr11:20387716-20509338 |
| region5000 | chr11:20382716-20514338 |
| regionname0 | PRMT3_chr11_20387716_20509338 |
| regionname5000 | PRMT3_chr11_20382716_20514338 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 531 | 335 | 75 | 60 | 151 | 14 | 33 | 118 | PRMT3_chr11_20382716_20514338 | PRMT3 | MCSLA others(526): Show |
chr11 | 20382716 | 20514338 |
| a0002 | 0/0 | 531 | 23 | 23 | 0 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | MCSLA others(526): Show |
chr11 | 20382716 | 20514338 |
| a0003 | 0/0 | 531 | 13 | 0 | 0 | 13 | 0 | 0 | 11 | PRMT3_chr11_20382716_20514338 | PRMT3 | MCSLA others(526): Show |
chr11 | 20382716 | 20514338 |
| a0004 | 0/0 | 531 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | MCSLA others(526): Show |
chr11 | 20382716 | 20514338 |
| a0005 | 0/0 | 531 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | MCSLA others(526): Show |
chr11 | 20382716 | 20514338 |
| a0006 | 0/0 | 531 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | MCSLA others(526): Show |
chr11 | 20382716 | 20514338 |
| a0007 | 0/0 | 531 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | MCSLA others(526): Show |
chr11 | 20382716 | 20514338 |
| a0008 | 0/0 | 531 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | MCSLA others(526): Show |
chr11 | 20382716 | 20514338 |
| a0009 | 0/0 | 531 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | MCSLA others(526): Show |
chr11 | 20382716 | 20514338 |
| a0010 | 0/0 | 531 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | MCSLA others(526): Show |
chr11 | 20382716 | 20514338 |
| a0011 | 0/0 | 531 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | MCSLA others(526): Show |
chr11 | 20382716 | 20514338 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1593 | 326 | 71 | 60 | 146 | 14 | 33 | PRMT3_chr11_20382716_20514338 | PRMT3 | ATGTG others(1588): Show |
chr11 | 20382716 | 20514338 | ||
| a0001c0004 | 0/0 | 1593 | 4 | 0 | 0 | 4 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | ATGTG others(1588): Show |
chr11 | 20382716 | 20514338 | ||
| a0001c0005 | 0/0 | 1593 | 3 | 3 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | ATGTG others(1588): Show |
chr11 | 20382716 | 20514338 | ||
| a0001c0009 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | ATGTG others(1588): Show |
chr11 | 20382716 | 20514338 | ||
| a0001c0013 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | ATGTG others(1588): Show |
chr11 | 20382716 | 20514338 | ||
| a0002c0002 | 0/0 | 1593 | 23 | 23 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | ATGTG others(1588): Show |
chr11 | 20382716 | 20514338 | ||
| a0003c0003 | 0/0 | 1593 | 13 | 0 | 0 | 13 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | ATGTG others(1588): Show |
chr11 | 20382716 | 20514338 | ||
| a0004c0006 | 0/0 | 1593 | 2 | 0 | 0 | 2 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | ATGTG others(1588): Show |
chr11 | 20382716 | 20514338 | ||
| a0005c0015 | 0/0 | 1593 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | ATGTG others(1588): Show |
chr11 | 20382716 | 20514338 | ||
| a0006c0007 | 0/0 | 1593 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | ATGTG others(1588): Show |
chr11 | 20382716 | 20514338 | ||
| a0007c0010 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | ATGTG others(1588): Show |
chr11 | 20382716 | 20514338 | ||
| a0008c0014 | 0/0 | 1593 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | ATGTG others(1588): Show |
chr11 | 20382716 | 20514338 | ||
| a0009c0008 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | ATGTG others(1588): Show |
chr11 | 20382716 | 20514338 | ||
| a0010c0011 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | ATGTG others(1588): Show |
chr11 | 20382716 | 20514338 | ||
| a0011c0012 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | ATGTG others(1588): Show |
chr11 | 20382716 | 20514338 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2550 | 211 | 52 | 44 | 69 | 14 | 31 | PRMT3_chr11_20382716_20514338 | PRMT3 | AGACA others(2545): Show |
chr11 | 20382716 | 20514338 |
| a0001c0001t0002 | 1/0 | 2552 | 106 | 11 | 16 | 76 | 0 | 2 | PRMT3_chr11_20382716_20514338 | PRMT3 | AGACA others(2547): Show |
chr11 | 20382716 | 20514338 |
| a0001c0001t0004 | 0/0 | 2552 | 7 | 7 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | AGACA others(2547): Show |
chr11 | 20382716 | 20514338 |
| a0001c0001t0006 | 0/0 | 2552 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | AGACA others(2547): Show |
chr11 | 20382716 | 20514338 |
| a0001c0001t0007 | 0/0 | 2550 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | AGACA others(2545): Show |
chr11 | 20382716 | 20514338 |
| a0001c0004t0001 | 0/0 | 2550 | 4 | 0 | 0 | 4 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | AGACA others(2545): Show |
chr11 | 20382716 | 20514338 |
| a0001c0005t0001 | 0/0 | 2550 | 3 | 3 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | AGACA others(2545): Show |
chr11 | 20382716 | 20514338 |
| a0001c0009t0001 | 0/0 | 2550 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | AGACA others(2545): Show |
chr11 | 20382716 | 20514338 |
| a0001c0013t0002 | 0/0 | 2552 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | AGACA others(2547): Show |
chr11 | 20382716 | 20514338 |
| a0002c0002t0002 | 0/0 | 2552 | 4 | 4 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | AGACA others(2547): Show |
chr11 | 20382716 | 20514338 |
| a0002c0002t0003 | 0/0 | 2552 | 17 | 17 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | AGACA others(2547): Show |
chr11 | 20382716 | 20514338 |
| a0002c0002t0005 | 0/0 | 2552 | 2 | 2 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | AGACA others(2547): Show |
chr11 | 20382716 | 20514338 |
| a0003c0003t0002 | 0/0 | 2552 | 13 | 0 | 0 | 13 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | AGACA others(2547): Show |
chr11 | 20382716 | 20514338 |
| a0004c0006t0002 | 0/0 | 2552 | 2 | 0 | 0 | 2 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | AGACA others(2547): Show |
chr11 | 20382716 | 20514338 |
| a0005c0015t0002 | 0/0 | 2552 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | AGACA others(2547): Show |
chr11 | 20382716 | 20514338 |
| a0006c0007t0002 | 0/0 | 2552 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | AGACA others(2547): Show |
chr11 | 20382716 | 20514338 |
| a0007c0010t0002 | 0/0 | 2552 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | AGACA others(2547): Show |
chr11 | 20382716 | 20514338 |
| a0008c0014t0002 | 0/0 | 2552 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | AGACA others(2547): Show |
chr11 | 20382716 | 20514338 |
| a0009c0008t0001 | 0/0 | 2550 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | AGACA others(2545): Show |
chr11 | 20382716 | 20514338 |
| a0010c0011t0001 | 0/0 | 2550 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | AGACA others(2545): Show |
chr11 | 20382716 | 20514338 |
| a0011c0012t0001 | 0/0 | 2550 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | AGACA others(2545): Show |
chr11 | 20382716 | 20514338 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0301 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0002g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0004g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0006g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0001t0007g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0004t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0004t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0004t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0004t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0005t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0005t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0005t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0009t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0001c0013t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0002c0002t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0002c0002t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0002c0002t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0002c0002t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0002c0002t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0002c0002t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0002c0002t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0002c0002t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0002c0002t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0002c0002t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0002c0002t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0002c0002t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0002c0002t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0002c0002t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0002c0002t0003g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0002c0002t0003g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0002c0002t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0002c0002t0003g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0002c0002t0003g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0002c0002t0003g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0002c0002t0003g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0002c0002t0005g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0002c0002t0005g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0003c0003t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0003c0003t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0003c0003t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0003c0003t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0003c0003t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0003c0003t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0003c0003t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0003c0003t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0003c0003t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0003c0003t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0003c0003t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0003c0003t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0003c0003t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0004c0006t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0004c0006t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0005c0015t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0006c0007t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0007c0010t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0008c0014t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0009c0008t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0010c0011t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| a0011c0012t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | GBR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0259 | EUR | GBR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | FIN | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0249 | EUR | FIN | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | FIN | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | FIN | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | CHS | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00609 | hp2 | a0003 | c0003 | t0002 | g0320 | EAS | CHS | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00621 | hp2 | a0004 | c0006 | t0002 | g0321 | EAS | CHS | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | CHS | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0356 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0287 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0353 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0365 | AMR | PUR | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0364 | AMR | CLM | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | CLM | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0263 | EUR | IBS | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0258 | EUR | IBS | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0261 | EUR | IBS | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0264 | EUR | IBS | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0328 | AMR | PEL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0331 | AMR | PEL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | PEL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0329 | AMR | PEL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01978 | hp2 | a0005 | c0015 | t0002 | g0330 | AMR | PEL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0282 | AMR | PEL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01993 | hp1 | a0006 | c0007 | t0002 | g0283 | AMR | PEL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02056 | hp1 | a0001 | c0001 | t0006 | g0026 | EAS | KHV | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02071 | hp1 | a0003 | c0003 | t0002 | g0295 | EAS | KHV | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | KHV | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | KHV | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | KHV | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02132 | hp2 | a0004 | c0006 | t0002 | g0293 | EAS | KHV | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02135 | hp2 | a0001 | c0004 | t0001 | g0150 | EAS | KHV | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0354 | AFR | ACB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0066 | AFR | ACB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | CDX | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | CDX | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CDX | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CDX | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02258 | hp1 | a0002 | c0002 | t0003 | g0342 | AFR | ACB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0278 | AMR | PEL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02280 | hp1 | a0001 | c0005 | t0001 | g0367 | AFR | ACB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0361 | AFR | ACB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02523 | hp1 | a0007 | c0010 | t0002 | g0015 | EAS | KHV | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02572 | hp1 | a0002 | c0002 | t0003 | g0273 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0370 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0337 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0371 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0335 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02647 | hp1 | a0002 | c0002 | t0003 | g0341 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0355 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0062 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0332 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0363 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02886 | hp1 | a0002 | c0002 | t0003 | g0270 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02895 | hp1 | a0002 | c0002 | t0003 | g0269 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0359 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02896 | hp2 | a0002 | c0002 | t0003 | g0344 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02897 | hp1 | a0002 | c0002 | t0003 | g0343 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0011 | AFR | ESN | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | ESN | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02970 | hp1 | a0001 | c0009 | t0001 | g0090 | AFR | ESN | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0360 | AFR | ESN | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03041 | hp2 | a0002 | c0002 | t0003 | g0346 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0358 | AFR | MSL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0065 | AFR | ESN | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03139 | hp2 | a0002 | c0002 | t0005 | g0334 | AFR | ESN | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03195 | hp1 | a0002 | c0002 | t0003 | g0271 | AFR | ESN | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0276 | AFR | MSL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03209 | hp2 | a0002 | c0002 | t0003 | g0274 | AFR | MSL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03225 | hp1 | a0002 | c0002 | t0003 | g0340 | AFR | MSL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0064 | AFR | MSL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03453 | hp2 | a0002 | c0002 | t0003 | g0272 | AFR | MSL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03516 | hp2 | a0002 | c0002 | t0003 | g0347 | AFR | ESN | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | GWD | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03579 | hp2 | a0001 | c0005 | t0001 | g0368 | AFR | MSL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03831 | hp2 | a0008 | c0014 | t0002 | g0322 | SAS | BEB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | BEB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | BEB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | BEB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | STU | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | STU | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | STU | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | STU | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | STU | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | STU | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0366 | AFR | YRI | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | CHB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | CHB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18906 | hp1 | a0002 | c0002 | t0002 | g0009 | AFR | YRI | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0362 | AFR | YRI | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18940 | hp1 | a0003 | c0003 | t0002 | g0318 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18940 | hp2 | a0001 | c0004 | t0001 | g0101 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18942 | hp2 | a0009 | c0008 | t0001 | g0195 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0351 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0352 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18964 | hp2 | a0001 | c0004 | t0001 | g0040 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18965 | hp2 | a0003 | c0003 | t0002 | g0289 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18969 | hp2 | a0003 | c0003 | t0002 | g0325 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18972 | hp2 | a0001 | c0004 | t0001 | g0102 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18979 | hp1 | a0003 | c0003 | t0002 | g0315 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18980 | hp2 | a0003 | c0003 | t0002 | g0313 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18983 | hp2 | a0003 | c0003 | t0002 | g0309 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18985 | hp2 | a0010 | c0011 | t0001 | g0234 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18991 | hp1 | a0003 | c0003 | t0002 | g0326 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0349 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18994 | hp2 | a0003 | c0003 | t0002 | g0314 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18999 | hp1 | a0011 | c0012 | t0001 | g0078 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0372 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | LWK | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0357 | AFR | LWK | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19074 | hp2 | a0003 | c0003 | t0002 | g0294 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19085 | hp1 | a0001 | c0013 | t0002 | g0277 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19086 | hp2 | a0003 | c0003 | t0002 | g0303 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19090 | hp2 | a0003 | c0003 | t0002 | g0316 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0350 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19240 | hp1 | a0002 | c0002 | t0003 | g0336 | AFR | YRI | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | YRI | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA20129 | hp1 | a0002 | c0002 | t0003 | g0339 | AFR | ASW | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ASW | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0250 | EUR | TSI | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | TSI | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0254 | EUR | TSI | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02109 | hp1 | a0001 | c0005 | t0001 | g0369 | AFR | ACB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0067 | AFR | ACB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0063 | AFR | ACB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG02559 | hp2 | a0002 | c0002 | t0003 | g0333 | AFR | ACB | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03471 | hp1 | a0002 | c0002 | t0005 | g0338 | AFR | MSL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | USA | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| HG06807 | hp2 | a0002 | c0002 | t0003 | g0345 | AFR | USA | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | USA | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | USA | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | LWK | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | LWK | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0105 | REF | REF | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0301 | REF | REF | PRMT3_chr11_20382716_20514338 | PRMT3 | chr11 | 20382716 | 20514338 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:20388120 | G | T | 1 | a0005 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.130G>T | p.Gly44Cys | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 2/16 | 161/2552 | 130/1596 | 44/531 | chr11 | 20388120 | |||
| chr11:20395857 | T | C | 1 | a0006 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.455T>C | p.Leu152Pro | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 6/16 | 486/2552 | 455/1596 | 152/531 | chr11 | 20395857 | |||
| chr11:20395860 | G | T | 1 | a0008 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.458G>T | p.Ser153Ile | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 6/16 | 489/2552 | 458/1596 | 153/531 | chr11 | 20395860 | |||
| chr11:20397645 | C | A | 1 | a0009 | 1 | NA18942.hp2 | missense_variant | MODERATE | c.629C>A | p.Ala210Glu | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/16 | 660/2552 | 629/1596 | 210/531 | chr11 | 20397645 | |||
| chr11:20462133 | C | T | 1 | a0011 | 1 | NA18999.hp1 | missense_variant | MODERATE | c.1226C>T | p.Pro409Leu | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/16 | 1257/2552 | 1226/1596 | 409/531 | chr11 | 20462133 | |||
| chr11:20464515 | C | A | 1 | a0007 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.1316C>A | p.Thr439Asn | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/16 | 1347/2552 | 1316/1596 | 439/531 | chr11 | 20464515 | |||
| chr11:20464517 | C | G | 2 | a0003 a0008 |
14 | HG00609.hp2 HG02071.hp1 HG03831.hp2 others(11): Show |
missense_variant | MODERATE | c.1318C>G | p.Leu440Val | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/16 | 1349/2552 | 1318/1596 | 440/531 | chr11 | 20464517 | |||
| chr11:20508340 | A | G | 1 | a0004 | 2 | HG00621.hp2 HG02132.hp2 |
missense_variant | MODERATE | c.1523A>G | p.Asn508Ser | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 16/16 | 1554/2552 | 1523/1596 | 508/531 | chr11 | 20508340 | |||
| chr11:20508346 | A | G | 1 | a0002 | 23 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(20): Show |
missense_variant | MODERATE | c.1529A>G | p.Lys510Arg | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 16/16 | 1560/2552 | 1529/1596 | 510/531 | chr11 | 20508346 | |||
| chr11:20508390 | A | C | 1 | a0010 | 1 | NA18985.hp2 | missense_variant | MODERATE | c.1573A>C | p.Thr525Pro | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 16/16 | 1604/2552 | 1573/1596 | 525/531 | chr11 | 20508390 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:20392974 | A | G | 1 | a0001c0005 | 3 | HG02109.hp1 HG02280.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.375A>G | p.Leu125Leu | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/16 | 406/2552 | 375/1596 | 125/531 | chr11 | 20392974 | |||
| chr11:20395954 | A | G | 1 | a0001c0013 | 1 | NA19085.hp1 | synonymous_variant | LOW | c.552A>G | p.Gln184Gln | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 6/16 | 583/2552 | 552/1596 | 184/531 | chr11 | 20395954 | |||
| chr11:20462134 | G | A | 1 | a0001c0009 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.1227G>A | p.Pro409Pro | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/16 | 1258/2552 | 1227/1596 | 409/531 | chr11 | 20462134 | |||
| chr11:20464480 | G | A | 1 | a0001c0004 | 4 | HG02135.hp2 NA18940.hp2 NA18964.hp2 others(1): Show |
synonymous_variant | LOW | c.1281G>A | p.Thr427Thr | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/16 | 1312/2552 | 1281/1596 | 427/531 | chr11 | 20464480 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:20508633 | G | A | 2 | a0002c0002t0003 a0002c0002t0005 |
19 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*220G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 16/16 | 220 | chr11 | 20508633 | ||||||
| chr11:20508960 | A | G | 1 | a0002c0002t0005 | 2 | HG03139.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*547A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 16/16 | 547 | chr11 | 20508960 | ||||||
| chr11:20509038 | T | C | 1 | a0001c0001t0004 | 7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*625T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 16/16 | 625 | chr11 | 20509038 | ||||||
| chr11:20509158 | A | G | 1 | a0001c0001t0007 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*745A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 16/16 | 745 | chr11 | 20509158 | ||||||
| chr11:20509183 | G | A | 1 | a0001c0001t0006 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*770G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 16/16 | 770 | chr11 | 20509183 | ||||||
| chr11:20509270 | CAA | C | 8 | a0001c0001t0001 a0001c0001t0007 a0001c0004t0001 others(5): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*858_*859delAA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 16/16 | 858 | chr11 | 20509270 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:20387805 | C | T | 1 | a0001c0001t0002g0372 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.28+31C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 1/15 | chr11 | 20387805 | |||||||
| chr11:20387944 | A | G | 1 | a0001c0001t0004g0371 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.29-75A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 1/15 | chr11 | 20387944 | |||||||
| chr11:20387994 | T | G | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.29-25T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 1/15 | chr11 | 20387994 | |||||||
| chr11:20388487 | T | C | 1 | a0001c0001t0001g0012 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.164+333T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 2/15 | chr11 | 20388487 | |||||||
| chr11:20388806 | A | G | 5 | a0001c0001t0001g0366 a0001c0001t0007g0370 a0001c0005t0001g0367 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.164+652A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 2/15 | chr11 | 20388806 | |||||||
| chr11:20389046 | C | A | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.165-698C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 2/15 | chr11 | 20389046 | |||||||
| chr11:20389075 | G | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.165-669G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 2/15 | chr11 | 20389075 | |||||||
| chr11:20389094 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.165-650A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 2/15 | chr11 | 20389094 | |||||||
| chr11:20389372 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.165-372A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 2/15 | chr11 | 20389372 | |||||||
| chr11:20389423 | T | C | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | NA18964.hp1 NA19079.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.165-321T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 2/15 | chr11 | 20389423 | |||||||
| chr11:20389429 | G | A | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG01891.hp1 HG02622.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.165-315G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 2/15 | chr11 | 20389429 | |||||||
| chr11:20389436 | ACT | A | 14 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(11): Show |
15 | HG01928.hp2 HG01952.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.165-305_165-304del others(2): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr11 | 20389436 | ||||||
| chr11:20389533 | T | C | 2 | a0002c0002t0003g0269 a0002c0002t0003g0270 |
2 | HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.165-211T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 2/15 | chr11 | 20389533 | |||||||
| chr11:20389651 | G | C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(8): Show |
12 | HG01928.hp2 HG01952.hp1 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.165-93G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 2/15 | chr11 | 20389651 | |||||||
| chr11:20389653 | T | TA | 50 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(47): Show |
50 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(47): Show |
intron_variant | MODIFIER | c.165-76dupA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr11 | 20389653 | ||||||
| chr11:20389653 | TA | T | 22 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(19): Show |
22 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.165-76delA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr11 | 20389653 | ||||||
| chr11:20389653 | TAAAA | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.165-79_165-76delAA others(2): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr11 | 20389653 | ||||||
| chr11:20389684 | G | A | 5 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-60G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 2/15 | chr11 | 20389684 | |||||||
| chr11:20389829 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02818.hp1 | splice_region_variant&intron_variant | LOW | c.247+3G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20389829 | |||||||
| chr11:20389872 | G | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.247+46G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20389872 | |||||||
| chr11:20389878 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.247+52A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20389878 | |||||||
| chr11:20389957 | G | A | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(200): Show |
210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.247+131G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20389957 | |||||||
| chr11:20389970 | G | A | 56 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(53): Show |
56 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.247+144G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20389970 | |||||||
| chr11:20390059 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.247+233G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20390059 | |||||||
| chr11:20390149 | C | CA | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.247+337dupA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr11 | 20390149 | ||||||
| chr11:20390149 | CA | C | 48 | a0001c0001t0002g0014 a0001c0001t0002g0016 a0001c0001t0002g0017 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.247+337delA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr11 | 20390149 | ||||||
| chr11:20390224 | A | G | 4 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0057 others(1): Show |
4 | NA18994.hp1 NA19006.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.247+398A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20390224 | |||||||
| chr11:20390358 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.247+532A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20390358 | |||||||
| chr11:20390512 | C | T | 22 | a0001c0001t0001g0348 a0001c0001t0002g0335 a0001c0001t0002g0337 others(19): Show |
22 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(19): Show |
intron_variant | MODIFIER | c.247+686C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20390512 | |||||||
| chr11:20390518 | T | C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG02257.hp2 HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.247+692T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20390518 | |||||||
| chr11:20390527 | T | C | 1 | a0001c0001t0002g0014 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.247+701T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20390527 | |||||||
| chr11:20390621 | C | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG02257.hp2 HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.247+795C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20390621 | |||||||
| chr11:20390634 | C | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0086 others(83): Show |
88 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.247+808C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20390634 | |||||||
| chr11:20390710 | T | A | 1 | a0002c0002t0002g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.247+884T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20390710 | |||||||
| chr11:20390724 | G | A | 1 | a0001c0013t0002g0277 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.247+898G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20390724 | |||||||
| chr11:20390731 | A | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0092 others(76): Show |
81 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.247+905A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20390731 | |||||||
| chr11:20390837 | T | G | 1 | a0002c0002t0002g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.247+1011T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20390837 | |||||||
| chr11:20390846 | C | T | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.247+1020C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20390846 | |||||||
| chr11:20390907 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.247+1081G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20390907 | |||||||
| chr11:20391044 | C | T | 4 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(1): Show |
4 | HG01928.hp2 HG01952.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.248-1167C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20391044 | |||||||
| chr11:20391049 | CA | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.248-1149delA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr11 | 20391049 | ||||||
| chr11:20391063 | T | A | 53 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(50): Show |
53 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(50): Show |
intron_variant | MODIFIER | c.248-1148T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20391063 | |||||||
| chr11:20391079 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.248-1132C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20391079 | |||||||
| chr11:20391101 | G | A | 1 | a0001c0001t0004g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.248-1110G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20391101 | |||||||
| chr11:20391128 | TACTA | T | 38 | a0001c0001t0001g0348 a0001c0001t0001g0362 a0001c0001t0001g0363 others(35): Show |
38 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.248-1080_248-1077d others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr11 | 20391128 | ||||||
| chr11:20391207 | G | A | 11 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 others(8): Show |
11 | HG01175.hp2 HG01981.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.248-1004G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20391207 | |||||||
| chr11:20391314 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.248-897C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20391314 | |||||||
| chr11:20391335 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.248-876T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20391335 | |||||||
| chr11:20391348 | T | A | 7 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(4): Show |
7 | HG02055.hp1 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.248-863T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20391348 | |||||||
| chr11:20391371 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.248-840A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20391371 | |||||||
| chr11:20391395 | G | A | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.248-816G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20391395 | |||||||
| chr11:20391454 | G | C | 1 | a0001c0001t0001g0173 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.248-757G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20391454 | |||||||
| chr11:20391491 | C | T | 1 | a0001c0001t0001g0348 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.248-720C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20391491 | |||||||
| chr11:20391533 | G | C | 2 | a0001c0001t0002g0016 a0007c0010t0002g0015 |
2 | HG00544.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.248-678G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20391533 | |||||||
| chr11:20391652 | T | C | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.248-559T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20391652 | |||||||
| chr11:20391663 | CAA | C | 5 | a0001c0001t0001g0366 a0001c0001t0007g0370 a0001c0005t0001g0367 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.248-547_248-546del others(2): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20391663 | |||||||
| chr11:20391687 | G | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG02257.hp2 HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.248-524G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20391687 | |||||||
| chr11:20391762 | C | G | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.248-449C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20391762 | |||||||
| chr11:20391886 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.248-325A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20391886 | |||||||
| chr11:20391915 | CT | C | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.248-294delT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr11 | 20391915 | ||||||
| chr11:20391976 | T | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.248-235T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20391976 | |||||||
| chr11:20391994 | C | A | 1 | a0001c0001t0001g0096 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.248-217C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20391994 | |||||||
| chr11:20392017 | T | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.248-194T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20392017 | |||||||
| chr11:20392033 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.248-178A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20392033 | |||||||
| chr11:20392090 | T | G | 17 | a0001c0001t0002g0335 a0001c0001t0002g0337 a0002c0002t0002g0276 others(14): Show |
17 | HG02258.hp1 HG02559.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.248-121T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 3/15 | chr11 | 20392090 | |||||||
| chr11:20392466 | G | A | 1 | a0001c0001t0002g0353 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.297+206G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 4/15 | chr11 | 20392466 | |||||||
| chr11:20392467 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.297+207C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 4/15 | chr11 | 20392467 | |||||||
| chr11:20392483 | C | T | 5 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(2): Show |
5 | HG01884.hp1 HG03130.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+223C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 4/15 | chr11 | 20392483 | |||||||
| chr11:20392497 | A | G | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.297+237A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 4/15 | chr11 | 20392497 | |||||||
| chr11:20392550 | C | G | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.297+290C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 4/15 | chr11 | 20392550 | |||||||
| chr11:20392592 | T | C | 17 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(14): Show |
18 | HG01516.hp1 HG01517.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.298-305T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 4/15 | chr11 | 20392592 | |||||||
| chr11:20392622 | G | GT | 14 | a0001c0001t0001g0093 a0001c0001t0001g0160 a0001c0001t0001g0161 others(11): Show |
14 | HG01175.hp2 HG02486.hp2 HG03209.hp2 others(11): Show |
intron_variant | MODIFIER | c.298-260dupT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr11 | 20392622 | ||||||
| chr11:20392622 | G | T | 4 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(1): Show |
4 | HG01243.hp2 HG01255.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.298-275G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 4/15 | chr11 | 20392622 | |||||||
| chr11:20393017 | G | A | 1 | a0001c0001t0001g0362 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.400+18G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20393017 | |||||||
| chr11:20393050 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.400+51A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20393050 | |||||||
| chr11:20393053 | G | A | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.400+54G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20393053 | |||||||
| chr11:20393244 | C | T | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.400+245C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20393244 | |||||||
| chr11:20393245 | A | G | 1 | a0001c0001t0001g0260 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.400+246A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20393245 | |||||||
| chr11:20393369 | C | T | 1 | a0001c0001t0002g0353 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.400+370C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20393369 | |||||||
| chr11:20393378 | C | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0168 |
2 | NA18995.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.400+379C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20393378 | |||||||
| chr11:20393533 | C | T | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.400+534C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20393533 | |||||||
| chr11:20393971 | A | G | 2 | a0002c0002t0003g0343 a0002c0002t0003g0344 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.400+972A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20393971 | |||||||
| chr11:20394019 | A | C | 1 | a0001c0001t0002g0051 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.400+1020A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20394019 | |||||||
| chr11:20394089 | T | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.400+1090T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20394089 | |||||||
| chr11:20394115 | T | C | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.400+1116T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20394115 | |||||||
| chr11:20394187 | T | A | 1 | a0001c0001t0001g0085 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.400+1188T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20394187 | |||||||
| chr11:20394359 | T | C | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.400+1360T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20394359 | |||||||
| chr11:20394427 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.401-1376C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20394427 | |||||||
| chr11:20394435 | A | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.401-1368A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20394435 | |||||||
| chr11:20394523 | G | C | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.401-1280G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20394523 | |||||||
| chr11:20394653 | C | T | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.401-1150C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20394653 | |||||||
| chr11:20394889 | A | G | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG01192.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.401-914A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20394889 | |||||||
| chr11:20394935 | A | G | 4 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(1): Show |
4 | HG01928.hp2 HG01952.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.401-868A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20394935 | |||||||
| chr11:20395043 | T | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0174 a0001c0001t0001g0175 others(3): Show |
7 | HG00733.hp2 HG00741.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.401-760T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20395043 | |||||||
| chr11:20395494 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.401-309T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20395494 | |||||||
| chr11:20395650 | G | C | 3 | a0002c0002t0003g0272 a0002c0002t0003g0273 a0002c0002t0003g0274 |
3 | HG02572.hp1 HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.401-153G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20395650 | |||||||
| chr11:20395726 | G | A | 47 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(44): Show |
47 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.401-77G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20395726 | |||||||
| chr11:20395738 | A | C | 1 | a0001c0001t0001g0154 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.401-65A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20395738 | |||||||
| chr11:20395784 | T | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG00738.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.401-19T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 5/15 | chr11 | 20395784 | |||||||
| chr11:20396649 | T | TG | 22 | a0001c0001t0001g0348 a0001c0001t0002g0335 a0001c0001t0002g0337 others(19): Show |
22 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(19): Show |
intron_variant | MODIFIER | c.560+694dupG | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr11 | 20396649 | ||||||
| chr11:20396651 | G | A | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.560+689G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 6/15 | chr11 | 20396651 | |||||||
| chr11:20396706 | A | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(237): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.560+744A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 6/15 | chr11 | 20396706 | |||||||
| chr11:20396742 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.560+780A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 6/15 | chr11 | 20396742 | |||||||
| chr11:20396773 | C | T | 4 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-804C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 6/15 | chr11 | 20396773 | |||||||
| chr11:20396793 | G | C | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.561-784G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 6/15 | chr11 | 20396793 | |||||||
| chr11:20396912 | G | A | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG01891.hp1 HG02622.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-665G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 6/15 | chr11 | 20396912 | |||||||
| chr11:20397140 | G | A | 1 | a0002c0002t0003g0345 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.561-437G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 6/15 | chr11 | 20397140 | |||||||
| chr11:20397192 | A | G | 1 | a0002c0002t0002g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.561-385A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 6/15 | chr11 | 20397192 | |||||||
| chr11:20397380 | AGTAT | A | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.561-192_561-189del others(4): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr11 | 20397380 | ||||||
| chr11:20397410 | T | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.561-167T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 6/15 | chr11 | 20397410 | |||||||
| chr11:20397482 | T | C | 180 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
187 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.561-95T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 6/15 | chr11 | 20397482 | |||||||
| chr11:20397743 | G | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG02257.hp2 HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.705+22G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20397743 | |||||||
| chr11:20397883 | A | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.705+162A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20397883 | |||||||
| chr11:20397916 | G | A | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.705+195G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20397916 | |||||||
| chr11:20398012 | T | TA | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(198): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.705+312dupA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr11 | 20398012 | ||||||
| chr11:20398012 | T | TAA | 10 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(7): Show |
10 | HG00738.hp2 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.705+311_705+312dup others(2): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr11 | 20398012 | ||||||
| chr11:20398012 | TA | T | 18 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(15): Show |
18 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.705+312delA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr11 | 20398012 | ||||||
| chr11:20398115 | G | A | 1 | a0001c0001t0002g0017 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.705+394G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20398115 | |||||||
| chr11:20398151 | A | G | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.705+430A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20398151 | |||||||
| chr11:20398159 | G | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.705+438G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20398159 | |||||||
| chr11:20398186 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.705+465A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20398186 | |||||||
| chr11:20398235 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.705+514G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20398235 | |||||||
| chr11:20398316 | GTTTTTTA others(12): Show |
G | 1 | a0001c0001t0001g0185 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.705+598_705+616del others(19): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr11 | 20398316 | ||||||
| chr11:20398428 | G | C | 1 | a0001c0001t0001g0366 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.705+707G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20398428 | |||||||
| chr11:20398459 | T | G | 58 | a0001c0001t0001g0186 a0001c0001t0001g0256 a0001c0001t0002g0013 others(55): Show |
58 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(55): Show |
intron_variant | MODIFIER | c.705+738T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20398459 | |||||||
| chr11:20398485 | C | T | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.705+764C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20398485 | |||||||
| chr11:20398578 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.705+857G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20398578 | |||||||
| chr11:20399005 | A | G | 14 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(11): Show |
14 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.705+1284A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20399005 | |||||||
| chr11:20399018 | G | A | 14 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(11): Show |
14 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.705+1297G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20399018 | |||||||
| chr11:20399037 | G | A | 1 | a0002c0002t0003g0333 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.705+1316G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20399037 | |||||||
| chr11:20399117 | G | A | 1 | a0007c0010t0002g0015 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.705+1396G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20399117 | |||||||
| chr11:20399128 | A | C | 4 | a0001c0001t0002g0328 a0001c0001t0002g0329 a0001c0001t0002g0331 others(1): Show |
4 | HG01928.hp1 HG01943.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.705+1407A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20399128 | |||||||
| chr11:20399320 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.705+1599A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20399320 | |||||||
| chr11:20399404 | A | T | 1 | a0001c0001t0001g0157 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.705+1683A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20399404 | |||||||
| chr11:20399405 | C | T | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.705+1684C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20399405 | |||||||
| chr11:20399453 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.705+1732A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20399453 | |||||||
| chr11:20399484 | T | G | 1 | a0002c0002t0002g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.705+1763T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20399484 | |||||||
| chr11:20399525 | A | T | 16 | a0001c0001t0002g0335 a0001c0001t0002g0337 a0002c0002t0003g0269 others(13): Show |
16 | HG02258.hp1 HG02559.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.705+1804A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20399525 | |||||||
| chr11:20399606 | A | G | 1 | a0001c0001t0002g0275 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.705+1885A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20399606 | |||||||
| chr11:20399791 | C | T | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.705+2070C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20399791 | |||||||
| chr11:20400044 | C | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(8): Show |
12 | HG01928.hp2 HG01952.hp1 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.705+2323C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20400044 | |||||||
| chr11:20400145 | C | G | 1 | a0001c0004t0001g0150 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.705+2424C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20400145 | |||||||
| chr11:20400327 | A | C | 5 | a0001c0001t0001g0366 a0001c0001t0007g0370 a0001c0005t0001g0367 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.706-2592A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20400327 | |||||||
| chr11:20400390 | G | A | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(271): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.706-2529G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20400390 | |||||||
| chr11:20400461 | C | G | 1 | a0001c0001t0001g0184 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.706-2458C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20400461 | |||||||
| chr11:20400659 | T | TAAAAACA others(342): Show |
1 | a0001c0001t0002g0018 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.706-2244_706-2243i others(351): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr11 | 20400659 | ||||||
| chr11:20400854 | T | A | 1 | a0001c0001t0001g0188 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.706-2065T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20400854 | |||||||
| chr11:20400878 | A | T | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(271): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.706-2041A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20400878 | |||||||
| chr11:20400890 | G | A | 1 | a0001c0001t0002g0353 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.706-2029G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20400890 | |||||||
| chr11:20400955 | G | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.706-1964G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20400955 | |||||||
| chr11:20400966 | T | G | 1 | a0001c0001t0001g0266 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.706-1953T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20400966 | |||||||
| chr11:20400972 | AT | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.706-1935delT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr11 | 20400972 | ||||||
| chr11:20400984 | T | C | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG00099.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.706-1935T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20400984 | |||||||
| chr11:20401055 | A | G | 1 | a0001c0001t0004g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.706-1864A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20401055 | |||||||
| chr11:20401146 | G | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.706-1773G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20401146 | |||||||
| chr11:20401184 | G | T | 58 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(55): Show |
58 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(55): Show |
intron_variant | MODIFIER | c.706-1735G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20401184 | |||||||
| chr11:20401185 | A | T | 58 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(55): Show |
58 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(55): Show |
intron_variant | MODIFIER | c.706-1734A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20401185 | |||||||
| chr11:20401189 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.706-1730A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20401189 | |||||||
| chr11:20401445 | G | A | 3 | a0001c0004t0001g0101 a0001c0004t0001g0102 a0001c0004t0001g0150 |
3 | HG02135.hp2 NA18940.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.706-1474G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20401445 | |||||||
| chr11:20401469 | A | C | 1 | a0001c0001t0001g0268 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.706-1450A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20401469 | |||||||
| chr11:20401558 | G | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.706-1361G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20401558 | |||||||
| chr11:20401629 | T | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.706-1290T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20401629 | |||||||
| chr11:20401741 | C | T | 1 | a0001c0001t0002g0240 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.706-1178C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20401741 | |||||||
| chr11:20401825 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.706-1094A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20401825 | |||||||
| chr11:20401945 | A | G | 5 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(2): Show |
5 | HG01884.hp1 HG03130.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.706-974A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20401945 | |||||||
| chr11:20402036 | C | T | 1 | a0002c0002t0002g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.706-883C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20402036 | |||||||
| chr11:20402107 | ATTTTTG | A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(8): Show |
12 | HG01928.hp2 HG01952.hp1 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.706-800_706-795del others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr11 | 20402107 | ||||||
| chr11:20402149 | C | A | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.706-770C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20402149 | |||||||
| chr11:20402150 | G | A | 21 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(18): Show |
21 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.706-769G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20402150 | |||||||
| chr11:20402205 | C | T | 6 | a0001c0001t0002g0017 a0001c0001t0002g0046 a0001c0001t0002g0055 others(3): Show |
6 | NA18952.hp1 NA18994.hp1 NA19006.hp1 others(3): Show |
intron_variant | MODIFIER | c.706-714C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20402205 | |||||||
| chr11:20402210 | C | T | 1 | a0002c0002t0002g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.706-709C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20402210 | |||||||
| chr11:20402212 | C | G | 14 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(11): Show |
14 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.706-707C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20402212 | |||||||
| chr11:20402263 | G | A | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(199): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.706-656G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20402263 | |||||||
| chr11:20402274 | C | T | 14 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(11): Show |
15 | HG01928.hp2 HG01952.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.706-645C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20402274 | |||||||
| chr11:20402299 | A | G | 5 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(2): Show |
5 | HG00408.hp1 NA18943.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.706-620A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20402299 | |||||||
| chr11:20402339 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.706-580G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20402339 | |||||||
| chr11:20402453 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.706-466G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20402453 | |||||||
| chr11:20402591 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.706-328A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20402591 | |||||||
| chr11:20402614 | ATC | A | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.706-303_706-302del others(2): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr11 | 20402614 | ||||||
| chr11:20402663 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.706-256C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20402663 | |||||||
| chr11:20402780 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.706-139A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20402780 | |||||||
| chr11:20402817 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.706-102A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20402817 | |||||||
| chr11:20402884 | C | T | 1 | a0001c0001t0007g0370 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.706-35C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20402884 | |||||||
| chr11:20402898 | G | A | 4 | a0001c0001t0007g0370 a0001c0005t0001g0367 a0001c0005t0001g0368 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.706-21G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 7/15 | chr11 | 20402898 | |||||||
| chr11:20403010 | T | C | 3 | a0001c0001t0001g0181 a0001c0001t0001g0191 a0001c0001t0001g0241 |
3 | HG03490.hp2 HG03492.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.771+26T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20403010 | |||||||
| chr11:20403047 | C | A | 2 | a0001c0001t0004g0063 a0001c0001t0004g0064 |
2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.771+63C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20403047 | |||||||
| chr11:20403229 | T | G | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(200): Show |
210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.771+245T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20403229 | |||||||
| chr11:20403305 | T | G | 57 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(54): Show |
57 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(54): Show |
intron_variant | MODIFIER | c.771+321T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20403305 | |||||||
| chr11:20403432 | T | C | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG01192.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.771+448T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20403432 | |||||||
| chr11:20403533 | A | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0241 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.771+549A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20403533 | |||||||
| chr11:20403634 | C | T | 3 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG02258.hp2 HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.771+650C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20403634 | |||||||
| chr11:20403638 | T | C | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.771+654T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20403638 | |||||||
| chr11:20403679 | C | T | 1 | a0001c0013t0002g0277 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.771+695C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20403679 | |||||||
| chr11:20403775 | C | T | 2 | a0003c0003t0002g0325 a0003c0003t0002g0326 |
2 | NA18969.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.771+791C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20403775 | |||||||
| chr11:20404056 | A | C | 1 | a0001c0001t0002g0045 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.771+1072A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20404056 | |||||||
| chr11:20404161 | G | GT | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.771+1186dupT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr11 | 20404161 | ||||||
| chr11:20404205 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.771+1221T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20404205 | |||||||
| chr11:20404211 | G | GT | 23 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0288 others(20): Show |
23 | HG00609.hp2 HG00621.hp2 HG03831.hp2 others(20): Show |
intron_variant | MODIFIER | c.771+1268dupT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr11 | 20404211 | ||||||
| chr11:20404211 | G | GTTTTTTT others(6): Show |
1 | a0001c0001t0002g0324 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.771+1256_771+1268d others(15): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr11 | 20404211 | ||||||
| chr11:20404211 | GT | G | 6 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(3): Show |
6 | HG00735.hp2 HG01175.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.771+1268delT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr11 | 20404211 | ||||||
| chr11:20404211 | GTTTT | G | 6 | a0001c0001t0001g0075 a0001c0001t0001g0079 a0001c0001t0001g0082 others(3): Show |
6 | HG01928.hp2 HG01952.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.771+1265_771+1268d others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr11 | 20404211 | ||||||
| chr11:20404211 | GTTTTT | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0076 a0001c0001t0001g0077 others(7): Show |
11 | HG01516.hp1 HG01517.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.771+1264_771+1268d others(7): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr11 | 20404211 | ||||||
| chr11:20404211 | GTTTTTT | G | 6 | a0001c0001t0002g0354 a0001c0001t0002g0355 a0002c0002t0003g0270 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.771+1263_771+1268d others(8): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr11 | 20404211 | ||||||
| chr11:20404211 | GTTTTTTT | G | 8 | a0001c0001t0002g0337 a0002c0002t0003g0269 a0002c0002t0003g0273 others(5): Show |
8 | HG02572.hp1 HG02622.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.771+1262_771+1268d others(9): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr11 | 20404211 | ||||||
| chr11:20404211 | GTTTTTTT others(1): Show |
G | 10 | a0001c0001t0001g0106 a0001c0001t0001g0348 a0001c0001t0002g0335 others(7): Show |
10 | HG02630.hp2 HG02886.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.771+1261_771+1268d others(10): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr11 | 20404211 | ||||||
| chr11:20404211 | GTTTTTTT others(2): Show |
G | 52 | a0001c0001t0001g0012 a0001c0001t0001g0070 a0001c0001t0001g0071 others(49): Show |
52 | HG00544.hp2 HG00642.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.771+1260_771+1268d others(11): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr11 | 20404211 | ||||||
| chr11:20404211 | GTTTTTTT others(3): Show |
G | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.771+1259_771+1268d others(12): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr11 | 20404211 | ||||||
| chr11:20404211 | GTTTTTTT others(4): Show |
G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG01975.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.771+1258_771+1268d others(13): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr11 | 20404211 | ||||||
| chr11:20404211 | GTTTTTTT others(7): Show |
G | 1 | a0001c0001t0002g0278 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.771+1255_771+1268d others(16): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr11 | 20404211 | ||||||
| chr11:20404217 | T | G | 1 | a0002c0002t0002g0009 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.771+1233T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20404217 | |||||||
| chr11:20404217 | T | TTTTGTTT others(12): Show |
10 | a0001c0001t0002g0013 a0001c0001t0002g0019 a0001c0001t0002g0020 others(7): Show |
10 | HG01192.hp2 HG01981.hp1 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.771+1236_771+1237i others(21): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr11 | 20404217 | ||||||
| chr11:20404218 | T | G | 2 | a0002c0002t0002g0010 a0002c0002t0002g0011 |
2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.771+1234T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20404218 | |||||||
| chr11:20404218 | T | TTTGTTTT others(11): Show |
37 | a0001c0001t0002g0014 a0001c0001t0002g0016 a0001c0001t0002g0017 others(34): Show |
37 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.771+1236_771+1237i others(20): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr11 | 20404218 | ||||||
| chr11:20404219 | T | TTGTTTTG others(10): Show |
1 | a0001c0001t0002g0044 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.771+1236_771+1237i others(19): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr11 | 20404219 | ||||||
| chr11:20404221 | T | G | 6 | a0001c0001t0001g0075 a0001c0001t0001g0079 a0001c0001t0001g0082 others(3): Show |
6 | HG01928.hp2 HG01952.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.771+1237T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20404221 | |||||||
| chr11:20404222 | T | G | 17 | a0001c0001t0001g0001 a0001c0001t0001g0076 a0001c0001t0001g0077 others(14): Show |
18 | HG01192.hp2 HG01981.hp1 HG02148.hp1 others(15): Show |
intron_variant | MODIFIER | c.771+1238T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20404222 | |||||||
| chr11:20404223 | T | G | 42 | a0001c0001t0002g0014 a0001c0001t0002g0016 a0001c0001t0002g0017 others(39): Show |
42 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.771+1239T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20404223 | |||||||
| chr11:20404224 | T | G | 4 | a0001c0001t0002g0044 a0001c0001t0004g0067 a0002c0002t0002g0010 others(1): Show |
4 | HG02109.hp2 HG02922.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.771+1240T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20404224 | |||||||
| chr11:20404225 | T | G | 1 | a0001c0001t0001g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.771+1241T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20404225 | |||||||
| chr11:20404226 | T | G | 52 | a0001c0001t0001g0012 a0001c0001t0001g0070 a0001c0001t0001g0071 others(49): Show |
52 | HG00544.hp2 HG00642.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.771+1242T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20404226 | |||||||
| chr11:20404227 | T | G | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.771+1243T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20404227 | |||||||
| chr11:20404228 | T | G | 39 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0002g0014 others(36): Show |
39 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(36): Show |
intron_variant | MODIFIER | c.771+1244T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20404228 | |||||||
| chr11:20404229 | T | G | 1 | a0001c0001t0002g0044 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.771+1245T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20404229 | |||||||
| chr11:20404232 | T | G | 10 | a0001c0001t0002g0013 a0001c0001t0002g0019 a0001c0001t0002g0020 others(7): Show |
10 | HG01192.hp2 HG01981.hp1 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.771+1248T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20404232 | |||||||
| chr11:20404233 | T | G | 37 | a0001c0001t0002g0014 a0001c0001t0002g0016 a0001c0001t0002g0017 others(34): Show |
37 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.771+1249T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20404233 | |||||||
| chr11:20404234 | T | G | 1 | a0001c0001t0002g0044 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.771+1250T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20404234 | |||||||
| chr11:20404237 | T | G | 1 | a0001c0001t0002g0013 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.771+1253T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20404237 | |||||||
| chr11:20404238 | T | G | 8 | a0001c0001t0002g0014 a0001c0001t0002g0017 a0001c0001t0002g0025 others(5): Show |
8 | HG02056.hp1 HG03834.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.771+1254T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20404238 | |||||||
| chr11:20404242 | T | G | 1 | a0001c0001t0002g0013 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.771+1258T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20404242 | |||||||
| chr11:20404483 | C | T | 1 | a0001c0001t0002g0356 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.771+1499C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20404483 | |||||||
| chr11:20404544 | G | A | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.771+1560G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20404544 | |||||||
| chr11:20404558 | A | G | 1 | a0001c0001t0004g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.771+1574A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20404558 | |||||||
| chr11:20404954 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.771+1970A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20404954 | |||||||
| chr11:20405169 | A | T | 1 | a0001c0001t0001g0096 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.771+2185A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20405169 | |||||||
| chr11:20405352 | CTCA | C | 22 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(19): Show |
22 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.771+2373_771+2375d others(5): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr11 | 20405352 | ||||||
| chr11:20405363 | A | T | 1 | a0001c0001t0001g0227 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.771+2379A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20405363 | |||||||
| chr11:20405478 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.772-2433A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20405478 | |||||||
| chr11:20405775 | T | A | 1 | a0001c0001t0001g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.772-2136T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20405775 | |||||||
| chr11:20405778 | T | C | 55 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(52): Show |
55 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(52): Show |
intron_variant | MODIFIER | c.772-2133T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20405778 | |||||||
| chr11:20405914 | A | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.772-1997A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20405914 | |||||||
| chr11:20405940 | G | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(66): Show |
70 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(67): Show |
intron_variant | MODIFIER | c.772-1971G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20405940 | |||||||
| chr11:20406378 | G | A | 89 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(86): Show |
94 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.772-1533G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20406378 | |||||||
| chr11:20406414 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0002g0043 |
2 | HG03669.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.772-1497C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20406414 | |||||||
| chr11:20406474 | A | G | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.772-1437A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20406474 | |||||||
| chr11:20406632 | G | T | 14 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(11): Show |
15 | HG01928.hp2 HG01952.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.772-1279G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20406632 | |||||||
| chr11:20406647 | C | A | 1 | a0001c0001t0001g0080 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.772-1264C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20406647 | |||||||
| chr11:20406734 | A | G | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.772-1177A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20406734 | |||||||
| chr11:20406968 | C | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG02257.hp2 HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.772-943C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20406968 | |||||||
| chr11:20407407 | C | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.772-504C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20407407 | |||||||
| chr11:20407450 | A | T | 1 | a0001c0001t0001g0159 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.772-461A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20407450 | |||||||
| chr11:20407496 | A | G | 1 | a0001c0001t0002g0355 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.772-415A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20407496 | |||||||
| chr11:20407633 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.772-278A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20407633 | |||||||
| chr11:20407692 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.772-219A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20407692 | |||||||
| chr11:20407695 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.772-216C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20407695 | |||||||
| chr11:20407731 | G | A | 21 | a0001c0001t0002g0335 a0001c0001t0002g0337 a0002c0002t0003g0269 others(18): Show |
21 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.772-180G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20407731 | |||||||
| chr11:20407908 | T | C | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
splice_region_variant&intron_variant | LOW | c.772-3T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 8/15 | chr11 | 20407908 | |||||||
| chr11:20408133 | A | G | 4 | a0001c0001t0002g0013 a0001c0001t0002g0052 a0001c0001t0002g0053 others(1): Show |
4 | NA18966.hp2 NA19065.hp1 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.893+101A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20408133 | |||||||
| chr11:20408261 | A | T | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.893+229A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20408261 | |||||||
| chr11:20408304 | T | C | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.893+272T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20408304 | |||||||
| chr11:20408450 | G | A | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.893+418G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20408450 | |||||||
| chr11:20408629 | C | G | 1 | a0001c0001t0001g0244 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.893+597C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20408629 | |||||||
| chr11:20408673 | C | T | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(175): Show |
185 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.893+641C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20408673 | |||||||
| chr11:20408674 | G | A | 1 | a0007c0010t0002g0015 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.893+642G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20408674 | |||||||
| chr11:20408729 | G | T | 14 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(11): Show |
14 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.893+697G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20408729 | |||||||
| chr11:20408888 | G | A | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.893+856G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20408888 | |||||||
| chr11:20408929 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.893+897T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20408929 | |||||||
| chr11:20408957 | C | A | 1 | a0001c0001t0001g0109 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.893+925C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20408957 | |||||||
| chr11:20409046 | G | A | 5 | a0001c0001t0001g0366 a0001c0001t0007g0370 a0001c0005t0001g0367 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.893+1014G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20409046 | |||||||
| chr11:20409059 | C | T | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.893+1027C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20409059 | |||||||
| chr11:20409060 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.893+1028G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20409060 | |||||||
| chr11:20409237 | T | A | 1 | a0001c0001t0002g0029 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.893+1205T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20409237 | |||||||
| chr11:20409300 | A | T | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.893+1268A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20409300 | |||||||
| chr11:20409313 | C | T | 2 | a0002c0002t0003g0343 a0002c0002t0003g0344 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.893+1281C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20409313 | |||||||
| chr11:20409346 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.893+1314T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20409346 | |||||||
| chr11:20409352 | T | G | 2 | a0001c0001t0004g0063 a0001c0001t0004g0064 |
2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.893+1320T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20409352 | |||||||
| chr11:20409451 | A | G | 1 | a0001c0001t0002g0323 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.893+1419A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20409451 | |||||||
| chr11:20409470 | C | A | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.893+1438C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20409470 | |||||||
| chr11:20409470 | C | G | 1 | a0001c0001t0002g0224 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.893+1438C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20409470 | |||||||
| chr11:20409480 | T | C | 14 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(11): Show |
14 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.893+1448T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20409480 | |||||||
| chr11:20409648 | T | TACACACA others(3): Show |
1 | a0001c0001t0001g0178 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.893+1621_893+1622i others(12): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20409648 | ||||||
| chr11:20409654 | A | AAC | 52 | a0001c0001t0001g0075 a0001c0001t0001g0080 a0001c0001t0001g0095 others(49): Show |
52 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.893+1659_893+1660d others(4): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20409654 | ||||||
| chr11:20409654 | A | AACAC | 41 | a0001c0001t0001g0003 a0001c0001t0001g0073 a0001c0001t0001g0086 others(38): Show |
42 | HG00558.hp1 HG01106.hp1 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.893+1657_893+1660d others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20409654 | ||||||
| chr11:20409654 | A | AACACAC | 16 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0094 others(13): Show |
16 | HG01099.hp2 HG02280.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.893+1655_893+1660d others(8): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20409654 | ||||||
| chr11:20409654 | A | AACACACA others(1): Show |
45 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(42): Show |
49 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.893+1653_893+1660d others(10): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20409654 | ||||||
| chr11:20409654 | A | AACACACA others(3): Show |
25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0074 others(22): Show |
27 | HG00099.hp1 HG00408.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.893+1651_893+1660d others(12): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20409654 | ||||||
| chr11:20409654 | A | AACACACA others(5): Show |
9 | a0001c0001t0001g0012 a0001c0001t0001g0093 a0001c0001t0001g0141 others(6): Show |
9 | HG01261.hp1 HG01884.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.893+1649_893+1660d others(14): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20409654 | ||||||
| chr11:20409654 | A | ACACACAC others(4): Show |
1 | a0001c0001t0001g0236 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.893+1622_893+1623i others(13): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20409654 | |||||||
| chr11:20409654 | A | C | 2 | a0001c0001t0001g0178 a0001c0001t0001g0223 |
2 | HG00639.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.893+1622A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20409654 | |||||||
| chr11:20409654 | AAC | A | 29 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(26): Show |
29 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.893+1659_893+1660d others(4): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20409654 | ||||||
| chr11:20409654 | AACAC | A | 12 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0250 others(9): Show |
12 | HG01167.hp1 HG01496.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.893+1657_893+1660d others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20409654 | ||||||
| chr11:20409654 | AACACAC | A | 6 | a0001c0001t0002g0019 a0001c0001t0002g0030 a0001c0001t0002g0031 others(3): Show |
6 | HG01952.hp2 HG01981.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.893+1655_893+1660d others(8): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20409654 | ||||||
| chr11:20409654 | AACACACA others(1): Show |
A | 49 | a0001c0001t0001g0261 a0001c0001t0001g0362 a0001c0001t0001g0363 others(46): Show |
49 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(46): Show |
intron_variant | MODIFIER | c.893+1653_893+1660d others(10): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20409654 | ||||||
| chr11:20409742 | C | T | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0041 others(1): Show |
4 | NA18945.hp2 NA18963.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.893+1710C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20409742 | |||||||
| chr11:20409792 | A | G | 7 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 others(4): Show |
7 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.893+1760A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20409792 | |||||||
| chr11:20410227 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.893+2195T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20410227 | |||||||
| chr11:20410500 | T | TAGTC | 56 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(53): Show |
56 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.893+2470_893+2471i others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20410500 | ||||||
| chr11:20410500 | T | TGGTC | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.893+2468_893+2469i others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20410500 | |||||||
| chr11:20410503 | G | A | 14 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(11): Show |
14 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.893+2471G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20410503 | |||||||
| chr11:20410672 | T | C | 2 | a0001c0001t0001g0193 a0001c0001t0001g0202 |
2 | HG02071.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.893+2640T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20410672 | |||||||
| chr11:20410692 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.893+2660A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20410692 | |||||||
| chr11:20410698 | A | G | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.893+2666A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20410698 | |||||||
| chr11:20410774 | A | G | 1 | a0001c0001t0001g0201 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.893+2742A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20410774 | |||||||
| chr11:20410803 | A | G | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.893+2771A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20410803 | |||||||
| chr11:20410987 | T | A | 4 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(1): Show |
4 | HG01243.hp2 HG01255.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.893+2955T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20410987 | |||||||
| chr11:20410993 | ATACT | A | 4 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(1): Show |
4 | HG01243.hp2 HG01255.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.893+2965_893+2968d others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20410993 | ||||||
| chr11:20411251 | G | A | 56 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(53): Show |
56 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.893+3219G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20411251 | |||||||
| chr11:20411262 | C | G | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(199): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.893+3230C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20411262 | |||||||
| chr11:20411281 | G | C | 1 | a0001c0001t0001g0082 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.893+3249G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20411281 | |||||||
| chr11:20411327 | A | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.893+3295A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20411327 | |||||||
| chr11:20411346 | G | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.893+3314G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20411346 | |||||||
| chr11:20411358 | T | C | 2 | a0002c0002t0003g0343 a0002c0002t0003g0344 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.893+3326T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20411358 | |||||||
| chr11:20411473 | C | G | 1 | a0001c0004t0001g0102 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.893+3441C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20411473 | |||||||
| chr11:20411760 | G | T | 14 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(11): Show |
14 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.893+3728G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20411760 | |||||||
| chr11:20411780 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.893+3748C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20411780 | |||||||
| chr11:20411804 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.893+3772A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20411804 | |||||||
| chr11:20411937 | A | G | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(199): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.893+3905A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20411937 | |||||||
| chr11:20411978 | C | G | 1 | a0001c0001t0001g0235 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.893+3946C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20411978 | |||||||
| chr11:20412024 | A | T | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.893+3992A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20412024 | |||||||
| chr11:20412139 | A | C | 1 | a0001c0001t0002g0284 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.893+4107A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20412139 | |||||||
| chr11:20412164 | C | G | 1 | a0001c0001t0001g0079 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.893+4132C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20412164 | |||||||
| chr11:20412293 | G | C | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG01891.hp1 HG02622.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.893+4261G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20412293 | |||||||
| chr11:20412397 | AC | A | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
217 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.893+4375delC | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20412397 | ||||||
| chr11:20412397 | ACC | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0068 a0001c0001t0001g0069 others(89): Show |
93 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.893+4374_893+4375d others(4): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20412397 | ||||||
| chr11:20412401 | C | A | 55 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(52): Show |
55 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(52): Show |
intron_variant | MODIFIER | c.893+4369C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20412401 | |||||||
| chr11:20412404 | C | A | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 |
3 | HG02055.hp1 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.893+4372C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20412404 | |||||||
| chr11:20412410 | C | T | 7 | a0001c0001t0001g0179 a0001c0001t0001g0220 a0001c0001t0001g0221 others(4): Show |
7 | HG00738.hp1 HG01071.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.893+4378C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20412410 | |||||||
| chr11:20412453 | A | C | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.893+4421A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20412453 | |||||||
| chr11:20412528 | A | G | 4 | a0001c0001t0001g0004 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.893+4496A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20412528 | |||||||
| chr11:20412529 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.893+4497A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20412529 | |||||||
| chr11:20412539 | AT | A | 4 | a0001c0001t0002g0291 a0001c0001t0002g0349 a0001c0001t0002g0350 others(1): Show |
4 | NA18954.hp1 NA18973.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.893+4515delT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20412539 | ||||||
| chr11:20412733 | ATTAAT | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.893+4705_893+4709d others(7): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20412733 | ||||||
| chr11:20413029 | T | A | 1 | a0001c0001t0001g0079 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.893+4997T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20413029 | |||||||
| chr11:20413069 | T | A | 1 | a0001c0001t0001g0261 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.893+5037T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20413069 | |||||||
| chr11:20413079 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.893+5047T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20413079 | |||||||
| chr11:20413083 | T | TA | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.893+5051_893+5052i others(3): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20413083 | |||||||
| chr11:20413194 | T | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.893+5162T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20413194 | |||||||
| chr11:20413235 | T | A | 1 | a0001c0001t0002g0054 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.893+5203T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20413235 | |||||||
| chr11:20413418 | C | G | 2 | a0001c0001t0004g0063 a0001c0001t0004g0064 |
2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.893+5386C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20413418 | |||||||
| chr11:20413473 | A | T | 2 | a0001c0001t0001g0185 a0001c0001t0002g0240 |
2 | HG00558.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.893+5441A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20413473 | |||||||
| chr11:20413562 | A | G | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.893+5530A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20413562 | |||||||
| chr11:20413601 | G | C | 55 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(52): Show |
55 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(52): Show |
intron_variant | MODIFIER | c.893+5569G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20413601 | |||||||
| chr11:20413628 | G | A | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.893+5596G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20413628 | |||||||
| chr11:20413681 | CTG | C | 5 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0237 others(2): Show |
5 | HG01071.hp1 HG01123.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.893+5652_893+5653d others(4): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20413681 | ||||||
| chr11:20413751 | T | C | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.893+5719T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20413751 | |||||||
| chr11:20413755 | C | A | 1 | a0002c0002t0002g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.893+5723C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20413755 | |||||||
| chr11:20413809 | T | G | 8 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0119 others(5): Show |
8 | HG01891.hp2 HG02809.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.893+5777T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20413809 | |||||||
| chr11:20413819 | T | C | 14 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(11): Show |
14 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.893+5787T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20413819 | |||||||
| chr11:20413832 | T | C | 17 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(14): Show |
18 | HG01516.hp1 HG01517.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.893+5800T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20413832 | |||||||
| chr11:20414278 | A | G | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.893+6246A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20414278 | |||||||
| chr11:20414309 | T | C | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.893+6277T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20414309 | |||||||
| chr11:20414372 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.893+6340T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20414372 | |||||||
| chr11:20414565 | C | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.893+6533C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20414565 | |||||||
| chr11:20414942 | G | T | 4 | a0001c0001t0002g0335 a0001c0001t0002g0337 a0002c0002t0005g0334 others(1): Show |
4 | HG02622.hp2 HG02630.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.893+6910G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20414942 | |||||||
| chr11:20415017 | G | GGT | 121 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0012 others(118): Show |
123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.893+7022_893+7023d others(4): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20415017 | ||||||
| chr11:20415017 | G | GGTGT | 53 | a0001c0001t0001g0003 a0001c0001t0001g0071 a0001c0001t0001g0072 others(50): Show |
54 | HG00323.hp2 HG00544.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.893+7020_893+7023d others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20415017 | ||||||
| chr11:20415017 | G | GGTGTGT | 36 | a0001c0001t0001g0004 a0001c0001t0001g0074 a0001c0001t0001g0087 others(33): Show |
37 | HG00642.hp2 HG01106.hp2 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.893+7018_893+7023d others(8): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20415017 | ||||||
| chr11:20415017 | G | GGTGTGTG others(1): Show |
24 | a0001c0001t0001g0161 a0001c0001t0001g0348 a0001c0001t0002g0018 others(21): Show |
24 | HG01255.hp1 HG01952.hp2 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.893+7016_893+7023d others(10): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20415017 | ||||||
| chr11:20415017 | G | GGTGTGTG others(3): Show |
8 | a0001c0001t0002g0019 a0001c0001t0002g0031 a0001c0001t0002g0038 others(5): Show |
8 | HG01981.hp1 HG02015.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.893+7014_893+7023d others(12): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20415017 | ||||||
| chr11:20415017 | G | GGTGTGTG others(5): Show |
5 | a0001c0001t0002g0049 a0001c0001t0002g0335 a0001c0001t0002g0337 others(2): Show |
5 | HG02155.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.893+7012_893+7023d others(14): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20415017 | ||||||
| chr11:20415017 | GGT | G | 5 | a0001c0001t0001g0113 a0001c0001t0001g0245 a0001c0001t0002g0242 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.893+7022_893+7023d others(4): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20415017 | ||||||
| chr11:20415036 | G | A | 1 | a0001c0001t0002g0242 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.893+7004G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20415036 | |||||||
| chr11:20415036 | G | GTA | 48 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0085 others(45): Show |
50 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.893+7005_893+7006i others(4): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20415036 | ||||||
| chr11:20415068 | T | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.893+7036T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20415068 | |||||||
| chr11:20415213 | A | T | 1 | a0001c0001t0001g0080 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.893+7181A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20415213 | |||||||
| chr11:20415232 | A | G | 1 | a0001c0005t0001g0368 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.893+7200A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20415232 | |||||||
| chr11:20415356 | G | A | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.893+7324G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20415356 | |||||||
| chr11:20415365 | A | G | 5 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(2): Show |
5 | HG01884.hp1 HG03130.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.893+7333A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20415365 | |||||||
| chr11:20415506 | CAGGCAGA others(73): Show |
C | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.893+7480_893+7559d others(82): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20415506 | ||||||
| chr11:20415558 | T | C | 5 | a0001c0001t0001g0099 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG02809.hp2 HG02970.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.893+7526T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20415558 | |||||||
| chr11:20415580 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.893+7548A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20415580 | |||||||
| chr11:20415611 | C | T | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.893+7579C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20415611 | |||||||
| chr11:20415628 | G | A | 1 | a0002c0002t0005g0334 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.893+7596G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20415628 | |||||||
| chr11:20415637 | A | T | 5 | a0001c0001t0001g0098 a0001c0001t0001g0118 a0001c0001t0001g0129 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.893+7605A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20415637 | |||||||
| chr11:20415684 | GT | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.893+7654delT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20415684 | ||||||
| chr11:20415811 | T | C | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.893+7779T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20415811 | |||||||
| chr11:20415915 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.893+7883A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20415915 | |||||||
| chr11:20416029 | A | G | 4 | a0002c0002t0003g0269 a0002c0002t0003g0270 a0002c0002t0003g0339 others(1): Show |
4 | HG02647.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.893+7997A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20416029 | |||||||
| chr11:20416171 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.893+8139A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20416171 | |||||||
| chr11:20416250 | G | A | 14 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(11): Show |
15 | HG01928.hp2 HG01952.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.893+8218G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20416250 | |||||||
| chr11:20416336 | A | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(8): Show |
12 | HG01928.hp2 HG01952.hp1 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.893+8304A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20416336 | |||||||
| chr11:20416477 | A | G | 1 | a0002c0002t0002g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.893+8445A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20416477 | |||||||
| chr11:20416517 | G | T | 14 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(11): Show |
14 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.893+8485G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20416517 | |||||||
| chr11:20416560 | T | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.893+8528T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20416560 | |||||||
| chr11:20416604 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.893+8572G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20416604 | |||||||
| chr11:20416732 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.893+8700A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20416732 | |||||||
| chr11:20416750 | T | C | 2 | a0002c0002t0003g0343 a0002c0002t0003g0344 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.893+8718T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20416750 | |||||||
| chr11:20416768 | G | C | 1 | a0001c0001t0002g0353 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.893+8736G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20416768 | |||||||
| chr11:20416930 | A | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.893+8898A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20416930 | |||||||
| chr11:20417018 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.893+8986C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20417018 | |||||||
| chr11:20417046 | A | G | 2 | a0001c0001t0001g0166 a0001c0001t0002g0043 |
2 | HG03579.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.893+9014A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20417046 | |||||||
| chr11:20417097 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.893+9065G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20417097 | |||||||
| chr11:20417113 | G | T | 21 | a0001c0001t0002g0335 a0001c0001t0002g0337 a0002c0002t0003g0269 others(18): Show |
21 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.893+9081G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20417113 | |||||||
| chr11:20417133 | A | C | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG01891.hp1 HG02622.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.893+9101A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20417133 | |||||||
| chr11:20417162 | T | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.893+9130T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20417162 | |||||||
| chr11:20417173 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.893+9141T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20417173 | |||||||
| chr11:20417505 | C | A | 1 | a0001c0001t0001g0161 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.894-9261C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20417505 | |||||||
| chr11:20417607 | A | C | 2 | a0001c0001t0002g0013 a0001c0001t0002g0053 |
2 | NA19076.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.894-9159A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20417607 | |||||||
| chr11:20417774 | T | TCA | 10 | a0001c0001t0001g0081 a0001c0001t0002g0032 a0001c0001t0002g0038 others(7): Show |
10 | HG01123.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.894-8969_894-8968d others(4): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20417774 | ||||||
| chr11:20417774 | T | TCACACA | 29 | a0001c0001t0001g0348 a0001c0001t0001g0362 a0001c0001t0001g0363 others(26): Show |
29 | HG00735.hp2 HG01243.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.894-8973_894-8968d others(8): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20417774 | ||||||
| chr11:20417774 | T | TCACACAC others(3): Show |
6 | a0002c0002t0002g0276 a0002c0002t0003g0272 a0002c0002t0003g0273 others(3): Show |
6 | HG02572.hp1 HG03041.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.894-8977_894-8968d others(12): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20417774 | ||||||
| chr11:20417774 | TCA | T | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.894-8969_894-8968d others(4): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20417774 | ||||||
| chr11:20417833 | C | T | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.894-8933C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20417833 | |||||||
| chr11:20417971 | C | T | 26 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0012 others(23): Show |
28 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.894-8795C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20417971 | |||||||
| chr11:20418042 | G | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | NA18970.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.894-8724G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20418042 | |||||||
| chr11:20418097 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.894-8669A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20418097 | |||||||
| chr11:20418126 | GA | G | 37 | a0001c0001t0001g0348 a0001c0001t0001g0362 a0001c0001t0001g0363 others(34): Show |
37 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.894-8635delA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20418126 | ||||||
| chr11:20418337 | C | T | 14 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(11): Show |
15 | HG01516.hp1 HG01517.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.894-8429C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20418337 | |||||||
| chr11:20418382 | T | C | 179 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
186 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.894-8384T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20418382 | |||||||
| chr11:20418757 | C | A | 1 | a0001c0001t0001g0099 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.894-8009C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20418757 | |||||||
| chr11:20418928 | A | G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(11): Show |
15 | HG01516.hp1 HG01517.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.894-7838A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20418928 | |||||||
| chr11:20419089 | T | G | 2 | a0001c0001t0004g0063 a0001c0001t0004g0064 |
2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.894-7677T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20419089 | |||||||
| chr11:20419145 | A | G | 91 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(88): Show |
96 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.894-7621A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20419145 | |||||||
| chr11:20419151 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.894-7615T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20419151 | |||||||
| chr11:20419180 | A | G | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.894-7586A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20419180 | |||||||
| chr11:20419499 | T | G | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.894-7267T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20419499 | |||||||
| chr11:20419629 | C | T | 5 | a0001c0001t0001g0366 a0001c0001t0007g0370 a0001c0005t0001g0367 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.894-7137C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20419629 | |||||||
| chr11:20419690 | C | T | 1 | a0001c0001t0004g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.894-7076C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20419690 | |||||||
| chr11:20419910 | G | C | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.894-6856G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20419910 | |||||||
| chr11:20419923 | A | G | 1 | a0001c0001t0002g0323 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.894-6843A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20419923 | |||||||
| chr11:20419936 | T | C | 37 | a0001c0001t0001g0348 a0001c0001t0001g0362 a0001c0001t0001g0363 others(34): Show |
37 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.894-6830T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20419936 | |||||||
| chr11:20419957 | A | C | 1 | a0001c0001t0001g0161 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.894-6809A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20419957 | |||||||
| chr11:20419959 | G | T | 1 | a0001c0001t0001g0246 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.894-6807G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20419959 | |||||||
| chr11:20419970 | G | A | 1 | a0001c0001t0002g0310 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.894-6796G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20419970 | |||||||
| chr11:20419970 | G | T | 1 | a0001c0001t0002g0304 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.894-6796G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20419970 | |||||||
| chr11:20420127 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.894-6639G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20420127 | |||||||
| chr11:20420491 | C | T | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.894-6275C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20420491 | |||||||
| chr11:20420499 | C | T | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.894-6267C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20420499 | |||||||
| chr11:20420500 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.894-6266G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20420500 | |||||||
| chr11:20420513 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.894-6253A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20420513 | |||||||
| chr11:20420586 | G | A | 14 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(11): Show |
15 | HG01928.hp2 HG01952.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.894-6180G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20420586 | |||||||
| chr11:20420834 | C | A | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | NA18964.hp1 NA19079.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.894-5932C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20420834 | |||||||
| chr11:20420848 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.894-5918A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20420848 | |||||||
| chr11:20421007 | C | T | 14 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(11): Show |
14 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.894-5759C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20421007 | |||||||
| chr11:20421095 | C | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.894-5671C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20421095 | |||||||
| chr11:20421162 | C | T | 1 | a0002c0002t0003g0345 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.894-5604C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20421162 | |||||||
| chr11:20421163 | G | A | 1 | a0001c0001t0001g0366 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.894-5603G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20421163 | |||||||
| chr11:20421192 | C | T | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.894-5574C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20421192 | |||||||
| chr11:20421193 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.894-5573G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20421193 | |||||||
| chr11:20421573 | A | T | 1 | a0001c0001t0001g0366 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.894-5193A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20421573 | |||||||
| chr11:20421642 | C | T | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.894-5124C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20421642 | |||||||
| chr11:20422010 | G | A | 1 | a0001c0001t0002g0311 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.894-4756G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20422010 | |||||||
| chr11:20422076 | A | G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(11): Show |
15 | HG01516.hp1 HG01517.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.894-4690A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20422076 | |||||||
| chr11:20422119 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.894-4647C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20422119 | |||||||
| chr11:20422329 | G | A | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0086 others(80): Show |
85 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.894-4437G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20422329 | |||||||
| chr11:20422463 | C | G | 11 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 others(8): Show |
11 | HG01175.hp2 HG01981.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.894-4303C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20422463 | |||||||
| chr11:20422560 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.894-4206A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20422560 | |||||||
| chr11:20422598 | C | A | 2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.894-4168C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20422598 | |||||||
| chr11:20422627 | C | T | 3 | a0001c0001t0002g0013 a0001c0001t0002g0052 a0001c0001t0002g0053 |
3 | NA19065.hp1 NA19076.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.894-4139C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20422627 | |||||||
| chr11:20423070 | T | C | 1 | a0001c0001t0001g0348 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.894-3696T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20423070 | |||||||
| chr11:20423193 | C | G | 22 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(19): Show |
22 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.894-3573C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20423193 | |||||||
| chr11:20423335 | C | T | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG01891.hp1 HG02622.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.894-3431C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20423335 | |||||||
| chr11:20423506 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.894-3260A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20423506 | |||||||
| chr11:20423524 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.894-3242G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20423524 | |||||||
| chr11:20423698 | A | G | 7 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(4): Show |
7 | HG02055.hp1 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.894-3068A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20423698 | |||||||
| chr11:20423828 | C | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(8): Show |
12 | HG01928.hp2 HG01952.hp1 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.894-2938C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20423828 | |||||||
| chr11:20423873 | T | TA | 24 | a0001c0001t0001g0348 a0001c0001t0002g0275 a0001c0001t0002g0278 others(21): Show |
24 | HG01175.hp2 HG02132.hp2 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.894-2864dupA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20423873 | ||||||
| chr11:20423873 | T | TAAAAAAA others(3): Show |
6 | a0001c0001t0001g0363 a0001c0001t0001g0364 a0001c0001t0001g0365 others(3): Show |
6 | HG01243.hp2 HG01255.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.894-2873_894-2864d others(12): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20423873 | ||||||
| chr11:20423873 | T | TAAAAAAA others(4): Show |
2 | a0001c0001t0001g0362 a0001c0001t0002g0358 |
2 | HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.894-2874_894-2864d others(13): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20423873 | ||||||
| chr11:20423873 | T | TAAAAAAA others(5): Show |
1 | a0001c0001t0002g0332 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.894-2875_894-2864d others(14): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20423873 | ||||||
| chr11:20423873 | TA | T | 66 | a0001c0001t0001g0068 a0001c0001t0001g0071 a0001c0001t0001g0085 others(63): Show |
66 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.894-2864delA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20423873 | ||||||
| chr11:20423873 | TAA | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.894-2865_894-2864d others(4): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20423873 | ||||||
| chr11:20423873 | TAAAA | T | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.894-2867_894-2864d others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20423873 | ||||||
| chr11:20423873 | TAAAAAAA others(5): Show |
T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(8): Show |
12 | HG01928.hp2 HG01952.hp1 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.894-2875_894-2864d others(14): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20423873 | ||||||
| chr11:20423873 | TAAAAAAA others(6): Show |
T | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.894-2876_894-2864d others(15): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20423873 | ||||||
| chr11:20423912 | C | T | 62 | a0001c0001t0001g0003 a0001c0001t0001g0097 a0001c0001t0001g0099 others(59): Show |
63 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.894-2854C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20423912 | |||||||
| chr11:20423922 | C | T | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.894-2844C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20423922 | |||||||
| chr11:20423990 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0200 a0001c0001t0001g0227 |
4 | HG00639.hp1 HG01081.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.894-2776C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20423990 | |||||||
| chr11:20424057 | G | A | 1 | a0001c0001t0002g0285 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.894-2709G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20424057 | |||||||
| chr11:20424139 | G | C | 2 | a0001c0005t0001g0367 a0001c0005t0001g0369 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.894-2627G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20424139 | |||||||
| chr11:20424183 | CA | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(240): Show |
251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.894-2565delA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20424183 | ||||||
| chr11:20424183 | CAA | C | 13 | a0001c0001t0001g0100 a0001c0001t0001g0103 a0001c0001t0001g0112 others(10): Show |
13 | HG00323.hp1 HG01081.hp2 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.894-2566_894-2565d others(4): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20424183 | ||||||
| chr11:20424262 | T | C | 1 | a0001c0013t0002g0277 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.894-2504T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20424262 | |||||||
| chr11:20424269 | G | GCA | 22 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(19): Show |
22 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.894-2497_894-2496i others(4): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20424269 | |||||||
| chr11:20424270 | T | C | 22 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(19): Show |
22 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.894-2496T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20424270 | |||||||
| chr11:20424270 | T | TAC | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
259 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.894-2495_894-2494d others(4): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20424270 | ||||||
| chr11:20424292 | A | G | 4 | a0001c0001t0004g0065 a0001c0001t0004g0066 a0001c0001t0004g0067 others(1): Show |
4 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.894-2474A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20424292 | |||||||
| chr11:20424300 | C | A | 14 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(11): Show |
14 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.894-2466C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20424300 | |||||||
| chr11:20424352 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.894-2414G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20424352 | |||||||
| chr11:20424364 | G | T | 1 | a0002c0002t0002g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.894-2402G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20424364 | |||||||
| chr11:20424417 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.894-2349A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20424417 | |||||||
| chr11:20424435 | G | A | 1 | a0001c0001t0004g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.894-2331G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20424435 | |||||||
| chr11:20424577 | A | G | 1 | a0001c0001t0002g0016 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.894-2189A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20424577 | |||||||
| chr11:20424632 | T | C | 1 | a0003c0003t0002g0313 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.894-2134T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20424632 | |||||||
| chr11:20424942 | A | G | 14 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(11): Show |
14 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.894-1824A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20424942 | |||||||
| chr11:20425036 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0255 |
2 | HG00544.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.894-1730G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20425036 | |||||||
| chr11:20425045 | G | A | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.894-1721G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20425045 | |||||||
| chr11:20425106 | T | TA | 20 | a0001c0001t0001g0262 a0001c0001t0001g0348 a0001c0001t0002g0335 others(17): Show |
20 | HG02258.hp1 HG02559.hp1 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.894-1644dupA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20425106 | ||||||
| chr11:20425106 | TA | T | 60 | a0001c0001t0001g0140 a0001c0001t0001g0162 a0001c0001t0001g0188 others(57): Show |
60 | HG00544.hp1 HG00639.hp2 HG01074.hp1 others(57): Show |
intron_variant | MODIFIER | c.894-1644delA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr11 | 20425106 | ||||||
| chr11:20425168 | A | G | 1 | a0002c0002t0003g0339 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.894-1598A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20425168 | |||||||
| chr11:20425277 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.894-1489G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20425277 | |||||||
| chr11:20425406 | T | C | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.894-1360T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20425406 | |||||||
| chr11:20425793 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.894-973A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20425793 | |||||||
| chr11:20425798 | C | G | 5 | a0001c0001t0001g0366 a0001c0001t0007g0370 a0001c0005t0001g0367 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.894-968C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20425798 | |||||||
| chr11:20425832 | G | A | 14 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(11): Show |
14 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.894-934G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20425832 | |||||||
| chr11:20425873 | T | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.894-893T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20425873 | |||||||
| chr11:20425909 | G | T | 1 | a0001c0001t0001g0202 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.894-857G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20425909 | |||||||
| chr11:20426060 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.894-706G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20426060 | |||||||
| chr11:20426086 | A | G | 37 | a0001c0001t0001g0348 a0001c0001t0001g0362 a0001c0001t0001g0363 others(34): Show |
37 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.894-680A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20426086 | |||||||
| chr11:20426092 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.894-674T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 9/15 | chr11 | 20426092 | |||||||
| chr11:20426952 | G | C | 14 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(11): Show |
14 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.993+87G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20426952 | |||||||
| chr11:20426985 | G | A | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.993+120G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20426985 | |||||||
| chr11:20427353 | G | C | 2 | a0001c0001t0002g0310 a0001c0001t0002g0323 |
2 | NA18975.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.993+488G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20427353 | |||||||
| chr11:20427398 | A | G | 1 | a0001c0001t0002g0351 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.993+533A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20427398 | |||||||
| chr11:20427417 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.993+552A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20427417 | |||||||
| chr11:20427444 | T | G | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.993+579T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20427444 | |||||||
| chr11:20427449 | G | A | 5 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(2): Show |
5 | HG01884.hp1 HG03130.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.993+584G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20427449 | |||||||
| chr11:20427572 | A | C | 90 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): Show |
95 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.993+707A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20427572 | |||||||
| chr11:20427837 | T | C | 5 | a0001c0001t0004g0062 a0001c0001t0004g0065 a0001c0001t0004g0066 others(2): Show |
5 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.993+972T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20427837 | |||||||
| chr11:20427858 | G | A | 1 | a0002c0002t0003g0339 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.993+993G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20427858 | |||||||
| chr11:20427866 | ATTTT | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.993+1002_993+1005d others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20427866 | |||||||
| chr11:20427891 | T | G | 1 | a0001c0001t0001g0225 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.993+1026T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20427891 | |||||||
| chr11:20427919 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.993+1054T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20427919 | |||||||
| chr11:20428061 | T | C | 50 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0085 others(47): Show |
52 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.993+1196T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20428061 | |||||||
| chr11:20428145 | C | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.993+1280C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20428145 | |||||||
| chr11:20428703 | C | G | 1 | a0001c0001t0002g0353 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.993+1838C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20428703 | |||||||
| chr11:20428729 | C | T | 5 | a0001c0001t0002g0014 a0001c0001t0002g0025 a0001c0001t0002g0027 others(2): Show |
5 | HG02056.hp1 NA18612.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.993+1864C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20428729 | |||||||
| chr11:20428970 | A | T | 85 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(82): Show |
90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.993+2105A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20428970 | |||||||
| chr11:20429180 | T | C | 3 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0260 |
3 | HG00621.hp1 HG04228.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.993+2315T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20429180 | |||||||
| chr11:20429349 | G | A | 1 | a0001c0001t0002g0356 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.993+2484G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20429349 | |||||||
| chr11:20429583 | C | T | 1 | a0001c0013t0002g0277 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.993+2718C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20429583 | |||||||
| chr11:20429625 | A | G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(11): Show |
15 | HG01516.hp1 HG01517.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.993+2760A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20429625 | |||||||
| chr11:20429633 | G | A | 14 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(11): Show |
14 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.993+2768G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20429633 | |||||||
| chr11:20429753 | G | C | 1 | a0001c0001t0001g0097 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.993+2888G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20429753 | |||||||
| chr11:20429785 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.993+2920A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20429785 | |||||||
| chr11:20429902 | A | C | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.993+3037A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20429902 | |||||||
| chr11:20429991 | TAAAC | T | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.993+3130_993+3133d others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20429991 | ||||||
| chr11:20430183 | C | G | 5 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(2): Show |
5 | HG00408.hp1 NA18943.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.993+3318C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20430183 | |||||||
| chr11:20430247 | GA | G | 4 | a0001c0001t0002g0335 a0001c0001t0002g0337 a0002c0002t0005g0334 others(1): Show |
4 | HG02622.hp2 HG02630.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.993+3385delA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20430247 | ||||||
| chr11:20430260 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.993+3395A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20430260 | |||||||
| chr11:20430333 | T | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.993+3468T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20430333 | |||||||
| chr11:20430443 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.993+3578A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20430443 | |||||||
| chr11:20430458 | A | G | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.993+3593A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20430458 | |||||||
| chr11:20430517 | C | T | 23 | a0001c0001t0001g0348 a0001c0001t0002g0335 a0001c0001t0002g0337 others(20): Show |
23 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.993+3652C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20430517 | |||||||
| chr11:20430530 | A | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG00323.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.993+3665A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20430530 | |||||||
| chr11:20430595 | A | C | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.993+3730A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20430595 | |||||||
| chr11:20430745 | C | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.993+3880C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20430745 | |||||||
| chr11:20431081 | G | A | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.993+4216G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20431081 | |||||||
| chr11:20431140 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.993+4275G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20431140 | |||||||
| chr11:20431158 | T | C | 6 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0028 others(3): Show |
6 | HG01106.hp2 HG01192.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.993+4293T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20431158 | |||||||
| chr11:20431376 | G | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(210): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.993+4511G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20431376 | |||||||
| chr11:20431399 | A | G | 1 | a0004c0006t0002g0321 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.993+4534A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20431399 | |||||||
| chr11:20431402 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0200 a0001c0001t0001g0227 |
4 | HG00639.hp1 HG01081.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.993+4537C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20431402 | |||||||
| chr11:20431845 | C | T | 1 | a0001c0001t0004g0066 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.993+4980C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20431845 | |||||||
| chr11:20431913 | G | T | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.993+5048G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20431913 | |||||||
| chr11:20431914 | T | A | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.993+5049T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20431914 | |||||||
| chr11:20431915 | A | C | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.993+5050A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20431915 | |||||||
| chr11:20432188 | A | T | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.993+5323A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20432188 | |||||||
| chr11:20432204 | C | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0174 a0001c0001t0001g0175 |
4 | HG01071.hp2 HG01081.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.993+5339C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20432204 | |||||||
| chr11:20432318 | A | G | 21 | a0001c0001t0002g0335 a0001c0001t0002g0337 a0002c0002t0003g0269 others(18): Show |
21 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.993+5453A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20432318 | |||||||
| chr11:20432350 | A | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0241 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.993+5485A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20432350 | |||||||
| chr11:20432398 | A | G | 2 | a0001c0001t0001g0134 a0001c0001t0001g0138 |
2 | HG02698.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.993+5533A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20432398 | |||||||
| chr11:20432402 | G | T | 1 | a0002c0002t0002g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.993+5537G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20432402 | |||||||
| chr11:20432568 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0200 a0001c0001t0001g0227 |
4 | HG00639.hp1 HG01081.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.993+5703A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20432568 | |||||||
| chr11:20432578 | G | A | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.993+5713G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20432578 | |||||||
| chr11:20432625 | G | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.993+5760G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20432625 | |||||||
| chr11:20432683 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0085 others(91): Show |
96 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.993+5818T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20432683 | |||||||
| chr11:20432697 | C | T | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.993+5832C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20432697 | |||||||
| chr11:20432832 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.993+5967C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20432832 | |||||||
| chr11:20433008 | T | C | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.993+6143T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20433008 | |||||||
| chr11:20433138 | T | G | 1 | a0002c0002t0002g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.993+6273T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20433138 | |||||||
| chr11:20433188 | T | C | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.993+6323T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20433188 | |||||||
| chr11:20433291 | T | C | 4 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0057 others(1): Show |
4 | NA18994.hp1 NA19006.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.993+6426T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20433291 | |||||||
| chr11:20433292 | G | A | 4 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0057 others(1): Show |
4 | NA18994.hp1 NA19006.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.993+6427G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20433292 | |||||||
| chr11:20433294 | G | A | 4 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0057 others(1): Show |
4 | NA18994.hp1 NA19006.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.993+6429G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20433294 | |||||||
| chr11:20433301 | T | C | 4 | a0002c0002t0003g0269 a0002c0002t0003g0270 a0002c0002t0003g0339 others(1): Show |
4 | HG02647.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.993+6436T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20433301 | |||||||
| chr11:20433430 | A | G | 14 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(11): Show |
14 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.993+6565A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20433430 | |||||||
| chr11:20433614 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.993+6749G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20433614 | |||||||
| chr11:20433629 | T | C | 6 | a0001c0001t0002g0353 a0001c0001t0002g0356 a0001c0001t0002g0358 others(3): Show |
6 | HG00735.hp2 HG01243.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.993+6764T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20433629 | |||||||
| chr11:20433646 | G | C | 45 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0174 others(42): Show |
47 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.993+6781G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20433646 | |||||||
| chr11:20433680 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG00099.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.993+6815G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20433680 | |||||||
| chr11:20433690 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.993+6825G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20433690 | |||||||
| chr11:20433711 | C | G | 3 | a0001c0001t0001g0106 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG02886.hp2 NA18970.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.993+6846C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20433711 | |||||||
| chr11:20433935 | T | G | 1 | a0001c0001t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.993+7070T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20433935 | |||||||
| chr11:20433952 | A | G | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.993+7087A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20433952 | |||||||
| chr11:20433955 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.993+7090A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20433955 | |||||||
| chr11:20433957 | A | G | 2 | a0001c0001t0001g0192 a0001c0001t0001g0196 |
2 | HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.993+7092A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20433957 | |||||||
| chr11:20434088 | A | T | 1 | a0001c0001t0001g0225 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.993+7223A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20434088 | |||||||
| chr11:20434369 | CTTTAG | C | 6 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0235 others(3): Show |
6 | HG01106.hp1 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.993+7509_993+7513d others(7): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20434369 | ||||||
| chr11:20434427 | A | G | 180 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
187 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.993+7562A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20434427 | |||||||
| chr11:20434724 | C | T | 1 | a0001c0001t0002g0327 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.993+7859C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20434724 | |||||||
| chr11:20434976 | G | A | 1 | a0001c0001t0002g0328 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.993+8111G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20434976 | |||||||
| chr11:20435037 | A | G | 2 | a0001c0001t0001g0209 a0001c0001t0001g0222 |
2 | NA18989.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.993+8172A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20435037 | |||||||
| chr11:20435211 | G | T | 1 | a0001c0001t0002g0058 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.993+8346G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20435211 | |||||||
| chr11:20435213 | TA | T | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.993+8349delA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20435213 | |||||||
| chr11:20435240 | C | T | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.993+8375C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20435240 | |||||||
| chr11:20435273 | C | T | 1 | a0001c0001t0002g0282 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.993+8408C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20435273 | |||||||
| chr11:20435394 | G | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.993+8529G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20435394 | |||||||
| chr11:20435522 | T | G | 5 | a0002c0002t0003g0272 a0002c0002t0003g0273 a0002c0002t0003g0274 others(2): Show |
5 | HG02572.hp1 HG03041.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.993+8657T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20435522 | |||||||
| chr11:20435539 | T | TTTTG | 22 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(19): Show |
22 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.993+8691_993+8694d others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20435539 | ||||||
| chr11:20435610 | A | G | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.993+8745A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20435610 | |||||||
| chr11:20435858 | C | T | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.993+8993C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20435858 | |||||||
| chr11:20435866 | G | T | 1 | a0001c0001t0002g0042 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.993+9001G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20435866 | |||||||
| chr11:20436027 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.993+9162A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20436027 | |||||||
| chr11:20436195 | C | T | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.993+9330C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20436195 | |||||||
| chr11:20436312 | G | A | 7 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(4): Show |
7 | HG01243.hp2 HG01255.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.993+9447G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20436312 | |||||||
| chr11:20436317 | G | T | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.993+9452G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20436317 | |||||||
| chr11:20436440 | G | T | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(305): Show |
315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.993+9575G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20436440 | |||||||
| chr11:20436740 | G | T | 5 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(2): Show |
5 | HG00408.hp1 NA18943.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.993+9875G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20436740 | |||||||
| chr11:20436797 | A | T | 12 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(9): Show |
12 | HG00099.hp2 HG00280.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.993+9932A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20436797 | |||||||
| chr11:20436892 | A | G | 92 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
97 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.993+10027A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20436892 | |||||||
| chr11:20436952 | G | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.993+10087G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20436952 | |||||||
| chr11:20437384 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.993+10519G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20437384 | |||||||
| chr11:20437398 | T | C | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.993+10533T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20437398 | |||||||
| chr11:20437405 | C | T | 1 | a0002c0002t0003g0346 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.993+10540C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20437405 | |||||||
| chr11:20437460 | T | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.993+10595T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20437460 | |||||||
| chr11:20437596 | G | T | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.993+10731G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20437596 | |||||||
| chr11:20437652 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG00597.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.993+10787C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20437652 | |||||||
| chr11:20437719 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.993+10854A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20437719 | |||||||
| chr11:20437720 | G | T | 1 | a0001c0001t0001g0098 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.993+10855G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20437720 | |||||||
| chr11:20437769 | T | C | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.993+10904T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20437769 | |||||||
| chr11:20437771 | A | G | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.993+10906A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20437771 | |||||||
| chr11:20437808 | C | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0085 others(89): Show |
94 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.993+10943C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20437808 | |||||||
| chr11:20437832 | G | A | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
184 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.993+10967G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20437832 | |||||||
| chr11:20437836 | G | T | 2 | a0002c0002t0003g0333 a0002c0002t0003g0342 |
2 | HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.993+10971G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20437836 | |||||||
| chr11:20437840 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.993+10975C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20437840 | |||||||
| chr11:20437849 | A | C | 1 | a0001c0001t0001g0348 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.993+10984A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20437849 | |||||||
| chr11:20437923 | G | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.993+11058G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20437923 | |||||||
| chr11:20437978 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.993+11113A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20437978 | |||||||
| chr11:20438129 | A | G | 1 | a0003c0003t0002g0320 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.993+11264A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20438129 | |||||||
| chr11:20438157 | A | G | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | NA18970.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.993+11292A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20438157 | |||||||
| chr11:20438178 | A | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG00323.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.993+11313A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20438178 | |||||||
| chr11:20438183 | G | A | 1 | a0001c0001t0001g0348 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.993+11318G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20438183 | |||||||
| chr11:20438206 | CTG | C | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.993+11344_993+1134 others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20438206 | ||||||
| chr11:20438244 | G | A | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.993+11379G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20438244 | |||||||
| chr11:20438345 | ACT | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.993+11483_993+1148 others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20438345 | ||||||
| chr11:20438379 | C | T | 1 | a0002c0002t0003g0341 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.993+11514C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20438379 | |||||||
| chr11:20438404 | A | G | 4 | a0001c0001t0002g0335 a0001c0001t0002g0337 a0002c0002t0005g0334 others(1): Show |
4 | HG02622.hp2 HG02630.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.993+11539A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20438404 | |||||||
| chr11:20438536 | G | T | 1 | a0002c0002t0003g0341 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.993+11671G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20438536 | |||||||
| chr11:20438547 | G | C | 2 | a0001c0001t0001g0185 a0001c0001t0002g0240 |
2 | HG00558.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.993+11682G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20438547 | |||||||
| chr11:20438548 | G | A | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.993+11683G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20438548 | |||||||
| chr11:20438675 | C | G | 3 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG02258.hp2 HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.993+11810C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20438675 | |||||||
| chr11:20438825 | A | G | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.993+11960A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20438825 | |||||||
| chr11:20438833 | G | A | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.993+11968G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20438833 | |||||||
| chr11:20439039 | G | A | 4 | a0001c0001t0002g0291 a0001c0001t0002g0349 a0001c0001t0002g0350 others(1): Show |
4 | NA18954.hp1 NA18973.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.993+12174G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20439039 | |||||||
| chr11:20439076 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.993+12211A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20439076 | |||||||
| chr11:20439318 | T | TC | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(139): Show |
145 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.993+12454dupC | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20439318 | ||||||
| chr11:20439322 | C | G | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.993+12457C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20439322 | |||||||
| chr11:20439585 | C | T | 23 | a0001c0001t0001g0348 a0001c0001t0002g0335 a0001c0001t0002g0337 others(20): Show |
23 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.994-12545C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20439585 | |||||||
| chr11:20439712 | C | G | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.994-12418C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20439712 | |||||||
| chr11:20439737 | G | A | 1 | a0001c0001t0002g0332 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.994-12393G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20439737 | |||||||
| chr11:20439812 | C | G | 5 | a0001c0001t0001g0110 a0001c0001t0004g0065 a0001c0001t0004g0066 others(2): Show |
5 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.994-12318C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20439812 | |||||||
| chr11:20439950 | T | C | 25 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0163 others(22): Show |
25 | HG00735.hp2 HG01243.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.994-12180T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20439950 | |||||||
| chr11:20440079 | T | C | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(315): Show |
325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.994-12051T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20440079 | |||||||
| chr11:20440203 | T | C | 2 | a0002c0002t0003g0272 a0002c0002t0003g0274 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.994-11927T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20440203 | |||||||
| chr11:20440371 | T | C | 48 | a0001c0001t0001g0161 a0001c0001t0002g0013 a0001c0001t0002g0014 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.994-11759T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20440371 | |||||||
| chr11:20440373 | T | C | 51 | a0001c0001t0001g0085 a0001c0001t0001g0161 a0001c0001t0002g0013 others(48): Show |
51 | HG00544.hp1 HG00597.hp2 HG01106.hp2 others(48): Show |
intron_variant | MODIFIER | c.994-11757T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20440373 | |||||||
| chr11:20440374 | G | A | 14 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(11): Show |
14 | HG00544.hp1 HG02056.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.994-11756G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20440374 | |||||||
| chr11:20440417 | G | A | 3 | a0001c0001t0004g0065 a0001c0001t0004g0066 a0001c0001t0004g0371 |
3 | HG02145.hp2 HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.994-11713G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20440417 | |||||||
| chr11:20440428 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.994-11702G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20440428 | |||||||
| chr11:20440461 | C | A | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.994-11669C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20440461 | |||||||
| chr11:20440473 | A | G | 6 | a0001c0001t0001g0192 a0001c0001t0001g0221 a0001c0001t0001g0238 others(3): Show |
6 | HG00735.hp2 HG01071.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.994-11657A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20440473 | |||||||
| chr11:20440483 | A | C | 1 | a0001c0001t0001g0257 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.994-11647A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20440483 | |||||||
| chr11:20440489 | C | CA | 108 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(105): Show |
113 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.994-11620dupA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20440489 | ||||||
| chr11:20440489 | C | CAA | 18 | a0001c0001t0001g0187 a0001c0001t0001g0190 a0001c0001t0001g0194 others(15): Show |
18 | HG00609.hp1 HG00609.hp2 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.994-11621_994-1162 others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20440489 | ||||||
| chr11:20440489 | C | T | 1 | a0001c0001t0002g0319 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.994-11641C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20440489 | |||||||
| chr11:20440489 | CAA | C | 9 | a0001c0001t0001g0167 a0001c0001t0002g0017 a0001c0001t0002g0025 others(6): Show |
9 | HG01255.hp1 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.994-11621_994-1162 others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20440489 | ||||||
| chr11:20440489 | CAAA | C | 44 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(41): Show |
44 | HG00544.hp1 HG01106.hp2 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.994-11622_994-1162 others(7): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20440489 | ||||||
| chr11:20440489 | CAAAAAA | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0086 a0001c0001t0001g0087 others(84): Show |
88 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.994-11625_994-1162 others(10): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20440489 | ||||||
| chr11:20440489 | CAAAAAAA others(1): Show |
C | 46 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(43): Show |
46 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.994-11627_994-1162 others(12): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20440489 | ||||||
| chr11:20440621 | AATG | A | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.994-11501_994-1149 others(7): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20440621 | ||||||
| chr11:20440667 | TCTA | T | 47 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(44): Show |
47 | HG00544.hp1 HG01106.hp2 HG01192.hp2 others(44): Show |
intron_variant | MODIFIER | c.994-11459_994-1145 others(7): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20440667 | ||||||
| chr11:20440732 | A | G | 2 | a0001c0001t0004g0063 a0001c0001t0004g0064 |
2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.994-11398A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20440732 | |||||||
| chr11:20440762 | G | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0199 a0001c0001t0001g0204 others(1): Show |
5 | HG02165.hp1 NA18612.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.994-11368G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20440762 | |||||||
| chr11:20440996 | CT | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(218): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.994-11125delT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20440996 | ||||||
| chr11:20441075 | A | G | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.994-11055A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20441075 | |||||||
| chr11:20441192 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.994-10938C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20441192 | |||||||
| chr11:20441263 | T | TTTTA | 4 | a0001c0001t0001g0132 a0001c0001t0001g0170 a0001c0004t0001g0150 others(1): Show |
4 | HG00597.hp1 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.994-10817_994-1081 others(8): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20441263 | ||||||
| chr11:20441263 | TTTTA | T | 187 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(184): Show |
190 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.994-10817_994-1081 others(8): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20441263 | ||||||
| chr11:20441263 | TTTTATTT others(1): Show |
T | 110 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0068 others(107): Show |
112 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.994-10821_994-1081 others(12): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20441263 | ||||||
| chr11:20441263 | TTTTATTT others(5): Show |
T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0076 a0001c0001t0001g0079 others(12): Show |
16 | HG01928.hp2 HG01952.hp1 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.994-10825_994-1081 others(16): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20441263 | ||||||
| chr11:20441263 | TTTTATTT others(9): Show |
T | 1 | a0001c0001t0001g0142 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.994-10829_994-1081 others(20): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20441263 | ||||||
| chr11:20441301 | TTATTTAT others(9): Show |
T | 4 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(1): Show |
4 | HG01243.hp2 HG01255.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.994-10823_994-1080 others(20): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20441301 | ||||||
| chr11:20441303 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.994-10827A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20441303 | |||||||
| chr11:20441309 | T | A | 1 | a0001c0001t0001g0008 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.994-10821T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20441309 | |||||||
| chr11:20441366 | C | T | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.994-10764C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20441366 | |||||||
| chr11:20441377 | C | T | 1 | a0001c0001t0004g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.994-10753C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20441377 | |||||||
| chr11:20441542 | C | T | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.994-10588C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20441542 | |||||||
| chr11:20441566 | C | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.994-10564C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20441566 | |||||||
| chr11:20441590 | A | C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0085 a0001c0001t0001g0092 others(76): Show |
80 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.994-10540A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20441590 | |||||||
| chr11:20441596 | C | T | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.994-10534C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20441596 | |||||||
| chr11:20441644 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.994-10486A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20441644 | |||||||
| chr11:20441659 | G | A | 1 | a0001c0001t0002g0275 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.994-10471G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20441659 | |||||||
| chr11:20441689 | CTT | C | 22 | a0001c0001t0002g0335 a0001c0001t0002g0337 a0002c0002t0002g0276 others(19): Show |
22 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(19): Show |
intron_variant | MODIFIER | c.994-10439_994-1043 others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20441689 | ||||||
| chr11:20441788 | G | GT | 24 | a0001c0001t0002g0275 a0001c0001t0002g0287 a0001c0001t0002g0335 others(21): Show |
24 | HG01175.hp2 HG02145.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.994-10321dupT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20441788 | ||||||
| chr11:20441788 | G | GTTT | 44 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(41): Show |
44 | HG00544.hp1 HG01123.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.994-10323_994-1032 others(7): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20441788 | ||||||
| chr11:20441788 | GT | G | 29 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(26): Show |
30 | HG01928.hp2 HG01952.hp1 HG01993.hp2 others(27): Show |
intron_variant | MODIFIER | c.994-10321delT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20441788 | ||||||
| chr11:20441789 | T | TG | 6 | a0001c0001t0001g0156 a0001c0001t0001g0232 a0001c0001t0001g0248 others(3): Show |
6 | HG00099.hp2 HG01074.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.994-10341_994-1034 others(5): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20441789 | |||||||
| chr11:20441790 | T | G | 193 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
200 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.994-10340T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20441790 | |||||||
| chr11:20441791 | T | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(17): Show |
21 | HG01928.hp2 HG01952.hp1 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.994-10339T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20441791 | |||||||
| chr11:20442005 | C | G | 14 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(11): Show |
14 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.994-10125C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20442005 | |||||||
| chr11:20442163 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0152 |
2 | NA18965.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.994-9967A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20442163 | |||||||
| chr11:20442230 | A | G | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.994-9900A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20442230 | |||||||
| chr11:20442363 | G | A | 22 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(19): Show |
22 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.994-9767G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20442363 | |||||||
| chr11:20442373 | A | T | 1 | a0002c0002t0002g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.994-9757A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20442373 | |||||||
| chr11:20442381 | T | G | 22 | a0001c0001t0002g0335 a0001c0001t0002g0337 a0002c0002t0002g0276 others(19): Show |
22 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(19): Show |
intron_variant | MODIFIER | c.994-9749T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20442381 | |||||||
| chr11:20442416 | A | G | 1 | a0001c0001t0002g0242 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.994-9714A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20442416 | |||||||
| chr11:20442543 | G | A | 4 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(1): Show |
4 | HG01243.hp2 HG01255.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.994-9587G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20442543 | |||||||
| chr11:20442759 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.994-9371A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20442759 | |||||||
| chr11:20442923 | A | T | 1 | a0001c0001t0002g0361 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.994-9207A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20442923 | |||||||
| chr11:20443016 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.994-9114G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20443016 | |||||||
| chr11:20443428 | T | A | 14 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(11): Show |
15 | HG01516.hp1 HG01517.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.994-8702T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20443428 | |||||||
| chr11:20443473 | G | A | 2 | a0001c0001t0004g0063 a0001c0001t0004g0064 |
2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.994-8657G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20443473 | |||||||
| chr11:20443622 | A | G | 6 | a0001c0001t0002g0036 a0001c0001t0002g0038 a0001c0001t0002g0039 others(3): Show |
6 | HG02015.hp1 NA18948.hp1 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.994-8508A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20443622 | |||||||
| chr11:20444035 | C | T | 5 | a0001c0001t0004g0062 a0001c0001t0004g0065 a0001c0001t0004g0066 others(2): Show |
5 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.994-8095C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20444035 | |||||||
| chr11:20444136 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.994-7994A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20444136 | |||||||
| chr11:20444144 | T | C | 1 | a0001c0001t0002g0240 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.994-7986T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20444144 | |||||||
| chr11:20444152 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.994-7978T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20444152 | |||||||
| chr11:20444212 | A | C | 1 | a0002c0002t0002g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.994-7918A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20444212 | |||||||
| chr11:20444346 | C | T | 1 | a0001c0001t0001g0002 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.994-7784C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20444346 | |||||||
| chr11:20444422 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG00738.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.994-7708G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20444422 | |||||||
| chr11:20444451 | T | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(250): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.994-7679T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20444451 | |||||||
| chr11:20445001 | T | C | 2 | a0001c0001t0001g0104 a0001c0001t0002g0327 |
2 | HG00673.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.994-7129T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20445001 | |||||||
| chr11:20445015 | G | A | 1 | a0010c0011t0001g0234 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.994-7115G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20445015 | |||||||
| chr11:20445080 | AACATAGG others(2): Show |
A | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(218): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.994-7048_994-7040d others(11): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20445080 | ||||||
| chr11:20445094 | G | C | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.994-7036G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20445094 | |||||||
| chr11:20445177 | A | T | 50 | a0001c0001t0001g0206 a0001c0001t0002g0013 a0001c0001t0002g0014 others(47): Show |
50 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(47): Show |
intron_variant | MODIFIER | c.994-6953A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20445177 | |||||||
| chr11:20445738 | C | A | 14 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(11): Show |
15 | HG01516.hp1 HG01517.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.994-6392C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20445738 | |||||||
| chr11:20445900 | A | G | 10 | a0001c0001t0002g0332 a0001c0001t0002g0353 a0001c0001t0002g0354 others(7): Show |
10 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.994-6230A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20445900 | |||||||
| chr11:20445925 | T | A | 3 | a0001c0001t0001g0213 a0001c0001t0001g0223 a0001c0001t0001g0243 |
3 | HG00639.hp2 HG03654.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.994-6205T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20445925 | |||||||
| chr11:20446015 | T | G | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.994-6115T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20446015 | |||||||
| chr11:20446031 | G | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0123 |
2 | HG00558.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.994-6099G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20446031 | |||||||
| chr11:20446127 | G | T | 1 | a0001c0001t0001g0212 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.994-6003G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20446127 | |||||||
| chr11:20446307 | G | A | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.994-5823G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20446307 | |||||||
| chr11:20446355 | CT | C | 367 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(364): Show |
375 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(372): Show |
intron_variant | MODIFIER | c.994-5763delT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20446355 | ||||||
| chr11:20446383 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.994-5747T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20446383 | |||||||
| chr11:20446415 | A | T | 1 | a0001c0001t0001g0085 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.994-5715A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20446415 | |||||||
| chr11:20446434 | A | G | 32 | a0001c0001t0002g0332 a0001c0001t0002g0335 a0001c0001t0002g0337 others(29): Show |
32 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.994-5696A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20446434 | |||||||
| chr11:20446564 | A | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0241 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.994-5566A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20446564 | |||||||
| chr11:20446726 | A | G | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.994-5404A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20446726 | |||||||
| chr11:20446774 | C | A | 1 | a0001c0001t0001g0002 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.994-5356C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20446774 | |||||||
| chr11:20446836 | T | C | 2 | a0001c0001t0001g0229 a0001c0001t0001g0232 |
2 | HG03927.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.994-5294T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20446836 | |||||||
| chr11:20447002 | G | A | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.994-5128G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20447002 | |||||||
| chr11:20447161 | T | C | 1 | a0001c0001t0002g0279 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.994-4969T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20447161 | |||||||
| chr11:20447246 | A | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.994-4884A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20447246 | |||||||
| chr11:20447287 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.994-4843T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20447287 | |||||||
| chr11:20447338 | T | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.994-4792T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20447338 | |||||||
| chr11:20447458 | A | G | 5 | a0001c0001t0002g0291 a0001c0001t0002g0323 a0001c0001t0002g0349 others(2): Show |
5 | NA18954.hp1 NA18973.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.994-4672A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20447458 | |||||||
| chr11:20447726 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0138 |
2 | HG02698.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.994-4404C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20447726 | |||||||
| chr11:20447814 | A | G | 11 | a0001c0001t0001g0007 a0001c0001t0001g0182 a0001c0001t0001g0183 others(8): Show |
12 | HG00738.hp2 HG02071.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.994-4316A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20447814 | |||||||
| chr11:20448010 | G | T | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(306): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.994-4120G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20448010 | |||||||
| chr11:20448146 | AT | A | 86 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(83): Show |
91 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.994-3974delT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20448146 | ||||||
| chr11:20448201 | G | T | 48 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(45): Show |
48 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.994-3929G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20448201 | |||||||
| chr11:20448205 | T | G | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.994-3925T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20448205 | |||||||
| chr11:20448256 | A | C | 1 | a0001c0001t0001g0096 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.994-3874A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20448256 | |||||||
| chr11:20448596 | T | C | 97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0085 others(94): Show |
99 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.994-3534T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20448596 | |||||||
| chr11:20448783 | A | T | 1 | a0001c0001t0001g0191 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.994-3347A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20448783 | |||||||
| chr11:20448793 | A | G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(11): Show |
15 | HG01516.hp1 HG01517.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.994-3337A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20448793 | |||||||
| chr11:20448976 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.994-3154G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20448976 | |||||||
| chr11:20449018 | C | G | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.994-3112C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20449018 | |||||||
| chr11:20449050 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.994-3080T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20449050 | |||||||
| chr11:20449132 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.994-2998C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20449132 | |||||||
| chr11:20449215 | T | C | 1 | a0002c0002t0003g0336 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.994-2915T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20449215 | |||||||
| chr11:20449426 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.994-2704A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20449426 | |||||||
| chr11:20449436 | A | G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(11): Show |
15 | HG01516.hp1 HG01517.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.994-2694A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20449436 | |||||||
| chr11:20449479 | C | T | 32 | a0001c0001t0002g0332 a0001c0001t0002g0335 a0001c0001t0002g0337 others(29): Show |
32 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.994-2651C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20449479 | |||||||
| chr11:20449660 | C | T | 3 | a0001c0001t0001g0180 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02683.hp1 HG03490.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.994-2470C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20449660 | |||||||
| chr11:20449771 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.994-2359T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20449771 | |||||||
| chr11:20449772 | A | T | 1 | a0001c0001t0001g0115 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.994-2358A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20449772 | |||||||
| chr11:20449773 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.994-2357T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20449773 | |||||||
| chr11:20449799 | T | A | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.994-2331T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20449799 | |||||||
| chr11:20449829 | A | G | 3 | a0001c0001t0001g0110 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG02647.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.994-2301A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20449829 | |||||||
| chr11:20449955 | A | G | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.994-2175A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20449955 | |||||||
| chr11:20450182 | A | G | 3 | a0001c0001t0002g0354 a0001c0001t0002g0355 a0001c0001t0002g0357 |
3 | HG02145.hp1 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.994-1948A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20450182 | |||||||
| chr11:20450190 | T | G | 22 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(19): Show |
22 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.994-1940T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20450190 | |||||||
| chr11:20450193 | A | T | 1 | a0001c0001t0001g0115 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.994-1937A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20450193 | |||||||
| chr11:20450293 | C | T | 1 | a0002c0002t0002g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.994-1837C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20450293 | |||||||
| chr11:20450355 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.994-1775A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20450355 | |||||||
| chr11:20450376 | A | G | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.994-1754A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20450376 | |||||||
| chr11:20450387 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.994-1743T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20450387 | |||||||
| chr11:20450404 | C | A | 1 | a0001c0001t0007g0370 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.994-1726C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20450404 | |||||||
| chr11:20450564 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.994-1566T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20450564 | |||||||
| chr11:20450571 | T | C | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.994-1559T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20450571 | |||||||
| chr11:20450637 | A | G | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | NA18943.hp1 NA18949.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.994-1493A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20450637 | |||||||
| chr11:20450672 | G | A | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.994-1458G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20450672 | |||||||
| chr11:20450696 | T | C | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0085 others(82): Show |
87 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.994-1434T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20450696 | |||||||
| chr11:20451080 | A | G | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG01071.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.994-1050A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20451080 | |||||||
| chr11:20451310 | A | T | 1 | a0001c0001t0001g0115 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.994-820A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20451310 | |||||||
| chr11:20451456 | A | C | 1 | a0001c0001t0002g0312 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.994-674A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20451456 | |||||||
| chr11:20451494 | G | GT | 9 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(6): Show |
9 | HG00323.hp1 HG01884.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.994-625dupT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr11 | 20451494 | ||||||
| chr11:20451501 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.994-629T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20451501 | |||||||
| chr11:20451517 | G | C | 22 | a0001c0001t0002g0335 a0001c0001t0002g0337 a0002c0002t0002g0276 others(19): Show |
22 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(19): Show |
intron_variant | MODIFIER | c.994-613G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20451517 | |||||||
| chr11:20451636 | T | C | 1 | a0001c0001t0002g0032 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.994-494T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20451636 | |||||||
| chr11:20451872 | G | T | 5 | a0001c0001t0001g0366 a0001c0001t0007g0370 a0001c0005t0001g0367 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.994-258G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20451872 | |||||||
| chr11:20452034 | T | G | 1 | a0001c0001t0001g0366 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.994-96T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20452034 | |||||||
| chr11:20452058 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.994-72G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20452058 | |||||||
| chr11:20452109 | T | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(218): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.994-21T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 10/15 | chr11 | 20452109 | |||||||
| chr11:20452313 | G | C | 1 | a0001c0001t0001g0262 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1072+105G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20452313 | |||||||
| chr11:20452564 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1072+356A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20452564 | |||||||
| chr11:20452571 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1072+363A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20452571 | |||||||
| chr11:20452769 | C | T | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1072+561C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20452769 | |||||||
| chr11:20452774 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1072+566C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20452774 | |||||||
| chr11:20452781 | A | G | 20 | a0001c0001t0002g0335 a0001c0001t0002g0337 a0002c0002t0003g0269 others(17): Show |
20 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.1072+573A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20452781 | |||||||
| chr11:20453219 | G | A | 1 | a0001c0001t0001g0366 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1072+1011G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20453219 | |||||||
| chr11:20453318 | T | TA | 20 | a0001c0001t0001g0071 a0001c0001t0001g0075 a0001c0001t0001g0093 others(17): Show |
20 | HG01123.hp2 HG01167.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1072+1132dupA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr11 | 20453318 | ||||||
| chr11:20453318 | T | TAA | 17 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(14): Show |
17 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(14): Show |
intron_variant | MODIFIER | c.1072+1131_1072+113 others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr11 | 20453318 | ||||||
| chr11:20453318 | TA | T | 61 | a0001c0001t0001g0128 a0001c0001t0001g0218 a0001c0001t0001g0227 others(58): Show |
61 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(58): Show |
intron_variant | MODIFIER | c.1072+1132delA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr11 | 20453318 | ||||||
| chr11:20453386 | A | G | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1072+1178A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20453386 | |||||||
| chr11:20453482 | A | G | 52 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(49): Show |
52 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.1072+1274A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20453482 | |||||||
| chr11:20453889 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1072+1681T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20453889 | |||||||
| chr11:20453974 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1072+1766C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20453974 | |||||||
| chr11:20454003 | A | G | 1 | a0002c0002t0002g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1072+1795A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20454003 | |||||||
| chr11:20454014 | C | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
206 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.1072+1806C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20454014 | |||||||
| chr11:20454189 | C | G | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
195 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1072+1981C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20454189 | |||||||
| chr11:20454316 | A | G | 2 | a0001c0001t0001g0259 a0001c0001t0001g0268 |
2 | HG00099.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.1072+2108A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20454316 | |||||||
| chr11:20454417 | A | G | 1 | a0002c0002t0002g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1072+2209A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20454417 | |||||||
| chr11:20454562 | A | G | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1072+2354A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20454562 | |||||||
| chr11:20454567 | A | G | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1072+2359A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20454567 | |||||||
| chr11:20454637 | G | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(9): Show |
13 | HG01243.hp1 HG01928.hp2 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.1072+2429G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20454637 | |||||||
| chr11:20455328 | C | G | 5 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1072+3120C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20455328 | |||||||
| chr11:20455364 | G | A | 1 | a0001c0001t0002g0032 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1072+3156G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20455364 | |||||||
| chr11:20455882 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1072+3674A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20455882 | |||||||
| chr11:20456093 | C | G | 1 | a0001c0001t0002g0353 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1072+3885C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20456093 | |||||||
| chr11:20456300 | TAAG | T | 3 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 |
3 | HG02486.hp1 HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1072+4095_1072+409 others(7): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr11 | 20456300 | ||||||
| chr11:20456763 | G | T | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1072+4555G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20456763 | |||||||
| chr11:20456828 | G | A | 50 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0174 others(47): Show |
52 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1072+4620G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20456828 | |||||||
| chr11:20457074 | G | C | 1 | a0002c0002t0002g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1072+4866G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20457074 | |||||||
| chr11:20457130 | G | A | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(305): Show |
315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.1073-4850G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20457130 | |||||||
| chr11:20457369 | T | A | 1 | a0001c0001t0001g0221 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1073-4611T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20457369 | |||||||
| chr11:20457511 | A | G | 1 | a0002c0002t0003g0336 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1073-4469A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20457511 | |||||||
| chr11:20457546 | C | G | 2 | a0001c0001t0002g0359 a0001c0001t0002g0361 |
2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1073-4434C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20457546 | |||||||
| chr11:20457796 | A | C | 5 | a0001c0001t0001g0119 a0001c0001t0001g0362 a0001c0001t0001g0363 others(2): Show |
5 | HG01243.hp2 HG01255.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1073-4184A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20457796 | |||||||
| chr11:20458003 | C | T | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1073-3977C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20458003 | |||||||
| chr11:20458253 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1073-3727A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20458253 | |||||||
| chr11:20458494 | C | T | 1 | a0001c0001t0002g0029 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1073-3486C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20458494 | |||||||
| chr11:20458778 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1073-3202T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20458778 | |||||||
| chr11:20459013 | AT | A | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.1073-2959delT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr11 | 20459013 | ||||||
| chr11:20459163 | G | C | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1073-2817G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20459163 | |||||||
| chr11:20459179 | GGGCCATA | G | 4 | a0001c0001t0002g0014 a0001c0001t0002g0025 a0001c0001t0002g0027 others(1): Show |
4 | NA18612.hp2 NA18969.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.1073-2799_1073-279 others(11): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr11 | 20459179 | ||||||
| chr11:20459230 | C | A | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1073-2750C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20459230 | |||||||
| chr11:20459250 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1073-2730T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20459250 | |||||||
| chr11:20459563 | T | A | 55 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0098 others(52): Show |
56 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.1073-2417T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20459563 | |||||||
| chr11:20459653 | G | A | 1 | a0001c0001t0002g0291 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1073-2327G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20459653 | |||||||
| chr11:20459705 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1073-2275G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20459705 | |||||||
| chr11:20459783 | G | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(274): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.1073-2197G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20459783 | |||||||
| chr11:20459851 | A | G | 2 | a0001c0001t0001g0246 a0001c0001t0001g0252 |
2 | HG01258.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1073-2129A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20459851 | |||||||
| chr11:20460059 | A | G | 32 | a0001c0001t0002g0332 a0001c0001t0002g0335 a0001c0001t0002g0337 others(29): Show |
32 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.1073-1921A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20460059 | |||||||
| chr11:20460102 | T | C | 21 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(18): Show |
21 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.1073-1878T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20460102 | |||||||
| chr11:20460177 | C | T | 2 | a0001c0001t0001g0185 a0001c0001t0002g0240 |
2 | HG00558.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.1073-1803C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20460177 | |||||||
| chr11:20460298 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(217): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.1073-1682T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20460298 | |||||||
| chr11:20460300 | A | T | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1073-1680A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20460300 | |||||||
| chr11:20460406 | C | G | 32 | a0001c0001t0002g0332 a0001c0001t0002g0335 a0001c0001t0002g0337 others(29): Show |
32 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.1073-1574C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20460406 | |||||||
| chr11:20460461 | ACTTAC | A | 4 | a0001c0001t0002g0358 a0001c0001t0002g0359 a0001c0001t0002g0360 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1073-1515_1073-151 others(9): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr11 | 20460461 | ||||||
| chr11:20460553 | C | G | 89 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(86): Show |
94 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.1073-1427C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20460553 | |||||||
| chr11:20460670 | TTTTA | T | 47 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(44): Show |
47 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.1073-1306_1073-130 others(8): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr11 | 20460670 | ||||||
| chr11:20460724 | C | T | 47 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(44): Show |
47 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.1073-1256C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20460724 | |||||||
| chr11:20460842 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1073-1138A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20460842 | |||||||
| chr11:20460877 | T | G | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(219): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1073-1103T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20460877 | |||||||
| chr11:20460882 | T | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
10 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.1073-1098T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20460882 | |||||||
| chr11:20460886 | A | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
10 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.1073-1094A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20460886 | |||||||
| chr11:20460908 | C | T | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1073-1072C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20460908 | |||||||
| chr11:20461017 | C | A | 22 | a0001c0001t0002g0335 a0001c0001t0002g0337 a0002c0002t0002g0276 others(19): Show |
22 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(19): Show |
intron_variant | MODIFIER | c.1073-963C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20461017 | |||||||
| chr11:20461255 | C | G | 54 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0098 others(51): Show |
55 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.1073-725C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20461255 | |||||||
| chr11:20461561 | C | A | 4 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0364 others(1): Show |
4 | HG01243.hp2 HG01255.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1073-419C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20461561 | |||||||
| chr11:20461702 | T | C | 4 | a0001c0001t0004g0065 a0001c0001t0004g0066 a0001c0001t0004g0067 others(1): Show |
4 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1073-278T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20461702 | |||||||
| chr11:20461719 | T | C | 4 | a0001c0001t0004g0065 a0001c0001t0004g0066 a0001c0001t0004g0067 others(1): Show |
4 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1073-261T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 11/15 | chr11 | 20461719 | |||||||
| chr11:20462202 | T | C | 89 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(86): Show |
94 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.1260+35T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20462202 | |||||||
| chr11:20462430 | T | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(219): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1260+263T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20462430 | |||||||
| chr11:20462497 | C | T | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1260+330C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20462497 | |||||||
| chr11:20462537 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1260+370G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20462537 | |||||||
| chr11:20462586 | G | A | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1260+419G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20462586 | |||||||
| chr11:20462588 | G | T | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1260+421G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20462588 | |||||||
| chr11:20462596 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1260+429A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20462596 | |||||||
| chr11:20462598 | T | G | 2 | a0001c0001t0002g0020 a0001c0001t0002g0047 |
2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1260+431T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20462598 | |||||||
| chr11:20462616 | A | G | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1260+449A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20462616 | |||||||
| chr11:20462776 | C | T | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(306): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.1260+609C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20462776 | |||||||
| chr11:20462920 | C | CA | 21 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(18): Show |
22 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.1260+754dupA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr11 | 20462920 | ||||||
| chr11:20462924 | G | A | 45 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0017 others(42): Show |
45 | HG01106.hp2 HG01123.hp1 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.1260+757G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20462924 | |||||||
| chr11:20462930 | A | G | 1 | a0001c0001t0002g0372 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1260+763A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20462930 | |||||||
| chr11:20463008 | G | A | 21 | a0001c0001t0002g0335 a0001c0001t0002g0337 a0002c0002t0003g0269 others(18): Show |
21 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.1260+841G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20463008 | |||||||
| chr11:20463067 | T | C | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1260+900T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20463067 | |||||||
| chr11:20463101 | T | G | 7 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(4): Show |
7 | HG02055.hp1 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1260+934T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20463101 | |||||||
| chr11:20463174 | A | G | 1 | a0001c0001t0002g0312 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1260+1007A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20463174 | |||||||
| chr11:20463340 | C | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG01071.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1261-1120C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20463340 | |||||||
| chr11:20463377 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1261-1083T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20463377 | |||||||
| chr11:20463574 | CT | C | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(291): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1261-873delT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr11 | 20463574 | ||||||
| chr11:20463574 | CTT | C | 11 | a0001c0001t0001g0229 a0001c0001t0001g0232 a0001c0001t0002g0059 others(8): Show |
11 | HG01496.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1261-874_1261-873d others(4): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr11 | 20463574 | ||||||
| chr11:20463606 | T | TA | 10 | a0001c0001t0002g0332 a0001c0001t0002g0353 a0001c0001t0002g0354 others(7): Show |
10 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1261-853dupA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr11 | 20463606 | ||||||
| chr11:20463624 | C | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1261-836C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20463624 | |||||||
| chr11:20463651 | G | T | 1 | a0001c0001t0001g0075 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1261-809G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20463651 | |||||||
| chr11:20463830 | A | G | 1 | a0002c0002t0003g0347 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1261-630A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20463830 | |||||||
| chr11:20463854 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1261-606C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20463854 | |||||||
| chr11:20463884 | T | G | 48 | a0001c0001t0001g0187 a0001c0001t0002g0013 a0001c0001t0002g0014 others(45): Show |
48 | HG00544.hp1 HG00609.hp1 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.1261-576T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20463884 | |||||||
| chr11:20463898 | GA | G | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(271): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.1261-559delA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr11 | 20463898 | ||||||
| chr11:20463942 | T | A | 1 | a0001c0001t0002g0296 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1261-518T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20463942 | |||||||
| chr11:20463990 | A | G | 1 | a0002c0002t0003g0272 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1261-470A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20463990 | |||||||
| chr11:20464011 | A | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
193 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1261-449A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20464011 | |||||||
| chr11:20464098 | G | A | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.1261-362G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20464098 | |||||||
| chr11:20464352 | G | A | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1261-108G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20464352 | |||||||
| chr11:20464401 | G | GT | 13 | a0001c0001t0001g0151 a0001c0001t0001g0186 a0001c0001t0002g0050 others(10): Show |
13 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1261-47dupT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr11 | 20464401 | ||||||
| chr11:20464412 | T | G | 1 | a0001c0001t0002g0023 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1261-48T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 12/15 | chr11 | 20464412 | |||||||
| chr11:20464847 | A | G | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1347+301A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20464847 | |||||||
| chr11:20464855 | A | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(206): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1347+309A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20464855 | |||||||
| chr11:20464912 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0241 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1347+366G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20464912 | |||||||
| chr11:20465094 | C | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG02257.hp2 HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1347+548C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20465094 | |||||||
| chr11:20465191 | G | A | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.1347+645G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20465191 | |||||||
| chr11:20465213 | A | G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.1347+667A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20465213 | |||||||
| chr11:20465517 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1347+971T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20465517 | |||||||
| chr11:20465907 | G | A | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(306): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.1347+1361G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20465907 | |||||||
| chr11:20466023 | C | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(217): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1347+1477C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20466023 | |||||||
| chr11:20466188 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0200 a0001c0001t0001g0233 |
4 | HG00639.hp1 HG01081.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1347+1642G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20466188 | |||||||
| chr11:20466196 | T | G | 1 | a0001c0001t0002g0350 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1347+1650T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20466196 | |||||||
| chr11:20466265 | A | T | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(306): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.1347+1719A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20466265 | |||||||
| chr11:20466338 | T | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(215): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1347+1792T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20466338 | |||||||
| chr11:20466652 | G | A | 1 | a0001c0001t0002g0054 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1347+2106G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20466652 | |||||||
| chr11:20466690 | A | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(215): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1347+2144A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20466690 | |||||||
| chr11:20466895 | GAA | G | 21 | a0001c0001t0002g0335 a0001c0001t0002g0337 a0002c0002t0003g0269 others(18): Show |
21 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.1347+2353_1347+235 others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20466895 | ||||||
| chr11:20466907 | A | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(204): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1347+2361A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20466907 | |||||||
| chr11:20466968 | G | A | 4 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(1): Show |
4 | HG01928.hp2 HG01952.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1347+2422G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20466968 | |||||||
| chr11:20467132 | C | T | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1347+2586C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20467132 | |||||||
| chr11:20467186 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1347+2640T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20467186 | |||||||
| chr11:20467231 | A | G | 3 | a0001c0001t0001g0172 a0001c0001t0001g0215 a0001c0001t0001g0231 |
3 | NA18975.hp1 NA19004.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1347+2685A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20467231 | |||||||
| chr11:20467473 | T | TA | 22 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(19): Show |
22 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.1347+2928dupA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20467473 | ||||||
| chr11:20467492 | G | C | 2 | a0001c0001t0001g0151 a0001c0001t0001g0267 |
2 | NA18946.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.1347+2946G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20467492 | |||||||
| chr11:20467627 | TA | T | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(306): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.1347+3083delA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20467627 | ||||||
| chr11:20467657 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0230 |
2 | HG00323.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.1347+3111G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20467657 | |||||||
| chr11:20467775 | A | T | 2 | a0002c0002t0003g0343 a0002c0002t0003g0344 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1347+3229A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20467775 | |||||||
| chr11:20467803 | C | T | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1347+3257C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20467803 | |||||||
| chr11:20467976 | A | T | 1 | a0001c0001t0001g0225 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1347+3430A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20467976 | |||||||
| chr11:20468049 | G | A | 21 | a0001c0001t0002g0335 a0001c0001t0002g0337 a0002c0002t0003g0269 others(18): Show |
21 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.1347+3503G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20468049 | |||||||
| chr11:20468360 | TTTTG | T | 3 | a0001c0001t0001g0252 a0001c0001t0002g0059 a0001c0001t0002g0060 |
3 | HG01258.hp2 HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1347+3834_1347+383 others(8): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20468360 | ||||||
| chr11:20468360 | TTTTGTTT others(1): Show |
T | 3 | a0001c0001t0001g0213 a0001c0001t0001g0223 a0001c0001t0001g0243 |
3 | HG00639.hp2 HG03654.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1347+3830_1347+383 others(12): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20468360 | ||||||
| chr11:20468377 | T | A | 4 | a0001c0001t0002g0358 a0001c0001t0002g0359 a0001c0001t0002g0360 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347+3831T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20468377 | |||||||
| chr11:20468455 | G | A | 47 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(44): Show |
47 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.1347+3909G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20468455 | |||||||
| chr11:20468518 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1347+3972G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20468518 | |||||||
| chr11:20468654 | C | A | 22 | a0001c0001t0002g0335 a0001c0001t0002g0337 a0002c0002t0002g0276 others(19): Show |
22 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(19): Show |
intron_variant | MODIFIER | c.1347+4108C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20468654 | |||||||
| chr11:20468656 | A | G | 31 | a0001c0001t0002g0335 a0001c0001t0002g0337 a0001c0001t0002g0353 others(28): Show |
31 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.1347+4110A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20468656 | |||||||
| chr11:20468818 | T | A | 1 | a0001c0001t0001g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1347+4272T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20468818 | |||||||
| chr11:20468819 | A | T | 1 | a0001c0001t0001g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1347+4273A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20468819 | |||||||
| chr11:20468821 | C | T | 3 | a0001c0001t0001g0180 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02683.hp1 HG03490.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1347+4275C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20468821 | |||||||
| chr11:20468924 | G | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG00323.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1347+4378G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20468924 | |||||||
| chr11:20468993 | G | GTCTTGAA | 4 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0033 others(1): Show |
4 | HG01106.hp2 HG01192.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347+4457_1347+446 others(11): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20468993 | ||||||
| chr11:20469158 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1347+4612A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20469158 | |||||||
| chr11:20469247 | G | A | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1347+4701G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20469247 | |||||||
| chr11:20469280 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1347+4734A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20469280 | |||||||
| chr11:20469334 | C | A | 1 | a0001c0001t0001g0227 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1347+4788C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20469334 | |||||||
| chr11:20469347 | T | G | 1 | a0001c0013t0002g0277 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1347+4801T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20469347 | |||||||
| chr11:20469473 | G | T | 1 | a0001c0001t0001g0114 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1347+4927G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20469473 | |||||||
| chr11:20469540 | C | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1347+4994C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20469540 | |||||||
| chr11:20469636 | A | C | 1 | a0001c0001t0002g0035 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1347+5090A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20469636 | |||||||
| chr11:20469708 | T | G | 1 | a0001c0001t0002g0308 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1347+5162T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20469708 | |||||||
| chr11:20469813 | C | CTT | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1347+5270_1347+527 others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20469813 | ||||||
| chr11:20470184 | A | G | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1347+5638A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20470184 | |||||||
| chr11:20470272 | G | A | 15 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(12): Show |
15 | HG00544.hp2 HG00673.hp2 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.1347+5726G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20470272 | |||||||
| chr11:20470380 | C | T | 21 | a0001c0001t0002g0335 a0001c0001t0002g0337 a0002c0002t0002g0276 others(18): Show |
21 | HG02258.hp1 HG02559.hp2 HG02622.hp2 others(18): Show |
intron_variant | MODIFIER | c.1347+5834C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20470380 | |||||||
| chr11:20470509 | G | A | 2 | a0001c0001t0004g0063 a0001c0001t0004g0064 |
2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1347+5963G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20470509 | |||||||
| chr11:20470585 | A | G | 48 | a0001c0001t0001g0187 a0001c0001t0002g0013 a0001c0001t0002g0014 others(45): Show |
48 | HG00544.hp1 HG00609.hp1 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.1347+6039A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20470585 | |||||||
| chr11:20470595 | A | G | 1 | a0002c0002t0002g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1347+6049A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20470595 | |||||||
| chr11:20470763 | A | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0085 a0001c0001t0001g0092 others(84): Show |
88 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.1347+6217A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20470763 | |||||||
| chr11:20470871 | C | T | 10 | a0001c0001t0002g0332 a0001c0001t0002g0353 a0001c0001t0002g0354 others(7): Show |
10 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1347+6325C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20470871 | |||||||
| chr11:20470984 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1347+6438T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20470984 | |||||||
| chr11:20471310 | T | C | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1347+6764T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20471310 | |||||||
| chr11:20471443 | G | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(215): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1347+6897G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20471443 | |||||||
| chr11:20471498 | G | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG00597.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1347+6952G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20471498 | |||||||
| chr11:20471527 | T | C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1347+6981T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20471527 | |||||||
| chr11:20471555 | C | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0115 a0001c0001t0002g0278 others(10): Show |
14 | HG01175.hp2 HG01981.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.1347+7009C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20471555 | |||||||
| chr11:20471556 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1347+7010G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20471556 | |||||||
| chr11:20471594 | ATGCTGTT others(8): Show |
A | 1 | a0002c0002t0005g0338 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1347+7051_1347+706 others(19): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20471594 | ||||||
| chr11:20471611 | G | A | 1 | a0002c0002t0005g0338 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1347+7065G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20471611 | |||||||
| chr11:20471769 | T | C | 51 | a0001c0001t0001g0006 a0001c0001t0001g0107 a0001c0001t0001g0200 others(48): Show |
52 | HG00544.hp1 HG00639.hp1 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.1347+7223T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20471769 | |||||||
| chr11:20471853 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1347+7307T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20471853 | |||||||
| chr11:20471924 | G | A | 4 | a0001c0001t0007g0370 a0001c0005t0001g0367 a0001c0005t0001g0368 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1347+7378G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20471924 | |||||||
| chr11:20471943 | A | AT | 11 | a0001c0001t0002g0332 a0001c0001t0002g0353 a0001c0001t0002g0354 others(8): Show |
11 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1347+7406dupT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20471943 | ||||||
| chr11:20472052 | G | A | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(306): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.1347+7506G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20472052 | |||||||
| chr11:20472313 | T | G | 36 | a0001c0001t0001g0075 a0001c0001t0002g0332 a0001c0001t0002g0335 others(33): Show |
36 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(33): Show |
intron_variant | MODIFIER | c.1347+7767T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20472313 | |||||||
| chr11:20472328 | C | CTG | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1347+7785_1347+778 others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20472328 | ||||||
| chr11:20472377 | A | C | 2 | a0001c0001t0001g0244 a0001c0001t0001g0255 |
2 | HG00544.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.1347+7831A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20472377 | |||||||
| chr11:20472574 | A | G | 15 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(12): Show |
15 | HG00544.hp2 HG00673.hp2 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.1347+8028A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20472574 | |||||||
| chr11:20472578 | T | G | 11 | a0001c0001t0001g0075 a0001c0001t0002g0332 a0001c0001t0002g0353 others(8): Show |
11 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1347+8032T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20472578 | |||||||
| chr11:20472586 | A | T | 1 | a0001c0001t0004g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1347+8040A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20472586 | |||||||
| chr11:20472617 | TTGGCCTG others(34): Show |
T | 51 | a0001c0001t0001g0006 a0001c0001t0001g0179 a0001c0001t0001g0200 others(48): Show |
52 | HG00544.hp1 HG00639.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.1347+8083_1347+812 others(45): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20472617 | ||||||
| chr11:20472658 | C | T | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(255): Show |
264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.1347+8112C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20472658 | |||||||
| chr11:20472691 | T | C | 50 | a0001c0001t0001g0006 a0001c0001t0001g0200 a0001c0001t0001g0233 others(47): Show |
51 | HG00544.hp1 HG00639.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.1347+8145T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20472691 | |||||||
| chr11:20472714 | A | C | 1 | a0001c0001t0001g0252 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1347+8168A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20472714 | |||||||
| chr11:20472831 | G | A | 1 | a0001c0001t0001g0366 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1347+8285G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20472831 | |||||||
| chr11:20472867 | G | C | 3 | a0001c0001t0001g0110 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG02647.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1347+8321G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20472867 | |||||||
| chr11:20472869 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1347+8323G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20472869 | |||||||
| chr11:20472900 | A | G | 4 | a0001c0001t0002g0291 a0001c0001t0002g0349 a0001c0001t0002g0350 others(1): Show |
4 | NA18954.hp1 NA18973.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347+8354A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20472900 | |||||||
| chr11:20473131 | C | A | 50 | a0001c0001t0001g0006 a0001c0001t0001g0200 a0001c0001t0001g0233 others(47): Show |
51 | HG00544.hp1 HG00639.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.1347+8585C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20473131 | |||||||
| chr11:20473157 | G | A | 2 | a0001c0005t0001g0367 a0001c0005t0001g0369 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1347+8611G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20473157 | |||||||
| chr11:20473172 | A | G | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0004g0062 others(6): Show |
9 | HG00099.hp1 HG01496.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1347+8626A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20473172 | |||||||
| chr11:20473223 | A | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(21): Show |
25 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1347+8677A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20473223 | |||||||
| chr11:20473259 | T | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(194): Show |
202 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.1347+8713T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20473259 | |||||||
| chr11:20473276 | G | T | 1 | a0003c0003t0002g0325 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1347+8730G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20473276 | |||||||
| chr11:20473302 | G | A | 10 | a0001c0001t0002g0332 a0001c0001t0002g0353 a0001c0001t0002g0354 others(7): Show |
10 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1347+8756G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20473302 | |||||||
| chr11:20473395 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG01192.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1347+8849C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20473395 | |||||||
| chr11:20473505 | G | C | 201 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
206 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.1347+8959G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20473505 | |||||||
| chr11:20473683 | G | A | 204 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(201): Show |
209 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.1347+9137G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20473683 | |||||||
| chr11:20473751 | TCTCAGCC others(12): Show |
T | 1 | a0001c0001t0002g0354 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1347+9221_1347+923 others(23): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20473751 | ||||||
| chr11:20473859 | G | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
199 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.1347+9313G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20473859 | |||||||
| chr11:20473936 | C | T | 50 | a0001c0001t0001g0006 a0001c0001t0001g0200 a0001c0001t0001g0233 others(47): Show |
51 | HG00544.hp1 HG00639.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.1347+9390C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20473936 | |||||||
| chr11:20474178 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1347+9632C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20474178 | |||||||
| chr11:20474335 | A | C | 204 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(201): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1347+9789A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20474335 | |||||||
| chr11:20474357 | CCT | C | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1347+9816_1347+981 others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20474357 | ||||||
| chr11:20474408 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG00099.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1347+9862G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20474408 | |||||||
| chr11:20474515 | C | A | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1347+9969C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20474515 | |||||||
| chr11:20474727 | C | T | 1 | a0001c0001t0002g0317 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1347+10181C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20474727 | |||||||
| chr11:20474741 | C | T | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1347+10195C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20474741 | |||||||
| chr11:20474775 | A | G | 104 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(101): Show |
108 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1347+10229A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20474775 | |||||||
| chr11:20474810 | A | T | 1 | a0001c0001t0001g0233 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1347+10264A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20474810 | |||||||
| chr11:20474823 | G | T | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1347+10277G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20474823 | |||||||
| chr11:20474938 | A | C | 10 | a0001c0001t0002g0332 a0001c0001t0002g0353 a0001c0001t0002g0354 others(7): Show |
10 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1347+10392A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20474938 | |||||||
| chr11:20475263 | A | C | 1 | a0001c0001t0001g0207 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1347+10717A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20475263 | |||||||
| chr11:20475375 | A | G | 1 | a0001c0001t0002g0029 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1347+10829A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20475375 | |||||||
| chr11:20475572 | T | TA | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(211): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1347+11031dupA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20475572 | ||||||
| chr11:20475606 | GT | G | 3 | a0003c0003t0002g0289 a0003c0003t0002g0309 a0003c0003t0002g0315 |
3 | NA18965.hp2 NA18979.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1347+11061delT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20475606 | |||||||
| chr11:20475650 | G | T | 1 | a0001c0001t0002g0308 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1347+11104G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20475650 | |||||||
| chr11:20475652 | C | CT | 7 | a0001c0001t0001g0081 a0001c0001t0002g0043 a0001c0001t0002g0059 others(4): Show |
7 | HG01496.hp2 HG02148.hp1 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.1347+11125dupT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20475652 | ||||||
| chr11:20475652 | CT | C | 79 | a0001c0001t0001g0006 a0001c0001t0001g0147 a0001c0001t0001g0196 others(76): Show |
80 | HG00544.hp1 HG00639.hp1 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.1347+11125delT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20475652 | ||||||
| chr11:20475652 | CTT | C | 193 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
198 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.1347+11124_1347+11 others(8): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20475652 | ||||||
| chr11:20475735 | C | T | 1 | a0001c0001t0002g0224 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1347+11189C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20475735 | |||||||
| chr11:20475794 | A | G | 60 | a0001c0001t0001g0006 a0001c0001t0001g0200 a0001c0001t0001g0233 others(57): Show |
61 | HG00544.hp1 HG00639.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.1347+11248A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20475794 | |||||||
| chr11:20475804 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1347+11258G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20475804 | |||||||
| chr11:20475888 | C | T | 1 | a0002c0002t0002g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1347+11342C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20475888 | |||||||
| chr11:20475906 | C | A | 1 | a0002c0002t0002g0009 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1347+11360C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20475906 | |||||||
| chr11:20475915 | A | T | 1 | a0002c0002t0002g0009 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1347+11369A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20475915 | |||||||
| chr11:20475965 | C | T | 4 | a0001c0001t0002g0335 a0001c0001t0002g0337 a0002c0002t0005g0334 others(1): Show |
4 | HG02622.hp2 HG02630.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1347+11419C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20475965 | |||||||
| chr11:20475966 | G | A | 1 | a0001c0001t0004g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1347+11420G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20475966 | |||||||
| chr11:20476066 | A | G | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1347+11520A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20476066 | |||||||
| chr11:20476120 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1347+11574C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20476120 | |||||||
| chr11:20476121 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1347+11575G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20476121 | |||||||
| chr11:20476252 | C | T | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1347+11706C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20476252 | |||||||
| chr11:20476390 | T | A | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.1347+11844T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20476390 | |||||||
| chr11:20476477 | G | A | 4 | a0001c0004t0001g0040 a0001c0004t0001g0101 a0001c0004t0001g0102 others(1): Show |
4 | HG02135.hp2 NA18940.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.1347+11931G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20476477 | |||||||
| chr11:20476510 | G | T | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.1347+11964G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20476510 | |||||||
| chr11:20476527 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1347+11981G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20476527 | |||||||
| chr11:20476641 | T | A | 10 | a0001c0001t0001g0100 a0001c0001t0001g0103 a0001c0001t0001g0104 others(7): Show |
10 | HG00558.hp1 HG02015.hp2 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.1347+12095T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20476641 | |||||||
| chr11:20476646 | T | C | 10 | a0001c0001t0002g0332 a0001c0001t0002g0353 a0001c0001t0002g0354 others(7): Show |
10 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1347+12100T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20476646 | |||||||
| chr11:20476682 | G | A | 2 | a0001c0001t0001g0209 a0001c0001t0001g0222 |
2 | NA18989.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1347+12136G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20476682 | |||||||
| chr11:20476712 | T | C | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1347+12166T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20476712 | |||||||
| chr11:20476754 | A | AG | 23 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(20): Show |
24 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.1347+12209dupG | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20476754 | ||||||
| chr11:20476755 | G | GT | 287 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(284): Show |
294 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.1347+12216dupT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20476755 | ||||||
| chr11:20476830 | A | G | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1347+12284A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20476830 | |||||||
| chr11:20476877 | CCTTTT | C | 3 | a0002c0002t0003g0272 a0002c0002t0003g0273 a0002c0002t0003g0274 |
3 | HG02572.hp1 HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1347+12332_1347+12 others(11): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20476877 | |||||||
| chr11:20476892 | A | AT | 10 | a0001c0001t0002g0332 a0001c0001t0002g0353 a0001c0001t0002g0354 others(7): Show |
10 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1347+12351dupT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20476892 | ||||||
| chr11:20477045 | C | A | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1347+12499C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20477045 | |||||||
| chr11:20477065 | A | T | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1347+12519A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20477065 | |||||||
| chr11:20477094 | T | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0075 others(71): Show |
76 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1347+12548T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20477094 | |||||||
| chr11:20477164 | C | T | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1347+12618C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20477164 | |||||||
| chr11:20477231 | T | G | 1 | a0001c0001t0001g0219 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1347+12685T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20477231 | |||||||
| chr11:20477268 | A | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1347+12722A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20477268 | |||||||
| chr11:20477318 | G | A | 1 | a0001c0001t0004g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1347+12772G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20477318 | |||||||
| chr11:20477380 | A | C | 1 | a0001c0001t0004g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1347+12834A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20477380 | |||||||
| chr11:20477555 | C | CA | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0075 others(71): Show |
76 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1347+13019dupA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20477555 | ||||||
| chr11:20477566 | G | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1347+13020G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20477566 | |||||||
| chr11:20477783 | A | G | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1347+13237A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20477783 | |||||||
| chr11:20477802 | A | AC | 27 | a0001c0001t0001g0094 a0001c0001t0001g0145 a0001c0001t0001g0213 others(24): Show |
27 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.1347+13268dupC | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20477802 | ||||||
| chr11:20477802 | A | C | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1347+13256A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20477802 | |||||||
| chr11:20477802 | AC | A | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(138): Show |
144 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.1347+13268delC | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20477802 | ||||||
| chr11:20477814 | C | A | 1 | a0001c0001t0002g0280 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1347+13268C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20477814 | |||||||
| chr11:20477814 | C | G | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1347+13268C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20477814 | |||||||
| chr11:20477866 | G | A | 95 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(92): Show |
99 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1347+13320G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20477866 | |||||||
| chr11:20477909 | G | A | 10 | a0001c0001t0002g0332 a0001c0001t0002g0353 a0001c0001t0002g0354 others(7): Show |
10 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1347+13363G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20477909 | |||||||
| chr11:20478013 | A | G | 10 | a0001c0001t0002g0332 a0001c0001t0002g0353 a0001c0001t0002g0354 others(7): Show |
10 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1347+13467A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20478013 | |||||||
| chr11:20478049 | C | T | 10 | a0001c0001t0002g0332 a0001c0001t0002g0353 a0001c0001t0002g0354 others(7): Show |
10 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1347+13503C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20478049 | |||||||
| chr11:20478238 | T | C | 10 | a0001c0001t0002g0332 a0001c0001t0002g0353 a0001c0001t0002g0354 others(7): Show |
10 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1347+13692T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20478238 | |||||||
| chr11:20478318 | C | T | 22 | a0001c0001t0002g0335 a0001c0001t0002g0337 a0002c0002t0002g0276 others(19): Show |
22 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(19): Show |
intron_variant | MODIFIER | c.1347+13772C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20478318 | |||||||
| chr11:20478325 | AT | A | 11 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(8): Show |
11 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1347+13782delT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20478325 | ||||||
| chr11:20478533 | T | TA | 17 | a0001c0001t0001g0184 a0001c0001t0002g0021 a0001c0001t0002g0332 others(14): Show |
17 | HG00735.hp2 HG00738.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1347+14003dupA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20478533 | ||||||
| chr11:20478533 | TA | T | 9 | a0001c0001t0001g0125 a0001c0001t0002g0305 a0001c0001t0004g0063 others(6): Show |
9 | HG00323.hp2 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1347+14003delA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20478533 | ||||||
| chr11:20478630 | G | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1347+14084G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20478630 | |||||||
| chr11:20478910 | A | G | 10 | a0001c0001t0002g0332 a0001c0001t0002g0353 a0001c0001t0002g0354 others(7): Show |
10 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1347+14364A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20478910 | |||||||
| chr11:20478951 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1347+14405G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20478951 | |||||||
| chr11:20479106 | C | G | 111 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(108): Show |
115 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1347+14560C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20479106 | |||||||
| chr11:20479148 | C | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG00099.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1347+14602C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20479148 | |||||||
| chr11:20479296 | A | G | 1 | a0001c0013t0002g0277 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1348-14623A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20479296 | |||||||
| chr11:20479528 | G | A | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1348-14391G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20479528 | |||||||
| chr11:20479697 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1348-14222T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20479697 | |||||||
| chr11:20479758 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1348-14161A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20479758 | |||||||
| chr11:20479794 | CAT | C | 17 | a0001c0001t0001g0001 a0001c0001t0001g0076 a0001c0001t0001g0077 others(14): Show |
18 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.1348-14124_1348-14 others(8): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20479794 | |||||||
| chr11:20479861 | T | A | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1348-14058T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20479861 | |||||||
| chr11:20480109 | C | T | 3 | a0002c0002t0003g0271 a0002c0002t0003g0343 a0002c0002t0003g0344 |
3 | HG02896.hp2 HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1348-13810C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20480109 | |||||||
| chr11:20480126 | T | C | 15 | a0001c0001t0001g0007 a0001c0001t0001g0182 a0001c0001t0001g0183 others(12): Show |
16 | HG00639.hp2 HG00738.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1348-13793T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20480126 | |||||||
| chr11:20480341 | G | A | 6 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0028 others(3): Show |
6 | HG01106.hp2 HG01192.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1348-13578G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20480341 | |||||||
| chr11:20480442 | T | C | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.1348-13477T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20480442 | |||||||
| chr11:20480462 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1348-13457A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20480462 | |||||||
| chr11:20480525 | G | A | 3 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG02258.hp2 HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1348-13394G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20480525 | |||||||
| chr11:20480543 | T | C | 50 | a0001c0001t0001g0006 a0001c0001t0001g0200 a0001c0001t0001g0233 others(47): Show |
51 | HG00544.hp1 HG00639.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.1348-13376T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20480543 | |||||||
| chr11:20480645 | G | A | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1348-13274G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20480645 | |||||||
| chr11:20480714 | C | G | 2 | a0002c0002t0003g0343 a0002c0002t0003g0344 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1348-13205C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20480714 | |||||||
| chr11:20480796 | A | G | 1 | a0001c0001t0002g0324 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1348-13123A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20480796 | |||||||
| chr11:20480820 | T | C | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.1348-13099T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20480820 | |||||||
| chr11:20480843 | C | CCTGT | 8 | a0001c0001t0001g0075 a0001c0001t0004g0062 a0001c0001t0004g0063 others(5): Show |
8 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1348-13074_1348-13 others(10): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20480843 | ||||||
| chr11:20480890 | G | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0170 a0001c0001t0001g0171 others(2): Show |
6 | HG01517.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1348-13029G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20480890 | |||||||
| chr11:20481146 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1348-12773A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20481146 | |||||||
| chr11:20481160 | C | G | 179 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
185 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.1348-12759C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20481160 | |||||||
| chr11:20481188 | T | A | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1348-12731T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20481188 | |||||||
| chr11:20481262 | T | TA | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1348-12644dupA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20481262 | ||||||
| chr11:20481262 | T | TAA | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0085 others(95): Show |
100 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.1348-12645_1348-12 others(8): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20481262 | ||||||
| chr11:20481576 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1348-12343T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20481576 | |||||||
| chr11:20481650 | C | A | 1 | a0001c0001t0002g0016 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1348-12269C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20481650 | |||||||
| chr11:20481885 | C | T | 1 | a0002c0002t0003g0336 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1348-12034C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20481885 | |||||||
| chr11:20481923 | G | GGAAACAT others(17): Show |
3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1348-11995_1348-11 others(30): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20481923 | ||||||
| chr11:20481984 | T | C | 4 | a0001c0001t0001g0080 a0001c0001t0001g0262 a0001c0001t0001g0263 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1348-11935T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20481984 | |||||||
| chr11:20482000 | T | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0083 |
2 | HG01928.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1348-11919T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20482000 | |||||||
| chr11:20482069 | A | G | 1 | a0002c0002t0002g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1348-11850A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20482069 | |||||||
| chr11:20482120 | G | A | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1348-11799G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20482120 | |||||||
| chr11:20482231 | T | TATCAGCA others(39): Show |
10 | a0001c0001t0002g0332 a0001c0001t0002g0353 a0001c0001t0002g0354 others(7): Show |
10 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1348-11687_1348-11 others(52): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20482231 | ||||||
| chr11:20482282 | A | G | 1 | a0001c0001t0001g0250 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1348-11637A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20482282 | |||||||
| chr11:20482292 | T | C | 1 | a0001c0001t0002g0304 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1348-11627T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20482292 | |||||||
| chr11:20482333 | T | C | 50 | a0001c0001t0001g0006 a0001c0001t0001g0200 a0001c0001t0001g0233 others(47): Show |
51 | HG00544.hp1 HG00639.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.1348-11586T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20482333 | |||||||
| chr11:20482351 | A | G | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1348-11568A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20482351 | |||||||
| chr11:20482371 | G | A | 4 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0254 others(1): Show |
4 | HG01167.hp1 HG01516.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.1348-11548G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20482371 | |||||||
| chr11:20482565 | A | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0241 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1348-11354A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20482565 | |||||||
| chr11:20482619 | T | G | 3 | a0001c0001t0002g0354 a0001c0001t0002g0355 a0001c0001t0002g0357 |
3 | HG02145.hp1 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1348-11300T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20482619 | |||||||
| chr11:20482812 | ATGGAAAG others(19): Show |
A | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.1348-11080_1348-11 others(32): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20482812 | ||||||
| chr11:20483003 | T | C | 24 | a0001c0001t0001g0075 a0001c0001t0001g0106 a0001c0001t0002g0335 others(21): Show |
24 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.1348-10916T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20483003 | |||||||
| chr11:20483098 | G | C | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.1348-10821G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20483098 | |||||||
| chr11:20483338 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1348-10581T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20483338 | |||||||
| chr11:20483554 | CAA | C | 45 | a0001c0001t0001g0075 a0001c0001t0001g0082 a0001c0001t0001g0106 others(42): Show |
45 | HG00735.hp2 HG01243.hp1 HG01952.hp1 others(42): Show |
intron_variant | MODIFIER | c.1348-10348_1348-10 others(8): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20483554 | ||||||
| chr11:20483554 | CAAA | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1348-10349_1348-10 others(9): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20483554 | ||||||
| chr11:20483554 | CAAAA | C | 51 | a0001c0001t0001g0006 a0001c0001t0001g0126 a0001c0001t0001g0200 others(48): Show |
52 | HG00544.hp1 HG00639.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.1348-10350_1348-10 others(10): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20483554 | ||||||
| chr11:20483617 | T | G | 1 | a0001c0001t0001g0158 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1348-10302T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20483617 | |||||||
| chr11:20483627 | T | C | 2 | a0001c0001t0004g0063 a0001c0001t0004g0064 |
2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1348-10292T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20483627 | |||||||
| chr11:20483641 | T | C | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1348-10278T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20483641 | |||||||
| chr11:20483642 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1348-10277A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20483642 | |||||||
| chr11:20483681 | A | G | 12 | a0001c0001t0001g0074 a0001c0001t0001g0233 a0001c0001t0002g0332 others(9): Show |
12 | HG00735.hp2 HG01243.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.1348-10238A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20483681 | |||||||
| chr11:20483690 | C | G | 1 | a0001c0001t0002g0311 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1348-10229C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20483690 | |||||||
| chr11:20483847 | T | A | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.1348-10072T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20483847 | |||||||
| chr11:20483942 | G | C | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.1348-9977G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20483942 | |||||||
| chr11:20483950 | G | A | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1348-9969G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20483950 | |||||||
| chr11:20484062 | A | G | 51 | a0001c0001t0001g0006 a0001c0001t0001g0200 a0001c0001t0001g0233 others(48): Show |
52 | HG00544.hp1 HG00639.hp1 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.1348-9857A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20484062 | |||||||
| chr11:20484245 | A | T | 51 | a0001c0001t0001g0006 a0001c0001t0001g0200 a0001c0001t0001g0233 others(48): Show |
52 | HG00544.hp1 HG00639.hp1 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.1348-9674A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20484245 | |||||||
| chr11:20484281 | G | A | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1348-9638G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20484281 | |||||||
| chr11:20484433 | A | AATCTC | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.1348-9482_1348-948 others(9): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20484433 | ||||||
| chr11:20484758 | A | G | 2 | a0001c0001t0002g0354 a0001c0001t0002g0357 |
2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1348-9161A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20484758 | |||||||
| chr11:20484827 | C | T | 20 | a0001c0001t0001g0001 a0001c0001t0001g0076 a0001c0001t0001g0077 others(17): Show |
21 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1348-9092C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20484827 | |||||||
| chr11:20484909 | G | A | 1 | a0002c0002t0002g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1348-9010G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20484909 | |||||||
| chr11:20484916 | A | G | 1 | a0008c0014t0002g0322 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1348-9003A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20484916 | |||||||
| chr11:20484958 | T | C | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1348-8961T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20484958 | |||||||
| chr11:20485236 | CA | C | 51 | a0001c0001t0001g0006 a0001c0001t0001g0200 a0001c0001t0001g0233 others(48): Show |
52 | HG00544.hp1 HG00639.hp1 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.1348-8678delA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20485236 | ||||||
| chr11:20485306 | C | G | 1 | a0001c0001t0001g0366 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1348-8613C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20485306 | |||||||
| chr11:20485634 | A | G | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0085 others(81): Show |
86 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1348-8285A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20485634 | |||||||
| chr11:20486068 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1348-7851A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20486068 | |||||||
| chr11:20486077 | C | T | 10 | a0001c0001t0002g0332 a0001c0001t0002g0353 a0001c0001t0002g0354 others(7): Show |
10 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1348-7842C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20486077 | |||||||
| chr11:20486078 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1348-7841G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20486078 | |||||||
| chr11:20486306 | T | C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1348-7613T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20486306 | |||||||
| chr11:20486341 | A | G | 3 | a0001c0001t0002g0354 a0001c0001t0002g0355 a0001c0001t0002g0357 |
3 | HG02145.hp1 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1348-7578A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20486341 | |||||||
| chr11:20486371 | G | A | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(310): Show |
321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.1348-7548G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20486371 | |||||||
| chr11:20486649 | T | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1348-7270T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20486649 | |||||||
| chr11:20486673 | G | T | 1 | a0001c0001t0001g0366 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1348-7246G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20486673 | |||||||
| chr11:20486814 | C | T | 4 | a0001c0001t0002g0335 a0001c0001t0002g0337 a0002c0002t0005g0334 others(1): Show |
4 | HG02622.hp2 HG02630.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1348-7105C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20486814 | |||||||
| chr11:20486815 | G | C | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1348-7104G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20486815 | |||||||
| chr11:20486874 | C | T | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1348-7045C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20486874 | |||||||
| chr11:20486913 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1348-7006C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20486913 | |||||||
| chr11:20486967 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1348-6952G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20486967 | |||||||
| chr11:20487059 | GA | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(217): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.1348-6848delA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20487059 | ||||||
| chr11:20487069 | A | G | 1 | a0001c0004t0001g0150 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1348-6850A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20487069 | |||||||
| chr11:20487069 | AAAG | A | 10 | a0001c0001t0002g0332 a0001c0001t0002g0353 a0001c0001t0002g0354 others(7): Show |
10 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1348-6838_1348-683 others(7): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20487069 | ||||||
| chr11:20487550 | G | T | 4 | a0001c0001t0004g0065 a0001c0001t0004g0066 a0001c0001t0004g0067 others(1): Show |
4 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1348-6369G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20487550 | |||||||
| chr11:20487555 | T | C | 22 | a0001c0001t0002g0335 a0001c0001t0002g0337 a0002c0002t0002g0276 others(19): Show |
22 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(19): Show |
intron_variant | MODIFIER | c.1348-6364T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20487555 | |||||||
| chr11:20487644 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0085 others(91): Show |
96 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.1348-6275T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20487644 | |||||||
| chr11:20487836 | A | G | 2 | a0001c0001t0002g0028 a0001c0001t0002g0034 |
2 | NA18942.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1348-6083A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20487836 | |||||||
| chr11:20487899 | G | T | 1 | a0001c0001t0001g0159 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1348-6020G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20487899 | |||||||
| chr11:20488063 | A | C | 1 | a0001c0001t0001g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1348-5856A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20488063 | |||||||
| chr11:20488152 | AAAAG | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG02895.hp2 HG02897.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1348-5761_1348-575 others(8): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20488152 | ||||||
| chr11:20488194 | A | G | 22 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(19): Show |
23 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.1348-5725A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20488194 | |||||||
| chr11:20488253 | T | C | 1 | a0001c0001t0002g0359 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1348-5666T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20488253 | |||||||
| chr11:20488411 | T | C | 15 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(12): Show |
15 | HG00544.hp2 HG00673.hp2 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.1348-5508T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20488411 | |||||||
| chr11:20488451 | C | T | 51 | a0001c0001t0001g0006 a0001c0001t0001g0200 a0001c0001t0001g0233 others(48): Show |
52 | HG00544.hp1 HG00639.hp1 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.1348-5468C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20488451 | |||||||
| chr11:20488730 | T | A | 1 | a0001c0001t0002g0240 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1348-5189T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20488730 | |||||||
| chr11:20488779 | A | G | 11 | a0001c0001t0001g0261 a0001c0001t0002g0332 a0001c0001t0002g0353 others(8): Show |
11 | HG00735.hp2 HG01243.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.1348-5140A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20488779 | |||||||
| chr11:20488850 | T | C | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG01071.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.1348-5069T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20488850 | |||||||
| chr11:20489176 | TCTCA | T | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1348-4739_1348-473 others(8): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20489176 | ||||||
| chr11:20489271 | C | T | 1 | a0001c0001t0001g0228 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1348-4648C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20489271 | |||||||
| chr11:20489317 | T | G | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1348-4602T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20489317 | |||||||
| chr11:20489318 | C | T | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1348-4601C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20489318 | |||||||
| chr11:20489321 | C | A | 1 | a0001c0001t0001g0092 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1348-4598C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20489321 | |||||||
| chr11:20489596 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1348-4323A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20489596 | |||||||
| chr11:20489769 | G | GT | 7 | a0001c0001t0001g0073 a0001c0001t0001g0082 a0001c0001t0002g0025 others(4): Show |
7 | HG01891.hp1 HG01952.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1348-4139dupT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20489769 | ||||||
| chr11:20490030 | G | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1348-3889G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20490030 | |||||||
| chr11:20490186 | G | A | 10 | a0001c0001t0002g0332 a0001c0001t0002g0353 a0001c0001t0002g0354 others(7): Show |
10 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1348-3733G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20490186 | |||||||
| chr11:20490520 | TAATCCCA others(39): Show |
T | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1348-3393_1348-334 others(50): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20490520 | ||||||
| chr11:20490668 | A | T | 90 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(87): Show |
94 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.1348-3251A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20490668 | |||||||
| chr11:20490766 | A | G | 22 | a0001c0001t0002g0335 a0001c0001t0002g0337 a0002c0002t0002g0276 others(19): Show |
22 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(19): Show |
intron_variant | MODIFIER | c.1348-3153A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20490766 | |||||||
| chr11:20490814 | C | CTTG | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.1348-3099_1348-309 others(7): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20490814 | ||||||
| chr11:20490944 | T | C | 50 | a0001c0001t0001g0006 a0001c0001t0001g0200 a0001c0001t0001g0233 others(47): Show |
51 | HG00544.hp1 HG00639.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.1348-2975T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20490944 | |||||||
| chr11:20491026 | G | T | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1348-2893G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20491026 | |||||||
| chr11:20491033 | A | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0115 a0001c0001t0001g0116 |
4 | NA18944.hp1 NA18991.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.1348-2886A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20491033 | |||||||
| chr11:20491290 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1348-2629T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20491290 | |||||||
| chr11:20491385 | ATTTGAGA others(7): Show |
A | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1348-2531_1348-251 others(18): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20491385 | ||||||
| chr11:20491477 | A | C | 1 | a0001c0001t0001g0366 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1348-2442A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20491477 | |||||||
| chr11:20491612 | T | C | 1 | a0001c0001t0002g0305 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1348-2307T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20491612 | |||||||
| chr11:20491638 | C | A | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(310): Show |
321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.1348-2281C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20491638 | |||||||
| chr11:20491688 | T | C | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1348-2231T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20491688 | |||||||
| chr11:20491714 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0085 others(90): Show |
95 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.1348-2205A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20491714 | |||||||
| chr11:20491752 | A | G | 1 | a0001c0001t0002g0029 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1348-2167A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20491752 | |||||||
| chr11:20491837 | C | T | 1 | a0001c0001t0002g0014 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1348-2082C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20491837 | |||||||
| chr11:20491846 | T | G | 1 | a0001c0001t0001g0266 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1348-2073T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20491846 | |||||||
| chr11:20491964 | G | A | 1 | a0001c0001t0001g0348 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1348-1955G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20491964 | |||||||
| chr11:20492134 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1348-1785A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20492134 | |||||||
| chr11:20492179 | C | G | 19 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(16): Show |
20 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1348-1740C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20492179 | |||||||
| chr11:20492184 | A | C | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1348-1735A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20492184 | |||||||
| chr11:20492366 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1348-1553C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20492366 | |||||||
| chr11:20492446 | T | C | 1 | a0002c0002t0002g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1348-1473T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20492446 | |||||||
| chr11:20492475 | C | A | 1 | a0001c0001t0001g0110 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1348-1444C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20492475 | |||||||
| chr11:20492490 | T | C | 1 | a0002c0002t0002g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1348-1429T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20492490 | |||||||
| chr11:20492651 | TA | T | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1348-1263delA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20492651 | ||||||
| chr11:20492668 | C | G | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG01891.hp1 HG02622.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1348-1251C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20492668 | |||||||
| chr11:20492742 | C | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0085 others(90): Show |
95 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.1348-1177C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20492742 | |||||||
| chr11:20492811 | C | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0076 a0001c0001t0001g0079 others(1): Show |
5 | HG02273.hp1 HG02300.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.1348-1108C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20492811 | |||||||
| chr11:20492897 | A | G | 1 | a0001c0001t0002g0307 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1348-1022A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20492897 | |||||||
| chr11:20492931 | C | T | 1 | a0003c0003t0002g0316 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1348-988C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20492931 | |||||||
| chr11:20492987 | C | T | 1 | a0002c0002t0002g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1348-932C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20492987 | |||||||
| chr11:20493062 | G | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(216): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1348-857G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20493062 | |||||||
| chr11:20493131 | C | CA | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(216): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1348-775dupA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr11 | 20493131 | ||||||
| chr11:20493163 | A | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0085 others(89): Show |
94 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.1348-756A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20493163 | |||||||
| chr11:20493286 | A | T | 5 | a0001c0001t0001g0098 a0001c0001t0001g0118 a0001c0001t0001g0129 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1348-633A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20493286 | |||||||
| chr11:20493321 | T | C | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1348-598T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20493321 | |||||||
| chr11:20493339 | T | G | 4 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0057 others(1): Show |
4 | NA18994.hp1 NA19006.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1348-580T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20493339 | |||||||
| chr11:20493357 | A | G | 4 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0057 others(1): Show |
4 | NA18994.hp1 NA19006.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1348-562A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20493357 | |||||||
| chr11:20493508 | C | T | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1348-411C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20493508 | |||||||
| chr11:20493518 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1348-401G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20493518 | |||||||
| chr11:20493640 | T | TTG | 22 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(19): Show |
23 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.1348-279_1348-278i others(4): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20493640 | |||||||
| chr11:20493685 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1348-234G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20493685 | |||||||
| chr11:20493806 | G | C | 1 | a0001c0001t0002g0279 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1348-113G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 13/15 | chr11 | 20493806 | |||||||
| chr11:20494056 | G | C | 1 | a0001c0001t0002g0312 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1398+87G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 14/15 | chr11 | 20494056 | |||||||
| chr11:20494098 | G | A | 50 | a0001c0001t0001g0006 a0001c0001t0001g0200 a0001c0001t0001g0233 others(47): Show |
51 | HG00544.hp1 HG00639.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.1399-69G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 14/15 | chr11 | 20494098 | |||||||
| chr11:20494439 | T | G | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1486+185T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20494439 | |||||||
| chr11:20494468 | G | T | 47 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(44): Show |
47 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.1486+214G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20494468 | |||||||
| chr11:20494481 | A | G | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(219): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1486+227A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20494481 | |||||||
| chr11:20494490 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0170 a0001c0001t0001g0171 others(2): Show |
6 | HG01517.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1486+236C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20494490 | |||||||
| chr11:20494577 | G | A | 3 | a0001c0001t0002g0296 a0001c0001t0002g0297 a0001c0001t0002g0311 |
3 | NA18970.hp1 NA19058.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1486+323G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20494577 | |||||||
| chr11:20494798 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(216): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1486+544A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20494798 | |||||||
| chr11:20494829 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1486+575T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20494829 | |||||||
| chr11:20494936 | G | C | 1 | a0001c0001t0001g0079 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1486+682G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20494936 | |||||||
| chr11:20494964 | T | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1486+710T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20494964 | |||||||
| chr11:20495051 | G | A | 3 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 |
3 | HG01516.hp1 HG01517.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1486+797G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20495051 | |||||||
| chr11:20495075 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1486+821C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20495075 | |||||||
| chr11:20495294 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1486+1040A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20495294 | |||||||
| chr11:20495312 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1486+1058A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20495312 | |||||||
| chr11:20495337 | A | C | 1 | a0001c0001t0002g0017 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1486+1083A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20495337 | |||||||
| chr11:20495625 | A | G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(18): Show |
22 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.1486+1371A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20495625 | |||||||
| chr11:20496008 | G | A | 1 | a0002c0002t0005g0334 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1486+1754G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20496008 | |||||||
| chr11:20496662 | G | A | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(310): Show |
321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.1486+2408G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20496662 | |||||||
| chr11:20496784 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0094 |
2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1486+2530C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20496784 | |||||||
| chr11:20496879 | C | G | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1486+2625C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20496879 | |||||||
| chr11:20496949 | G | C | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(233): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1486+2695G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20496949 | |||||||
| chr11:20496966 | C | G | 1 | a0003c0003t0002g0294 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1486+2712C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20496966 | |||||||
| chr11:20497069 | A | G | 1 | a0001c0001t0001g0002 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1486+2815A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20497069 | |||||||
| chr11:20497191 | A | AT | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0085 others(91): Show |
96 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.1486+2938dupT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20497191 | ||||||
| chr11:20497512 | T | TGTAA | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(230): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1486+3261_1486+326 others(8): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20497512 | ||||||
| chr11:20497575 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1486+3321A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20497575 | |||||||
| chr11:20497842 | G | C | 4 | a0001c0001t0004g0065 a0001c0001t0004g0066 a0001c0001t0004g0067 others(1): Show |
4 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1486+3588G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20497842 | |||||||
| chr11:20497923 | G | A | 54 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0174 others(51): Show |
56 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.1486+3669G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20497923 | |||||||
| chr11:20498549 | C | A | 19 | a0002c0002t0003g0269 a0002c0002t0003g0270 a0002c0002t0003g0271 others(16): Show |
19 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.1486+4295C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20498549 | |||||||
| chr11:20498550 | G | A | 4 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0335 others(1): Show |
4 | HG01496.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1486+4296G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20498550 | |||||||
| chr11:20498551 | A | G | 1 | a0001c0001t0001g0366 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1486+4297A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20498551 | |||||||
| chr11:20498622 | C | T | 3 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0253 |
3 | HG00733.hp1 HG01099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1486+4368C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20498622 | |||||||
| chr11:20498631 | G | A | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | NA18964.hp1 NA19079.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1486+4377G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20498631 | |||||||
| chr11:20498799 | A | G | 3 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0253 |
3 | HG00733.hp1 HG01099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1486+4545A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20498799 | |||||||
| chr11:20498915 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.1486+4661T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20498915 | |||||||
| chr11:20499261 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1486+5007C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20499261 | |||||||
| chr11:20499468 | T | A | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(219): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1486+5214T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20499468 | |||||||
| chr11:20499469 | T | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0188 |
2 | HG01099.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1486+5215T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20499469 | |||||||
| chr11:20499604 | G | T | 6 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 others(3): Show |
6 | NA18957.hp2 NA18960.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.1486+5350G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20499604 | |||||||
| chr11:20499826 | G | A | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1486+5572G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20499826 | |||||||
| chr11:20499910 | G | A | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1486+5656G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20499910 | |||||||
| chr11:20500120 | A | G | 19 | a0001c0001t0001g0002 a0001c0001t0001g0092 a0001c0001t0001g0093 others(16): Show |
20 | HG00642.hp2 HG01192.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.1486+5866A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20500120 | |||||||
| chr11:20500275 | A | C | 47 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(44): Show |
47 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.1486+6021A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20500275 | |||||||
| chr11:20500278 | G | A | 1 | a0001c0001t0002g0285 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1486+6024G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20500278 | |||||||
| chr11:20500475 | G | A | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1486+6221G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20500475 | |||||||
| chr11:20500586 | C | T | 2 | a0001c0001t0001g0364 a0001c0001t0001g0365 |
2 | HG01243.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1486+6332C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20500586 | |||||||
| chr11:20500744 | G | A | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1486+6490G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20500744 | |||||||
| chr11:20500787 | A | G | 1 | a0002c0002t0005g0334 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1486+6533A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20500787 | |||||||
| chr11:20500843 | C | T | 1 | a0001c0001t0001g0362 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1486+6589C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20500843 | |||||||
| chr11:20500923 | C | CCTTA | 4 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0335 others(1): Show |
4 | HG01496.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1486+6671_1486+667 others(8): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20500923 | ||||||
| chr11:20500927 | T | C | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1486+6673T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20500927 | |||||||
| chr11:20500965 | C | A | 4 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0335 others(1): Show |
4 | HG01496.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1486+6711C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20500965 | |||||||
| chr11:20501282 | C | T | 1 | a0001c0001t0001g0348 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1487-7022C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20501282 | |||||||
| chr11:20501369 | T | G | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
215 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1487-6935T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20501369 | |||||||
| chr11:20501395 | A | G | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1487-6909A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20501395 | |||||||
| chr11:20501465 | C | T | 1 | a0001c0001t0002g0048 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1487-6839C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20501465 | |||||||
| chr11:20501467 | A | G | 3 | a0001c0001t0001g0181 a0001c0001t0001g0191 a0001c0001t0001g0241 |
3 | HG03490.hp2 HG03492.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1487-6837A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20501467 | |||||||
| chr11:20501601 | A | G | 4 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0335 others(1): Show |
4 | HG01496.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1487-6703A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20501601 | |||||||
| chr11:20501655 | G | A | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG01257.hp2 HG01258.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1487-6649G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20501655 | |||||||
| chr11:20501669 | A | C | 4 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0335 others(1): Show |
4 | HG01496.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1487-6635A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20501669 | |||||||
| chr11:20501782 | C | A | 1 | a0001c0001t0002g0312 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1487-6522C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20501782 | |||||||
| chr11:20501891 | A | T | 2 | a0001c0001t0004g0063 a0001c0001t0004g0064 |
2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1487-6413A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20501891 | |||||||
| chr11:20502079 | A | G | 4 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0335 others(1): Show |
4 | HG01496.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1487-6225A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20502079 | |||||||
| chr11:20502111 | A | G | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.1487-6193A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20502111 | |||||||
| chr11:20502113 | A | G | 4 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0335 others(1): Show |
4 | HG01496.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1487-6191A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20502113 | |||||||
| chr11:20502125 | G | A | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0041 others(1): Show |
4 | NA18945.hp2 NA18963.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1487-6179G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20502125 | |||||||
| chr11:20502256 | C | G | 1 | a0001c0001t0001g0348 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1487-6048C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20502256 | |||||||
| chr11:20502287 | TTTAG | T | 3 | a0001c0001t0001g0114 a0001c0001t0001g0122 a0001c0001t0001g0123 |
3 | HG00558.hp1 HG02165.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1487-6012_1487-600 others(8): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20502287 | ||||||
| chr11:20502447 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1487-5857A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20502447 | |||||||
| chr11:20502581 | G | T | 1 | a0001c0001t0001g0267 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1487-5723G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20502581 | |||||||
| chr11:20502582 | T | C | 4 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0335 others(1): Show |
4 | HG01496.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1487-5722T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20502582 | |||||||
| chr11:20502732 | A | C | 1 | a0009c0008t0001g0195 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1487-5572A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20502732 | |||||||
| chr11:20502739 | A | G | 2 | a0001c0001t0002g0335 a0001c0001t0002g0337 |
2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1487-5565A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20502739 | |||||||
| chr11:20502846 | AAAG | A | 11 | a0001c0001t0001g0261 a0001c0001t0002g0332 a0001c0001t0002g0353 others(8): Show |
11 | HG00735.hp2 HG01243.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.1487-5454_1487-545 others(7): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20502846 | ||||||
| chr11:20502865 | A | T | 1 | a0001c0001t0004g0063 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1487-5439A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20502865 | |||||||
| chr11:20502940 | G | A | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1487-5364G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20502940 | |||||||
| chr11:20503078 | T | TA | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
193 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1487-5220dupA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20503078 | ||||||
| chr11:20503093 | A | G | 4 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0335 others(1): Show |
4 | HG01496.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1487-5211A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20503093 | |||||||
| chr11:20503199 | GTCTGGCT others(12): Show |
G | 1 | a0001c0001t0001g0075 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1487-5103_1487-508 others(23): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20503199 | ||||||
| chr11:20503293 | T | C | 4 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0335 others(1): Show |
4 | HG01496.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1487-5011T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20503293 | |||||||
| chr11:20503518 | G | A | 4 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0335 others(1): Show |
4 | HG01496.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1487-4786G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20503518 | |||||||
| chr11:20503630 | A | AT | 64 | a0001c0001t0001g0138 a0001c0001t0001g0217 a0001c0001t0001g0235 others(61): Show |
64 | HG00544.hp1 HG01106.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.1487-4662dupT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20503630 | ||||||
| chr11:20503650 | T | G | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.1487-4654T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20503650 | |||||||
| chr11:20503723 | C | T | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1487-4581C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20503723 | |||||||
| chr11:20503962 | C | T | 3 | a0001c0001t0002g0279 a0001c0001t0002g0285 a0001c0001t0002g0288 |
3 | NA18995.hp2 NA19000.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1487-4342C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20503962 | |||||||
| chr11:20503967 | G | A | 4 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0335 others(1): Show |
4 | HG01496.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1487-4337G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20503967 | |||||||
| chr11:20504016 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1487-4288G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20504016 | |||||||
| chr11:20504513 | G | C | 7 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1487-3791G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20504513 | |||||||
| chr11:20504628 | A | T | 1 | a0001c0001t0001g0245 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1487-3676A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20504628 | |||||||
| chr11:20504684 | T | TTG | 4 | a0001c0001t0001g0095 a0001c0001t0001g0107 a0001c0001t0001g0180 others(1): Show |
4 | HG01975.hp2 HG02683.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1487-3618_1487-361 others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504684 | ||||||
| chr11:20504684 | TTGTA | T | 4 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0335 others(1): Show |
4 | HG01496.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1487-3616_1487-361 others(8): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504684 | ||||||
| chr11:20504686 | GTA | G | 75 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0085 others(72): Show |
77 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.1487-3616_1487-361 others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504686 | ||||||
| chr11:20504688 | A | ATG | 5 | a0001c0001t0002g0299 a0001c0001t0002g0300 a0001c0001t0002g0306 others(2): Show |
5 | HG03225.hp1 NA18957.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.1487-3597_1487-359 others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504688 | ||||||
| chr11:20504688 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(153): Show |
162 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1487-3616A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20504688 | |||||||
| chr11:20504705 | T | TGA | 6 | a0001c0001t0001g0084 a0001c0001t0001g0249 a0001c0001t0001g0262 others(3): Show |
6 | HG00280.hp2 HG01074.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1487-3598_1487-359 others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504705 | ||||||
| chr11:20504705 | T | TGAGAGA | 3 | a0001c0001t0001g0077 a0001c0001t0001g0263 a0001c0001t0001g0264 |
3 | HG01516.hp1 HG01517.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1487-3598_1487-359 others(10): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504705 | ||||||
| chr11:20504705 | TGTGAGAG others(9): Show |
T | 1 | a0001c0001t0001g0203 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1487-3597_1487-358 others(20): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504705 | ||||||
| chr11:20504707 | T | A | 14 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0081 others(11): Show |
14 | HG00280.hp2 HG01074.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.1487-3597T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20504707 | |||||||
| chr11:20504707 | T | TGA | 13 | a0001c0001t0001g0119 a0001c0001t0001g0130 a0001c0001t0001g0251 others(10): Show |
13 | HG00621.hp2 HG01167.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.1487-3559_1487-355 others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504707 | ||||||
| chr11:20504707 | T | TGAGA | 3 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0364 |
3 | HG01255.hp2 HG02273.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1487-3561_1487-355 others(8): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504707 | ||||||
| chr11:20504707 | T | TGAGAGAG others(3): Show |
1 | a0001c0001t0002g0357 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1487-3567_1487-355 others(14): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504707 | ||||||
| chr11:20504707 | T | TGAGAGAG others(15): Show |
1 | a0001c0001t0001g0092 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1487-3579_1487-355 others(26): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504707 | ||||||
| chr11:20504707 | T | TGAGAGAG others(25): Show |
1 | a0001c0001t0001g0093 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1487-3589_1487-355 others(36): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504707 | ||||||
| chr11:20504707 | T | TGTGA | 7 | a0001c0001t0001g0001 a0001c0001t0001g0068 a0001c0001t0001g0091 others(4): Show |
8 | HG01258.hp2 HG02818.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1487-3596_1487-359 others(8): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504707 | ||||||
| chr11:20504707 | T | TGTGAGA | 5 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0173 others(2): Show |
5 | HG00544.hp2 HG02523.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.1487-3596_1487-359 others(10): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504707 | ||||||
| chr11:20504707 | T | TGTGAGAG others(3): Show |
1 | a0001c0001t0002g0332 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1487-3596_1487-359 others(14): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504707 | ||||||
| chr11:20504707 | T | TGTGAGAG others(5): Show |
1 | a0001c0001t0002g0353 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1487-3596_1487-359 others(16): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504707 | ||||||
| chr11:20504707 | T | TGTGAGAG others(9): Show |
1 | a0001c0001t0002g0354 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1487-3596_1487-359 others(20): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504707 | ||||||
| chr11:20504707 | T | TGTGAGAG others(11): Show |
3 | a0001c0001t0001g0086 a0001c0001t0001g0366 a0001c0001t0002g0355 |
3 | HG02451.hp2 HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1487-3596_1487-359 others(22): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504707 | ||||||
| chr11:20504707 | T | TGTGAGAG others(15): Show |
2 | a0001c0001t0001g0088 a0001c0001t0002g0361 |
2 | HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1487-3596_1487-359 others(26): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504707 | ||||||
| chr11:20504707 | T | TGTGAGAG others(19): Show |
2 | a0001c0001t0002g0358 a0001c0001t0002g0359 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1487-3596_1487-359 others(30): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504707 | ||||||
| chr11:20504707 | T | TGTGAGAG others(21): Show |
1 | a0001c0001t0001g0087 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1487-3596_1487-359 others(32): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504707 | ||||||
| chr11:20504707 | T | TGTGAGAG others(23): Show |
1 | a0001c0001t0001g0089 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1487-3596_1487-359 others(34): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504707 | ||||||
| chr11:20504707 | T | TGTGTGAG others(17): Show |
1 | a0001c0001t0002g0360 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1487-3596_1487-359 others(28): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504707 | ||||||
| chr11:20504707 | T | TGTGTGAG others(29): Show |
1 | a0001c0001t0001g0094 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1487-3596_1487-359 others(40): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504707 | ||||||
| chr11:20504707 | T | TGTGTGTG others(3): Show |
1 | a0002c0002t0002g0011 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1487-3596_1487-359 others(14): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504707 | ||||||
| chr11:20504707 | TGA | T | 6 | a0001c0001t0002g0017 a0001c0001t0002g0056 a0001c0001t0004g0062 others(3): Show |
6 | HG02717.hp2 HG03130.hp1 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.1487-3559_1487-355 others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504707 | ||||||
| chr11:20504707 | TGAGA | T | 77 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0012 others(74): Show |
79 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1487-3561_1487-355 others(8): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504707 | ||||||
| chr11:20504707 | TGAGAGA | T | 47 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0071 others(44): Show |
49 | HG00099.hp1 HG00639.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.1487-3563_1487-355 others(10): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504707 | ||||||
| chr11:20504707 | TGAGAGAG others(1): Show |
T | 6 | a0001c0001t0001g0144 a0001c0001t0001g0172 a0001c0001t0001g0202 others(3): Show |
6 | HG02071.hp2 HG02148.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.1487-3565_1487-355 others(12): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504707 | ||||||
| chr11:20504707 | TGAGAGAG others(3): Show |
T | 1 | a0001c0001t0001g0229 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1487-3567_1487-355 others(14): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504707 | ||||||
| chr11:20504707 | TGAGAGAG others(7): Show |
T | 1 | a0001c0001t0001g0260 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1487-3571_1487-355 others(18): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504707 | ||||||
| chr11:20504709 | A | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(98): Show |
104 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.1487-3595A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20504709 | |||||||
| chr11:20504711 | A | T | 25 | a0001c0001t0001g0110 a0001c0001t0002g0017 a0001c0001t0002g0056 others(22): Show |
25 | HG02145.hp2 HG02258.hp1 HG02559.hp2 others(22): Show |
intron_variant | MODIFIER | c.1487-3593A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20504711 | |||||||
| chr11:20504713 | A | T | 79 | a0001c0001t0001g0007 a0001c0001t0001g0193 a0001c0001t0001g0194 others(76): Show |
80 | HG00544.hp1 HG00735.hp2 HG01071.hp1 others(77): Show |
intron_variant | MODIFIER | c.1487-3591A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20504713 | |||||||
| chr11:20504715 | A | T | 54 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(51): Show |
54 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(51): Show |
intron_variant | MODIFIER | c.1487-3589A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20504715 | |||||||
| chr11:20504717 | A | T | 8 | a0001c0001t0001g0202 a0001c0001t0002g0023 a0001c0001t0002g0024 others(5): Show |
8 | HG02071.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1487-3587A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20504717 | |||||||
| chr11:20504719 | A | T | 3 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0042 |
3 | NA18963.hp1 NA18981.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1487-3585A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20504719 | |||||||
| chr11:20504741 | A | C | 1 | a0001c0001t0001g0012 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1487-3563A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20504741 | |||||||
| chr11:20504745 | A | AGAGAGAG others(9): Show |
2 | a0001c0005t0001g0367 a0001c0005t0001g0368 |
2 | HG02280.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1487-3558_1487-355 others(20): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504745 | ||||||
| chr11:20504745 | A | AGAGAGAG others(7): Show |
1 | a0001c0005t0001g0369 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1487-3558_1487-355 others(18): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20504745 | ||||||
| chr11:20504745 | A | C | 1 | a0001c0001t0001g0366 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1487-3559A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20504745 | |||||||
| chr11:20504747 | C | A | 9 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1487-3557C>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20504747 | |||||||
| chr11:20504765 | G | T | 1 | a0001c0001t0001g0348 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1487-3539G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20504765 | |||||||
| chr11:20504772 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1487-3532C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20504772 | |||||||
| chr11:20505358 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1487-2946G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20505358 | |||||||
| chr11:20505369 | G | T | 1 | a0001c0001t0002g0357 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1487-2935G>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20505369 | |||||||
| chr11:20505409 | T | G | 1 | a0001c0001t0001g0012 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1487-2895T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20505409 | |||||||
| chr11:20505678 | T | C | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1487-2626T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20505678 | |||||||
| chr11:20505778 | G | A | 23 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 others(20): Show |
23 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.1487-2526G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20505778 | |||||||
| chr11:20505865 | CA | C | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(279): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1487-2427delA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20505865 | ||||||
| chr11:20505892 | C | T | 20 | a0002c0002t0002g0276 a0002c0002t0003g0269 a0002c0002t0003g0270 others(17): Show |
20 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.1487-2412C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20505892 | |||||||
| chr11:20505920 | A | C | 1 | a0001c0001t0001g0205 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1487-2384A>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20505920 | |||||||
| chr11:20506037 | C | T | 1 | a0004c0006t0002g0321 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1487-2267C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20506037 | |||||||
| chr11:20506111 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1487-2193C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20506111 | |||||||
| chr11:20506135 | T | A | 1 | a0001c0001t0001g0173 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1487-2169T>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20506135 | |||||||
| chr11:20506215 | A | G | 10 | a0001c0001t0002g0332 a0001c0001t0002g0353 a0001c0001t0002g0354 others(7): Show |
10 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487-2089A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20506215 | |||||||
| chr11:20506232 | A | T | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1487-2072A>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20506232 | |||||||
| chr11:20506344 | A | G | 1 | a0002c0002t0003g0345 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1487-1960A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20506344 | |||||||
| chr11:20506394 | G | C | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.1487-1910G>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20506394 | |||||||
| chr11:20506411 | T | G | 2 | a0001c0001t0001g0213 a0001c0001t0001g0223 |
2 | HG00639.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1487-1893T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20506411 | |||||||
| chr11:20506453 | CTATTATT others(26): Show |
C | 47 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(44): Show |
47 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.1487-1849_1487-181 others(37): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20506453 | ||||||
| chr11:20506659 | G | A | 11 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 others(8): Show |
11 | HG01175.hp2 HG01981.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.1487-1645G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20506659 | |||||||
| chr11:20506738 | C | G | 1 | a0001c0001t0001g0252 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1487-1566C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20506738 | |||||||
| chr11:20506841 | TAAAATAA others(5): Show |
T | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0041 others(1): Show |
4 | NA18945.hp2 NA18963.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1487-1459_1487-144 others(16): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20506841 | ||||||
| chr11:20507050 | G | A | 5 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(2): Show |
5 | HG00408.hp1 NA18943.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.1487-1254G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20507050 | |||||||
| chr11:20507051 | C | T | 1 | a0001c0001t0004g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1487-1253C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20507051 | |||||||
| chr11:20507414 | A | G | 47 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(44): Show |
47 | HG00544.hp1 HG01106.hp2 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.1487-890A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20507414 | |||||||
| chr11:20507455 | GTAGT | G | 181 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
188 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1487-843_1487-840d others(6): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20507455 | ||||||
| chr11:20507502 | G | A | 1 | a0001c0001t0002g0287 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1487-802G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20507502 | |||||||
| chr11:20507548 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1487-756G>A | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20507548 | |||||||
| chr11:20507587 | C | G | 5 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(2): Show |
5 | HG01884.hp1 HG03130.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1487-717C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20507587 | |||||||
| chr11:20507638 | T | G | 4 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0335 others(1): Show |
4 | HG01496.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1487-666T>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20507638 | |||||||
| chr11:20507761 | C | G | 1 | a0001c0001t0001g0257 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1487-543C>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20507761 | |||||||
| chr11:20507793 | GA | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(218): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1487-508delA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20507793 | ||||||
| chr11:20507837 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1487-467T>C | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20507837 | |||||||
| chr11:20507846 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1487-458C>T | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20507846 | |||||||
| chr11:20508043 | TTGCAGTG others(37): Show |
T | 1 | a0001c0001t0002g0311 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1487-250_1487-207d others(46): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20508043 | ||||||
| chr11:20508149 | T | TA | 15 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0296 others(12): Show |
15 | HG01496.hp2 HG01943.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1487-134dupA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20508149 | ||||||
| chr11:20508149 | TA | T | 63 | a0001c0001t0001g0001 a0001c0001t0001g0076 a0001c0001t0001g0077 others(60): Show |
64 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1487-134delA | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20508149 | ||||||
| chr11:20508149 | TAA | T | 53 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0084 others(50): Show |
55 | HG00099.hp1 HG00621.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1487-135_1487-134d others(4): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20508149 | ||||||
| chr11:20508149 | TAAA | T | 153 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(150): Show |
158 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.1487-136_1487-134d others(5): Show |
PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20508149 | ||||||
| chr11:20508239 | A | G | 3 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0011 |
3 | HG02922.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1487-65A>G | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | chr11 | 20508239 | |||||||
| chr11:20508295 | G | GT | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0235 |
3 | HG01106.hp1 HG02698.hp2 HG03017.hp1 |
splice_region_variant&intron_variant | LOW | c.1487-5dupT | PRMT3 | ENSG00000185238.13 | transcript | ENST00000331079.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr11 | 20508295 |