Item | Value |
---|---|
geneid | 675 |
ensemblid | ENSG00000139618.18 |
hgncid | 1101 |
symbol | BRCA2 |
name | BRCA2 DNA repair associated |
refseq_nuc | NM_000059.4 |
refseq_prot | NP_000050.3 |
ensembl_nuc | ENST00000380152.8 |
ensembl_prot | ENSP00000369497.3 |
mane_status | MANE Select |
chr | chr13 |
start | 32315508 |
end | 32400268 |
strand | + |
ver | v1.2 |
region | chr13:32315508-32400268 |
region5000 | chr13:32310508-32405268 |
regionname0 | BRCA2_chr13_32315508_32400268 |
regionname5000 | BRCA2_chr13_32310508_32405268 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 3418 | 202 | 45 | 36 | 91 | 7 | 23 | 73 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0002 | 0/1 | 3418 | 72 | 3 | 13 | 40 | 4 | 11 | 31 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0003 | 0/0 | 3418 | 40 | 3 | 6 | 22 | 1 | 8 | 17 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0004 | 0/0 | 3418 | 17 | 9 | 6 | 2 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0005 | 1/0 | 3418 | 9 | 7 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0006 | 0/0 | 3418 | 7 | 0 | 6 | 0 | 0 | 1 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0007 | 0/0 | 3418 | 7 | 0 | 0 | 7 | 0 | 0 | 7 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0008 | 0/0 | 3418 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0009 | 0/0 | 3418 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0010 | 0/0 | 3418 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0011 | 0/0 | 3418 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0012 | 0/0 | 3418 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0013 | 0/0 | 3418 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0014 | 0/0 | 3418 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0015 | 0/0 | 3418 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0016 | 0/0 | 3418 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0017 | 0/0 | 3418 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0018 | 0/0 | 3418 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0019 | 0/0 | 3418 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0020 | 0/0 | 3418 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0021 | 0/0 | 3418 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0022 | 0/0 | 3418 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0023 | 0/0 | 3418 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0024 | 0/0 | 3418 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0025 | 0/0 | 3418 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0026 | 0/0 | 3418 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0027 | 0/0 | 3418 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0028 | 0/0 | 3418 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0029 | 0/0 | 3418 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0030 | 0/0 | 3418 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0031 | 0/0 | 3418 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0032 | 0/0 | 3418 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0033 | 0/0 | 3418 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0034 | 0/0 | 3418 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0035 | 0/0 | 3418 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0036 | 0/0 | 3418 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0037 | 0/0 | 3418 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
a0038 | 0/0 | 3418 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | MPIGS others(3413): Show |
chr13 | 32310508 | 32405268 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 10254 | 90 | 16 | 8 | 56 | 2 | 8 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0001c0003 | 0/0 | 10254 | 55 | 17 | 20 | 8 | 2 | 8 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0001c0004 | 0/0 | 10254 | 46 | 6 | 6 | 27 | 2 | 5 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0001c0010 | 0/0 | 10254 | 6 | 1 | 2 | 0 | 1 | 2 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0001c0011 | 0/0 | 10254 | 4 | 4 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0001c0033 | 0/0 | 10254 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0002c0002 | 0/1 | 10254 | 71 | 3 | 13 | 39 | 4 | 11 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0002c0048 | 0/0 | 10254 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0003c0005 | 0/0 | 10254 | 37 | 1 | 6 | 21 | 1 | 8 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0003c0023 | 0/0 | 10254 | 2 | 2 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0003c0051 | 0/0 | 10254 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0004c0006 | 0/0 | 10254 | 10 | 3 | 5 | 2 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0004c0012 | 0/0 | 10254 | 4 | 4 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0004c0019 | 0/0 | 10254 | 2 | 2 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0004c0031 | 0/0 | 10254 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0005c0007 | 1/0 | 10254 | 7 | 5 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0005c0024 | 0/0 | 10254 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0005c0037 | 0/0 | 10254 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0006c0009 | 0/0 | 10254 | 7 | 0 | 6 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0007c0008 | 0/0 | 10254 | 7 | 0 | 0 | 7 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0008c0013 | 0/0 | 10254 | 4 | 0 | 4 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0009c0015 | 0/0 | 10254 | 3 | 0 | 0 | 3 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0010c0014 | 0/0 | 10254 | 3 | 3 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0011c0021 | 0/0 | 10254 | 2 | 1 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0012c0020 | 0/0 | 10254 | 2 | 0 | 2 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0013c0018 | 0/0 | 10254 | 2 | 1 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0014c0017 | 0/0 | 10254 | 2 | 2 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0015c0022 | 0/0 | 10254 | 2 | 0 | 0 | 2 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0016c0016 | 0/0 | 10254 | 2 | 0 | 0 | 2 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0017c0026 | 0/0 | 10254 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0018c0040 | 0/0 | 10254 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0019c0044 | 0/0 | 10254 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0020c0038 | 0/0 | 10254 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0021c0025 | 0/0 | 10254 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0022c0035 | 0/0 | 10254 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0023c0027 | 0/0 | 10254 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0024c0045 | 0/0 | 10254 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0025c0029 | 0/0 | 10254 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0026c0030 | 0/0 | 10254 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0027c0043 | 0/0 | 10254 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0028c0049 | 0/0 | 10254 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0029c0032 | 0/0 | 10254 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0030c0028 | 0/0 | 10254 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0031c0036 | 0/0 | 10254 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0032c0050 | 0/0 | 10254 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0033c0041 | 0/0 | 10254 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0034c0034 | 0/0 | 10254 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0035c0046 | 0/0 | 10254 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0036c0047 | 0/0 | 10254 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0037c0039 | 0/0 | 10254 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 | ||
a0038c0042 | 0/0 | 10254 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | ATGCC others(10249): Show |
chr13 | 32310508 | 32405268 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 11953 | 67 | 5 | 4 | 49 | 1 | 8 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11948): Show |
chr13 | 32310508 | 32405268 |
a0001c0001t0008 | 0/0 | 11953 | 10 | 9 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11948): Show |
chr13 | 32310508 | 32405268 |
a0001c0001t0009 | 0/0 | 11953 | 7 | 1 | 3 | 2 | 1 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11948): Show |
chr13 | 32310508 | 32405268 |
a0001c0001t0013 | 0/0 | 11953 | 5 | 1 | 0 | 4 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11948): Show |
chr13 | 32310508 | 32405268 |
a0001c0001t0017 | 0/0 | 11954 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0001c0003t0004 | 0/0 | 11955 | 42 | 8 | 18 | 7 | 2 | 7 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11950): Show |
chr13 | 32310508 | 32405268 |
a0001c0003t0010 | 0/0 | 11954 | 4 | 3 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0001c0003t0014 | 0/0 | 11954 | 3 | 3 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0001c0003t0021 | 0/0 | 11955 | 2 | 0 | 2 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11950): Show |
chr13 | 32310508 | 32405268 |
a0001c0003t0034 | 0/0 | 11955 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11950): Show |
chr13 | 32310508 | 32405268 |
a0001c0003t0035 | 0/0 | 11955 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11950): Show |
chr13 | 32310508 | 32405268 |
a0001c0003t0036 | 0/0 | 11954 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0001c0003t0038 | 0/0 | 11954 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0001c0004t0003 | 0/0 | 11954 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0001c0004t0005 | 0/0 | 11954 | 32 | 0 | 5 | 21 | 2 | 4 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0001c0004t0006 | 0/0 | 11954 | 6 | 0 | 0 | 6 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0001c0004t0012 | 0/0 | 11954 | 5 | 5 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0001c0004t0040 | 0/0 | 11954 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0001c0004t0041 | 0/0 | 11955 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11950): Show |
chr13 | 32310508 | 32405268 |
a0001c0010t0011 | 0/0 | 11954 | 4 | 1 | 1 | 0 | 0 | 2 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0001c0010t0017 | 0/0 | 11954 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0001c0010t0039 | 0/0 | 11954 | 1 | 0 | 0 | 0 | 1 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0001c0011t0004 | 0/0 | 11955 | 2 | 2 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11950): Show |
chr13 | 32310508 | 32405268 |
a0001c0011t0019 | 0/0 | 11955 | 2 | 2 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11950): Show |
chr13 | 32310508 | 32405268 |
a0001c0033t0004 | 0/0 | 11955 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11950): Show |
chr13 | 32310508 | 32405268 |
a0002c0002t0002 | 0/0 | 11954 | 48 | 3 | 8 | 29 | 2 | 6 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0002c0002t0004 | 0/0 | 11955 | 3 | 0 | 1 | 0 | 2 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11950): Show |
chr13 | 32310508 | 32405268 |
a0002c0002t0006 | 0/0 | 11954 | 13 | 0 | 2 | 7 | 0 | 4 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0002c0002t0011 | 0/0 | 11954 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0002c0002t0024 | 0/1 | 11954 | 1 | 0 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0002c0002t0025 | 0/0 | 11954 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0002c0002t0028 | 0/0 | 11955 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11950): Show |
chr13 | 32310508 | 32405268 |
a0002c0002t0029 | 0/0 | 11954 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0002c0002t0030 | 0/0 | 11954 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0002c0002t0037 | 0/0 | 11955 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11950): Show |
chr13 | 32310508 | 32405268 |
a0002c0048t0002 | 0/0 | 11954 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0003c0005t0003 | 0/0 | 11954 | 31 | 0 | 5 | 19 | 1 | 6 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0003c0005t0007 | 0/0 | 11954 | 2 | 1 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0003c0005t0010 | 0/0 | 11954 | 2 | 0 | 0 | 0 | 0 | 2 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0003c0005t0032 | 0/0 | 11954 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0003c0005t0033 | 0/0 | 11954 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0003c0023t0007 | 0/0 | 11954 | 2 | 2 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0003c0051t0003 | 0/0 | 11954 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0004c0006t0003 | 0/0 | 11954 | 4 | 3 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0004c0006t0007 | 0/0 | 11954 | 6 | 0 | 4 | 2 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0004c0012t0007 | 0/0 | 11954 | 4 | 4 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0004c0019t0016 | 0/0 | 11954 | 2 | 2 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0004c0031t0007 | 0/0 | 11954 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0005c0007t0002 | 1/0 | 11954 | 1 | 0 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0005c0007t0003 | 0/0 | 11954 | 5 | 4 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0005c0007t0026 | 0/0 | 11954 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0005c0024t0003 | 0/0 | 11954 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0005c0037t0003 | 0/0 | 11954 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0006c0009t0003 | 0/0 | 11954 | 6 | 0 | 6 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0006c0009t0027 | 0/0 | 11955 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11950): Show |
chr13 | 32310508 | 32405268 |
a0007c0008t0001 | 0/0 | 11953 | 6 | 0 | 0 | 6 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11948): Show |
chr13 | 32310508 | 32405268 |
a0007c0008t0009 | 0/0 | 11953 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11948): Show |
chr13 | 32310508 | 32405268 |
a0008c0013t0002 | 0/0 | 11954 | 4 | 0 | 4 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0009c0015t0002 | 0/0 | 11954 | 3 | 0 | 0 | 3 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0010c0014t0015 | 0/0 | 11955 | 3 | 3 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11950): Show |
chr13 | 32310508 | 32405268 |
a0011c0021t0020 | 0/0 | 11954 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0011c0021t0023 | 0/0 | 11954 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0012c0020t0001 | 0/0 | 11953 | 2 | 0 | 2 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11948): Show |
chr13 | 32310508 | 32405268 |
a0013c0018t0003 | 0/0 | 11954 | 2 | 1 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0014c0017t0018 | 0/0 | 11954 | 2 | 2 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0015c0022t0001 | 0/0 | 11953 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11948): Show |
chr13 | 32310508 | 32405268 |
a0015c0022t0022 | 0/0 | 11954 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0016c0016t0005 | 0/0 | 11954 | 2 | 0 | 0 | 2 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0017c0026t0001 | 0/0 | 11953 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11948): Show |
chr13 | 32310508 | 32405268 |
a0018c0040t0011 | 0/0 | 11954 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0019c0044t0001 | 0/0 | 11953 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11948): Show |
chr13 | 32310508 | 32405268 |
a0020c0038t0004 | 0/0 | 11955 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11950): Show |
chr13 | 32310508 | 32405268 |
a0021c0025t0003 | 0/0 | 11954 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0022c0035t0004 | 0/0 | 11955 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11950): Show |
chr13 | 32310508 | 32405268 |
a0023c0027t0013 | 0/0 | 11953 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11948): Show |
chr13 | 32310508 | 32405268 |
a0024c0045t0020 | 0/0 | 11954 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0025c0029t0001 | 0/0 | 11953 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11948): Show |
chr13 | 32310508 | 32405268 |
a0026c0030t0003 | 0/0 | 11954 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0027c0043t0031 | 0/0 | 11954 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0028c0049t0010 | 0/0 | 11954 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0029c0032t0012 | 0/0 | 11954 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0030c0028t0005 | 0/0 | 11954 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0031c0036t0004 | 0/0 | 11955 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11950): Show |
chr13 | 32310508 | 32405268 |
a0032c0050t0003 | 0/0 | 11954 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0033c0041t0003 | 0/0 | 11954 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0034c0034t0006 | 0/0 | 11954 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0035c0046t0002 | 0/0 | 11954 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0036c0047t0002 | 0/0 | 11954 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0037c0039t0010 | 0/0 | 11954 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11949): Show |
chr13 | 32310508 | 32405268 |
a0038c0042t0004 | 0/0 | 11955 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | AGAGG others(11950): Show |
chr13 | 32310508 | 32405268 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0008g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0008g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0008g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0008g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0008g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0008g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0008g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0008g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0008g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0008g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0009g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0009g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0009g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0009g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0009g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0009g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0009g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0013g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0013g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0013g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0013g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0013g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0001t0017g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0004g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0010g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0010g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0010g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0010g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0014g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0014g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0014g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0021g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0021g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0034g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0035g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0036g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0003t0038g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0005g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0006g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0006g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0006g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0006g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0012g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0012g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0012g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0012g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0012g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0040g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0004t0041g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0010t0011g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0010t0011g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0010t0011g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0010t0011g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0010t0017g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0010t0039g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0011t0004g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0011t0004g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0011t0019g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0011t0019g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0001c0033t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0005 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0002g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0004g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0004g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0004g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0006g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0006g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0006g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0006g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0006g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0006g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0006g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0006g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0006g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0006g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0011g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0024g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0025g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0028g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0029g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0030g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0002t0037g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0002c0048t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0007g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0010g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0010g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0032g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0005t0033g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0023t0007g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0003c0051t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0004c0006t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0004c0006t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0004c0006t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0004c0006t0003g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0004c0006t0007g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0004c0006t0007g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0004c0006t0007g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0004c0006t0007g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0004c0006t0007g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0004c0006t0007g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0004c0012t0007g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0004c0012t0007g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0004c0012t0007g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0004c0019t0016g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0004c0019t0016g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0004c0031t0007g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0005c0007t0002g0297 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0005c0007t0003g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0005c0007t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0005c0007t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0005c0007t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0005c0007t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0005c0007t0026g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0005c0024t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0005c0037t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0006c0009t0003g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0006c0009t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0006c0009t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0006c0009t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0006c0009t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0006c0009t0027g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0007c0008t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0007c0008t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0007c0008t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0007c0008t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0007c0008t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0007c0008t0009g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0008c0013t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0008c0013t0002g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0008c0013t0002g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0009c0015t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0009c0015t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0009c0015t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0010c0014t0015g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0010c0014t0015g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0011c0021t0020g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0011c0021t0023g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0012c0020t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0012c0020t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0013c0018t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0013c0018t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0014c0017t0018g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0014c0017t0018g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0015c0022t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0015c0022t0022g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0016c0016t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0016c0016t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0017c0026t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0018c0040t0011g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0019c0044t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0020c0038t0004g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0021c0025t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0022c0035t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0023c0027t0013g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0024c0045t0020g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0025c0029t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0026c0030t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0027c0043t0031g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0028c0049t0010g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0029c0032t0012g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0030c0028t0005g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0031c0036t0004g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0032c0050t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0033c0041t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0034c0034t0006g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0035c0046t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0036c0047t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0037c0039t0010g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
a0038c0042t0004g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0004 | g0127 | EUR | GBR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00099 | hp2 | a0001 | c0003 | t0004 | g0320 | EUR | GBR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00280 | hp1 | a0001 | c0004 | t0005 | g0113 | EUR | FIN | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00280 | hp2 | a0002 | c0002 | t0002 | g0005 | EUR | FIN | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00323 | hp1 | a0002 | c0002 | t0004 | g0348 | EUR | FIN | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0021 | EUR | FIN | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00408 | hp1 | a0004 | c0006 | t0007 | g0010 | EAS | CHS | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00423 | hp1 | a0009 | c0015 | t0002 | g0157 | EAS | CHS | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00558 | hp1 | a0001 | c0003 | t0004 | g0075 | EAS | CHS | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0180 | EAS | CHS | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00597 | hp1 | a0017 | c0026 | t0001 | g0001 | EAS | CHS | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00597 | hp2 | a0001 | c0003 | t0004 | g0304 | EAS | CHS | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00609 | hp2 | a0001 | c0004 | t0005 | g0016 | EAS | CHS | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00621 | hp2 | a0001 | c0004 | t0005 | g0112 | EAS | CHS | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0166 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00639 | hp2 | a0003 | c0005 | t0003 | g0051 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00642 | hp1 | a0004 | c0006 | t0007 | g0119 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00733 | hp1 | a0001 | c0003 | t0004 | g0328 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00733 | hp2 | a0001 | c0001 | t0009 | g0069 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00735 | hp1 | a0006 | c0009 | t0003 | g0026 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00735 | hp2 | a0001 | c0003 | t0021 | g0319 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0162 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00738 | hp2 | a0001 | c0003 | t0004 | g0327 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0176 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01069 | hp1 | a0001 | c0010 | t0017 | g0369 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01069 | hp2 | a0001 | c0004 | t0040 | g0108 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01070 | hp2 | a0001 | c0003 | t0004 | g0317 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01071 | hp1 | a0001 | c0003 | t0004 | g0318 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01071 | hp2 | a0001 | c0010 | t0011 | g0368 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01074 | hp1 | a0001 | c0003 | t0021 | g0307 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01074 | hp2 | a0001 | c0003 | t0004 | g0210 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01099 | hp1 | a0002 | c0002 | t0002 | g0167 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01099 | hp2 | a0001 | c0003 | t0004 | g0313 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01106 | hp1 | a0001 | c0001 | t0008 | g0347 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01106 | hp2 | a0018 | c0040 | t0011 | g0014 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01167 | hp1 | a0001 | c0001 | t0009 | g0068 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01167 | hp2 | a0006 | c0009 | t0003 | g0027 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01168 | hp1 | a0001 | c0004 | t0005 | g0109 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01168 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01169 | hp1 | a0001 | c0001 | t0009 | g0067 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01169 | hp2 | a0001 | c0004 | t0005 | g0102 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01175 | hp1 | a0005 | c0007 | t0003 | g0294 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01175 | hp2 | a0001 | c0004 | t0005 | g0111 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01192 | hp1 | a0003 | c0005 | t0003 | g0023 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01192 | hp2 | a0001 | c0003 | t0004 | g0013 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01243 | hp1 | a0004 | c0006 | t0003 | g0118 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01243 | hp2 | a0011 | c0021 | t0023 | g0279 | AMR | PUR | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01255 | hp1 | a0002 | c0002 | t0030 | g0355 | AMR | CLM | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01255 | hp2 | a0001 | c0003 | t0004 | g0213 | AMR | CLM | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01256 | hp1 | a0002 | c0002 | t0006 | g0011 | AMR | CLM | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0161 | AMR | CLM | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01257 | hp1 | a0001 | c0003 | t0004 | g0018 | AMR | CLM | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01257 | hp2 | a0006 | c0009 | t0003 | g0007 | AMR | CLM | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01258 | hp1 | a0002 | c0002 | t0006 | g0011 | AMR | CLM | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01258 | hp2 | a0001 | c0003 | t0004 | g0018 | AMR | CLM | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01261 | hp1 | a0012 | c0020 | t0001 | g0366 | AMR | CLM | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01261 | hp2 | a0003 | c0005 | t0032 | g0362 | AMR | CLM | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01346 | hp1 | a0012 | c0020 | t0001 | g0367 | AMR | CLM | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01346 | hp2 | a0006 | c0009 | t0003 | g0007 | AMR | CLM | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01358 | hp1 | a0002 | c0002 | t0025 | g0165 | AMR | CLM | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01358 | hp2 | a0001 | c0003 | t0004 | g0209 | AMR | CLM | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01361 | hp1 | a0002 | c0002 | t0004 | g0175 | AMR | CLM | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01361 | hp2 | a0001 | c0003 | t0004 | g0314 | AMR | CLM | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01496 | hp1 | a0001 | c0003 | t0004 | g0013 | AMR | CLM | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01496 | hp2 | a0013 | c0018 | t0003 | g0073 | AMR | CLM | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01515 | hp1 | a0003 | c0005 | t0003 | g0054 | EUR | IBS | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | IBS | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01516 | hp1 | a0001 | c0001 | t0009 | g0139 | EUR | IBS | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01516 | hp2 | a0001 | c0010 | t0039 | g0257 | EUR | IBS | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01884 | hp1 | a0001 | c0003 | t0004 | g0324 | AFR | ACB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01884 | hp2 | a0001 | c0001 | t0008 | g0291 | AFR | ACB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01928 | hp1 | a0006 | c0009 | t0003 | g0024 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0173 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01934 | hp2 | a0019 | c0044 | t0001 | g0254 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01943 | hp1 | a0001 | c0003 | t0004 | g0211 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01943 | hp2 | a0008 | c0013 | t0002 | g0020 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01952 | hp1 | a0008 | c0013 | t0002 | g0020 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01952 | hp2 | a0004 | c0006 | t0007 | g0121 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01975 | hp1 | a0008 | c0013 | t0002 | g0359 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01975 | hp2 | a0020 | c0038 | t0004 | g0312 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01978 | hp1 | a0021 | c0025 | t0003 | g0215 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01981 | hp1 | a0001 | c0004 | t0005 | g0093 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01981 | hp2 | a0003 | c0005 | t0003 | g0035 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01993 | hp1 | a0001 | c0003 | t0004 | g0206 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG01993 | hp2 | a0003 | c0005 | t0003 | g0039 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02004 | hp1 | a0004 | c0006 | t0007 | g0120 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02004 | hp2 | a0001 | c0003 | t0004 | g0208 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02015 | hp1 | a0002 | c0002 | t0002 | g0153 | EAS | KHV | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02015 | hp2 | a0003 | c0005 | t0003 | g0003 | EAS | KHV | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02027 | hp1 | a0002 | c0002 | t0037 | g0183 | EAS | KHV | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02027 | hp2 | a0002 | c0002 | t0002 | g0160 | EAS | KHV | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02040 | hp1 | a0003 | c0005 | t0003 | g0003 | EAS | KHV | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02040 | hp2 | a0001 | c0003 | t0004 | g0302 | EAS | KHV | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02055 | hp2 | a0001 | c0003 | t0010 | g0316 | AFR | ACB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02071 | hp1 | a0022 | c0035 | t0004 | g0305 | EAS | KHV | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0156 | EAS | KHV | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02074 | hp1 | a0003 | c0005 | t0003 | g0050 | EAS | KHV | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0154 | EAS | KHV | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02083 | hp1 | a0001 | c0004 | t0006 | g0002 | EAS | KHV | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02129 | hp1 | a0002 | c0002 | t0002 | g0172 | EAS | KHV | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02132 | hp1 | a0001 | c0003 | t0004 | g0308 | EAS | KHV | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02132 | hp2 | a0001 | c0004 | t0006 | g0282 | EAS | KHV | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02135 | hp1 | a0001 | c0004 | t0005 | g0284 | EAS | KHV | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0145 | EAS | KHV | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02148 | hp1 | a0008 | c0013 | t0002 | g0358 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02148 | hp2 | a0004 | c0031 | t0007 | g0010 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02155 | hp1 | a0001 | c0004 | t0005 | g0016 | EAS | CDX | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02155 | hp2 | a0002 | c0002 | t0006 | g0133 | EAS | CDX | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02165 | hp1 | a0003 | c0005 | t0003 | g0003 | EAS | CDX | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02165 | hp2 | a0023 | c0027 | t0013 | g0205 | EAS | CDX | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02257 | hp1 | a0001 | c0003 | t0014 | g0080 | AFR | ACB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02257 | hp2 | a0004 | c0012 | t0007 | g0019 | AFR | ACB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02258 | hp1 | a0024 | c0045 | t0020 | g0352 | AFR | ACB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02258 | hp2 | a0002 | c0002 | t0002 | g0280 | AFR | ACB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02273 | hp1 | a0001 | c0003 | t0004 | g0207 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02273 | hp2 | a0003 | c0005 | t0003 | g0218 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02280 | hp1 | a0001 | c0001 | t0008 | g0055 | AFR | ACB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02280 | hp2 | a0001 | c0004 | t0003 | g0343 | AFR | ACB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02293 | hp1 | a0006 | c0009 | t0003 | g0025 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02293 | hp2 | a0001 | c0004 | t0005 | g0105 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02300 | hp1 | a0001 | c0003 | t0004 | g0212 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02300 | hp2 | a0004 | c0006 | t0007 | g0123 | AMR | PEL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02451 | hp1 | a0001 | c0003 | t0035 | g0287 | AFR | ACB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02451 | hp2 | a0002 | c0002 | t0002 | g0158 | AFR | ACB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02523 | hp1 | a0001 | c0004 | t0005 | g0283 | EAS | KHV | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02523 | hp2 | a0025 | c0029 | t0001 | g0263 | EAS | KHV | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02572 | hp1 | a0004 | c0006 | t0003 | g0344 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02572 | hp2 | a0005 | c0007 | t0003 | g0295 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02615 | hp1 | a0001 | c0001 | t0008 | g0361 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02615 | hp2 | a0001 | c0003 | t0004 | g0276 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02622 | hp1 | a0001 | c0003 | t0004 | g0333 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02622 | hp2 | a0001 | c0003 | t0010 | g0076 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02647 | hp1 | a0001 | c0001 | t0008 | g0290 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0357 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02698 | hp1 | a0003 | c0005 | t0003 | g0045 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02698 | hp2 | a0002 | c0002 | t0002 | g0126 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02723 | hp1 | a0001 | c0001 | t0009 | g0292 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02723 | hp2 | a0005 | c0007 | t0003 | g0301 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02735 | hp1 | a0001 | c0003 | t0004 | g0273 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02735 | hp2 | a0002 | c0002 | t0006 | g0136 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02738 | hp1 | a0001 | c0010 | t0011 | g0200 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02738 | hp2 | a0001 | c0004 | t0041 | g0107 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02809 | hp1 | a0004 | c0006 | t0003 | g0125 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02809 | hp2 | a0001 | c0003 | t0014 | g0079 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02818 | hp1 | a0003 | c0023 | t0007 | g0008 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02818 | hp2 | a0002 | c0002 | t0002 | g0168 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02886 | hp1 | a0013 | c0018 | t0003 | g0072 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02886 | hp2 | a0001 | c0004 | t0012 | g0341 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02895 | hp1 | a0004 | c0012 | t0007 | g0019 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02896 | hp1 | a0001 | c0011 | t0004 | g0364 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02896 | hp2 | a0014 | c0017 | t0018 | g0309 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02897 | hp1 | a0001 | c0011 | t0004 | g0365 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02922 | hp1 | a0026 | c0030 | t0003 | g0277 | AFR | ESN | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02922 | hp2 | a0004 | c0006 | t0003 | g0124 | AFR | ESN | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02965 | hp1 | a0001 | c0001 | t0008 | g0056 | AFR | ESN | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02965 | hp2 | a0010 | c0014 | t0015 | g0017 | AFR | ESN | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02970 | hp1 | a0001 | c0004 | t0012 | g0082 | AFR | ESN | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02970 | hp2 | a0027 | c0043 | t0031 | g0285 | AFR | ESN | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02976 | hp1 | a0001 | c0003 | t0004 | g0321 | AFR | ESN | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02976 | hp2 | a0001 | c0001 | t0008 | g0293 | AFR | ESN | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03017 | hp1 | a0003 | c0005 | t0010 | g0140 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03017 | hp2 | a0001 | c0003 | t0034 | g0214 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03041 | hp1 | a0005 | c0007 | t0003 | g0299 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03041 | hp2 | a0004 | c0019 | t0016 | g0065 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03130 | hp1 | a0004 | c0012 | t0007 | g0345 | AFR | ESN | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03130 | hp2 | a0001 | c0003 | t0038 | g0322 | AFR | ESN | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03139 | hp1 | a0001 | c0011 | t0019 | g0274 | AFR | ESN | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03139 | hp2 | a0001 | c0004 | t0012 | g0084 | AFR | ESN | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03195 | hp1 | a0001 | c0001 | t0008 | g0278 | AFR | ESN | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03195 | hp2 | a0001 | c0001 | t0008 | g0064 | AFR | ESN | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03209 | hp1 | a0005 | c0024 | t0003 | g0071 | AFR | MSL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03209 | hp2 | a0014 | c0017 | t0018 | g0311 | AFR | MSL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03225 | hp1 | a0004 | c0019 | t0016 | g0059 | AFR | MSL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03225 | hp2 | a0001 | c0001 | t0008 | g0063 | AFR | MSL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03239 | hp1 | a0002 | c0002 | t0002 | g0138 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03239 | hp2 | a0001 | c0010 | t0011 | g0014 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03486 | hp1 | a0028 | c0049 | t0010 | g0340 | AFR | MSL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03486 | hp2 | a0001 | c0003 | t0004 | g0326 | AFR | MSL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03490 | hp1 | a0001 | c0004 | t0005 | g0009 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03491 | hp1 | a0002 | c0002 | t0029 | g0354 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03491 | hp2 | a0003 | c0005 | t0003 | g0029 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03492 | hp1 | a0001 | c0004 | t0005 | g0009 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03492 | hp2 | a0003 | c0005 | t0003 | g0030 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03516 | hp1 | a0001 | c0003 | t0010 | g0077 | AFR | ESN | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03516 | hp2 | a0001 | c0004 | t0012 | g0085 | AFR | ESN | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03540 | hp1 | a0003 | c0023 | t0007 | g0008 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03540 | hp2 | a0011 | c0021 | t0020 | g0281 | AFR | GWD | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03579 | hp1 | a0029 | c0032 | t0012 | g0083 | AFR | MSL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03579 | hp2 | a0010 | c0014 | t0015 | g0286 | AFR | MSL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03654 | hp1 | a0001 | c0003 | t0004 | g0330 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03654 | hp2 | a0002 | c0002 | t0006 | g0135 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03669 | hp1 | a0001 | c0003 | t0004 | g0339 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03669 | hp2 | a0001 | c0004 | t0005 | g0091 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03688 | hp1 | a0002 | c0002 | t0006 | g0131 | SAS | STU | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03688 | hp2 | a0001 | c0003 | t0004 | g0303 | SAS | STU | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03704 | hp1 | a0030 | c0028 | t0005 | g0094 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03704 | hp2 | a0003 | c0005 | t0003 | g0031 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03710 | hp1 | a0002 | c0002 | t0002 | g0356 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03831 | hp2 | a0003 | c0005 | t0010 | g0141 | SAS | BEB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03834 | hp1 | a0006 | c0009 | t0027 | g0288 | SAS | BEB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0351 | SAS | BEB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03927 | hp1 | a0031 | c0036 | t0004 | g0334 | SAS | BEB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | BEB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03942 | hp2 | a0003 | c0005 | t0003 | g0053 | SAS | BEB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG04115 | hp1 | a0001 | c0003 | t0004 | g0360 | SAS | STU | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG04115 | hp2 | a0002 | c0002 | t0002 | g0178 | SAS | STU | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG04184 | hp2 | a0001 | c0003 | t0004 | g0323 | SAS | BEB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | STU | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG04199 | hp2 | a0001 | c0003 | t0004 | g0074 | SAS | STU | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG04204 | hp1 | a0001 | c0004 | t0005 | g0115 | SAS | STU | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG04204 | hp2 | a0032 | c0050 | t0003 | g0052 | SAS | STU | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18522 | hp1 | a0001 | c0003 | t0004 | g0325 | AFR | YRI | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18522 | hp2 | a0001 | c0001 | t0013 | g0250 | AFR | YRI | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18612 | hp1 | a0003 | c0005 | t0003 | g0040 | EAS | CHB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18612 | hp2 | a0001 | c0004 | t0006 | g0002 | EAS | CHB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18906 | hp1 | a0033 | c0041 | t0003 | g0022 | AFR | YRI | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18906 | hp2 | a0003 | c0005 | t0007 | g0028 | AFR | YRI | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18939 | hp2 | a0002 | c0002 | t0028 | g0152 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18941 | hp1 | a0003 | c0005 | t0003 | g0042 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18941 | hp2 | a0007 | c0008 | t0001 | g0001 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18942 | hp1 | a0001 | c0004 | t0005 | g0100 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18943 | hp1 | a0002 | c0002 | t0006 | g0129 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18944 | hp1 | a0001 | c0004 | t0005 | g0104 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18944 | hp2 | a0007 | c0008 | t0001 | g0253 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18945 | hp1 | a0003 | c0005 | t0003 | g0038 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18945 | hp2 | a0001 | c0001 | t0013 | g0256 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18946 | hp2 | a0003 | c0005 | t0003 | g0047 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18948 | hp1 | a0034 | c0034 | t0006 | g0310 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18949 | hp2 | a0002 | c0002 | t0002 | g0159 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18950 | hp2 | a0015 | c0022 | t0022 | g0229 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18951 | hp1 | a0001 | c0004 | t0006 | g0117 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18951 | hp2 | a0003 | c0005 | t0003 | g0202 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18952 | hp1 | a0001 | c0001 | t0009 | g0061 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18953 | hp2 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18954 | hp1 | a0007 | c0008 | t0001 | g0001 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18954 | hp2 | a0002 | c0002 | t0002 | g0155 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18956 | hp2 | a0035 | c0046 | t0002 | g0350 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18957 | hp2 | a0003 | c0005 | t0003 | g0043 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18959 | hp1 | a0002 | c0002 | t0011 | g0201 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18962 | hp1 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18963 | hp1 | a0001 | c0004 | t0005 | g0114 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18963 | hp2 | a0003 | c0005 | t0003 | g0036 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18965 | hp1 | a0003 | c0005 | t0007 | g0289 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18965 | hp2 | a0036 | c0047 | t0002 | g0181 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18966 | hp1 | a0001 | c0004 | t0005 | g0092 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18967 | hp1 | a0009 | c0015 | t0002 | g0142 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18967 | hp2 | a0001 | c0001 | t0013 | g0187 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18969 | hp1 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18970 | hp2 | a0002 | c0002 | t0006 | g0134 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18971 | hp2 | a0001 | c0004 | t0005 | g0110 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18972 | hp2 | a0001 | c0004 | t0005 | g0097 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18973 | hp1 | a0002 | c0002 | t0002 | g0148 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18979 | hp1 | a0002 | c0002 | t0006 | g0132 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18979 | hp2 | a0003 | c0005 | t0003 | g0044 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18980 | hp1 | a0001 | c0004 | t0005 | g0116 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18983 | hp2 | a0016 | c0016 | t0005 | g0096 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18986 | hp1 | a0016 | c0016 | t0005 | g0095 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18986 | hp2 | a0007 | c0008 | t0001 | g0251 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18987 | hp2 | a0001 | c0004 | t0005 | g0099 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18990 | hp1 | a0001 | c0003 | t0004 | g0332 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18990 | hp2 | a0002 | c0002 | t0002 | g0353 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18992 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18993 | hp1 | a0001 | c0004 | t0005 | g0090 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18994 | hp2 | a0001 | c0004 | t0005 | g0002 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18995 | hp1 | a0003 | c0005 | t0003 | g0041 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18998 | hp1 | a0002 | c0002 | t0006 | g0137 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18999 | hp1 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19001 | hp1 | a0001 | c0001 | t0017 | g0217 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19001 | hp2 | a0003 | c0005 | t0033 | g0037 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19003 | hp1 | a0001 | c0001 | t0013 | g0062 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19003 | hp2 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19004 | hp1 | a0007 | c0008 | t0009 | g0004 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19004 | hp2 | a0009 | c0015 | t0002 | g0150 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19005 | hp1 | a0002 | c0002 | t0002 | g0147 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19005 | hp2 | a0004 | c0006 | t0007 | g0122 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19006 | hp1 | a0001 | c0004 | t0005 | g0088 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19006 | hp2 | a0003 | c0005 | t0003 | g0049 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19007 | hp2 | a0007 | c0008 | t0001 | g0246 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19009 | hp1 | a0037 | c0039 | t0010 | g0315 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19010 | hp2 | a0001 | c0004 | t0006 | g0098 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19012 | hp1 | a0001 | c0004 | t0005 | g0089 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19030 | hp1 | a0001 | c0003 | t0014 | g0078 | AFR | LWK | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19030 | hp2 | a0001 | c0004 | t0012 | g0086 | AFR | LWK | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19043 | hp1 | a0001 | c0033 | t0004 | g0298 | AFR | LWK | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19043 | hp2 | a0001 | c0003 | t0036 | g0081 | AFR | LWK | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19054 | hp1 | a0007 | c0008 | t0001 | g0245 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19054 | hp2 | a0001 | c0003 | t0004 | g0306 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19055 | hp1 | a0038 | c0042 | t0004 | g0335 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19056 | hp1 | a0001 | c0001 | t0009 | g0066 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19056 | hp2 | a0002 | c0002 | t0002 | g0170 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19057 | hp2 | a0001 | c0003 | t0004 | g0336 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19058 | hp1 | a0003 | c0005 | t0003 | g0032 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19058 | hp2 | a0001 | c0004 | t0006 | g0342 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19060 | hp2 | a0001 | c0004 | t0005 | g0087 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19062 | hp2 | a0002 | c0002 | t0006 | g0128 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19065 | hp1 | a0003 | c0005 | t0003 | g0046 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19065 | hp2 | a0002 | c0048 | t0002 | g0169 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19066 | hp2 | a0001 | c0004 | t0005 | g0002 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19067 | hp1 | a0001 | c0003 | t0010 | g0337 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19070 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19072 | hp1 | a0003 | c0005 | t0003 | g0048 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19072 | hp2 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19074 | hp2 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19077 | hp1 | a0002 | c0002 | t0002 | g0171 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19077 | hp2 | a0001 | c0001 | t0013 | g0188 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19080 | hp2 | a0003 | c0005 | t0003 | g0338 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19081 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19085 | hp2 | a0001 | c0004 | t0005 | g0103 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19087 | hp1 | a0003 | c0005 | t0003 | g0216 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19087 | hp2 | a0015 | c0022 | t0001 | g0228 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19091 | hp1 | a0001 | c0004 | t0005 | g0106 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA20129 | hp2 | a0001 | c0003 | t0004 | g0331 | AFR | ASW | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA20805 | hp1 | a0001 | c0003 | t0004 | g0329 | EUR | TSI | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA20805 | hp2 | a0001 | c0004 | t0005 | g0101 | EUR | TSI | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA20905 | hp1 | a0002 | c0002 | t0006 | g0130 | SAS | GIH | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA20905 | hp2 | a0003 | c0005 | t0003 | g0034 | SAS | GIH | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02486 | hp1 | a0001 | c0010 | t0011 | g0267 | AFR | ACB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG02486 | hp2 | a0005 | c0007 | t0026 | g0296 | AFR | ACB | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03471 | hp1 | a0004 | c0012 | t0007 | g0346 | AFR | MSL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
HG03471 | hp2 | a0001 | c0011 | t0019 | g0275 | AFR | MSL | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18955 | hp1 | a0003 | c0051 | t0003 | g0033 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA18955 | hp2 | a0002 | c0002 | t0006 | g0349 | EAS | JPT | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA20300 | hp1 | a0010 | c0014 | t0015 | g0017 | AFR | USA | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA20300 | hp2 | a0005 | c0007 | t0003 | g0300 | AFR | USA | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA21309 | hp1 | a0001 | c0003 | t0004 | g0363 | AFR | LWK | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
NA21309 | hp2 | a0005 | c0037 | t0003 | g0070 | AFR | LWK | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
homoSapiens | chm13v2 | a0002 | c0002 | t0024 | g0164 | REF | REF | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
homoSapiens | grch38p0 | a0005 | c0007 | t0002 | g0297 | REF | REF | BRCA2_chr13_32310508_32405268 | BRCA2 | chr13 | 32310508 | 32405268 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:32316513 | G | A | 1 | a0016 | 2 | NA18983.hp2 NA18986.hp1 |
missense_variant | MODERATE | c.53G>A | p.Arg18His | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/27 | 252/11954 | 53/10257 | 18/3418 | chr13 | 32316513 | |||
chr13:32326112 | T | C | 1 | a0021 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.437T>C | p.Leu146Pro | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 5/27 | 636/11954 | 437/10257 | 146/3418 | chr13 | 32326112 | |||
chr13:32332343 | A | C | 3 | a0003 a0006 a0032 |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
missense_variant | MODERATE | c.865A>C | p.Asn289His | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/27 | 1064/11954 | 865/10257 | 289/3418 | chr13 | 32332343 | |||
chr13:32332421 | T | A | 2 | a0017 a0023 |
2 | HG00597.hp1 HG02165.hp2 |
missense_variant | MODERATE | c.943T>A | p.Cys315Ser | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/27 | 1142/11954 | 943/10257 | 315/3418 | chr13 | 32332421 | |||
chr13:32332442 | A | C | 1 | a0015 | 2 | NA18950.hp2 NA19087.hp2 |
missense_variant | MODERATE | c.964A>C | p.Lys322Gln | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/27 | 1163/11954 | 964/10257 | 322/3418 | chr13 | 32332442 | |||
chr13:32332518 | A | G | 1 | a0028 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.1040A>G | p.Gln347Arg | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/27 | 1239/11954 | 1040/10257 | 347/3418 | chr13 | 32332518 | |||
chr13:32332563 | A | T | 1 | a0023 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.1085A>T | p.Asp362Val | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/27 | 1284/11954 | 1085/10257 | 362/3418 | chr13 | 32332563 | |||
chr13:32332592 | A | C | 7 | a0002 a0008 a0009 others(4): Show |
83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
missense_variant | MODERATE | c.1114A>C | p.Asn372His | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/27 | 1313/11954 | 1114/10257 | 372/3418 | chr13 | 32332592 | |||
chr13:32332689 | A | T | 1 | a0019 | 1 | HG01934.hp2 | missense_variant | MODERATE | c.1211A>T | p.Asn404Ile | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/27 | 1410/11954 | 1211/10257 | 404/3418 | chr13 | 32332689 | |||
chr13:32332925 | G | A | 1 | a0030 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.1447G>A | p.Ala483Thr | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/27 | 1646/11954 | 1447/10257 | 483/3418 | chr13 | 32332925 | |||
chr13:32333078 | G | A | 1 | a0025 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.1600G>A | p.Glu534Lys | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/27 | 1799/11954 | 1600/10257 | 534/3418 | chr13 | 32333078 | |||
chr13:32336705 | A | G | 2 | a0007 a0015 |
9 | NA18941.hp2 NA18944.hp2 NA18950.hp2 others(6): Show |
missense_variant | MODERATE | c.2350A>G | p.Met784Val | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 2549/11954 | 2350/10257 | 784/3418 | chr13 | 32336705 | |||
chr13:32337087 | A | G | 1 | a0038 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.2732A>G | p.Glu911Gly | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 2931/11954 | 2732/10257 | 911/3418 | chr13 | 32337087 | |||
chr13:32337141 | T | C | 1 | a0024 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.2786T>C | p.Leu929Ser | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 2985/11954 | 2786/10257 | 929/3418 | chr13 | 32337141 | |||
chr13:32337315 | A | T | 1 | a0024 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.2960A>T | p.Asn987Ile | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 3159/11954 | 2960/10257 | 987/3418 | chr13 | 32337315 | |||
chr13:32337326 | A | G | 4 | a0003 a0006 a0032 others(1): Show |
49 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(46): Show |
missense_variant | MODERATE | c.2971A>G | p.Asn991Asp | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 3170/11954 | 2971/10257 | 991/3418 | chr13 | 32337326 | |||
chr13:32338445 | A | C | 1 | a0010 | 3 | HG02965.hp2 HG03579.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.4090A>C | p.Ile1364Leu | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 4289/11954 | 4090/10257 | 1364/3418 | chr13 | 32338445 | |||
chr13:32338596 | C | T | 1 | a0033 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.4241C>T | p.Thr1414Met | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 4440/11954 | 4241/10257 | 1414/3418 | chr13 | 32338596 | |||
chr13:32339134 | A | C | 1 | a0032 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.4779A>C | p.Glu1593Asp | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 4978/11954 | 4779/10257 | 1593/3418 | chr13 | 32339134 | |||
chr13:32339995 | T | G | 1 | a0029 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.5640T>G | p.Asn1880Lys | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 5839/11954 | 5640/10257 | 1880/3418 | chr13 | 32339995 | |||
chr13:32340038 | G | A | 1 | a0034 | 1 | NA18948.hp1 | missense_variant | MODERATE | c.5683G>A | p.Glu1895Lys | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 5882/11954 | 5683/10257 | 1895/3418 | chr13 | 32340038 | |||
chr13:32340059 | G | A | 1 | a0033 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.5704G>A | p.Asp1902Asn | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 5903/11954 | 5704/10257 | 1902/3418 | chr13 | 32340059 | |||
chr13:32340099 | C | T | 1 | a0012 | 2 | HG01261.hp1 HG01346.hp1 |
missense_variant | MODERATE | c.5744C>T | p.Thr1915Met | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 5943/11954 | 5744/10257 | 1915/3418 | chr13 | 32340099 | |||
chr13:32340140 | A | G | 1 | a0037 | 1 | NA19009.hp1 | missense_variant | MODERATE | c.5785A>G | p.Ile1929Val | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 5984/11954 | 5785/10257 | 1929/3418 | chr13 | 32340140 | |||
chr13:32340486 | G | T | 1 | a0036 | 1 | NA18965.hp2 | missense_variant | MODERATE | c.6131G>T | p.Gly2044Val | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 6330/11954 | 6131/10257 | 2044/3418 | chr13 | 32340486 | |||
chr13:32340575 | C | A | 1 | a0014 | 2 | HG02896.hp2 HG03209.hp2 |
missense_variant | MODERATE | c.6220C>A | p.His2074Asn | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 6419/11954 | 6220/10257 | 2074/3418 | chr13 | 32340575 | |||
chr13:32340636 | A | G | 1 | a0020 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.6281A>G | p.Tyr2094Cys | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 6480/11954 | 6281/10257 | 2094/3418 | chr13 | 32340636 | |||
chr13:32340678 | G | A | 1 | a0027 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.6323G>A | p.Arg2108His | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 6522/11954 | 6323/10257 | 2108/3418 | chr13 | 32340678 | |||
chr13:32340680 | G | A | 1 | a0035 | 1 | NA18956.hp2 | missense_variant | MODERATE | c.6325G>A | p.Val2109Ile | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 6524/11954 | 6325/10257 | 2109/3418 | chr13 | 32340680 | |||
chr13:32354870 | G | C | 1 | a0026 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.7017G>C | p.Lys2339Asn | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 14/27 | 7216/11954 | 7017/10257 | 2339/3418 | chr13 | 32354870 | |||
chr13:32355154 | A | C | 1 | a0031 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.7301A>C | p.Lys2434Thr | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 14/27 | 7500/11954 | 7301/10257 | 2434/3418 | chr13 | 32355154 | |||
chr13:32355172 | A | G | 2 | a0026 a0027 |
2 | HG02922.hp1 HG02970.hp2 |
missense_variant | MODERATE | c.7319A>G | p.His2440Arg | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 14/27 | 7518/11954 | 7319/10257 | 2440/3418 | chr13 | 32355172 | |||
chr13:32355250 | T | C | 37 | a0001 a0002 a0003 others(34): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
missense_variant | MODERATE | c.7397T>C | p.Val2466Ala | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 14/27 | 7596/11954 | 7397/10257 | 2466/3418 | chr13 | 32355250 | |||
chr13:32356461 | T | C | 1 | a0008 | 4 | HG01943.hp2 HG01952.hp1 HG01975.hp1 others(1): Show |
missense_variant | MODERATE | c.7469T>C | p.Ile2490Thr | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 15/27 | 7668/11954 | 7469/10257 | 2490/3418 | chr13 | 32356461 | |||
chr13:32363351 | G | T | 1 | a0018 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.8149G>T | p.Ala2717Ser | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/27 | 8348/11954 | 8149/10257 | 2717/3418 | chr13 | 32363351 | |||
chr13:32363389 | G | T | 1 | a0009 | 3 | HG00423.hp1 NA18967.hp1 NA19004.hp2 |
missense_variant | MODERATE | c.8187G>T | p.Lys2729Asn | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/27 | 8386/11954 | 8187/10257 | 2729/3418 | chr13 | 32363389 | |||
chr13:32370971 | T | C | 1 | a0013 | 2 | HG01496.hp2 HG02886.hp1 |
missense_variant | MODERATE | c.8503T>C | p.Ser2835Pro | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/27 | 8702/11954 | 8503/10257 | 2835/3418 | chr13 | 32370971 | |||
chr13:32379392 | A | T | 2 | a0011 a0024 |
3 | HG01243.hp2 HG02258.hp1 HG03540.hp2 |
missense_variant | MODERATE | c.8830A>T | p.Ile2944Phe | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 22/27 | 9029/11954 | 8830/10257 | 2944/3418 | chr13 | 32379392 | |||
chr13:32379413 | G | A | 1 | a0006 | 7 | HG00735.hp1 HG01167.hp2 HG01257.hp2 others(4): Show |
missense_variant | MODERATE | c.8851G>A | p.Ala2951Thr | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 22/27 | 9050/11954 | 8851/10257 | 2951/3418 | chr13 | 32379413 | |||
chr13:32398203 | A | T | 1 | a0022 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.9690A>T | p.Leu3230Phe | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 27/27 | 9889/11954 | 9690/10257 | 3230/3418 | chr13 | 32398203 | |||
chr13:32398243 | G | A | 1 | a0026 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.9730G>A | p.Val3244Ile | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 27/27 | 9929/11954 | 9730/10257 | 3244/3418 | chr13 | 32398243 | |||
chr13:32398747 | A | G | 2 | a0004 a0021 |
18 | HG00408.hp1 HG00642.hp1 HG01243.hp1 others(15): Show |
missense_variant | MODERATE | c.10234A>G | p.Ile3412Val | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 27/27 | 10433/11954 | 10234/10257 | 3412/3418 | chr13 | 32398747 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:32319240 | T | G | 1 | a0005c0024 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.231T>G | p.Thr77Thr | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/27 | 430/11954 | 231/10257 | 77/3418 | chr13 | 32319240 | |||
chr13:32332753 | A | G | 2 | a0002c0048 a0027c0043 |
2 | HG02970.hp2 NA19065.hp2 |
synonymous_variant | LOW | c.1275A>G | p.Glu425Glu | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/27 | 1474/11954 | 1275/10257 | 425/3418 | chr13 | 32332753 | |||
chr13:32332843 | A | G | 5 | a0003c0005 a0003c0023 a0003c0051 others(2): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
synonymous_variant | LOW | c.1365A>G | p.Ser455Ser | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/27 | 1564/11954 | 1365/10257 | 455/3418 | chr13 | 32332843 | |||
chr13:32333266 | T | C | 1 | a0001c0011 | 4 | HG02896.hp1 HG02897.hp1 HG03139.hp1 others(1): Show |
synonymous_variant | LOW | c.1788T>C | p.Asp596Asp | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/27 | 1987/11954 | 1788/10257 | 596/3418 | chr13 | 32333266 | |||
chr13:32336266 | T | C | 1 | a0028c0049 | 1 | HG03486.hp1 | splice_region_variant&synonymous_variant | LOW | c.1911T>C | p.Gly637Gly | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 2110/11954 | 1911/10257 | 637/3418 | chr13 | 32336266 | |||
chr13:32336584 | T | C | 5 | a0003c0005 a0003c0023 a0003c0051 others(2): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
synonymous_variant | LOW | c.2229T>C | p.His743His | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 2428/11954 | 2229/10257 | 743/3418 | chr13 | 32336584 | |||
chr13:32336845 | C | T | 1 | a0003c0051 | 1 | NA18955.hp1 | synonymous_variant | LOW | c.2490C>T | p.Asn830Asn | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 2689/11954 | 2490/10257 | 830/3418 | chr13 | 32336845 | |||
chr13:32337619 | T | C | 1 | a0026c0030 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.3264T>C | p.Pro1088Pro | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 3463/11954 | 3264/10257 | 1088/3418 | chr13 | 32337619 | |||
chr13:32337751 | A | G | 11 | a0001c0001 a0001c0010 a0004c0019 others(8): Show |
114 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(111): Show |
synonymous_variant | LOW | c.3396A>G | p.Lys1132Lys | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 3595/11954 | 3396/10257 | 1132/3418 | chr13 | 32337751 | |||
chr13:32338162 | T | C | 8 | a0001c0004 a0004c0006 a0004c0012 others(5): Show |
66 | HG00280.hp1 HG00408.hp1 HG00609.hp2 others(63): Show |
synonymous_variant | LOW | c.3807T>C | p.Val1269Val | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 4006/11954 | 3807/10257 | 1269/3418 | chr13 | 32338162 | |||
chr13:32338918 | A | G | 48 | a0001c0001 a0001c0003 a0001c0004 others(45): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
synonymous_variant | LOW | c.4563A>G | p.Leu1521Leu | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 4762/11954 | 4563/10257 | 1521/3418 | chr13 | 32338918 | |||
chr13:32339213 | T | C | 1 | a0004c0031 | 1 | HG02148.hp2 | synonymous_variant | LOW | c.4858T>C | p.Leu1620Leu | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 5057/11954 | 4858/10257 | 1620/3418 | chr13 | 32339213 | |||
chr13:32339773 | A | G | 1 | a0026c0030 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.5418A>G | p.Glu1806Glu | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 5617/11954 | 5418/10257 | 1806/3418 | chr13 | 32339773 | |||
chr13:32340868 | G | C | 47 | a0001c0001 a0001c0003 a0001c0004 others(44): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
synonymous_variant | LOW | c.6513G>C | p.Val2171Val | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/27 | 6712/11954 | 6513/10257 | 2171/3418 | chr13 | 32340868 | |||
chr13:32355095 | A | G | 9 | a0001c0001 a0004c0019 a0007c0008 others(6): Show |
107 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(104): Show |
synonymous_variant | LOW | c.7242A>G | p.Ser2414Ser | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 14/27 | 7441/11954 | 7242/10257 | 2414/3418 | chr13 | 32355095 | |||
chr13:32370530 | A | C | 2 | a0004c0012 a0004c0019 |
6 | HG02257.hp2 HG02895.hp1 HG03041.hp2 others(3): Show |
synonymous_variant | LOW | c.8460A>C | p.Val2820Val | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 19/27 | 8659/11954 | 8460/10257 | 2820/3418 | chr13 | 32370530 | |||
chr13:32398356 | A | G | 1 | a0003c0023 | 2 | HG02818.hp1 HG03540.hp1 |
synonymous_variant | LOW | c.9843A>G | p.Pro3281Pro | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 27/27 | 10042/11954 | 9843/10257 | 3281/3418 | chr13 | 32398356 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:32315655 | A | G | 13 | a0001c0001t0013 a0001c0004t0005 a0001c0004t0040 others(10): Show |
59 | HG00280.hp1 HG00408.hp1 HG00609.hp2 others(56): Show |
5_prime_UTR_variant | MODIFIER | c.-52A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 1/27 | 806 | chr13 | 32315655 | ||||||
chr13:32316435 | G | A | 18 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0017 others(15): Show |
98 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(95): Show |
5_prime_UTR_variant | MODIFIER | c.-26G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/27 | 26 | chr13 | 32316435 | ||||||
chr13:32316446 | A | C | 1 | a0001c0003t0038 | 1 | HG03130.hp2 | 5_prime_UTR_variant | MODIFIER | c.-15A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/27 | 15 | chr13 | 32316446 | ||||||
chr13:32316450 | C | T | 1 | a0010c0014t0015 | 3 | HG02965.hp2 HG03579.hp2 NA20300.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-11C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/27 | chr13 | 32316450 | |||||||
chr13:32398875 | A | C | 10 | a0001c0001t0017 a0001c0004t0005 a0001c0004t0006 others(7): Show |
59 | HG00280.hp1 HG00609.hp2 HG00621.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*105A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 27/27 | 105 | chr13 | 32398875 | ||||||
chr13:32399065 | C | G | 2 | a0001c0003t0014 a0001c0003t0036 |
4 | HG02257.hp1 HG02809.hp2 NA19030.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*295C>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 27/27 | 295 | chr13 | 32399065 | ||||||
chr13:32399139 | A | G | 22 | a0001c0003t0004 a0001c0003t0010 a0001c0003t0021 others(19): Show |
75 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*369A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 27/27 | 369 | chr13 | 32399139 | ||||||
chr13:32399167 | C | A | 2 | a0001c0004t0012 a0029c0032t0012 |
6 | HG02886.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*397C>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 27/27 | 397 | chr13 | 32399167 | ||||||
chr13:32399302 | A | G | 12 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0013 others(9): Show |
94 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*532A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 27/27 | 532 | chr13 | 32399302 | ||||||
chr13:32399322 | G | A | 1 | a0001c0003t0036 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*552G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 27/27 | 552 | chr13 | 32399322 | ||||||
chr13:32399523 | C | T | 1 | a0003c0005t0033 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*753C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 27/27 | 753 | chr13 | 32399523 | ||||||
chr13:32399599 | AT | A | 14 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(11): Show |
106 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*839delT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 27/27 | 839 | INFO_REALIGN_3_PRIME | chr13 | 32399599 | |||||
chr13:32399611 | A | G | 1 | a0003c0005t0032 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*841A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 27/27 | 841 | chr13 | 32399611 | ||||||
chr13:32399612 | A | G | 1 | a0027c0043t0031 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*842A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 27/27 | 842 | chr13 | 32399612 | ||||||
chr13:32399625 | C | A | 1 | a0001c0011t0019 | 2 | HG03139.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*855C>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 27/27 | 855 | chr13 | 32399625 | ||||||
chr13:32399713 | C | A | 1 | a0001c0003t0034 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*943C>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 27/27 | 943 | chr13 | 32399713 | ||||||
chr13:32399747 | A | G | 2 | a0002c0002t0029 a0002c0002t0030 |
2 | HG01255.hp1 HG03491.hp1 |
3_prime_UTR_variant | MODIFIER | c.*977A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 27/27 | 977 | chr13 | 32399747 | ||||||
chr13:32399786 | C | CT | 19 | a0001c0003t0004 a0001c0003t0021 a0001c0003t0034 others(16): Show |
68 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1031dupT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 27/27 | 1032 | INFO_REALIGN_3_PRIME | chr13 | 32399786 | |||||
chr13:32399918 | T | G | 1 | a0002c0002t0025 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1148T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 27/27 | 1148 | chr13 | 32399918 | ||||||
chr13:32399959 | C | T | 1 | a0001c0003t0035 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1189C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 27/27 | 1189 | chr13 | 32399959 | ||||||
chr13:32400001 | G | A | 1 | a0002c0002t0029 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1231G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 27/27 | 1231 | chr13 | 32400001 | ||||||
chr13:32400081 | C | T | 1 | a0001c0003t0021 | 2 | HG00735.hp2 HG01074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1311C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 27/27 | 1311 | chr13 | 32400081 | ||||||
chr13:32400151 | T | A | 68 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(65): Show |
319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
3_prime_UTR_variant | MODIFIER | c.*1381T>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 27/27 | 1381 | chr13 | 32400151 | ||||||
chr13:32400233 | C | T | 1 | a0005c0007t0026 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1463C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 27/27 | 1463 | chr13 | 32400233 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:32315728 | G | A | 1 | a0002c0002t0002g0021 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-40+61G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 1/26 | chr13 | 32315728 | |||||||
chr13:32315831 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(282): Show |
304 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.-40+164G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 1/26 | chr13 | 32315831 | |||||||
chr13:32315859 | C | T | 4 | a0001c0004t0005g0016 a0001c0004t0005g0283 a0001c0004t0005g0284 others(1): Show |
5 | HG00609.hp2 HG02132.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.-40+192C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 1/26 | chr13 | 32315859 | |||||||
chr13:32315889 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0203 others(92): Show |
99 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.-40+222C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 1/26 | chr13 | 32315889 | |||||||
chr13:32316027 | G | A | 3 | a0010c0014t0015g0017 a0010c0014t0015g0286 a0027c0043t0031g0285 |
4 | HG02965.hp2 HG02970.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40+360G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 1/26 | chr13 | 32316027 | |||||||
chr13:32316041 | A | G | 1 | a0002c0002t0011g0201 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-40+374A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 1/26 | chr13 | 32316041 | |||||||
chr13:32316090 | G | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0185 others(91): Show |
97 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.-39-332G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 1/26 | chr13 | 32316090 | |||||||
chr13:32316211 | G | A | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-39-211G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 1/26 | chr13 | 32316211 | |||||||
chr13:32316292 | C | G | 1 | a0001c0001t0001g0184 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-39-130C>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 1/26 | chr13 | 32316292 | |||||||
chr13:32316307 | G | A | 1 | a0001c0001t0017g0217 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-39-115G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 1/26 | chr13 | 32316307 | |||||||
chr13:32316543 | A | G | 1 | a0001c0003t0004g0360 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.67+16A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/26 | chr13 | 32316543 | |||||||
chr13:32316853 | G | C | 1 | a0001c0003t0035g0287 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67+326G>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/26 | chr13 | 32316853 | |||||||
chr13:32317042 | A | G | 1 | a0003c0005t0003g0216 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.67+515A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/26 | chr13 | 32317042 | |||||||
chr13:32317113 | C | T | 1 | a0002c0002t0037g0183 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.67+586C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/26 | chr13 | 32317113 | |||||||
chr13:32317168 | T | C | 41 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(38): Show |
45 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(42): Show |
intron_variant | MODIFIER | c.67+641T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/26 | chr13 | 32317168 | |||||||
chr13:32317246 | T | A | 1 | a0027c0043t0031g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.67+719T>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/26 | chr13 | 32317246 | |||||||
chr13:32317314 | CAAGT | C | 81 | a0001c0001t0008g0278 a0001c0001t0008g0347 a0001c0001t0008g0361 others(78): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.67+788_67+791delAA others(2): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/26 | chr13 | 32317314 | |||||||
chr13:32317498 | T | G | 2 | a0001c0011t0004g0364 a0001c0011t0004g0365 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.67+971T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/26 | chr13 | 32317498 | |||||||
chr13:32317569 | A | G | 55 | a0001c0004t0003g0343 a0001c0004t0005g0002 a0001c0004t0005g0009 others(52): Show |
60 | HG00280.hp1 HG00408.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.67+1042A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/26 | chr13 | 32317569 | |||||||
chr13:32317629 | T | C | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.67+1102T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/26 | chr13 | 32317629 | |||||||
chr13:32317661 | T | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(106): Show |
113 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.67+1134T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/26 | chr13 | 32317661 | |||||||
chr13:32317793 | C | T | 2 | a0001c0001t0008g0278 a0001c0001t0008g0361 |
2 | HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.67+1266C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/26 | chr13 | 32317793 | |||||||
chr13:32318080 | C | T | 364 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(361): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.68-997C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/26 | chr13 | 32318080 | |||||||
chr13:32318103 | CAGT | C | 3 | a0001c0001t0009g0067 a0001c0001t0009g0068 a0001c0001t0009g0069 |
3 | HG00733.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.68-973_68-971delAG others(1): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/26 | chr13 | 32318103 | |||||||
chr13:32318399 | C | A | 1 | a0002c0002t0002g0126 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.68-678C>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/26 | chr13 | 32318399 | |||||||
chr13:32318439 | AT | A | 41 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(38): Show |
45 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(42): Show |
intron_variant | MODIFIER | c.68-625delT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 32318439 | ||||||
chr13:32318450 | T | C | 1 | a0001c0003t0035g0287 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.68-627T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/26 | chr13 | 32318450 | |||||||
chr13:32318532 | C | T | 3 | a0001c0001t0008g0278 a0001c0001t0008g0347 a0001c0001t0008g0361 |
3 | HG01106.hp1 HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.68-545C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/26 | chr13 | 32318532 | |||||||
chr13:32318557 | G | T | 41 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(38): Show |
45 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(42): Show |
intron_variant | MODIFIER | c.68-520G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/26 | chr13 | 32318557 | |||||||
chr13:32318598 | T | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(254): Show |
272 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(269): Show |
intron_variant | MODIFIER | c.68-479T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/26 | chr13 | 32318598 | |||||||
chr13:32318623 | A | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(106): Show |
113 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.68-454A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/26 | chr13 | 32318623 | |||||||
chr13:32318683 | T | C | 42 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(39): Show |
46 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.68-394T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/26 | chr13 | 32318683 | |||||||
chr13:32318738 | G | A | 4 | a0001c0003t0014g0078 a0001c0003t0014g0079 a0001c0003t0014g0080 others(1): Show |
4 | HG02257.hp1 HG02809.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-339G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/26 | chr13 | 32318738 | |||||||
chr13:32318748 | G | A | 1 | a0026c0030t0003g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.68-329G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 2/26 | chr13 | 32318748 | |||||||
chr13:32319433 | A | G | 3 | a0001c0003t0010g0076 a0001c0003t0010g0077 a0028c0049t0010g0340 |
3 | HG02622.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.316+108A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32319433 | |||||||
chr13:32319442 | G | C | 1 | a0005c0037t0003g0070 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.316+117G>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32319442 | |||||||
chr13:32319500 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.316+175G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32319500 | |||||||
chr13:32319508 | T | G | 1 | a0003c0005t0003g0023 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.316+183T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32319508 | |||||||
chr13:32319587 | G | A | 2 | a0002c0002t0004g0127 a0002c0002t0004g0348 |
2 | HG00099.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.316+262G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32319587 | |||||||
chr13:32319654 | A | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(217): Show |
231 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(228): Show |
intron_variant | MODIFIER | c.316+329A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32319654 | |||||||
chr13:32319686 | A | G | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.316+361A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32319686 | |||||||
chr13:32319771 | A | G | 1 | a0026c0030t0003g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.316+446A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32319771 | |||||||
chr13:32320129 | G | A | 2 | a0013c0018t0003g0072 a0013c0018t0003g0073 |
2 | HG01496.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.316+804G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32320129 | |||||||
chr13:32320188 | A | C | 1 | a0001c0003t0004g0339 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.316+863A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32320188 | |||||||
chr13:32320306 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.316+981T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32320306 | |||||||
chr13:32320347 | G | A | 14 | a0002c0002t0002g0126 a0002c0002t0006g0011 a0002c0002t0006g0128 others(11): Show |
15 | HG01256.hp1 HG01258.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.316+1022G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32320347 | |||||||
chr13:32320545 | C | T | 1 | a0001c0004t0006g0117 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.316+1220C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32320545 | |||||||
chr13:32320601 | G | A | 41 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(38): Show |
45 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(42): Show |
intron_variant | MODIFIER | c.316+1276G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32320601 | |||||||
chr13:32320668 | A | T | 3 | a0001c0001t0001g0220 a0001c0001t0001g0272 a0001c0001t0009g0066 |
3 | HG03710.hp2 HG04199.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.316+1343A>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32320668 | |||||||
chr13:32320728 | T | C | 3 | a0001c0001t0009g0139 a0002c0002t0002g0005 a0002c0002t0002g0138 |
5 | HG00280.hp2 HG00642.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.316+1403T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32320728 | |||||||
chr13:32320753 | A | G | 1 | a0003c0005t0003g0338 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.316+1428A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32320753 | |||||||
chr13:32320782 | G | A | 1 | a0001c0003t0035g0287 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.316+1457G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32320782 | |||||||
chr13:32320807 | G | A | 1 | a0027c0043t0031g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.316+1482G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32320807 | |||||||
chr13:32320840 | C | T | 6 | a0001c0004t0012g0082 a0001c0004t0012g0084 a0001c0004t0012g0085 others(3): Show |
6 | HG02886.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.316+1515C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32320840 | |||||||
chr13:32321240 | G | C | 364 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(361): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.316+1915G>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32321240 | |||||||
chr13:32321244 | T | C | 1 | a0001c0004t0003g0343 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.316+1919T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32321244 | |||||||
chr13:32321334 | T | A | 6 | a0006c0009t0003g0007 a0006c0009t0003g0024 a0006c0009t0003g0025 others(3): Show |
7 | HG00735.hp1 HG01167.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.316+2009T>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32321334 | |||||||
chr13:32321537 | C | T | 41 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(38): Show |
45 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(42): Show |
intron_variant | MODIFIER | c.316+2212C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32321537 | |||||||
chr13:32321612 | G | C | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.316+2287G>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32321612 | |||||||
chr13:32321859 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.316+2534G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32321859 | |||||||
chr13:32321936 | T | C | 1 | a0027c0043t0031g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.316+2611T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32321936 | |||||||
chr13:32322149 | C | A | 1 | a0001c0001t0017g0217 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.316+2824C>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32322149 | |||||||
chr13:32322150 | A | T | 1 | a0001c0001t0017g0217 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.316+2825A>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32322150 | |||||||
chr13:32322151 | T | A | 1 | a0001c0001t0017g0217 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.316+2826T>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32322151 | |||||||
chr13:32322152 | C | T | 3 | a0002c0002t0002g0280 a0011c0021t0020g0281 a0011c0021t0023g0279 |
3 | HG01243.hp2 HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.316+2827C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32322152 | |||||||
chr13:32322477 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.317-2599G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32322477 | |||||||
chr13:32322539 | G | A | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.317-2537G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32322539 | |||||||
chr13:32322585 | C | T | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.317-2491C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32322585 | |||||||
chr13:32322589 | G | T | 1 | a0004c0019t0016g0065 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.317-2487G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32322589 | |||||||
chr13:32322709 | G | A | 39 | a0001c0004t0005g0002 a0001c0004t0005g0009 a0001c0004t0005g0016 others(36): Show |
43 | HG00280.hp1 HG00609.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.317-2367G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32322709 | |||||||
chr13:32322960 | A | G | 2 | a0001c0003t0004g0336 a0001c0003t0010g0337 |
2 | NA19057.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.317-2116A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32322960 | |||||||
chr13:32323006 | A | G | 3 | a0001c0001t0008g0063 a0001c0001t0008g0064 a0001c0001t0008g0293 |
3 | HG02976.hp2 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.317-2070A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32323006 | |||||||
chr13:32323063 | C | T | 2 | a0001c0010t0011g0368 a0001c0010t0017g0369 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.317-2013C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32323063 | |||||||
chr13:32323072 | C | T | 1 | a0002c0002t0006g0011 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.317-2004C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32323072 | |||||||
chr13:32323151 | A | AT | 61 | a0001c0001t0001g0271 a0001c0003t0004g0075 a0001c0004t0003g0343 others(58): Show |
66 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.317-1907dupT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr13 | 32323151 | ||||||
chr13:32323151 | AT | A | 8 | a0001c0001t0008g0063 a0001c0001t0017g0217 a0001c0003t0004g0332 others(5): Show |
8 | HG02451.hp1 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.317-1907delT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr13 | 32323151 | ||||||
chr13:32323151 | ATT | A | 104 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(101): Show |
111 | HG00099.hp2 HG00597.hp2 HG00639.hp2 others(108): Show |
intron_variant | MODIFIER | c.317-1908_317-1907d others(4): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr13 | 32323151 | ||||||
chr13:32323151 | ATTTTTTT others(1): Show |
A | 18 | a0002c0002t0002g0005 a0002c0002t0002g0138 a0002c0002t0002g0143 others(15): Show |
20 | HG00280.hp2 HG00423.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.317-1914_317-1907d others(10): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr13 | 32323151 | ||||||
chr13:32323201 | G | A | 10 | a0001c0003t0004g0013 a0001c0003t0004g0206 a0001c0003t0004g0207 others(7): Show |
11 | HG01074.hp2 HG01192.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.317-1875G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32323201 | |||||||
chr13:32323301 | C | T | 1 | a0003c0005t0010g0141 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.317-1775C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32323301 | |||||||
chr13:32323302 | G | A | 1 | a0001c0003t0004g0206 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.317-1774G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32323302 | |||||||
chr13:32323396 | G | A | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.317-1680G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32323396 | |||||||
chr13:32323405 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.317-1671G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32323405 | |||||||
chr13:32323448 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.317-1628C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32323448 | |||||||
chr13:32323773 | T | G | 1 | a0003c0005t0010g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.317-1303T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32323773 | |||||||
chr13:32323775 | A | G | 1 | a0003c0005t0010g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.317-1301A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32323775 | |||||||
chr13:32324055 | A | G | 1 | a0004c0006t0003g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.317-1021A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32324055 | |||||||
chr13:32324101 | G | A | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.317-975G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32324101 | |||||||
chr13:32324252 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.317-824G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32324252 | |||||||
chr13:32324686 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.317-390G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32324686 | |||||||
chr13:32324693 | A | G | 3 | a0001c0003t0010g0076 a0001c0003t0010g0077 a0028c0049t0010g0340 |
3 | HG02622.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.317-383A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32324693 | |||||||
chr13:32324727 | A | G | 1 | a0001c0001t0001g0270 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.317-349A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32324727 | |||||||
chr13:32324978 | C | T | 1 | a0009c0015t0002g0157 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.317-98C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32324978 | |||||||
chr13:32325066 | A | G | 1 | a0001c0001t0001g0269 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.317-10A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 3/26 | chr13 | 32325066 | |||||||
chr13:32325251 | A | C | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.425+67A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 4/26 | chr13 | 32325251 | |||||||
chr13:32325307 | C | T | 1 | a0026c0030t0003g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.425+123C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 4/26 | chr13 | 32325307 | |||||||
chr13:32325331 | G | T | 7 | a0001c0003t0004g0018 a0001c0003t0004g0327 a0001c0003t0004g0328 others(4): Show |
8 | HG00733.hp1 HG00738.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.425+147G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 4/26 | chr13 | 32325331 | |||||||
chr13:32325418 | G | A | 2 | a0002c0002t0002g0159 a0002c0002t0002g0160 |
2 | HG02027.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.425+234G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 4/26 | chr13 | 32325418 | |||||||
chr13:32325430 | G | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(107): Show |
114 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.425+246G>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 4/26 | chr13 | 32325430 | |||||||
chr13:32325469 | C | T | 1 | a0027c0043t0031g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.425+285C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 4/26 | chr13 | 32325469 | |||||||
chr13:32325485 | A | G | 2 | a0001c0003t0004g0276 a0001c0003t0004g0326 |
2 | HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.425+301A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 4/26 | chr13 | 32325485 | |||||||
chr13:32325548 | G | GT | 11 | a0001c0001t0001g0222 a0001c0001t0009g0139 a0001c0003t0004g0276 others(8): Show |
11 | HG01516.hp1 HG01884.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.425+378dupT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr13 | 32325548 | ||||||
chr13:32325548 | G | T | 2 | a0001c0004t0005g0088 a0001c0004t0005g0116 |
2 | NA18980.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.425+364G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 4/26 | chr13 | 32325548 | |||||||
chr13:32325589 | G | A | 2 | a0001c0001t0009g0067 a0001c0001t0009g0068 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.425+405G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 4/26 | chr13 | 32325589 | |||||||
chr13:32325634 | G | A | 3 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 |
3 | NA18962.hp2 NA18964.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.425+450G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 4/26 | chr13 | 32325634 | |||||||
chr13:32325641 | C | T | 5 | a0002c0002t0002g0180 a0008c0013t0002g0020 a0008c0013t0002g0358 others(2): Show |
6 | HG00558.hp2 HG01943.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.425+457C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 4/26 | chr13 | 32325641 | |||||||
chr13:32325687 | C | T | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.426-414C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 4/26 | chr13 | 32325687 | |||||||
chr13:32325696 | A | G | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.426-405A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 4/26 | chr13 | 32325696 | |||||||
chr13:32325701 | C | T | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.426-400C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 4/26 | chr13 | 32325701 | |||||||
chr13:32325741 | C | T | 364 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(361): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.426-360C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 4/26 | chr13 | 32325741 | |||||||
chr13:32325750 | T | C | 1 | a0026c0030t0003g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.426-351T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 4/26 | chr13 | 32325750 | |||||||
chr13:32325762 | G | A | 2 | a0001c0001t0008g0278 a0001c0001t0008g0361 |
2 | HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.426-339G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 4/26 | chr13 | 32325762 | |||||||
chr13:32325765 | T | C | 2 | a0001c0003t0004g0302 a0026c0030t0003g0277 |
2 | HG02040.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.426-336T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 4/26 | chr13 | 32325765 | |||||||
chr13:32325828 | C | T | 1 | a0005c0007t0003g0301 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.426-273C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 4/26 | chr13 | 32325828 | |||||||
chr13:32325834 | C | T | 1 | a0002c0002t0002g0179 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.426-267C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 4/26 | chr13 | 32325834 | |||||||
chr13:32325840 | T | A | 1 | a0027c0043t0031g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.426-261T>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 4/26 | chr13 | 32325840 | |||||||
chr13:32326012 | T | C | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.426-89T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 4/26 | chr13 | 32326012 | |||||||
chr13:32326303 | A | T | 3 | a0001c0003t0010g0076 a0001c0003t0010g0077 a0028c0049t0010g0340 |
3 | HG02622.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.516+21A>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 6/26 | chr13 | 32326303 | |||||||
chr13:32326480 | C | T | 2 | a0005c0007t0003g0299 a0005c0007t0003g0300 |
2 | HG03041.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.517-19C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 6/26 | chr13 | 32326480 | |||||||
chr13:32326796 | T | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(152): Show |
163 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(160): Show |
intron_variant | MODIFIER | c.631+183T>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | chr13 | 32326796 | |||||||
chr13:32326867 | T | C | 1 | a0015c0022t0001g0228 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.631+254T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | chr13 | 32326867 | |||||||
chr13:32327066 | A | G | 1 | a0003c0005t0003g0054 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.631+453A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | chr13 | 32327066 | |||||||
chr13:32327154 | T | C | 4 | a0001c0011t0004g0364 a0001c0011t0004g0365 a0001c0011t0019g0274 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.631+541T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | chr13 | 32327154 | |||||||
chr13:32327293 | A | C | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.631+680A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | chr13 | 32327293 | |||||||
chr13:32327443 | G | A | 1 | a0015c0022t0022g0229 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.631+830G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | chr13 | 32327443 | |||||||
chr13:32327594 | C | T | 2 | a0013c0018t0003g0072 a0013c0018t0003g0073 |
2 | HG01496.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.631+981C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | chr13 | 32327594 | |||||||
chr13:32327601 | C | T | 1 | a0002c0002t0037g0183 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.631+988C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | chr13 | 32327601 | |||||||
chr13:32327672 | C | CA | 8 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(5): Show |
8 | HG00609.hp1 HG02273.hp1 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.631+1074dupA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr13 | 32327672 | ||||||
chr13:32327688 | T | A | 1 | a0001c0001t0001g0185 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.631+1075T>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | chr13 | 32327688 | |||||||
chr13:32327689 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.631+1076C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | chr13 | 32327689 | |||||||
chr13:32327768 | A | AT | 142 | a0001c0003t0014g0078 a0001c0003t0014g0079 a0001c0003t0014g0080 others(139): Show |
154 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.631+1169dupT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr13 | 32327768 | ||||||
chr13:32327930 | A | G | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.631+1317A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | chr13 | 32327930 | |||||||
chr13:32327943 | T | C | 7 | a0001c0001t0008g0055 a0001c0001t0008g0056 a0001c0001t0008g0063 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.631+1330T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | chr13 | 32327943 | |||||||
chr13:32328245 | G | GT | 17 | a0001c0003t0004g0013 a0001c0003t0004g0074 a0001c0003t0004g0213 others(14): Show |
18 | HG00280.hp1 HG00621.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.632-1184dupT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr13 | 32328245 | ||||||
chr13:32328257 | T | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(102): Show |
109 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.632-1186T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | chr13 | 32328257 | |||||||
chr13:32328367 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.632-1076G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | chr13 | 32328367 | |||||||
chr13:32328452 | G | A | 2 | a0001c0003t0004g0327 a0031c0036t0004g0334 |
2 | HG00738.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.632-991G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | chr13 | 32328452 | |||||||
chr13:32328571 | T | C | 1 | a0002c0002t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.632-872T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | chr13 | 32328571 | |||||||
chr13:32328594 | G | T | 1 | a0001c0001t0001g0266 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.632-849G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | chr13 | 32328594 | |||||||
chr13:32328640 | G | A | 1 | a0026c0030t0003g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.632-803G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | chr13 | 32328640 | |||||||
chr13:32328672 | A | T | 4 | a0001c0003t0014g0078 a0001c0003t0014g0079 a0001c0003t0014g0080 others(1): Show |
4 | HG02257.hp1 HG02809.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.632-771A>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | chr13 | 32328672 | |||||||
chr13:32328875 | A | AGT | 42 | a0001c0003t0010g0076 a0001c0003t0010g0077 a0001c0004t0005g0002 others(39): Show |
46 | HG00280.hp1 HG00609.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.632-551_632-550dup others(2): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr13 | 32328875 | ||||||
chr13:32328875 | AGT | A | 10 | a0001c0001t0001g0185 a0001c0001t0001g0233 a0001c0001t0001g0234 others(7): Show |
10 | HG00423.hp2 HG00621.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.632-551_632-550del others(2): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr13 | 32328875 | ||||||
chr13:32328941 | A | C | 1 | a0001c0004t0006g0342 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.632-502A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | chr13 | 32328941 | |||||||
chr13:32329132 | A | G | 1 | a0001c0001t0001g0015 | 2 | NA18971.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.632-311A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | chr13 | 32329132 | |||||||
chr13:32329344 | A | G | 1 | a0001c0001t0013g0062 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.632-99A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | chr13 | 32329344 | |||||||
chr13:32329434 | A | T | 1 | a0001c0001t0001g0239 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.632-9A>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 7/26 | chr13 | 32329434 | |||||||
chr13:32329548 | C | T | 66 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(63): Show |
69 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.681+56C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 8/26 | chr13 | 32329548 | |||||||
chr13:32329687 | T | G | 1 | a0001c0003t0035g0287 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.681+195T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 8/26 | chr13 | 32329687 | |||||||
chr13:32329701 | C | T | 3 | a0001c0001t0008g0278 a0001c0001t0008g0347 a0001c0001t0008g0361 |
3 | HG01106.hp1 HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.681+209C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 8/26 | chr13 | 32329701 | |||||||
chr13:32329726 | C | T | 1 | a0002c0002t0002g0160 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.681+234C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 8/26 | chr13 | 32329726 | |||||||
chr13:32329767 | T | A | 1 | a0028c0049t0010g0340 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.681+275T>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 8/26 | chr13 | 32329767 | |||||||
chr13:32329770 | C | A | 1 | a0002c0002t0002g0351 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.681+278C>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 8/26 | chr13 | 32329770 | |||||||
chr13:32329790 | T | A | 4 | a0001c0003t0014g0078 a0001c0003t0014g0079 a0001c0003t0014g0080 others(1): Show |
4 | HG02257.hp1 HG02809.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.681+298T>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 8/26 | chr13 | 32329790 | |||||||
chr13:32329806 | T | TTA | 55 | a0001c0004t0003g0343 a0001c0004t0005g0002 a0001c0004t0005g0009 others(52): Show |
60 | HG00280.hp1 HG00408.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.681+325_681+326dup others(2): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr13 | 32329806 | ||||||
chr13:32329935 | C | T | 1 | a0003c0005t0003g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.681+443C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 8/26 | chr13 | 32329935 | |||||||
chr13:32330162 | A | G | 2 | a0027c0043t0031g0285 a0033c0041t0003g0022 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.681+670A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 8/26 | chr13 | 32330162 | |||||||
chr13:32330189 | C | T | 1 | a0001c0004t0005g0113 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.681+697C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 8/26 | chr13 | 32330189 | |||||||
chr13:32330603 | G | A | 2 | a0012c0020t0001g0366 a0012c0020t0001g0367 |
2 | HG01261.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.682-316G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 8/26 | chr13 | 32330603 | |||||||
chr13:32330646 | G | C | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.682-273G>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 8/26 | chr13 | 32330646 | |||||||
chr13:32330889 | A | C | 1 | a0001c0003t0035g0287 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.682-30A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 8/26 | chr13 | 32330889 | |||||||
chr13:32331120 | G | A | 1 | a0002c0002t0002g0143 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.793+90G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 9/26 | chr13 | 32331120 | |||||||
chr13:32331128 | G | A | 364 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(361): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.793+98G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 9/26 | chr13 | 32331128 | |||||||
chr13:32331135 | C | T | 3 | a0002c0002t0002g0154 a0002c0002t0002g0155 a0002c0002t0002g0156 |
3 | HG02071.hp2 HG02074.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.793+105C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 9/26 | chr13 | 32331135 | |||||||
chr13:32331431 | G | T | 1 | a0026c0030t0003g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.793+401G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 9/26 | chr13 | 32331431 | |||||||
chr13:32331491 | C | A | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.793+461C>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 9/26 | chr13 | 32331491 | |||||||
chr13:32331778 | T | C | 4 | a0001c0003t0014g0078 a0001c0003t0014g0079 a0001c0003t0014g0080 others(1): Show |
4 | HG02257.hp1 HG02809.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-494T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 9/26 | chr13 | 32331778 | |||||||
chr13:32331802 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.794-470T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 9/26 | chr13 | 32331802 | |||||||
chr13:32331861 | A | G | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.794-411A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 9/26 | chr13 | 32331861 | |||||||
chr13:32332100 | G | C | 1 | a0001c0003t0004g0363 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.794-172G>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 9/26 | chr13 | 32332100 | |||||||
chr13:32333458 | T | C | 1 | a0001c0004t0005g0283 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1909+71T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | chr13 | 32333458 | |||||||
chr13:32333478 | ATATCT | A | 6 | a0001c0004t0012g0082 a0001c0004t0012g0084 a0001c0004t0012g0085 others(3): Show |
6 | HG02886.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1909+95_1909+99del others(5): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr13 | 32333478 | ||||||
chr13:32333619 | A | G | 1 | a0001c0003t0004g0302 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1909+232A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | chr13 | 32333619 | |||||||
chr13:32333630 | C | T | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.1909+243C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | chr13 | 32333630 | |||||||
chr13:32333651 | G | A | 1 | a0001c0004t0005g0089 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1909+264G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | chr13 | 32333651 | |||||||
chr13:32333719 | A | G | 9 | a0001c0003t0004g0276 a0001c0003t0004g0321 a0001c0003t0004g0324 others(6): Show |
10 | HG01884.hp1 HG02615.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1909+332A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | chr13 | 32333719 | |||||||
chr13:32333776 | C | T | 1 | a0005c0024t0003g0071 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1909+389C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | chr13 | 32333776 | |||||||
chr13:32333969 | A | G | 364 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(361): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.1909+582A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | chr13 | 32333969 | |||||||
chr13:32334210 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(151): Show |
162 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(159): Show |
intron_variant | MODIFIER | c.1909+823C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | chr13 | 32334210 | |||||||
chr13:32334492 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(107): Show |
114 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.1909+1105A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | chr13 | 32334492 | |||||||
chr13:32334587 | T | C | 1 | a0027c0043t0031g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1909+1200T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | chr13 | 32334587 | |||||||
chr13:32334699 | T | G | 1 | a0002c0002t0002g0160 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1909+1312T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | chr13 | 32334699 | |||||||
chr13:32334735 | G | A | 1 | a0001c0004t0005g0090 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1909+1348G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | chr13 | 32334735 | |||||||
chr13:32335313 | C | T | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1910-952C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | chr13 | 32335313 | |||||||
chr13:32335332 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1910-933G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | chr13 | 32335332 | |||||||
chr13:32335344 | C | CA | 21 | a0001c0001t0001g0186 a0001c0001t0001g0220 a0001c0003t0004g0321 others(18): Show |
21 | HG00738.hp1 HG01175.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.1910-902dupA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr13 | 32335344 | ||||||
chr13:32335344 | CA | C | 6 | a0001c0010t0017g0369 a0001c0011t0004g0365 a0002c0002t0002g0143 others(3): Show |
6 | HG01069.hp1 HG02451.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1910-902delA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr13 | 32335344 | ||||||
chr13:32335382 | T | C | 2 | a0001c0001t0001g0220 a0001c0001t0001g0272 |
2 | HG03710.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1910-883T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | chr13 | 32335382 | |||||||
chr13:32335478 | G | C | 1 | a0026c0030t0003g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1910-787G>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | chr13 | 32335478 | |||||||
chr13:32335723 | T | C | 1 | a0001c0001t0008g0055 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1910-542T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | chr13 | 32335723 | |||||||
chr13:32335744 | C | A | 2 | a0003c0005t0007g0028 a0003c0023t0007g0008 |
3 | HG02818.hp1 HG03540.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1910-521C>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | chr13 | 32335744 | |||||||
chr13:32335828 | GA | G | 4 | a0001c0003t0014g0078 a0001c0003t0014g0079 a0001c0003t0014g0080 others(1): Show |
4 | HG02257.hp1 HG02809.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1910-436delA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | chr13 | 32335828 | |||||||
chr13:32335919 | T | G | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.1910-346T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | chr13 | 32335919 | |||||||
chr13:32335965 | T | C | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1910-300T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | chr13 | 32335965 | |||||||
chr13:32336030 | C | T | 1 | a0001c0001t0008g0063 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1910-235C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | chr13 | 32336030 | |||||||
chr13:32336191 | T | C | 61 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(58): Show |
64 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.1910-74T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | chr13 | 32336191 | |||||||
chr13:32336214 | G | T | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.1910-51G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | chr13 | 32336214 | |||||||
chr13:32336222 | T | C | 1 | a0027c0043t0031g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1910-43T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 10/26 | chr13 | 32336222 | |||||||
chr13:32341273 | CAATT | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(107): Show |
114 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.6841+80_6841+83del others(4): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr13 | 32341273 | ||||||
chr13:32341387 | C | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(107): Show |
114 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.6841+191C>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32341387 | |||||||
chr13:32341421 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.6841+225T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32341421 | |||||||
chr13:32341461 | A | G | 1 | a0001c0001t0001g0199 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.6841+265A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32341461 | |||||||
chr13:32341669 | A | G | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.6841+473A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32341669 | |||||||
chr13:32341729 | G | A | 1 | a0002c0002t0002g0161 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.6841+533G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32341729 | |||||||
chr13:32341739 | G | A | 1 | a0006c0009t0027g0288 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.6841+543G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32341739 | |||||||
chr13:32341792 | T | C | 4 | a0003c0005t0003g0029 a0003c0005t0003g0030 a0003c0005t0003g0031 others(1): Show |
4 | HG03491.hp2 HG03492.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.6841+596T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32341792 | |||||||
chr13:32341836 | C | G | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.6841+640C>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32341836 | |||||||
chr13:32341867 | C | CA | 6 | a0001c0001t0008g0055 a0001c0001t0008g0056 a0001c0001t0008g0290 others(3): Show |
6 | HG01261.hp1 HG01884.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.6841+686dupA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr13 | 32341867 | ||||||
chr13:32341936 | A | G | 1 | a0001c0004t0005g0110 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.6841+740A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32341936 | |||||||
chr13:32342160 | C | A | 61 | a0001c0004t0003g0343 a0001c0004t0005g0002 a0001c0004t0005g0009 others(58): Show |
66 | HG00280.hp1 HG00408.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.6841+964C>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32342160 | |||||||
chr13:32342225 | A | G | 1 | a0001c0003t0004g0363 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.6841+1029A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32342225 | |||||||
chr13:32342233 | A | T | 1 | a0001c0001t0001g0232 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.6841+1037A>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32342233 | |||||||
chr13:32342240 | T | C | 1 | a0001c0001t0001g0241 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.6841+1044T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32342240 | |||||||
chr13:32342270 | C | CA | 50 | a0001c0004t0003g0343 a0001c0004t0005g0002 a0001c0004t0005g0009 others(47): Show |
55 | HG00280.hp1 HG00408.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.6841+1092dupA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr13 | 32342270 | ||||||
chr13:32342270 | C | CAA | 6 | a0001c0004t0005g0092 a0001c0004t0005g0093 a0003c0005t0003g0031 others(3): Show |
6 | HG00642.hp1 HG01515.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.6841+1091_6841+109 others(6): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr13 | 32342270 | ||||||
chr13:32342270 | C | CAAA | 42 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(39): Show |
46 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.6841+1090_6841+109 others(7): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr13 | 32342270 | ||||||
chr13:32342270 | CA | C | 81 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0008g0361 others(78): Show |
87 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.6841+1092delA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr13 | 32342270 | ||||||
chr13:32342270 | CAA | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(170): Show |
180 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(177): Show |
intron_variant | MODIFIER | c.6841+1091_6841+109 others(6): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr13 | 32342270 | ||||||
chr13:32342270 | CAAA | C | 9 | a0001c0003t0004g0313 a0001c0003t0004g0314 a0001c0003t0004g0317 others(6): Show |
9 | HG00099.hp2 HG00735.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.6841+1090_6841+109 others(7): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr13 | 32342270 | ||||||
chr13:32342322 | T | C | 1 | a0002c0002t0002g0138 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.6841+1126T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32342322 | |||||||
chr13:32342323 | A | G | 1 | a0002c0002t0002g0153 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.6841+1127A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32342323 | |||||||
chr13:32342540 | G | T | 3 | a0003c0005t0003g0003 a0003c0005t0003g0050 a0003c0005t0003g0338 |
5 | HG02015.hp2 HG02040.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.6841+1344G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32342540 | |||||||
chr13:32342608 | C | G | 1 | a0001c0001t0009g0061 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.6841+1412C>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32342608 | |||||||
chr13:32342652 | A | G | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.6841+1456A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32342652 | |||||||
chr13:32342915 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.6842-1643G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32342915 | |||||||
chr13:32342999 | A | G | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.6842-1559A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32342999 | |||||||
chr13:32343048 | G | GA | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01192.hp1 others(45): Show |
intron_variant | MODIFIER | c.6842-1496dupA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr13 | 32343048 | ||||||
chr13:32343048 | GA | G | 67 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(64): Show |
70 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.6842-1496delA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr13 | 32343048 | ||||||
chr13:32343174 | A | G | 1 | a0002c0002t0002g0176 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.6842-1384A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32343174 | |||||||
chr13:32343207 | T | C | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.6842-1351T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32343207 | |||||||
chr13:32343208 | T | C | 1 | a0001c0001t0001g0270 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.6842-1350T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32343208 | |||||||
chr13:32343436 | C | G | 1 | a0020c0038t0004g0312 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.6842-1122C>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32343436 | |||||||
chr13:32343709 | G | GA | 45 | a0001c0001t0001g0184 a0001c0004t0012g0082 a0003c0005t0003g0003 others(42): Show |
49 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.6842-839dupA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr13 | 32343709 | ||||||
chr13:32343709 | GA | G | 61 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(58): Show |
64 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.6842-839delA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr13 | 32343709 | ||||||
chr13:32344085 | A | G | 45 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(42): Show |
49 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.6842-473A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32344085 | |||||||
chr13:32344161 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0013g0062 |
2 | NA18987.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.6842-397G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32344161 | |||||||
chr13:32344166 | GA | G | 187 | a0001c0001t0001g0060 a0001c0001t0001g0244 a0001c0001t0001g0264 others(184): Show |
203 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.6842-375delA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr13 | 32344166 | ||||||
chr13:32344166 | GAA | G | 69 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(66): Show |
72 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.6842-376_6842-375d others(4): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr13 | 32344166 | ||||||
chr13:32344182 | A | G | 2 | a0001c0001t0001g0265 a0003c0005t0003g0048 |
2 | HG02647.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.6842-376A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32344182 | |||||||
chr13:32344280 | G | C | 2 | a0016c0016t0005g0095 a0016c0016t0005g0096 |
2 | NA18983.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.6842-278G>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32344280 | |||||||
chr13:32344344 | T | A | 1 | a0001c0003t0035g0287 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.6842-214T>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 11/26 | chr13 | 32344344 | |||||||
chr13:32344804 | A | G | 66 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(63): Show |
69 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.6937+151A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 12/26 | chr13 | 32344804 | |||||||
chr13:32344830 | G | A | 66 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(63): Show |
69 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.6937+177G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 12/26 | chr13 | 32344830 | |||||||
chr13:32344974 | T | C | 1 | a0027c0043t0031g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.6937+321T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 12/26 | chr13 | 32344974 | |||||||
chr13:32345062 | A | G | 1 | a0001c0004t0005g0115 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.6937+409A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 12/26 | chr13 | 32345062 | |||||||
chr13:32345093 | C | T | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.6937+440C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 12/26 | chr13 | 32345093 | |||||||
chr13:32345193 | T | C | 1 | a0007c0008t0001g0246 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.6937+540T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 12/26 | chr13 | 32345193 | |||||||
chr13:32345247 | T | G | 1 | a0001c0003t0004g0313 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.6937+594T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 12/26 | chr13 | 32345247 | |||||||
chr13:32345383 | C | T | 1 | a0014c0017t0018g0311 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.6937+730C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 12/26 | chr13 | 32345383 | |||||||
chr13:32345389 | A | T | 66 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(63): Show |
69 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.6937+736A>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 12/26 | chr13 | 32345389 | |||||||
chr13:32345500 | T | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(107): Show |
114 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.6937+847T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 12/26 | chr13 | 32345500 | |||||||
chr13:32345631 | A | T | 6 | a0001c0001t0001g0057 a0001c0001t0001g0060 a0001c0001t0001g0184 others(3): Show |
6 | HG01928.hp2 HG04184.hp1 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.6937+978A>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 12/26 | chr13 | 32345631 | |||||||
chr13:32345694 | T | C | 1 | a0001c0003t0004g0314 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.6937+1041T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 12/26 | chr13 | 32345694 | |||||||
chr13:32345739 | C | T | 1 | a0001c0001t0001g0269 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.6937+1086C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 12/26 | chr13 | 32345739 | |||||||
chr13:32345879 | G | A | 364 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(361): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.6938-948G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 12/26 | chr13 | 32345879 | |||||||
chr13:32345984 | C | T | 2 | a0004c0012t0007g0345 a0004c0012t0007g0346 |
2 | HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.6938-843C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 12/26 | chr13 | 32345984 | |||||||
chr13:32346073 | T | C | 1 | a0001c0003t0004g0314 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.6938-754T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 12/26 | chr13 | 32346073 | |||||||
chr13:32346203 | G | T | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.6938-624G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 12/26 | chr13 | 32346203 | |||||||
chr13:32346312 | G | C | 1 | a0026c0030t0003g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.6938-515G>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 12/26 | chr13 | 32346312 | |||||||
chr13:32346481 | G | A | 140 | a0001c0003t0014g0078 a0001c0003t0014g0079 a0001c0003t0014g0080 others(137): Show |
152 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.6938-346G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 12/26 | chr13 | 32346481 | |||||||
chr13:32346514 | C | T | 1 | a0001c0001t0001g0264 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.6938-313C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 12/26 | chr13 | 32346514 | |||||||
chr13:32346566 | C | A | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.6938-261C>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 12/26 | chr13 | 32346566 | |||||||
chr13:32346707 | T | C | 364 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(361): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.6938-120T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 12/26 | chr13 | 32346707 | |||||||
chr13:32346989 | G | A | 1 | a0001c0001t0008g0290 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.7007+93G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32346989 | |||||||
chr13:32347011 | T | TTTTATAA others(2): Show |
44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.7007+126_7007+134d others(11): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr13 | 32347011 | ||||||
chr13:32347053 | C | T | 4 | a0001c0001t0008g0055 a0001c0001t0008g0056 a0001c0001t0008g0290 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.7007+157C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32347053 | |||||||
chr13:32347162 | T | C | 1 | a0001c0003t0004g0213 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.7007+266T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32347162 | |||||||
chr13:32347169 | G | A | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.7007+273G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32347169 | |||||||
chr13:32347225 | T | C | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.7007+329T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32347225 | |||||||
chr13:32347278 | C | T | 1 | a0001c0003t0035g0287 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.7007+382C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32347278 | |||||||
chr13:32347376 | G | A | 1 | a0027c0043t0031g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.7007+480G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32347376 | |||||||
chr13:32347391 | A | T | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.7007+495A>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32347391 | |||||||
chr13:32347399 | A | G | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.7007+503A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32347399 | |||||||
chr13:32347584 | G | A | 3 | a0001c0001t0009g0067 a0001c0001t0009g0068 a0001c0001t0009g0069 |
3 | HG00733.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.7007+688G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32347584 | |||||||
chr13:32347695 | G | A | 1 | a0001c0003t0004g0323 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.7007+799G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32347695 | |||||||
chr13:32347699 | C | G | 2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | HG00423.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.7007+803C>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32347699 | |||||||
chr13:32347807 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(107): Show |
114 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.7007+911A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32347807 | |||||||
chr13:32347809 | G | C | 1 | a0001c0004t0003g0343 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7007+913G>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32347809 | |||||||
chr13:32347834 | C | T | 1 | a0003c0005t0007g0028 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.7007+938C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32347834 | |||||||
chr13:32347999 | C | T | 62 | a0001c0004t0003g0343 a0001c0004t0005g0002 a0001c0004t0005g0009 others(59): Show |
67 | HG00280.hp1 HG00408.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.7007+1103C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32347999 | |||||||
chr13:32348194 | A | C | 20 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0220 others(17): Show |
20 | HG00733.hp2 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.7007+1298A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32348194 | |||||||
chr13:32348295 | T | TAAAAGTT others(310): Show |
1 | a0006c0009t0003g0027 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.7007+1406_7007+140 others(321): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr13 | 32348295 | ||||||
chr13:32348295 | T | TAAAAGTT others(311): Show |
31 | a0003c0005t0003g0003 a0003c0005t0003g0029 a0003c0005t0003g0030 others(28): Show |
35 | HG00639.hp2 HG00735.hp1 HG01257.hp2 others(32): Show |
intron_variant | MODIFIER | c.7007+1406_7007+140 others(322): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr13 | 32348295 | ||||||
chr13:32348295 | T | TAAAAGTT others(312): Show |
9 | a0003c0005t0003g0023 a0003c0005t0003g0034 a0003c0005t0003g0035 others(6): Show |
9 | HG01192.hp1 HG01928.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.7007+1406_7007+140 others(323): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr13 | 32348295 | ||||||
chr13:32348295 | T | TAAAAGTT others(313): Show |
3 | a0003c0005t0003g0032 a0003c0005t0010g0140 a0003c0005t0010g0141 |
3 | HG03017.hp1 HG03831.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.7007+1406_7007+140 others(324): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr13 | 32348295 | ||||||
chr13:32348303 | C | T | 45 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(42): Show |
49 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.7007+1407C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32348303 | |||||||
chr13:32348329 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.7007+1433C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32348329 | |||||||
chr13:32348357 | C | T | 1 | a0006c0009t0027g0288 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.7007+1461C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32348357 | |||||||
chr13:32348361 | C | G | 1 | a0001c0001t0001g0261 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.7007+1465C>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32348361 | |||||||
chr13:32348465 | A | G | 2 | a0014c0017t0018g0309 a0014c0017t0018g0311 |
2 | HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.7007+1569A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32348465 | |||||||
chr13:32348708 | T | C | 1 | a0037c0039t0010g0315 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.7007+1812T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32348708 | |||||||
chr13:32348948 | C | T | 4 | a0003c0005t0003g0036 a0003c0005t0003g0046 a0003c0005t0003g0048 others(1): Show |
4 | NA18963.hp2 NA19006.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.7007+2052C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32348948 | |||||||
chr13:32348993 | G | T | 3 | a0001c0003t0010g0076 a0001c0003t0010g0077 a0028c0049t0010g0340 |
3 | HG02622.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.7007+2097G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32348993 | |||||||
chr13:32349216 | C | CA | 12 | a0001c0004t0005g0089 a0001c0004t0006g0342 a0001c0004t0012g0086 others(9): Show |
12 | HG01175.hp1 HG01243.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.7007+2343dupA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr13 | 32349216 | ||||||
chr13:32349216 | CA | C | 111 | a0001c0001t0008g0055 a0001c0001t0008g0056 a0001c0001t0008g0064 others(108): Show |
115 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.7007+2343delA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr13 | 32349216 | ||||||
chr13:32349216 | CAA | C | 7 | a0001c0001t0008g0278 a0001c0001t0008g0347 a0001c0001t0008g0361 others(4): Show |
7 | HG01106.hp1 HG01167.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.7007+2342_7007+234 others(6): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr13 | 32349216 | ||||||
chr13:32349216 | CAAAAAAA others(4): Show |
C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(98): Show |
105 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.7007+2333_7007+234 others(15): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr13 | 32349216 | ||||||
chr13:32349216 | CAAAAAAA others(5): Show |
C | 3 | a0001c0003t0010g0076 a0001c0003t0010g0077 a0028c0049t0010g0340 |
3 | HG02622.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.7007+2332_7007+234 others(16): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr13 | 32349216 | ||||||
chr13:32349217 | A | G | 1 | a0038c0042t0004g0335 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.7007+2321A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32349217 | |||||||
chr13:32349322 | C | A | 3 | a0001c0001t0001g0268 a0002c0002t0002g0126 a0002c0002t0002g0143 |
3 | HG02698.hp2 HG03942.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.7007+2426C>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32349322 | |||||||
chr13:32349322 | C | CA | 61 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(58): Show |
64 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.7007+2436dupA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr13 | 32349322 | ||||||
chr13:32349324 | A | C | 6 | a0001c0003t0014g0078 a0001c0003t0014g0079 a0001c0003t0014g0080 others(3): Show |
6 | HG02257.hp1 HG02698.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.7007+2428A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32349324 | |||||||
chr13:32349352 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.7007+2456C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32349352 | |||||||
chr13:32349428 | G | A | 1 | a0026c0030t0003g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.7007+2532G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32349428 | |||||||
chr13:32349553 | C | T | 65 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(62): Show |
68 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.7007+2657C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32349553 | |||||||
chr13:32349772 | G | A | 1 | a0029c0032t0012g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.7007+2876G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32349772 | |||||||
chr13:32349814 | C | CA | 138 | a0001c0004t0003g0343 a0001c0004t0005g0002 a0001c0004t0005g0009 others(135): Show |
150 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.7007+2936dupA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr13 | 32349814 | ||||||
chr13:32349814 | C | CAA | 47 | a0001c0003t0014g0078 a0001c0003t0014g0079 a0001c0003t0014g0080 others(44): Show |
51 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.7007+2935_7007+293 others(6): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr13 | 32349814 | ||||||
chr13:32349814 | CA | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(158): Show |
168 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.7007+2936delA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr13 | 32349814 | ||||||
chr13:32349851 | A | G | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.7007+2955A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32349851 | |||||||
chr13:32349878 | G | A | 1 | a0003c0005t0003g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.7007+2982G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32349878 | |||||||
chr13:32350055 | A | G | 20 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0220 others(17): Show |
20 | HG00733.hp2 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.7007+3159A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32350055 | |||||||
chr13:32350083 | G | A | 1 | a0038c0042t0004g0335 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.7007+3187G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32350083 | |||||||
chr13:32350130 | A | G | 1 | a0003c0005t0003g0050 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.7007+3234A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32350130 | |||||||
chr13:32350157 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.7007+3261C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32350157 | |||||||
chr13:32350182 | T | A | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | NA18948.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.7007+3286T>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32350182 | |||||||
chr13:32350183 | A | C | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | NA18948.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.7007+3287A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32350183 | |||||||
chr13:32350487 | C | T | 1 | a0001c0001t0008g0064 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.7007+3591C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32350487 | |||||||
chr13:32350510 | G | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(107): Show |
114 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.7007+3614G>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32350510 | |||||||
chr13:32350688 | G | T | 1 | a0003c0005t0003g0043 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.7007+3792G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32350688 | |||||||
chr13:32350747 | C | T | 75 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0012 others(72): Show |
82 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.7007+3851C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32350747 | |||||||
chr13:32350821 | A | G | 2 | a0002c0002t0006g0135 a0002c0002t0006g0136 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.7007+3925A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32350821 | |||||||
chr13:32350951 | T | G | 2 | a0001c0003t0004g0304 a0022c0035t0004g0305 |
2 | HG00597.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.7008-3910T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32350951 | |||||||
chr13:32351120 | C | A | 65 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(62): Show |
68 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.7008-3741C>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32351120 | |||||||
chr13:32351158 | C | T | 1 | a0001c0003t0004g0325 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.7008-3703C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32351158 | |||||||
chr13:32351239 | C | T | 2 | a0001c0010t0011g0014 a0018c0040t0011g0014 |
2 | HG01106.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.7008-3622C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32351239 | |||||||
chr13:32351338 | T | C | 5 | a0001c0003t0004g0302 a0001c0003t0004g0306 a0001c0003t0004g0332 others(2): Show |
5 | HG02040.hp2 NA18990.hp1 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.7008-3523T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32351338 | |||||||
chr13:32351343 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.7008-3518G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32351343 | |||||||
chr13:32351369 | C | A | 1 | a0001c0004t0005g0114 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.7008-3492C>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32351369 | |||||||
chr13:32351799 | A | AT | 3 | a0001c0003t0010g0076 a0001c0003t0010g0077 a0028c0049t0010g0340 |
3 | HG02622.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.7008-3059dupT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr13 | 32351799 | ||||||
chr13:32351870 | T | C | 1 | a0001c0001t0001g0249 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.7008-2991T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32351870 | |||||||
chr13:32351909 | C | G | 39 | a0003c0005t0003g0003 a0003c0005t0003g0029 a0003c0005t0003g0030 others(36): Show |
43 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.7008-2952C>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32351909 | |||||||
chr13:32351962 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.7008-2899C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32351962 | |||||||
chr13:32352070 | G | C | 1 | a0001c0001t0001g0232 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.7008-2791G>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32352070 | |||||||
chr13:32352100 | C | T | 1 | a0001c0004t0041g0107 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.7008-2761C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32352100 | |||||||
chr13:32352243 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.7008-2618A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32352243 | |||||||
chr13:32352395 | G | C | 1 | a0001c0004t0005g0009 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.7008-2466G>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32352395 | |||||||
chr13:32352517 | T | G | 45 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(42): Show |
49 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.7008-2344T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32352517 | |||||||
chr13:32352524 | C | T | 1 | a0026c0030t0003g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.7008-2337C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32352524 | |||||||
chr13:32352807 | A | G | 45 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(42): Show |
49 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.7008-2054A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32352807 | |||||||
chr13:32352880 | G | A | 9 | a0002c0002t0002g0021 a0002c0002t0002g0158 a0002c0002t0002g0162 others(6): Show |
9 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.7008-1981G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32352880 | |||||||
chr13:32353080 | T | G | 1 | a0029c0032t0012g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.7008-1781T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32353080 | |||||||
chr13:32353246 | A | G | 1 | a0001c0001t0008g0347 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.7008-1615A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32353246 | |||||||
chr13:32353385 | G | A | 1 | a0001c0003t0004g0074 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.7008-1476G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32353385 | |||||||
chr13:32353411 | A | T | 2 | a0002c0002t0002g0012 a0002c0002t0002g0179 |
3 | NA18962.hp1 NA18964.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.7008-1450A>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32353411 | |||||||
chr13:32353467 | C | CA | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(100): Show |
107 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.7008-1394_7008-139 others(5): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32353467 | |||||||
chr13:32353468 | T | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(100): Show |
107 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.7008-1393T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32353468 | |||||||
chr13:32353470 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(100): Show |
107 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.7008-1391A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32353470 | |||||||
chr13:32353471 | A | T | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(100): Show |
107 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.7008-1390A>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32353471 | |||||||
chr13:32353473 | G | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(100): Show |
107 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.7008-1388G>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32353473 | |||||||
chr13:32353474 | C | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(100): Show |
107 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.7008-1387C>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32353474 | |||||||
chr13:32353509 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.7008-1352C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32353509 | |||||||
chr13:32353519 | A | G | 1 | a0001c0003t0004g0327 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.7008-1342A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32353519 | |||||||
chr13:32353757 | C | T | 114 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(111): Show |
121 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.7008-1104C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32353757 | |||||||
chr13:32353780 | T | C | 1 | a0002c0002t0002g0353 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.7008-1081T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32353780 | |||||||
chr13:32353809 | G | A | 1 | a0001c0003t0004g0208 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.7008-1052G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32353809 | |||||||
chr13:32353908 | T | C | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.7008-953T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32353908 | |||||||
chr13:32353975 | G | A | 69 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(66): Show |
72 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.7008-886G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32353975 | |||||||
chr13:32354065 | A | G | 70 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(67): Show |
73 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.7008-796A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32354065 | |||||||
chr13:32354156 | A | G | 1 | a0001c0003t0004g0313 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.7008-705A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32354156 | |||||||
chr13:32354180 | T | C | 365 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(362): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.7008-681T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32354180 | |||||||
chr13:32354267 | T | C | 69 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(66): Show |
72 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.7008-594T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32354267 | |||||||
chr13:32354271 | G | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(216): Show |
230 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.7008-590G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32354271 | |||||||
chr13:32354726 | G | A | 1 | a0005c0007t0003g0294 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.7008-135G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32354726 | |||||||
chr13:32354799 | A | G | 2 | a0002c0002t0002g0166 a0002c0002t0002g0167 |
2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.7008-62A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 13/26 | chr13 | 32354799 | |||||||
chr13:32355332 | A | G | 1 | a0005c0037t0003g0070 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.7435+44A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 14/26 | chr13 | 32355332 | |||||||
chr13:32355341 | C | T | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.7435+53C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 14/26 | chr13 | 32355341 | |||||||
chr13:32355342 | G | A | 1 | a0001c0001t0001g0269 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.7435+54G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 14/26 | chr13 | 32355342 | |||||||
chr13:32355381 | G | A | 1 | a0002c0002t0002g0356 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.7435+93G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 14/26 | chr13 | 32355381 | |||||||
chr13:32355588 | G | A | 1 | a0002c0002t0002g0166 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.7435+300G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 14/26 | chr13 | 32355588 | |||||||
chr13:32355641 | CACCTGAG others(37): Show |
C | 3 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 |
3 | NA18962.hp2 NA18964.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.7435+357_7435+400d others(46): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr13 | 32355641 | ||||||
chr13:32355646 | G | A | 1 | a0001c0003t0004g0331 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.7435+358G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 14/26 | chr13 | 32355646 | |||||||
chr13:32355995 | A | G | 1 | a0001c0001t0001g0260 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.7436-433A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 14/26 | chr13 | 32355995 | |||||||
chr13:32356120 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.7436-308G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 14/26 | chr13 | 32356120 | |||||||
chr13:32356177 | G | A | 2 | a0001c0001t0013g0187 a0001c0001t0013g0188 |
2 | NA18967.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.7436-251G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 14/26 | chr13 | 32356177 | |||||||
chr13:32356233 | A | G | 1 | a0001c0003t0004g0308 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.7436-195A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 14/26 | chr13 | 32356233 | |||||||
chr13:32356237 | T | A | 4 | a0001c0001t0008g0063 a0001c0001t0008g0064 a0001c0001t0008g0293 others(1): Show |
4 | HG02976.hp2 HG03195.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.7436-191T>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 14/26 | chr13 | 32356237 | |||||||
chr13:32356272 | T | G | 3 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 |
3 | NA18962.hp2 NA18964.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.7436-156T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 14/26 | chr13 | 32356272 | |||||||
chr13:32356292 | A | C | 1 | a0038c0042t0004g0335 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.7436-136A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 14/26 | chr13 | 32356292 | |||||||
chr13:32356297 | C | T | 2 | a0004c0006t0003g0124 a0004c0006t0003g0344 |
2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.7436-131C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 14/26 | chr13 | 32356297 | |||||||
chr13:32356298 | G | A | 2 | a0001c0011t0004g0364 a0001c0011t0004g0365 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.7436-130G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 14/26 | chr13 | 32356298 | |||||||
chr13:32356757 | G | A | 2 | a0026c0030t0003g0277 a0027c0043t0031g0285 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.7617+148G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 15/26 | chr13 | 32356757 | |||||||
chr13:32356785 | G | A | 1 | a0028c0049t0010g0340 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.7617+176G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 15/26 | chr13 | 32356785 | |||||||
chr13:32356799 | G | A | 372 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(369): Show |
395 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(392): Show |
intron_variant | MODIFIER | c.7617+190G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 15/26 | chr13 | 32356799 | |||||||
chr13:32356844 | C | A | 2 | a0013c0018t0003g0072 a0013c0018t0003g0073 |
2 | HG01496.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.7617+235C>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 15/26 | chr13 | 32356844 | |||||||
chr13:32357107 | A | G | 1 | a0001c0001t0008g0347 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.7617+498A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 15/26 | chr13 | 32357107 | |||||||
chr13:32357158 | G | A | 2 | a0026c0030t0003g0277 a0027c0043t0031g0285 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.7617+549G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 15/26 | chr13 | 32357158 | |||||||
chr13:32357472 | TCCTCACA others(3): Show |
T | 1 | a0002c0002t0030g0355 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.7618-266_7618-257d others(12): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr13 | 32357472 | ||||||
chr13:32357492 | G | A | 1 | a0002c0002t0002g0168 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.7618-250G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 15/26 | chr13 | 32357492 | |||||||
chr13:32357952 | G | A | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.7805+23G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32357952 | |||||||
chr13:32357976 | A | G | 1 | a0001c0001t0001g0222 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.7805+47A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32357976 | |||||||
chr13:32358127 | A | G | 1 | a0001c0003t0034g0214 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.7805+198A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32358127 | |||||||
chr13:32358241 | C | T | 1 | a0001c0011t0019g0275 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.7805+312C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32358241 | |||||||
chr13:32358274 | G | T | 1 | a0001c0001t0001g0186 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.7805+345G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32358274 | |||||||
chr13:32358337 | G | A | 1 | a0003c0005t0003g0050 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.7805+408G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32358337 | |||||||
chr13:32358436 | A | G | 1 | a0027c0043t0031g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.7805+507A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32358436 | |||||||
chr13:32358468 | C | G | 1 | a0026c0030t0003g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.7805+539C>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32358468 | |||||||
chr13:32358476 | C | CA | 87 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(84): Show |
92 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.7805+561dupA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr13 | 32358476 | ||||||
chr13:32358491 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.7805+562G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32358491 | |||||||
chr13:32358492 | A | G | 1 | a0001c0001t0001g0057 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.7805+563A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32358492 | |||||||
chr13:32358600 | T | C | 1 | a0001c0033t0004g0298 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.7805+671T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32358600 | |||||||
chr13:32358687 | C | G | 1 | a0027c0043t0031g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.7805+758C>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32358687 | |||||||
chr13:32358691 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.7805+762G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32358691 | |||||||
chr13:32358855 | G | T | 7 | a0001c0001t0001g0186 a0001c0001t0001g0191 a0001c0001t0001g0192 others(4): Show |
7 | NA18972.hp1 NA19009.hp2 NA19012.hp2 others(4): Show |
intron_variant | MODIFIER | c.7805+926G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32358855 | |||||||
chr13:32358885 | G | T | 146 | a0001c0003t0014g0078 a0001c0003t0014g0079 a0001c0003t0014g0080 others(143): Show |
158 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.7805+956G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32358885 | |||||||
chr13:32358917 | G | C | 1 | a0029c0032t0012g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.7805+988G>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32358917 | |||||||
chr13:32358986 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.7805+1057T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32358986 | |||||||
chr13:32359222 | G | GA | 65 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(62): Show |
68 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.7805+1314dupA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr13 | 32359222 | ||||||
chr13:32359222 | GA | G | 143 | a0001c0003t0014g0078 a0001c0003t0014g0079 a0001c0003t0014g0080 others(140): Show |
155 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.7805+1314delA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr13 | 32359222 | ||||||
chr13:32359222 | GAA | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(105): Show |
112 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.7805+1313_7805+131 others(6): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr13 | 32359222 | ||||||
chr13:32359302 | A | G | 6 | a0003c0005t0003g0003 a0003c0005t0003g0050 a0003c0005t0003g0051 others(3): Show |
8 | HG00639.hp2 HG01261.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.7805+1373A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32359302 | |||||||
chr13:32359497 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.7805+1568A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32359497 | |||||||
chr13:32359662 | A | C | 1 | a0001c0004t0012g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.7805+1733A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32359662 | |||||||
chr13:32359696 | T | C | 2 | a0013c0018t0003g0072 a0013c0018t0003g0073 |
2 | HG01496.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.7805+1767T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32359696 | |||||||
chr13:32359789 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(100): Show |
107 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.7805+1860A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32359789 | |||||||
chr13:32359800 | A | G | 365 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(362): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.7805+1871A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32359800 | |||||||
chr13:32360294 | G | A | 2 | a0026c0030t0003g0277 a0027c0043t0031g0285 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.7806-2229G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32360294 | |||||||
chr13:32360373 | T | A | 2 | a0026c0030t0003g0277 a0027c0043t0031g0285 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.7806-2150T>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32360373 | |||||||
chr13:32360422 | C | T | 1 | a0003c0005t0003g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.7806-2101C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32360422 | |||||||
chr13:32360521 | G | A | 2 | a0026c0030t0003g0277 a0027c0043t0031g0285 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.7806-2002G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32360521 | |||||||
chr13:32360644 | C | T | 2 | a0013c0018t0003g0072 a0013c0018t0003g0073 |
2 | HG01496.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.7806-1879C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32360644 | |||||||
chr13:32360647 | T | C | 1 | a0002c0002t0006g0137 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.7806-1876T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32360647 | |||||||
chr13:32360755 | A | T | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.7806-1768A>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32360755 | |||||||
chr13:32360774 | G | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(100): Show |
107 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.7806-1749G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32360774 | |||||||
chr13:32360864 | G | A | 1 | a0001c0011t0019g0274 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.7806-1659G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32360864 | |||||||
chr13:32360873 | C | T | 3 | a0001c0003t0010g0076 a0001c0003t0010g0077 a0028c0049t0010g0340 |
3 | HG02622.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.7806-1650C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32360873 | |||||||
chr13:32360930 | G | A | 1 | a0004c0006t0003g0118 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.7806-1593G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32360930 | |||||||
chr13:32361269 | T | C | 46 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(43): Show |
48 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.7806-1254T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32361269 | |||||||
chr13:32361348 | C | T | 3 | a0009c0015t0002g0142 a0009c0015t0002g0150 a0009c0015t0002g0157 |
3 | HG00423.hp1 NA18967.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.7806-1175C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32361348 | |||||||
chr13:32361365 | G | A | 5 | a0003c0005t0003g0038 a0003c0005t0003g0042 a0003c0005t0003g0044 others(2): Show |
5 | NA18941.hp1 NA18945.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.7806-1158G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32361365 | |||||||
chr13:32361504 | G | A | 1 | a0026c0030t0003g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.7806-1019G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32361504 | |||||||
chr13:32362021 | T | G | 1 | a0001c0003t0010g0316 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.7806-502T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32362021 | |||||||
chr13:32362049 | G | A | 2 | a0013c0018t0003g0072 a0013c0018t0003g0073 |
2 | HG01496.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.7806-474G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32362049 | |||||||
chr13:32362062 | G | A | 2 | a0013c0018t0003g0072 a0013c0018t0003g0073 |
2 | HG01496.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.7806-461G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32362062 | |||||||
chr13:32362094 | C | G | 1 | a0001c0033t0004g0298 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.7806-429C>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32362094 | |||||||
chr13:32362136 | C | T | 1 | a0002c0002t0002g0143 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.7806-387C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32362136 | |||||||
chr13:32362483 | A | G | 3 | a0004c0012t0007g0019 a0004c0012t0007g0345 a0004c0012t0007g0346 |
4 | HG02257.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.7806-40A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32362483 | |||||||
chr13:32362509 | T | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(215): Show |
229 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.7806-14T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 16/26 | chr13 | 32362509 | |||||||
chr13:32362717 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.7976+24G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 17/26 | chr13 | 32362717 | |||||||
chr13:32363642 | G | A | 4 | a0001c0011t0004g0364 a0001c0011t0004g0365 a0001c0011t0019g0274 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.8331+109G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32363642 | |||||||
chr13:32363866 | A | G | 2 | a0026c0030t0003g0277 a0027c0043t0031g0285 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.8331+333A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32363866 | |||||||
chr13:32364036 | A | C | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.8331+503A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32364036 | |||||||
chr13:32364037 | C | G | 1 | a0005c0007t0003g0301 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.8331+504C>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32364037 | |||||||
chr13:32364066 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.8331+533A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32364066 | |||||||
chr13:32364315 | A | G | 5 | a0001c0003t0004g0302 a0001c0003t0004g0306 a0001c0003t0004g0332 others(2): Show |
5 | HG02040.hp2 NA18990.hp1 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.8331+782A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32364315 | |||||||
chr13:32364476 | T | G | 1 | a0005c0024t0003g0071 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.8331+943T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32364476 | |||||||
chr13:32364532 | T | A | 4 | a0001c0003t0014g0078 a0001c0003t0014g0079 a0001c0003t0014g0080 others(1): Show |
4 | HG02257.hp1 HG02809.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.8331+999T>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32364532 | |||||||
chr13:32364579 | T | G | 2 | a0001c0010t0011g0014 a0018c0040t0011g0014 |
2 | HG01106.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.8331+1046T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32364579 | |||||||
chr13:32364618 | C | CT | 67 | a0001c0004t0040g0108 a0001c0010t0011g0014 a0001c0010t0011g0200 others(64): Show |
73 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.8331+1086dupT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32364618 | ||||||
chr13:32364660 | G | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | NA18962.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.8331+1127G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32364660 | |||||||
chr13:32364744 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(100): Show |
107 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.8331+1211A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32364744 | |||||||
chr13:32364848 | C | T | 4 | a0001c0003t0014g0078 a0001c0003t0014g0079 a0001c0003t0014g0080 others(1): Show |
4 | HG02257.hp1 HG02809.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.8331+1315C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32364848 | |||||||
chr13:32364948 | C | T | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.8331+1415C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32364948 | |||||||
chr13:32365109 | C | CT | 63 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(60): Show |
66 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.8331+1604dupT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32365109 | ||||||
chr13:32365109 | C | CTT | 38 | a0001c0003t0004g0276 a0001c0003t0004g0327 a0003c0005t0003g0003 others(35): Show |
41 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.8331+1603_8331+160 others(6): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32365109 | ||||||
chr13:32365109 | C | CTTT | 8 | a0003c0005t0003g0041 a0003c0005t0003g0045 a0003c0005t0003g0049 others(5): Show |
9 | HG02698.hp1 HG02818.hp1 HG03540.hp1 others(6): Show |
intron_variant | MODIFIER | c.8331+1602_8331+160 others(7): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32365109 | ||||||
chr13:32365109 | CT | C | 67 | a0001c0003t0010g0076 a0001c0003t0010g0077 a0001c0004t0005g0112 others(64): Show |
72 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.8331+1604delT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32365109 | ||||||
chr13:32365109 | CTT | C | 76 | a0001c0001t0001g0186 a0001c0003t0014g0078 a0001c0003t0014g0079 others(73): Show |
82 | HG00280.hp1 HG00408.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.8331+1603_8331+160 others(6): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32365109 | ||||||
chr13:32365109 | CTTTT | C | 6 | a0001c0001t0001g0222 a0001c0001t0001g0230 a0001c0001t0001g0232 others(3): Show |
6 | HG00609.hp1 HG02647.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.8331+1601_8331+160 others(8): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32365109 | ||||||
chr13:32365109 | CTTTTT | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(81): Show |
88 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.8331+1600_8331+160 others(9): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32365109 | ||||||
chr13:32365109 | CTTTTTT | C | 11 | a0001c0001t0001g0234 a0001c0001t0008g0056 a0001c0001t0008g0064 others(8): Show |
11 | HG01106.hp1 HG01169.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.8331+1599_8331+160 others(10): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32365109 | ||||||
chr13:32365148 | C | T | 1 | a0001c0003t0004g0074 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.8331+1615C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32365148 | |||||||
chr13:32365149 | T | G | 67 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(64): Show |
70 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.8331+1616T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32365149 | |||||||
chr13:32365165 | G | A | 77 | a0001c0004t0003g0343 a0001c0004t0005g0002 a0001c0004t0005g0009 others(74): Show |
83 | HG00280.hp1 HG00408.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.8331+1632G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32365165 | |||||||
chr13:32365177 | C | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(212): Show |
226 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.8331+1644C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32365177 | |||||||
chr13:32365198 | C | G | 1 | a0002c0002t0006g0134 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.8331+1665C>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32365198 | |||||||
chr13:32365244 | C | G | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.8331+1711C>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32365244 | |||||||
chr13:32365441 | C | T | 1 | a0004c0006t0007g0123 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.8331+1908C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32365441 | |||||||
chr13:32365721 | C | CT | 156 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(153): Show |
166 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.8331+2209dupT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32365721 | ||||||
chr13:32365721 | C | CTT | 64 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0009g0066 others(61): Show |
67 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.8331+2208_8331+220 others(6): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32365721 | ||||||
chr13:32365721 | CT | C | 10 | a0001c0001t0013g0250 a0001c0003t0014g0079 a0001c0003t0014g0080 others(7): Show |
10 | HG00323.hp2 HG01168.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.8331+2209delT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32365721 | ||||||
chr13:32366019 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.8331+2486C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32366019 | |||||||
chr13:32366142 | G | A | 1 | a0004c0006t0003g0118 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.8331+2609G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32366142 | |||||||
chr13:32366208 | C | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(212): Show |
226 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.8331+2675C>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32366208 | |||||||
chr13:32366257 | A | C | 3 | a0004c0006t0003g0124 a0004c0006t0003g0125 a0004c0006t0003g0344 |
3 | HG02572.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.8331+2724A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32366257 | |||||||
chr13:32366385 | T | C | 1 | a0027c0043t0031g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.8331+2852T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32366385 | |||||||
chr13:32366564 | A | G | 1 | a0001c0001t0001g0249 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.8331+3031A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32366564 | |||||||
chr13:32366747 | G | T | 1 | a0003c0005t0003g0040 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.8331+3214G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32366747 | |||||||
chr13:32366751 | C | T | 67 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(64): Show |
70 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.8331+3218C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32366751 | |||||||
chr13:32366825 | GA | G | 7 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0003t0014g0078 others(4): Show |
7 | HG00423.hp2 HG02257.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.8331+3303delA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32366825 | ||||||
chr13:32366863 | A | G | 1 | a0002c0002t0002g0280 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.8331+3330A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32366863 | |||||||
chr13:32366868 | C | CA | 11 | a0001c0001t0001g0222 a0001c0001t0001g0231 a0001c0001t0013g0187 others(8): Show |
11 | HG00558.hp1 HG02040.hp2 HG03516.hp1 others(8): Show |
intron_variant | MODIFIER | c.8331+3351dupA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32366868 | ||||||
chr13:32366868 | CA | C | 143 | a0001c0001t0001g0247 a0001c0001t0001g0266 a0001c0003t0004g0323 others(140): Show |
156 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.8331+3351delA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32366868 | ||||||
chr13:32366868 | CAA | C | 6 | a0001c0001t0001g0248 a0001c0010t0011g0200 a0008c0013t0002g0359 others(3): Show |
6 | HG00423.hp1 HG01496.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.8331+3350_8331+335 others(6): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32366868 | ||||||
chr13:32366873 | A | C | 1 | a0009c0015t0002g0157 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.8331+3340A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32366873 | |||||||
chr13:32366979 | G | T | 3 | a0001c0001t0008g0278 a0001c0001t0008g0347 a0001c0001t0008g0361 |
3 | HG01106.hp1 HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.8332-3423G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32366979 | |||||||
chr13:32367008 | A | G | 3 | a0004c0006t0003g0124 a0004c0006t0003g0125 a0004c0006t0003g0344 |
3 | HG02572.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.8332-3394A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32367008 | |||||||
chr13:32367127 | T | C | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.8332-3275T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32367127 | |||||||
chr13:32367159 | G | T | 3 | a0001c0003t0010g0076 a0001c0003t0010g0077 a0028c0049t0010g0340 |
3 | HG02622.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.8332-3243G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32367159 | |||||||
chr13:32367262 | C | T | 2 | a0002c0002t0002g0166 a0002c0002t0002g0167 |
2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.8332-3140C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32367262 | |||||||
chr13:32367304 | C | T | 8 | a0004c0006t0007g0010 a0004c0006t0007g0119 a0004c0006t0007g0120 others(5): Show |
8 | HG00408.hp1 HG00642.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.8332-3098C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32367304 | |||||||
chr13:32367440 | GA | G | 45 | a0001c0003t0010g0077 a0003c0005t0003g0003 a0003c0005t0003g0023 others(42): Show |
49 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.8332-2952delA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32367440 | ||||||
chr13:32367486 | A | G | 3 | a0001c0003t0010g0076 a0001c0003t0010g0077 a0028c0049t0010g0340 |
3 | HG02622.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.8332-2916A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32367486 | |||||||
chr13:32367541 | C | T | 1 | a0001c0003t0004g0213 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.8332-2861C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32367541 | |||||||
chr13:32367579 | A | AGATGGCT others(2): Show |
215 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(212): Show |
226 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.8332-2823_8332-282 others(13): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32367579 | |||||||
chr13:32367696 | G | A | 1 | a0001c0003t0004g0328 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.8332-2706G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32367696 | |||||||
chr13:32367964 | C | T | 2 | a0001c0003t0004g0018 a0001c0003t0004g0328 |
3 | HG00733.hp1 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.8332-2438C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32367964 | |||||||
chr13:32368001 | C | CT | 31 | a0001c0004t0040g0108 a0001c0010t0011g0014 a0001c0010t0011g0200 others(28): Show |
33 | HG00738.hp1 HG01069.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.8332-2365dupT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32368001 | ||||||
chr13:32368001 | C | CTT | 14 | a0001c0010t0011g0267 a0001c0010t0011g0368 a0002c0002t0002g0012 others(11): Show |
15 | HG01071.hp2 HG01243.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.8332-2366_8332-236 others(6): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32368001 | ||||||
chr13:32368001 | CTTTTTTT | C | 21 | a0001c0001t0001g0057 a0001c0001t0001g0184 a0001c0001t0001g0186 others(18): Show |
21 | HG01346.hp1 HG01515.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.8332-2371_8332-236 others(11): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32368001 | ||||||
chr13:32368001 | CTTTTTTT others(1): Show |
C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(80): Show |
87 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.8332-2372_8332-236 others(12): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32368001 | ||||||
chr13:32368001 | CTTTTTTT others(2): Show |
C | 55 | a0001c0001t0001g0189 a0001c0001t0001g0241 a0001c0001t0001g0242 others(52): Show |
59 | HG00639.hp2 HG00738.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.8332-2373_8332-236 others(13): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32368001 | ||||||
chr13:32368001 | CTTTTTTT others(3): Show |
C | 118 | a0001c0001t0001g0224 a0001c0003t0004g0013 a0001c0003t0004g0018 others(115): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.8332-2374_8332-236 others(14): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32368001 | ||||||
chr13:32368001 | CTTTTTTT others(4): Show |
C | 5 | a0002c0002t0006g0130 a0004c0006t0007g0120 a0016c0016t0005g0095 others(2): Show |
5 | HG02004.hp1 HG02922.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.8332-2375_8332-236 others(15): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32368001 | ||||||
chr13:32368001 | CTTTTTTT others(8): Show |
C | 3 | a0001c0001t0008g0278 a0001c0001t0008g0347 a0001c0001t0008g0361 |
3 | HG01106.hp1 HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.8332-2379_8332-236 others(19): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32368001 | ||||||
chr13:32368001 | CTTTTTTT others(9): Show |
C | 5 | a0001c0003t0014g0078 a0001c0003t0014g0079 a0001c0003t0014g0080 others(2): Show |
5 | HG02257.hp1 HG02698.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.8332-2380_8332-236 others(20): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32368001 | ||||||
chr13:32368081 | A | T | 1 | a0002c0048t0002g0169 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.8332-2321A>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32368081 | |||||||
chr13:32368082 | C | T | 1 | a0002c0048t0002g0169 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.8332-2320C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32368082 | |||||||
chr13:32368169 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.8332-2233A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32368169 | |||||||
chr13:32368300 | T | G | 63 | a0002c0002t0002g0006 a0002c0002t0002g0012 a0002c0002t0002g0126 others(60): Show |
71 | HG00558.hp2 HG00639.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.8332-2102T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32368300 | |||||||
chr13:32368453 | T | C | 4 | a0001c0004t0005g0016 a0001c0004t0005g0283 a0001c0004t0005g0284 others(1): Show |
5 | HG00609.hp2 HG02132.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.8332-1949T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32368453 | |||||||
chr13:32368521 | A | AT | 7 | a0001c0003t0004g0213 a0001c0004t0012g0082 a0001c0004t0012g0084 others(4): Show |
7 | HG01255.hp2 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.8332-1869dupT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32368521 | ||||||
chr13:32368578 | C | T | 3 | a0001c0001t0009g0067 a0001c0001t0009g0068 a0001c0001t0009g0069 |
3 | HG00733.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.8332-1824C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32368578 | |||||||
chr13:32368798 | GT | G | 160 | a0001c0001t0008g0055 a0001c0001t0008g0056 a0001c0001t0008g0063 others(157): Show |
172 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.8332-1594delT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32368798 | ||||||
chr13:32368799 | T | G | 11 | a0001c0001t0009g0066 a0001c0003t0004g0313 a0001c0003t0004g0314 others(8): Show |
11 | HG00099.hp2 HG00735.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.8332-1603T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32368799 | |||||||
chr13:32368808 | T | G | 111 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(108): Show |
118 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.8332-1594T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32368808 | |||||||
chr13:32368809 | G | T | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.8332-1593G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32368809 | |||||||
chr13:32368810 | G | T | 108 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(105): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.8332-1592G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32368810 | |||||||
chr13:32368811 | T | G | 73 | a0001c0004t0003g0343 a0001c0004t0005g0002 a0001c0004t0005g0009 others(70): Show |
79 | HG00280.hp1 HG00408.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.8332-1591T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32368811 | |||||||
chr13:32368818 | T | G | 4 | a0001c0004t0005g0093 a0001c0004t0005g0104 a0001c0004t0005g0112 others(1): Show |
4 | HG00621.hp2 HG01981.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.8332-1584T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32368818 | |||||||
chr13:32368819 | G | GT | 90 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(87): Show |
94 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.8332-1573dupT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32368819 | ||||||
chr13:32368819 | G | T | 6 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0004t0005g0093 others(3): Show |
6 | HG00621.hp2 HG01981.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.8332-1583G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32368819 | |||||||
chr13:32368879 | C | T | 3 | a0001c0004t0005g0092 a0001c0004t0005g0099 a0034c0034t0006g0310 |
3 | NA18948.hp1 NA18966.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.8332-1523C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32368879 | |||||||
chr13:32368935 | C | T | 23 | a0001c0004t0005g0002 a0001c0004t0005g0087 a0001c0004t0005g0088 others(20): Show |
25 | HG00621.hp2 HG02083.hp1 NA18612.hp2 others(22): Show |
intron_variant | MODIFIER | c.8332-1467C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32368935 | |||||||
chr13:32368937 | A | C | 1 | a0001c0004t0005g0093 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.8332-1465A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32368937 | |||||||
chr13:32368970 | C | T | 1 | a0001c0003t0035g0287 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.8332-1432C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32368970 | |||||||
chr13:32368998 | C | T | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.8332-1404C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32368998 | |||||||
chr13:32369041 | C | G | 4 | a0001c0004t0005g0102 a0001c0004t0005g0109 a0001c0004t0005g0113 others(1): Show |
4 | HG00280.hp1 HG01069.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.8332-1361C>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32369041 | |||||||
chr13:32369205 | TAA | T | 10 | a0001c0003t0004g0313 a0001c0003t0004g0314 a0001c0003t0004g0317 others(7): Show |
10 | HG00099.hp2 HG00735.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.8332-1195_8332-119 others(6): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32369205 | ||||||
chr13:32369218 | AT | A | 45 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(42): Show |
49 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.8332-1173delT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr13 | 32369218 | ||||||
chr13:32369232 | T | C | 1 | a0001c0003t0004g0213 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.8332-1170T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32369232 | |||||||
chr13:32369605 | G | A | 2 | a0013c0018t0003g0072 a0013c0018t0003g0073 |
2 | HG01496.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.8332-797G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32369605 | |||||||
chr13:32369612 | C | A | 4 | a0001c0003t0014g0078 a0001c0003t0014g0079 a0001c0003t0014g0080 others(1): Show |
4 | HG02257.hp1 HG02809.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.8332-790C>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32369612 | |||||||
chr13:32369645 | C | T | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.8332-757C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32369645 | |||||||
chr13:32369699 | G | A | 10 | a0001c0003t0004g0013 a0001c0003t0004g0206 a0001c0003t0004g0207 others(7): Show |
11 | HG01074.hp2 HG01192.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.8332-703G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32369699 | |||||||
chr13:32369784 | G | A | 2 | a0002c0002t0006g0135 a0002c0002t0006g0136 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.8332-618G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32369784 | |||||||
chr13:32369919 | G | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(97): Show |
104 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.8332-483G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32369919 | |||||||
chr13:32369961 | G | A | 58 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(55): Show |
61 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.8332-441G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 18/26 | chr13 | 32369961 | |||||||
chr13:32370576 | A | G | 4 | a0001c0003t0014g0078 a0001c0003t0014g0079 a0001c0003t0014g0080 others(1): Show |
4 | HG02257.hp1 HG02809.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.8487+19A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 19/26 | chr13 | 32370576 | |||||||
chr13:32370604 | C | T | 6 | a0001c0004t0012g0082 a0001c0004t0012g0084 a0001c0004t0012g0085 others(3): Show |
6 | HG02886.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.8487+47C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 19/26 | chr13 | 32370604 | |||||||
chr13:32370639 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.8487+82G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 19/26 | chr13 | 32370639 | |||||||
chr13:32370951 | T | C | 1 | a0002c0002t0006g0131 | 1 | HG03688.hp1 | splice_region_variant&intron_variant | LOW | c.8488-5T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 19/26 | chr13 | 32370951 | |||||||
chr13:32371150 | G | A | 1 | a0034c0034t0006g0310 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.8632+50G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32371150 | |||||||
chr13:32371231 | T | TC | 3 | a0005c0007t0003g0294 a0005c0007t0003g0299 a0005c0007t0003g0300 |
3 | HG01175.hp1 HG03041.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.8632+132dupC | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 32371231 | ||||||
chr13:32371400 | A | T | 55 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(52): Show |
58 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.8632+300A>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32371400 | |||||||
chr13:32371492 | T | C | 2 | a0026c0030t0003g0277 a0027c0043t0031g0285 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.8632+392T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32371492 | |||||||
chr13:32371580 | A | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(97): Show |
104 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.8632+480A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32371580 | |||||||
chr13:32371704 | A | G | 1 | a0001c0003t0004g0320 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.8632+604A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32371704 | |||||||
chr13:32371795 | C | T | 66 | a0001c0004t0040g0108 a0001c0010t0011g0014 a0001c0010t0011g0200 others(63): Show |
72 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.8632+695C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32371795 | |||||||
chr13:32371842 | A | T | 3 | a0001c0003t0010g0076 a0001c0003t0010g0077 a0028c0049t0010g0340 |
3 | HG02622.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.8632+742A>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32371842 | |||||||
chr13:32371874 | A | G | 365 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(362): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.8632+774A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32371874 | |||||||
chr13:32372010 | A | C | 1 | a0007c0008t0001g0245 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.8632+910A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32372010 | |||||||
chr13:32372082 | G | A | 4 | a0001c0011t0004g0364 a0001c0011t0004g0365 a0001c0011t0019g0274 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.8632+982G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32372082 | |||||||
chr13:32372278 | C | T | 365 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(362): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.8632+1178C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32372278 | |||||||
chr13:32372283 | A | G | 4 | a0001c0003t0014g0078 a0001c0003t0014g0079 a0001c0003t0014g0080 others(1): Show |
4 | HG02257.hp1 HG02809.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.8632+1183A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32372283 | |||||||
chr13:32372447 | C | T | 3 | a0002c0002t0002g0351 a0002c0002t0002g0356 a0002c0002t0002g0357 |
3 | HG02683.hp1 HG03710.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.8632+1347C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32372447 | |||||||
chr13:32372453 | G | A | 1 | a0001c0003t0004g0332 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.8632+1353G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32372453 | |||||||
chr13:32372668 | G | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(87): Show |
94 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.8632+1568G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32372668 | |||||||
chr13:32372707 | C | T | 2 | a0016c0016t0005g0095 a0016c0016t0005g0096 |
2 | NA18983.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.8632+1607C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32372707 | |||||||
chr13:32372708 | G | A | 1 | a0001c0001t0001g0262 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.8632+1608G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32372708 | |||||||
chr13:32372719 | A | G | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.8632+1619A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32372719 | |||||||
chr13:32372857 | A | G | 1 | a0001c0004t0005g0104 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.8632+1757A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32372857 | |||||||
chr13:32372990 | A | G | 1 | a0001c0003t0035g0287 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.8632+1890A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32372990 | |||||||
chr13:32372996 | C | CT | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(105): Show |
112 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.8632+1910dupT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 32372996 | ||||||
chr13:32372996 | CT | C | 12 | a0002c0002t0002g0144 a0002c0002t0002g0146 a0002c0002t0002g0147 others(9): Show |
12 | HG02015.hp1 HG02071.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.8632+1910delT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 32372996 | ||||||
chr13:32373019 | G | A | 2 | a0001c0003t0004g0304 a0022c0035t0004g0305 |
2 | HG00597.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.8632+1919G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32373019 | |||||||
chr13:32373331 | C | T | 2 | a0005c0007t0003g0299 a0005c0007t0003g0300 |
2 | HG03041.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.8632+2231C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32373331 | |||||||
chr13:32373397 | T | C | 1 | a0020c0038t0004g0312 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.8632+2297T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32373397 | |||||||
chr13:32373524 | A | T | 10 | a0001c0003t0010g0076 a0001c0003t0010g0077 a0002c0002t0002g0173 others(7): Show |
11 | HG00735.hp1 HG01167.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.8632+2424A>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32373524 | |||||||
chr13:32373692 | C | G | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.8632+2592C>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32373692 | |||||||
chr13:32373717 | C | G | 4 | a0001c0011t0004g0364 a0001c0011t0004g0365 a0001c0011t0019g0274 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.8632+2617C>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32373717 | |||||||
chr13:32373858 | C | T | 1 | a0007c0008t0001g0246 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.8632+2758C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32373858 | |||||||
chr13:32374083 | T | G | 2 | a0001c0011t0019g0274 a0001c0011t0019g0275 |
2 | HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.8633-2587T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32374083 | |||||||
chr13:32374128 | A | G | 1 | a0026c0030t0003g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.8633-2542A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32374128 | |||||||
chr13:32374299 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.8633-2371A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32374299 | |||||||
chr13:32374878 | C | T | 1 | a0004c0019t0016g0065 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.8633-1792C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32374878 | |||||||
chr13:32374890 | A | G | 1 | a0001c0003t0004g0331 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.8633-1780A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32374890 | |||||||
chr13:32374976 | G | T | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.8633-1694G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32374976 | |||||||
chr13:32374977 | G | T | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.8633-1693G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32374977 | |||||||
chr13:32375245 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(211): Show |
225 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.8633-1425T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32375245 | |||||||
chr13:32375530 | C | G | 4 | a0001c0001t0001g0230 a0001c0001t0001g0244 a0001c0001t0001g0266 others(1): Show |
4 | HG00609.hp1 HG01934.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.8633-1140C>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32375530 | |||||||
chr13:32375563 | C | CT | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(209): Show |
223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.8633-1093dupT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 32375563 | ||||||
chr13:32375621 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.8633-1049C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32375621 | |||||||
chr13:32375662 | G | A | 2 | a0003c0005t0010g0140 a0003c0005t0010g0141 |
2 | HG03017.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.8633-1008G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32375662 | |||||||
chr13:32375718 | G | A | 2 | a0011c0021t0020g0281 a0011c0021t0023g0279 |
2 | HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.8633-952G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32375718 | |||||||
chr13:32375786 | C | T | 1 | a0002c0002t0002g0356 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.8633-884C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32375786 | |||||||
chr13:32375831 | A | ATTAC | 3 | a0001c0003t0004g0320 a0001c0003t0021g0307 a0001c0003t0021g0319 |
3 | HG00099.hp2 HG00735.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.8633-838_8633-835d others(6): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 32375831 | ||||||
chr13:32376115 | GTGAAA | G | 4 | a0001c0001t0008g0055 a0001c0001t0008g0056 a0001c0001t0008g0290 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.8633-553_8633-549d others(7): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 32376115 | ||||||
chr13:32376120 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(205): Show |
219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.8633-550A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32376120 | |||||||
chr13:32376181 | CT | C | 18 | a0003c0005t0003g0048 a0004c0006t0003g0118 a0004c0006t0003g0124 others(15): Show |
19 | HG00408.hp1 HG00642.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.8633-476delT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 32376181 | ||||||
chr13:32376413 | C | A | 2 | a0001c0011t0019g0274 a0001c0011t0019g0275 |
2 | HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.8633-257C>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | chr13 | 32376413 | |||||||
chr13:32376521 | C | CA | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(96): Show |
103 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.8633-135dupA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 32376521 | ||||||
chr13:32376521 | CA | C | 7 | a0001c0003t0014g0078 a0001c0003t0014g0079 a0001c0003t0014g0080 others(4): Show |
7 | HG02257.hp1 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.8633-135delA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 32376521 | ||||||
chr13:32376960 | A | G | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.8754+169A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 21/26 | chr13 | 32376960 | |||||||
chr13:32376974 | A | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(94): Show |
101 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.8754+183A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 21/26 | chr13 | 32376974 | |||||||
chr13:32376978 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(97): Show |
104 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.8754+187C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 21/26 | chr13 | 32376978 | |||||||
chr13:32377317 | C | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(87): Show |
94 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.8754+526C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 21/26 | chr13 | 32377317 | |||||||
chr13:32377390 | G | A | 1 | a0001c0003t0004g0329 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.8754+599G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 21/26 | chr13 | 32377390 | |||||||
chr13:32377452 | G | A | 1 | a0002c0002t0006g0134 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.8754+661G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 21/26 | chr13 | 32377452 | |||||||
chr13:32377459 | A | C | 67 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(64): Show |
70 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.8754+668A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 21/26 | chr13 | 32377459 | |||||||
chr13:32377582 | C | T | 3 | a0001c0003t0010g0076 a0001c0003t0010g0077 a0028c0049t0010g0340 |
3 | HG02622.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.8754+791C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 21/26 | chr13 | 32377582 | |||||||
chr13:32377590 | CA | C | 363 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(360): Show |
386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.8754+816delA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr13 | 32377590 | ||||||
chr13:32377974 | T | TA | 2 | a0002c0002t0002g0012 a0002c0002t0002g0179 |
3 | NA18962.hp1 NA18964.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.8754+1184dupA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr13 | 32377974 | ||||||
chr13:32378219 | T | C | 1 | a0003c0005t0003g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.8755-1098T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 21/26 | chr13 | 32378219 | |||||||
chr13:32378348 | A | G | 5 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0220 others(2): Show |
5 | HG01515.hp2 HG02683.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.8755-969A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 21/26 | chr13 | 32378348 | |||||||
chr13:32378476 | T | C | 3 | a0001c0001t0008g0278 a0001c0001t0008g0347 a0001c0001t0008g0361 |
3 | HG01106.hp1 HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.8755-841T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 21/26 | chr13 | 32378476 | |||||||
chr13:32378757 | G | A | 2 | a0014c0017t0018g0309 a0014c0017t0018g0311 |
2 | HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.8755-560G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 21/26 | chr13 | 32378757 | |||||||
chr13:32379045 | A | G | 30 | a0001c0003t0004g0013 a0001c0003t0004g0075 a0001c0003t0004g0206 others(27): Show |
31 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.8755-272A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 21/26 | chr13 | 32379045 | |||||||
chr13:32379128 | G | A | 5 | a0001c0003t0014g0078 a0001c0003t0014g0079 a0001c0003t0014g0080 others(2): Show |
5 | HG02257.hp1 HG02809.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.8755-189G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 21/26 | chr13 | 32379128 | |||||||
chr13:32379251 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(209): Show |
223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.8755-66T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 21/26 | chr13 | 32379251 | |||||||
chr13:32380001 | C | A | 1 | a0001c0001t0008g0064 | 1 | HG03195.hp2 | splice_region_variant&intron_variant | LOW | c.9118-6C>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 23/26 | chr13 | 32380001 | |||||||
chr13:32380213 | A | G | 1 | a0001c0001t0009g0066 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.9256+68A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32380213 | |||||||
chr13:32380284 | C | T | 1 | a0026c0030t0003g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.9256+139C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32380284 | |||||||
chr13:32380306 | A | G | 2 | a0003c0005t0003g0046 a0003c0005t0003g0049 |
2 | NA19006.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.9256+161A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32380306 | |||||||
chr13:32380424 | G | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(210): Show |
224 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.9256+279G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32380424 | |||||||
chr13:32380534 | C | CT | 166 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(163): Show |
173 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.9256+409dupT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr13 | 32380534 | ||||||
chr13:32380534 | C | CTT | 7 | a0001c0001t0001g0233 a0001c0003t0004g0303 a0001c0003t0004g0336 others(4): Show |
7 | HG01346.hp1 HG03486.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.9256+408_9256+409d others(4): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr13 | 32380534 | ||||||
chr13:32380554 | T | TC | 42 | a0001c0003t0004g0209 a0003c0005t0003g0003 a0003c0005t0003g0023 others(39): Show |
46 | HG00639.hp2 HG01167.hp2 HG01192.hp1 others(43): Show |
intron_variant | MODIFIER | c.9256+413dupC | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr13 | 32380554 | ||||||
chr13:32380559 | G | A | 2 | a0001c0003t0035g0287 a0001c0033t0004g0298 |
2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.9256+414G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32380559 | |||||||
chr13:32380604 | T | A | 365 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(362): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.9256+459T>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32380604 | |||||||
chr13:32380605 | A | G | 1 | a0001c0004t0012g0341 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.9256+460A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32380605 | |||||||
chr13:32380611 | G | A | 1 | a0002c0002t0002g0182 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.9256+466G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32380611 | |||||||
chr13:32380660 | C | T | 1 | a0001c0003t0004g0209 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.9256+515C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32380660 | |||||||
chr13:32380686 | A | C | 1 | a0026c0030t0003g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.9256+541A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32380686 | |||||||
chr13:32380725 | A | C | 1 | a0001c0003t0034g0214 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.9256+580A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32380725 | |||||||
chr13:32380775 | C | T | 6 | a0003c0005t0003g0038 a0003c0005t0003g0041 a0003c0005t0003g0042 others(3): Show |
6 | NA18941.hp1 NA18945.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.9256+630C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32380775 | |||||||
chr13:32380776 | G | A | 5 | a0002c0002t0006g0128 a0002c0002t0006g0129 a0002c0002t0006g0132 others(2): Show |
5 | NA18943.hp1 NA18955.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.9256+631G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32380776 | |||||||
chr13:32380880 | A | C | 5 | a0003c0005t0003g0029 a0003c0005t0003g0030 a0003c0005t0003g0031 others(2): Show |
5 | HG03491.hp2 HG03492.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.9256+735A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32380880 | |||||||
chr13:32381260 | C | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(208): Show |
222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.9256+1115C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32381260 | |||||||
chr13:32381563 | T | A | 1 | a0026c0030t0003g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.9256+1418T>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32381563 | |||||||
chr13:32381963 | G | A | 2 | a0001c0003t0004g0075 a0038c0042t0004g0335 |
2 | HG00558.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.9256+1818G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32381963 | |||||||
chr13:32381972 | G | A | 67 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(64): Show |
70 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.9256+1827G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32381972 | |||||||
chr13:32382007 | G | C | 3 | a0001c0003t0010g0076 a0001c0003t0010g0077 a0028c0049t0010g0340 |
3 | HG02622.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.9256+1862G>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32382007 | |||||||
chr13:32382030 | G | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0195 |
2 | NA18972.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.9256+1885G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32382030 | |||||||
chr13:32382033 | T | G | 1 | a0026c0030t0003g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.9256+1888T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32382033 | |||||||
chr13:32382146 | G | A | 64 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(61): Show |
67 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.9256+2001G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32382146 | |||||||
chr13:32382598 | A | AG | 3 | a0001c0003t0010g0076 a0001c0003t0010g0077 a0028c0049t0010g0340 |
3 | HG02622.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.9256+2454dupG | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr13 | 32382598 | ||||||
chr13:32382609 | G | A | 1 | a0001c0004t0012g0341 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.9256+2464G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32382609 | |||||||
chr13:32382620 | G | A | 80 | a0001c0001t0017g0217 a0001c0004t0003g0343 a0001c0004t0005g0002 others(77): Show |
86 | HG00280.hp1 HG00408.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.9256+2475G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32382620 | |||||||
chr13:32382624 | G | A | 1 | a0027c0043t0031g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.9256+2479G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32382624 | |||||||
chr13:32382821 | A | G | 1 | a0002c0002t0002g0180 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.9256+2676A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32382821 | |||||||
chr13:32382958 | A | G | 1 | a0005c0037t0003g0070 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.9256+2813A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32382958 | |||||||
chr13:32383099 | C | T | 1 | a0001c0003t0004g0323 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.9256+2954C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32383099 | |||||||
chr13:32383102 | C | CTGTAATC others(25): Show |
101 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(98): Show |
105 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.9256+2960_9256+299 others(36): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr13 | 32383102 | ||||||
chr13:32383177 | G | A | 4 | a0001c0001t0008g0055 a0001c0001t0008g0056 a0001c0001t0008g0290 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.9256+3032G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32383177 | |||||||
chr13:32383229 | G | A | 1 | a0003c0005t0007g0028 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.9256+3084G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32383229 | |||||||
chr13:32383682 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(97): Show |
104 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.9256+3537G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32383682 | |||||||
chr13:32383835 | G | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(97): Show |
104 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.9256+3690G>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32383835 | |||||||
chr13:32384015 | G | A | 1 | a0001c0003t0035g0287 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.9256+3870G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32384015 | |||||||
chr13:32384329 | T | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(97): Show |
104 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.9256+4184T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32384329 | |||||||
chr13:32384449 | G | C | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.9256+4304G>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32384449 | |||||||
chr13:32384512 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(97): Show |
104 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.9256+4367G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32384512 | |||||||
chr13:32384750 | G | A | 7 | a0001c0003t0004g0018 a0001c0003t0004g0327 a0001c0003t0004g0328 others(4): Show |
8 | HG00733.hp1 HG00738.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.9256+4605G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32384750 | |||||||
chr13:32384823 | A | C | 1 | a0001c0001t0001g0244 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.9256+4678A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32384823 | |||||||
chr13:32384860 | G | A | 8 | a0001c0001t0017g0217 a0002c0002t0006g0128 a0002c0002t0006g0129 others(5): Show |
8 | HG02027.hp1 NA18943.hp1 NA18955.hp2 others(5): Show |
intron_variant | MODIFIER | c.9256+4715G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32384860 | |||||||
chr13:32385055 | T | C | 1 | a0001c0001t0001g0057 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.9256+4910T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32385055 | |||||||
chr13:32385062 | C | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(209): Show |
223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.9256+4917C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32385062 | |||||||
chr13:32385099 | C | T | 4 | a0001c0001t0009g0067 a0001c0001t0009g0068 a0001c0001t0009g0069 others(1): Show |
4 | HG00733.hp2 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.9256+4954C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32385099 | |||||||
chr13:32385103 | C | A | 11 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0220 others(8): Show |
11 | HG00733.hp2 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.9256+4958C>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32385103 | |||||||
chr13:32385213 | G | A | 2 | a0001c0003t0004g0303 a0001c0003t0004g0360 |
2 | HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.9256+5068G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32385213 | |||||||
chr13:32385397 | A | G | 67 | a0001c0004t0040g0108 a0001c0010t0011g0014 a0001c0010t0011g0200 others(64): Show |
73 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.9256+5252A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32385397 | |||||||
chr13:32385415 | TTGTCTTT others(5): Show |
T | 1 | a0021c0025t0003g0215 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.9256+5289_9256+530 others(16): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr13 | 32385415 | ||||||
chr13:32385548 | G | A | 1 | a0002c0002t0006g0131 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.9256+5403G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32385548 | |||||||
chr13:32385652 | T | C | 80 | a0001c0001t0017g0217 a0001c0004t0003g0343 a0001c0004t0005g0002 others(77): Show |
86 | HG00280.hp1 HG00408.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.9256+5507T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32385652 | |||||||
chr13:32385702 | A | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(209): Show |
223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.9256+5557A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32385702 | |||||||
chr13:32385743 | A | G | 1 | a0030c0028t0005g0094 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.9256+5598A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32385743 | |||||||
chr13:32385807 | G | C | 1 | a0002c0002t0006g0134 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.9256+5662G>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32385807 | |||||||
chr13:32385907 | T | C | 3 | a0001c0003t0010g0076 a0001c0003t0010g0077 a0028c0049t0010g0340 |
3 | HG02622.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.9256+5762T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32385907 | |||||||
chr13:32386106 | C | A | 1 | a0027c0043t0031g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.9256+5961C>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32386106 | |||||||
chr13:32386150 | T | G | 2 | a0013c0018t0003g0072 a0013c0018t0003g0073 |
2 | HG01496.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.9256+6005T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32386150 | |||||||
chr13:32386226 | T | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(211): Show |
225 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.9256+6081T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32386226 | |||||||
chr13:32386265 | A | C | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.9256+6120A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32386265 | |||||||
chr13:32386531 | C | T | 3 | a0004c0006t0003g0124 a0004c0006t0003g0125 a0004c0006t0003g0344 |
3 | HG02572.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.9256+6386C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32386531 | |||||||
chr13:32386560 | A | G | 3 | a0001c0001t0008g0278 a0001c0001t0008g0347 a0001c0001t0008g0361 |
3 | HG01106.hp1 HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.9256+6415A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32386560 | |||||||
chr13:32386567 | AAAAACCA others(24): Show |
A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(97): Show |
104 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.9256+6423_9256+645 others(35): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32386567 | |||||||
chr13:32386596 | A | G | 2 | a0001c0010t0011g0014 a0018c0040t0011g0014 |
2 | HG01106.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.9256+6451A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32386596 | |||||||
chr13:32386851 | A | G | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.9256+6706A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32386851 | |||||||
chr13:32386891 | T | G | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.9256+6746T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32386891 | |||||||
chr13:32387015 | G | A | 1 | a0002c0002t0002g0178 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.9256+6870G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32387015 | |||||||
chr13:32387052 | G | GC | 365 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(362): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.9256+6908dupC | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr13 | 32387052 | ||||||
chr13:32387185 | G | A | 2 | a0001c0001t0001g0252 a0001c0001t0001g0255 |
2 | NA18973.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.9256+7040G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32387185 | |||||||
chr13:32387360 | C | T | 7 | a0001c0001t0017g0217 a0002c0002t0006g0128 a0002c0002t0006g0129 others(4): Show |
7 | HG02027.hp1 NA18943.hp1 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.9256+7215C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32387360 | |||||||
chr13:32387367 | A | G | 1 | a0005c0037t0003g0070 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.9256+7222A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32387367 | |||||||
chr13:32387447 | C | T | 1 | a0001c0004t0003g0343 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.9257-7242C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32387447 | |||||||
chr13:32387470 | C | T | 1 | a0032c0050t0003g0052 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.9257-7219C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32387470 | |||||||
chr13:32387742 | A | G | 1 | a0002c0002t0002g0170 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.9257-6947A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32387742 | |||||||
chr13:32387788 | C | T | 1 | a0008c0013t0002g0358 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.9257-6901C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32387788 | |||||||
chr13:32387908 | A | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(208): Show |
222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.9257-6781A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32387908 | |||||||
chr13:32387951 | C | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(209): Show |
223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.9257-6738C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32387951 | |||||||
chr13:32388063 | C | T | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.9257-6626C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32388063 | |||||||
chr13:32388121 | C | CT | 258 | a0001c0001t0017g0217 a0001c0003t0004g0013 a0001c0003t0004g0018 others(255): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.9257-6553dupT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr13 | 32388121 | ||||||
chr13:32388121 | CT | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(97): Show |
104 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.9257-6553delT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr13 | 32388121 | ||||||
chr13:32388181 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(209): Show |
223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.9257-6508T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32388181 | |||||||
chr13:32388406 | A | G | 2 | a0005c0007t0003g0299 a0005c0007t0003g0300 |
2 | HG03041.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.9257-6283A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32388406 | |||||||
chr13:32388542 | T | A | 56 | a0001c0003t0004g0013 a0001c0003t0004g0206 a0001c0003t0004g0207 others(53): Show |
61 | HG00639.hp2 HG00735.hp1 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.9257-6147T>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32388542 | |||||||
chr13:32388548 | C | T | 4 | a0001c0003t0014g0078 a0001c0003t0014g0079 a0001c0003t0014g0080 others(1): Show |
4 | HG02257.hp1 HG02809.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.9257-6141C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32388548 | |||||||
chr13:32388666 | C | CT | 110 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(107): Show |
117 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.9257-6010dupT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr13 | 32388666 | ||||||
chr13:32388666 | C | CTT | 87 | a0001c0001t0017g0217 a0001c0003t0014g0078 a0001c0003t0014g0079 others(84): Show |
93 | HG00280.hp1 HG00408.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.9257-6011_9257-601 others(6): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr13 | 32388666 | ||||||
chr13:32388666 | C | CTTT | 65 | a0001c0004t0005g0111 a0001c0004t0040g0108 a0001c0010t0011g0014 others(62): Show |
71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.9257-6012_9257-601 others(7): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr13 | 32388666 | ||||||
chr13:32388691 | T | C | 1 | a0001c0003t0010g0316 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.9257-5998T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32388691 | |||||||
chr13:32388785 | C | G | 1 | a0002c0002t0028g0152 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.9257-5904C>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32388785 | |||||||
chr13:32389051 | G | T | 1 | a0001c0001t0009g0139 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.9257-5638G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32389051 | |||||||
chr13:32389113 | T | A | 1 | a0002c0002t0037g0183 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.9257-5576T>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32389113 | |||||||
chr13:32389392 | C | G | 14 | a0001c0001t0017g0217 a0002c0002t0006g0011 a0002c0002t0006g0128 others(11): Show |
15 | HG01256.hp1 HG01258.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.9257-5297C>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32389392 | |||||||
chr13:32389570 | C | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(209): Show |
223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.9257-5119C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32389570 | |||||||
chr13:32389575 | T | C | 3 | a0002c0002t0002g0351 a0002c0002t0002g0356 a0002c0002t0002g0357 |
3 | HG02683.hp1 HG03710.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.9257-5114T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32389575 | |||||||
chr13:32389701 | A | G | 4 | a0001c0004t0005g0102 a0001c0004t0005g0109 a0001c0004t0005g0113 others(1): Show |
4 | HG00280.hp1 HG01069.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.9257-4988A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32389701 | |||||||
chr13:32389796 | T | C | 1 | a0001c0004t0003g0343 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.9257-4893T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32389796 | |||||||
chr13:32389810 | A | G | 3 | a0002c0002t0004g0127 a0002c0002t0004g0175 a0002c0002t0004g0348 |
3 | HG00099.hp1 HG00323.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.9257-4879A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32389810 | |||||||
chr13:32390265 | G | T | 1 | a0004c0006t0003g0124 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.9257-4424G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32390265 | |||||||
chr13:32390362 | C | T | 7 | a0001c0003t0004g0075 a0001c0003t0004g0302 a0001c0003t0004g0306 others(4): Show |
7 | HG00558.hp1 HG02040.hp2 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.9257-4327C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32390362 | |||||||
chr13:32390367 | C | T | 54 | a0001c0001t0017g0217 a0001c0004t0005g0002 a0001c0004t0005g0009 others(51): Show |
59 | HG00280.hp1 HG00609.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.9257-4322C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32390367 | |||||||
chr13:32390441 | A | G | 1 | a0003c0005t0003g0040 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.9257-4248A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32390441 | |||||||
chr13:32390498 | G | A | 1 | a0002c0002t0002g0178 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.9257-4191G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32390498 | |||||||
chr13:32390504 | T | C | 3 | a0001c0003t0010g0076 a0001c0003t0010g0077 a0028c0049t0010g0340 |
3 | HG02622.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.9257-4185T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32390504 | |||||||
chr13:32390684 | G | T | 1 | a0002c0002t0002g0177 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.9257-4005G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32390684 | |||||||
chr13:32391079 | G | A | 2 | a0013c0018t0003g0072 a0013c0018t0003g0073 |
2 | HG01496.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.9257-3610G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32391079 | |||||||
chr13:32391137 | A | T | 1 | a0009c0015t0002g0157 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.9257-3552A>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32391137 | |||||||
chr13:32391173 | G | A | 80 | a0001c0001t0017g0217 a0001c0004t0003g0343 a0001c0004t0005g0002 others(77): Show |
86 | HG00280.hp1 HG00408.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.9257-3516G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32391173 | |||||||
chr13:32391462 | G | C | 2 | a0013c0018t0003g0072 a0013c0018t0003g0073 |
2 | HG01496.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.9257-3227G>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32391462 | |||||||
chr13:32391514 | T | C | 365 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(362): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.9257-3175T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32391514 | |||||||
chr13:32391585 | C | T | 1 | a0001c0004t0012g0084 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.9257-3104C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32391585 | |||||||
chr13:32391627 | C | T | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.9257-3062C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32391627 | |||||||
chr13:32391658 | A | T | 4 | a0003c0005t0003g0003 a0003c0005t0003g0050 a0003c0005t0003g0051 others(1): Show |
6 | HG00639.hp2 HG02015.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.9257-3031A>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32391658 | |||||||
chr13:32391886 | C | T | 2 | a0015c0022t0001g0228 a0015c0022t0022g0229 |
2 | NA18950.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.9257-2803C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32391886 | |||||||
chr13:32391940 | A | C | 1 | a0001c0004t0006g0098 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.9257-2749A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32391940 | |||||||
chr13:32391943 | T | C | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.9257-2746T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32391943 | |||||||
chr13:32392243 | T | C | 1 | a0014c0017t0018g0309 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.9257-2446T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32392243 | |||||||
chr13:32392526 | G | A | 1 | a0006c0009t0027g0288 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.9257-2163G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32392526 | |||||||
chr13:32392531 | G | A | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.9257-2158G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32392531 | |||||||
chr13:32392589 | CA | C | 279 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0057 others(276): Show |
298 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(295): Show |
intron_variant | MODIFIER | c.9257-2082delA | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr13 | 32392589 | ||||||
chr13:32392589 | CAA | C | 74 | a0001c0001t0001g0058 a0001c0001t0008g0064 a0001c0001t0009g0069 others(71): Show |
77 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.9257-2083_9257-208 others(6): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr13 | 32392589 | ||||||
chr13:32392993 | C | T | 1 | a0002c0002t0006g0136 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.9257-1696C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32392993 | |||||||
chr13:32393109 | A | C | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.9257-1580A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32393109 | |||||||
chr13:32393164 | C | T | 2 | a0001c0003t0004g0303 a0001c0003t0004g0360 |
2 | HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.9257-1525C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32393164 | |||||||
chr13:32393166 | A | G | 4 | a0001c0003t0014g0078 a0001c0003t0014g0079 a0001c0003t0014g0080 others(1): Show |
4 | HG02257.hp1 HG02809.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.9257-1523A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32393166 | |||||||
chr13:32393237 | TC | T | 54 | a0001c0001t0017g0217 a0001c0004t0005g0002 a0001c0004t0005g0009 others(51): Show |
59 | HG00280.hp1 HG00609.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.9257-1451delC | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32393237 | |||||||
chr13:32393329 | A | G | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(209): Show |
223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.9257-1360A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32393329 | |||||||
chr13:32393659 | A | C | 1 | a0002c0002t0002g0147 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.9257-1030A>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32393659 | |||||||
chr13:32393672 | C | G | 54 | a0001c0001t0017g0217 a0001c0004t0005g0002 a0001c0004t0005g0009 others(51): Show |
59 | HG00280.hp1 HG00609.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.9257-1017C>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32393672 | |||||||
chr13:32393874 | T | C | 1 | a0001c0003t0004g0363 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.9257-815T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32393874 | |||||||
chr13:32394153 | C | G | 4 | a0001c0003t0014g0078 a0001c0003t0014g0079 a0001c0003t0014g0080 others(1): Show |
4 | HG02257.hp1 HG02809.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.9257-536C>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32394153 | |||||||
chr13:32394172 | A | G | 17 | a0004c0006t0003g0118 a0004c0006t0003g0124 a0004c0006t0003g0125 others(14): Show |
18 | HG00408.hp1 HG00642.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.9257-517A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32394172 | |||||||
chr13:32394312 | T | A | 3 | a0002c0002t0002g0154 a0002c0002t0002g0155 a0002c0002t0002g0156 |
3 | HG02071.hp2 HG02074.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.9257-377T>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32394312 | |||||||
chr13:32394327 | G | T | 1 | a0001c0004t0005g0110 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.9257-362G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32394327 | |||||||
chr13:32394448 | A | T | 1 | a0027c0043t0031g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.9257-241A>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32394448 | |||||||
chr13:32394454 | G | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(211): Show |
225 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.9257-235G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32394454 | |||||||
chr13:32394459 | C | T | 1 | a0002c0002t0002g0357 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.9257-230C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32394459 | |||||||
chr13:32394462 | A | G | 1 | a0001c0003t0004g0308 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.9257-227A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32394462 | |||||||
chr13:32394470 | A | G | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(209): Show |
223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.9257-219A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32394470 | |||||||
chr13:32394546 | T | A | 1 | a0001c0003t0004g0363 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.9257-143T>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32394546 | |||||||
chr13:32394606 | G | A | 18 | a0001c0004t0003g0343 a0004c0006t0003g0118 a0004c0006t0003g0124 others(15): Show |
19 | HG00408.hp1 HG00642.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.9257-83G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32394606 | |||||||
chr13:32394640 | T | C | 1 | a0001c0001t0001g0219 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.9257-49T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 24/26 | chr13 | 32394640 | |||||||
chr13:32395111 | A | G | 54 | a0001c0001t0017g0217 a0001c0004t0005g0002 a0001c0004t0005g0009 others(51): Show |
59 | HG00280.hp1 HG00609.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.9501+178A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 25/26 | chr13 | 32395111 | |||||||
chr13:32395894 | T | C | 70 | a0001c0003t0004g0013 a0001c0003t0004g0018 a0001c0003t0004g0074 others(67): Show |
73 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.9501+961T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 25/26 | chr13 | 32395894 | |||||||
chr13:32395918 | T | G | 3 | a0001c0001t0001g0232 a0001c0001t0001g0235 a0001c0001t0013g0256 |
3 | NA18945.hp2 NA18956.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.9502-980T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 25/26 | chr13 | 32395918 | |||||||
chr13:32395952 | C | T | 2 | a0001c0003t0004g0317 a0001c0003t0004g0318 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.9502-946C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 25/26 | chr13 | 32395952 | |||||||
chr13:32395960 | C | CT | 172 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(169): Show |
183 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(180): Show |
intron_variant | MODIFIER | c.9502-910dupT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr13 | 32395960 | ||||||
chr13:32395960 | C | CTT | 31 | a0001c0001t0001g0186 a0001c0001t0001g0190 a0001c0001t0001g0191 others(28): Show |
32 | HG00408.hp1 HG00423.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.9502-911_9502-910d others(4): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr13 | 32395960 | ||||||
chr13:32395960 | C | CTTT | 6 | a0001c0001t0001g0223 a0001c0001t0001g0259 a0001c0001t0008g0056 others(3): Show |
6 | HG01175.hp2 HG02055.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.9502-912_9502-910d others(5): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr13 | 32395960 | ||||||
chr13:32395960 | CT | C | 26 | a0001c0003t0014g0079 a0001c0011t0004g0365 a0002c0002t0004g0348 others(23): Show |
26 | HG00323.hp1 HG01167.hp2 HG01981.hp2 others(23): Show |
intron_variant | MODIFIER | c.9502-910delT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr13 | 32395960 | ||||||
chr13:32395963 | T | TC | 62 | a0001c0004t0006g0117 a0001c0004t0040g0108 a0001c0010t0011g0014 others(59): Show |
68 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.9502-935_9502-934i others(3): Show |
BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 25/26 | chr13 | 32395963 | |||||||
chr13:32395964 | T | C | 1 | a0002c0002t0002g0021 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.9502-934T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 25/26 | chr13 | 32395964 | |||||||
chr13:32396210 | G | T | 2 | a0014c0017t0018g0309 a0014c0017t0018g0311 |
2 | HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.9502-688G>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 25/26 | chr13 | 32396210 | |||||||
chr13:32396248 | A | G | 2 | a0026c0030t0003g0277 a0027c0043t0031g0285 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.9502-650A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 25/26 | chr13 | 32396248 | |||||||
chr13:32396296 | G | A | 3 | a0011c0021t0020g0281 a0011c0021t0023g0279 a0024c0045t0020g0352 |
3 | HG01243.hp2 HG02258.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.9502-602G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 25/26 | chr13 | 32396296 | |||||||
chr13:32396326 | T | A | 2 | a0007c0008t0001g0251 a0007c0008t0001g0253 |
2 | NA18944.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.9502-572T>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 25/26 | chr13 | 32396326 | |||||||
chr13:32396449 | A | G | 67 | a0001c0004t0040g0108 a0001c0010t0011g0014 a0001c0010t0011g0200 others(64): Show |
73 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.9502-449A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 25/26 | chr13 | 32396449 | |||||||
chr13:32396462 | A | G | 44 | a0003c0005t0003g0003 a0003c0005t0003g0023 a0003c0005t0003g0029 others(41): Show |
48 | HG00639.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.9502-436A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 25/26 | chr13 | 32396462 | |||||||
chr13:32396591 | A | G | 1 | a0001c0001t0001g0264 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.9502-307A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 25/26 | chr13 | 32396591 | |||||||
chr13:32396599 | G | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(209): Show |
223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.9502-299G>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 25/26 | chr13 | 32396599 | |||||||
chr13:32396749 | C | T | 1 | a0001c0001t0009g0139 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.9502-149C>T | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 25/26 | chr13 | 32396749 | |||||||
chr13:32396761 | C | A | 1 | a0022c0035t0004g0305 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.9502-137C>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 25/26 | chr13 | 32396761 | |||||||
chr13:32397148 | AT | A | 3 | a0001c0003t0010g0076 a0001c0003t0010g0077 a0028c0049t0010g0340 |
3 | HG02622.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.9648+106delT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr13 | 32397148 | ||||||
chr13:32397288 | T | C | 365 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(362): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.9648+244T>C | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 26/26 | chr13 | 32397288 | |||||||
chr13:32397328 | A | G | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.9648+284A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 26/26 | chr13 | 32397328 | |||||||
chr13:32397453 | A | G | 1 | a0033c0041t0003g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.9648+409A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 26/26 | chr13 | 32397453 | |||||||
chr13:32397555 | T | A | 1 | a0028c0049t0010g0340 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.9648+511T>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 26/26 | chr13 | 32397555 | |||||||
chr13:32397569 | AT | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(209): Show |
223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.9648+534delT | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr13 | 32397569 | ||||||
chr13:32397919 | T | G | 3 | a0003c0005t0003g0003 a0003c0005t0003g0050 a0003c0005t0003g0338 |
5 | HG02015.hp2 HG02040.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.9649-243T>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 26/26 | chr13 | 32397919 | |||||||
chr13:32398004 | A | G | 1 | a0002c0002t0006g0133 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.9649-158A>G | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 26/26 | chr13 | 32398004 | |||||||
chr13:32398143 | G | A | 2 | a0002c0002t0002g0147 a0002c0002t0002g0149 |
2 | NA18950.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.9649-19G>A | BRCA2 | ENSG00000139618.18 | transcript | ENST00000380152.8 | protein_coding | 26/26 | chr13 | 32398143 |